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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Bone marrow dosimetry in peptide receptor radionuclide therapy with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate</title><author><name sortKey="Forrer, Flavio" sort="Forrer, Flavio" uniqKey="Forrer F" first="Flavio" last="Forrer">Flavio Forrer</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Krenning, Eric P" sort="Krenning, Eric P" uniqKey="Krenning E" first="Eric P." last="Krenning">Eric P. Krenning</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kooij, Peter P" sort="Kooij, Peter P" uniqKey="Kooij P" first="Peter P." last="Kooij">Peter P. Kooij</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Bernard, Bert F" sort="Bernard, Bert F" uniqKey="Bernard B" first="Bert F." last="Bernard">Bert F. Bernard</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Konijnenberg, Mark" sort="Konijnenberg, Mark" uniqKey="Konijnenberg M" first="Mark" last="Konijnenberg">Mark Konijnenberg</name><affiliation><nlm:aff id="Aff2">Research and Development, Mallinckrodt Medical BV, Covidien, Petten, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Bakker, Willem H" sort="Bakker, Willem H" uniqKey="Bakker W" first="Willem H." last="Bakker">Willem H. Bakker</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Teunissen, Jaap J M" sort="Teunissen, Jaap J M" uniqKey="Teunissen J" first="Jaap J. M." last="Teunissen">Jaap J. M. Teunissen</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="De Jong, Marion" sort="De Jong, Marion" uniqKey="De Jong M" first="Marion" last="De Jong">Marion De Jong</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Lom, Kirsten" sort="Van Lom, Kirsten" uniqKey="Van Lom K" first="Kirsten" last="Van Lom">Kirsten Van Lom</name><affiliation><nlm:aff id="Aff3">Department of Haematology, Erasmus MC Rotterdam, Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="De Herder, Wouter W" sort="De Herder, Wouter W" uniqKey="De Herder W" first="Wouter W." last="De Herder">Wouter W. De Herder</name><affiliation><nlm:aff id="Aff4">Department of Internal Medicine, Erasmus MC Rotterdam, Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kwekkeboom, Dik J" sort="Kwekkeboom, Dik J" uniqKey="Kwekkeboom D" first="Dik J." last="Kwekkeboom">Dik J. Kwekkeboom</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">19247653</idno><idno type="pmc">2691529</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691529</idno><idno type="RBID">PMC:2691529</idno><idno type="doi">10.1007/s00259-009-1072-6</idno><date when="2009">2009</date><idno type="wicri:Area/Pmc/Corpus">000245</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Bone marrow dosimetry in peptide receptor radionuclide therapy with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate</title><author><name sortKey="Forrer, Flavio" sort="Forrer, Flavio" uniqKey="Forrer F" first="Flavio" last="Forrer">Flavio Forrer</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Krenning, Eric P" sort="Krenning, Eric P" uniqKey="Krenning E" first="Eric P." last="Krenning">Eric P. Krenning</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kooij, Peter P" sort="Kooij, Peter P" uniqKey="Kooij P" first="Peter P." last="Kooij">Peter P. Kooij</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Bernard, Bert F" sort="Bernard, Bert F" uniqKey="Bernard B" first="Bert F." last="Bernard">Bert F. Bernard</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Konijnenberg, Mark" sort="Konijnenberg, Mark" uniqKey="Konijnenberg M" first="Mark" last="Konijnenberg">Mark Konijnenberg</name><affiliation><nlm:aff id="Aff2">Research and Development, Mallinckrodt Medical BV, Covidien, Petten, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Bakker, Willem H" sort="Bakker, Willem H" uniqKey="Bakker W" first="Willem H." last="Bakker">Willem H. Bakker</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Teunissen, Jaap J M" sort="Teunissen, Jaap J M" uniqKey="Teunissen J" first="Jaap J. M." last="Teunissen">Jaap J. M. Teunissen</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="De Jong, Marion" sort="De Jong, Marion" uniqKey="De Jong M" first="Marion" last="De Jong">Marion De Jong</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Lom, Kirsten" sort="Van Lom, Kirsten" uniqKey="Van Lom K" first="Kirsten" last="Van Lom">Kirsten Van Lom</name><affiliation><nlm:aff id="Aff3">Department of Haematology, Erasmus MC Rotterdam, Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="De Herder, Wouter W" sort="De Herder, Wouter W" uniqKey="De Herder W" first="Wouter W." last="De Herder">Wouter W. De Herder</name><affiliation><nlm:aff id="Aff4">Department of Internal Medicine, Erasmus MC Rotterdam, Rotterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kwekkeboom, Dik J" sort="Kwekkeboom, Dik J" uniqKey="Kwekkeboom D" first="Dik J." last="Kwekkeboom">Dik J. Kwekkeboom</name><affiliation><nlm:aff id="Aff1">Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</nlm:aff></affiliation></author></analytic><series><title level="j">European Journal of Nuclear Medicine and Molecular Imaging</title><idno type="ISSN">1619-7070</idno><idno type="eISSN">1619-7089</idno><imprint><date when="2009">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Purpose</title><p>Adequate dosimetry is mandatory for effective and safe peptide receptor radionuclide therapy (PRRT). Besides the kidneys, the bone marrow is a potentially dose-limiting organ. The radiation dose to the bone marrow is usually calculated according to the MIRD scheme, where the accumulated activity in the bone marrow is calculated from the accumulated radioactivity of the radiopharmaceutical in the blood. This may underestimate the absorbed dose since stem cells express somatostatin receptors. We verified the blood-based method by comparing the activity in the blood with the radioactivity in bone marrow aspirates. Also, we evaluated the absorbed cross-dose from the source organs (liver, spleen, kidneys and blood), tumours and the so-called “remainder of the body” to the bone marrow.</p></sec><sec><title>Methods</title><p>Bone marrow aspirates were drawn in 15 patients after treatment with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate. Radioactivity in the bone marrow was compared with radioactivity in the blood drawn simultaneously. The nucleated cell fraction was isolated from the bone marrow aspirate and radioactivity was measured. The absorbed dose to the bone marrow was calculated. The results were correlated to the change in platelet counts 6 weeks after treatment.</p></sec><sec><title>Results</title><p>A strong linear correlation and high agreement between the measured radioactivities in the bone marrow aspirates and in the blood was found (<italic>r</italic>=0.914, <italic>p</italic><0.001). No correlation between the calculated absorbed dose in the bone marrow and the change in platelets was found. There was a considerable contribution from other organs and the remainder of the body to the bone marrow absorbed dose.</p></sec><sec><title>Conclusion</title><p>(1) After PRRT with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, the radioactivity concentration in the bone marrow is identical to that in the blood; (2) There is no significant binding of the radiopharmaceutical to bone marrow precursor stem cells; (3) The contribution of the cross dose from source organs and tumours to the bone marrow dose is significant; and (4) There is considerable variation in bone marrow absorbed dose between patients. These findings imply that for individual dose optimization, individual calculation of the bone marrow absorbed dose is necessary.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct></listBibl></div1></back></TEI><pmc xml:lang="EN" article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Eur J Nucl Med Mol Imaging</journal-id><journal-title>European Journal of Nuclear Medicine and Molecular Imaging</journal-title><issn pub-type="ppub">1619-7070</issn><issn pub-type="epub">1619-7089</issn><publisher><publisher-name>Springer-Verlag</publisher-name><publisher-loc>Berlin/Heidelberg</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">19247653</article-id><article-id pub-id-type="pmc">2691529</article-id><article-id pub-id-type="publisher-id">1072</article-id><article-id pub-id-type="doi">10.1007/s00259-009-1072-6</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject></subj-group></article-categories><title-group><article-title>Bone marrow dosimetry in peptide receptor radionuclide therapy with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name name-style="western"><surname>Forrer</surname><given-names>Flavio</given-names></name><address><phone>+31-104-634889</phone><fax>+31-104-635997</fax><email>fforrer@uhbs.ch</email></address><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Krenning</surname><given-names>Eric P.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Kooij</surname><given-names>Peter P.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Bernard</surname><given-names>Bert F.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Konijnenberg</surname><given-names>Mark</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Bakker</surname><given-names>Willem H.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Teunissen</surname><given-names>Jaap J. M.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>de Jong</surname><given-names>Marion</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>van Lom</surname><given-names>Kirsten</given-names></name><xref ref-type="aff" rid="Aff3">3</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>de Herder</surname><given-names>Wouter W.</given-names></name><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Kwekkeboom</surname><given-names>Dik J.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><aff id="Aff1"><label>1</label>Department of Nuclear Medicine, Erasmus MC Rotterdam, Dr. Molewaterplein 40, NL-3015 GD Rotterdam, The Netherlands</aff><aff id="Aff2"><label>2</label>Research and Development, Mallinckrodt Medical BV, Covidien, Petten, The Netherlands</aff><aff id="Aff3"><label>3</label>Department of Haematology, Erasmus MC Rotterdam, Rotterdam, The Netherlands</aff><aff id="Aff4"><label>4</label>Department of Internal Medicine, Erasmus MC Rotterdam, Rotterdam, The Netherlands</aff></contrib-group><pub-date pub-type="epub"><day>27</day><month>2</month><year>2009</year></pub-date><pub-date pub-type="ppub"><month>7</month><year>2009</year></pub-date><volume>36</volume><issue>7</issue><fpage>1138</fpage><lpage>1146</lpage><history><date date-type="received"><day>18</day><month>7</month><year>2008</year></date><date date-type="accepted"><day>30</day><month>12</month><year>2008</year></date></history><permissions><copyright-statement>© The Author(s) 2009</copyright-statement></permissions><abstract xml:lang="EN"><sec><title>Purpose</title><p>Adequate dosimetry is mandatory for effective and safe peptide receptor radionuclide therapy (PRRT). Besides the kidneys, the bone marrow is a potentially dose-limiting organ. The radiation dose to the bone marrow is usually calculated according to the MIRD scheme, where the accumulated activity in the bone marrow is calculated from the accumulated radioactivity of the radiopharmaceutical in the blood. This may underestimate the absorbed dose since stem cells express somatostatin receptors. We verified the blood-based method by comparing the activity in the blood with the radioactivity in bone marrow aspirates. Also, we evaluated the absorbed cross-dose from the source organs (liver, spleen, kidneys and blood), tumours and the so-called “remainder of the body” to the bone marrow.</p></sec><sec><title>Methods</title><p>Bone marrow aspirates were drawn in 15 patients after treatment with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate. Radioactivity in the bone marrow was compared with radioactivity in the blood drawn simultaneously. The nucleated cell fraction was isolated from the bone marrow aspirate and radioactivity was measured. The absorbed dose to the bone marrow was calculated. The results were correlated to the change in platelet counts 6 weeks after treatment.</p></sec><sec><title>Results</title><p>A strong linear correlation and high agreement between the measured radioactivities in the bone marrow aspirates and in the blood was found (<italic>r</italic>=0.914, <italic>p</italic><0.001). No correlation between the calculated absorbed dose in the bone marrow and the change in platelets was found. There was a considerable contribution from other organs and the remainder of the body to the bone marrow absorbed dose.</p></sec><sec><title>Conclusion</title><p>(1) After PRRT with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, the radioactivity concentration in the bone marrow is identical to that in the blood; (2) There is no significant binding of the radiopharmaceutical to bone marrow precursor stem cells; (3) The contribution of the cross dose from source organs and tumours to the bone marrow dose is significant; and (4) There is considerable variation in bone marrow absorbed dose between patients. These findings imply that for individual dose optimization, individual calculation of the bone marrow absorbed dose is necessary.</p></sec></abstract><kwd-group><title>Keywords</title><kwd>Dosimetry</kwd><kwd>Bone marrow</kwd><kwd>[<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate</kwd><kwd>Therapy</kwd><kwd>Somatostatin receptor</kwd></kwd-group><custom-meta-wrap><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© Springer-Verlag 2009</meta-value></custom-meta></custom-meta-wrap></article-meta></front><body><sec id="Sec1" sec-type="introduction"><title>Introduction</title><p>Peptide receptor radionuclide therapy (PRRT) with radiolabelled somatostatin analogues, such as [<sup>90</sup>Y-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotide (<sup>90</sup>Y-DOTATOC) or [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, has been shown to be an effective treatment in patients with metastatic neuroendocrine tumours [<xref ref-type="bibr" rid="CR1">1</xref>–<xref ref-type="bibr" rid="CR6">6</xref>]. The dose-limiting organs with this treatment are usually either the kidneys or the bone marrow [<xref ref-type="bibr" rid="CR7">7</xref>–<xref ref-type="bibr" rid="CR9">9</xref>]. In order to avoid toxicity due to absorbed radiation dose, dosimetry can be performed. While kidney dosimetry has been investigated extensively [<xref ref-type="bibr" rid="CR10">10</xref>–<xref ref-type="bibr" rid="CR12">12</xref>], less attention has been paid to bone marrow dosimetry.</p><p>In order to achieve a maximum antitumour effect, patients should be treated with the highest justifiable dose of the radiopharmaceutical that does not cause serious toxicity. Often the kidneys are the dose-limiting organ. However, recently it has been shown that the bone marrow has to be regarded as the dose-limiting organ in approximately 70% of patients treated with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate [<xref ref-type="bibr" rid="CR13">13</xref>]. Many studies with radiolabelled somatostatin analogues have shown that the myelotoxicity is generally mild and transient [<xref ref-type="bibr" rid="CR1">1</xref>–<xref ref-type="bibr" rid="CR3">3</xref>, <xref ref-type="bibr" rid="CR6">6</xref>]. However, in a phase 1 study with [<sup>111</sup>In-DTPA<sup>0</sup>]octreotide 3 out of 50 patients developed a myelodysplastic syndrome (MDS) which was probably related to the therapy [<xref ref-type="bibr" rid="CR14">14</xref>]. Calculations from these data resulted in an estimated radiation absorbed dose for the bone marrow of approximately 3 Gy. In another study with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, MDS was observed in a patient who had had chemotherapy with alkylating agents 2 years before study entry [<xref ref-type="bibr" rid="CR15">15</xref>]. In the latest update of our own records of 504 patients treated with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, four patients (including the patient mentioned above) developed MDS [<xref ref-type="bibr" rid="CR16">16</xref>].</p><p> To avoid hypoplasia, a maximum absorbed dose of 2 Gy to the bone marrow is generally accepted [<xref ref-type="bibr" rid="CR2">2</xref>, <xref ref-type="bibr" rid="CR17">17</xref>]. With a dose of 2 Gy, the probability for developing leukaemia is approximately 2% [<xref ref-type="bibr" rid="CR18">18</xref>]. In radioiodine therapy of metastatic thyroid cancer a threshold of 2 Gy to the blood as surrogate for bone marrow has been maintained since the pioneering work of Benua et al. in 1962 [<xref ref-type="bibr" rid="CR19">19</xref>]. More recent work has set this limit to as high as 3 Gy by using more patient-specific dosimetry techniques [<xref ref-type="bibr" rid="CR20">20</xref>]. Nevertheless, even if this limit is not exceeded the risk of the patient developing MDS cannot be excluded completely, but an accurate estimation of the absorbed dose to the bone marrow will help find an adequate dosage.</p><p>The absorbed dose to the bone marrow during radionuclide therapies may be estimated with the aid of the MIRD scheme [<xref ref-type="bibr" rid="CR21">21</xref>–<xref ref-type="bibr" rid="CR23">23</xref>]. Contributions to the red marrow dose (<italic>D</italic><sub><italic>rm</italic></sub>) arise from the accumulated activity in the marrow tissue itself <inline-formula id="IEq1"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq1.gif </pmc-comment><tex-math id="M1">\documentclass[12pt]{minimal}
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\begin{document}$$\left( {\tilde A_{rm} } \right)$$\end{document}</tex-math></inline-formula> (self-dose), in source organs (including tumours and blood) <inline-formula id="IEq2"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq2.gif </pmc-comment><tex-math id="M2">\documentclass[12pt]{minimal}
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\begin{document}$$\tilde A_h $$\end{document}</tex-math></inline-formula> and in the remainder of the body <inline-formula id="IEq3"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq3.gif </pmc-comment><tex-math id="M3">\documentclass[12pt]{minimal}
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\begin{document}$$\tilde A_{rb} $$\end{document}</tex-math></inline-formula>:
<disp-formula id="Equ1"><label>1</label><tex-math id="M4">\documentclass[12pt]{minimal}
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\begin{document}$$D_{rm} = \tilde A_{rm} S_{rm \leftarrow rm} + \sum {\tilde A_h S_{rm \leftarrow h} + \tilde A_{rb} S_{rm \leftarrow rb} } $$\end{document}</tex-math></disp-formula>with <italic>S</italic><sub><italic>rm←rm</italic></sub> the self-dose S-factor, <italic>S</italic><sub><italic>rm←h</italic></sub> the cross-dose S-factor of the source organs and <italic>S</italic><sub><italic>rm←rb</italic></sub> the cross-dose S-factor of the remainder of the body. The accumulated activity of the radiopharmaceutical in the bone marrow is calculated from the accumulated activity in the blood (Eq. <xref rid="Equ2" ref-type="">2</xref>)
<disp-formula id="Equ2"><label>2</label><tex-math id="M5">\documentclass[12pt]{minimal}
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\begin{document}$$\tilde{A}_{{rm}} = {\left[ {\tilde{A}} \right]}_{{bl}} \times RMBLR \times {\left\{ \begin{aligned} {1.3} \mathord{\left/ {\vphantom {{1.3} {57}}} \right. \kern-\nulldelimiterspace} {57}{\left( {female} \right)} \\ {1.1} \mathord{\left/ {\vphantom {{1.1} {74{\left( {male} \right)}}}} \right. \kern-\nulldelimiterspace} {74{\left( {male} \right)}} \\ \end{aligned} \right\}}\quad \times M_{{pat}}$$\end{document}</tex-math></disp-formula>where <inline-formula id="IEq4"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq4.gif </pmc-comment><tex-math id="M6">\documentclass[12pt]{minimal}
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\begin{document}$$[\tilde A]_{bl} $$\end{document}</tex-math></inline-formula> is the accumulated activity concentration in the blood, 1.3/57 and 1.1/74 are the ratios between the red marrow mass and the total body mass for the adult reference woman and the adult reference man, respectively, and <italic>M</italic><sub><italic>pat</italic></sub> is the mass of the patient in kilograms. Taking into consideration the red marrow to blood concentration ratio (RMBLR), a correction factor can be added depending on the vector used for treatment. This method has been validated by bone marrow aspiration for antibodies but not for radiopeptides [<xref ref-type="bibr" rid="CR24">24</xref>, <xref ref-type="bibr" rid="CR25">25</xref>].</p><p>For radiolabelled somatostatin analogues, the calculation usually deals with the assumption of absence of specific uptake of the radiolabel into the bone marrow. Since certain haematological cells (lymphocytes, monocytes) and haematopoietic progenitor cells express somatostatin receptors, mainly subtype 2 [<xref ref-type="bibr" rid="CR26">26</xref>–<xref ref-type="bibr" rid="CR28">28</xref>], this assumption may result in an underestimation of the absorbed radiation dose to the bone marrow. It is not known whether in patients a significantly higher radioactivity in the bone marrow, compared to the blood, may be present.</p><p>Relevant results for bone marrow dosimetry were obtained using <sup>86</sup>Y as a surrogate for <sup>90</sup>Y to calculate the accumulated dose in the red marrow by PET before treatment with <sup>90</sup>Y-DOTATOC. A region of interest (ROI) was drawn around a segment of the thoracic spine and rescaled for the whole red marrow mass using the standard fraction of active red marrow present in the thoracic spine [<xref ref-type="bibr" rid="CR29">29</xref>]. Recently a comparable calculation showing relevant results as well was presented for iodinated antibodies. Instead of a PET scan patients underwent a SPECT/CT scan during therapy [<xref ref-type="bibr" rid="CR30">30</xref>]. Acquiring a CT scan and using an integrated SPECT/CT camera allows the ROIs to be placed anatomically more accurately than using SPECT alone. This is especially important in radiopharmaceuticals, e.g. most radiopeptides, which do not show sufficiently high bone marrow uptake to be indisputably identified on the scans. In addition the CT scan provides an attenuation map that can be used to apply an attenuation correction. With three SPECT scans at different time-points after therapy, we investigated the feasibility of this calculation in a therapeutic setting in this study.</p><p>In order to verify whether the assumption of no specific uptake in the bone marrow can be applied with radiolabelled somatostatin analogues, we compared the radioactivity in bone marrow aspirates with the radioactivity in blood samples drawn simultaneously. In addition we determined the difference between the radioactivity in the nucleated cell fraction of the bone marrow, including the stem cells, and that in the blood to determine whether there was any difference that could be attributed to the specific binding of the radiopeptide to somatostatin receptor-positive cells in the bone marrow. Finally, the absorbed doses to the bone marrow calculated according to the MIRD scheme and from the SPECT scans were correlated with the change in the platelet counts 6 weeks after the treatment.</p></sec><sec id="Sec2" sec-type="materials|methods"><title>Materials and methods</title><sec id="Sec3"><title>Patients</title><p>Included in the study were 15 patients with somatostatin receptor-positive neuroendocrine tumours. All patients were admitted to our clinic for PRRT with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate and fulfilled the inclusion criteria as previously described [<xref ref-type="bibr" rid="CR6">6</xref>]. None of the patients had known bone metastases. All patients gave written informed consent to participate in the study, which was approved by the medical ethics committee of the hospital.</p></sec><sec id="Sec4"><title>Comparison of the radioactivity in the bone marrow and nucleated cell fraction with the radioactivity in the blood</title><p>In addition to the examinations, the treatment, and the scans that are performed routinely during and after the first treatment cycle with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, patients underwent bone marrow aspiration from the iliac crest 4 days (seven patients), 7 days (seven patients) or 8 days (one patient) after the treatment. A rough differential count of cells was performed on the bone marrow samples to prove the presence of a sufficient number of bone marrow cells and the samples were analysed for haematological abnormalities. The volume of aspirate was recorded and the radioactivity was measured in a gamma counter (Perkin Elmer, Groningen, The Netherlands). One patient (aspiration 4 days after treatment) was excluded because no bone marrow could be aspirated. In all patients, a blood sample was drawn simultaneously to determine the radioactivity in the blood.</p><p>Some of the bone marrow samples and blood samples were purified for the mononuclear cells (including the stem cells in the bone marrow samples). The samples (<italic>blood</italic> 8–48 mg, 26±12.2 mg, mean±SD; <italic>bone marrow</italic> 2–49 mg, 22±16.6 mg) were diluted with 5 ml Dispase (Roche Diagnostics, Almere, The Netherlands) and mixed for 20 min to suspend the cells. Then the samples were diluted with 50 ml phosphate-buffered saline (PBS) (pH 7.4) and centrifuged three times for 10 min at 2,500 rpm (about 60 <italic>g</italic>) each time with washing with 50 ml PBS after every step. The mononuclear cells, including the stem cells in the samples from the bone marrow, were isolated by Ficoll-Paque gradient sedimentation (density 1.077 g/ml; GE Healthcare Europe, Diegem, The Netherlands). The weight of the cell pellets was then determined and the radioactivity was measured in a gamma counter.</p></sec><sec id="Sec5"><title>Bone marrow dosimetry</title><p>For all patients the absorbed radiation dose to the bone marrow was calculated according to the MIRD scheme (Eq. <xref rid="Equ1" ref-type="">1</xref>). The radioactivity concentration in the red marrow was assumed to be equal to the radioactivity concentration measured in the blood (RMBLR = 1) [<xref ref-type="bibr" rid="CR24">24</xref>, <xref ref-type="bibr" rid="CR31">31</xref>]. This was based on at least five blood samples per patient drawn between 0 and 168 h after injection. Assuming no specific uptake in the red marrow, a uniform distribution of the radioactivity, and that the red marrow clearance was the same as in blood, the self-dose to the red marrow was calculated. The distribution in the remainder of the body besides source organs and tumour uptake was assumed to be homogeneous. In addition, cross-radiation from the liver, spleen, kidneys, tumour as well as blood was taken into account. At three different time-points between 24 and 168 h after the administration of [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, scans of tumour deposits, liver, kidney and spleen were acquired using a dual head camera (Picker Prism 2000 XP, Philips, Eindhoven, The Netherlands) using the 208-keV peak. The accumulated activity of the radiopharmaceutical in tumour and organs (liver, kidneys and spleen) was calculated from these scans. Attenuation correction was applied using the data from the pretreatment CT scan. It appeared that in our patient group there was a high degree of overprojection both for tumours and organs. As the S-factors of the liver, spleen and kidneys to the bone marrow were almost the same, the summation term in Eq. <xref rid="Equ1" ref-type="">1</xref> was regarded as a single source organ.</p><p>Urine was collected up to 24 h after treatment and the radioactivity was measured in a gamma counter. From these data the accumulated activity in the remainder of the body (i.e. injected activity minus accumulated activity in source organs and tumours and minus excreted radioactivity) was calculated, taking into account the fact that the radioactivity was overestimated since the urine was collected for 24 h only. In two patients the radioactivity in the remainder of the body could not be determined. The quotient of <inline-formula id="IEq5"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq5.gif </pmc-comment><tex-math id="M7">\documentclass[12pt]{minimal}
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\begin{document}$$\widetilde{\text{A}}$$\end{document}</tex-math></inline-formula> and the injected activity IA yields the residence time <inline-formula id="IEq6"><pmc-comment> Alternate image not processed: 259_2009_1072_Article_IEq6.gif </pmc-comment><tex-math id="M8">\documentclass[12pt]{minimal}
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\begin{document}$$\tau = {{\widetilde{\text{A}}} \mathord{\left/ {\vphantom {{\widetilde{\text{A}}} {{\text{IA}}}}} \right. \kern-\nulldelimiterspace} {{\text{IA}}}}$$\end{document}</tex-math></inline-formula> (in hours) for the different organs. The thus calculated residence times were used as input in the OLINDA program (Vanderbilt University, Nashville, USA).</p></sec><sec id="Sec6"><title>Bone marrow dosimetry using SPECT scans</title><p>In addition, at three different time-points between 24 and 168 h after treatment, SPECT scans of the thorax were acquired (energy window 208 keV ±10%, matrix 128×128, 120 projections, 20 s/ per projection).</p></sec><sec id="Sec7"><title>Correlation with haematological response</title><p>Six weeks after the treatment, blood was drawn from 13 patients to determine haematological toxicity after the treatment. For one patient no blood results were available. All values were correlated with the decrease in platelet counts expressed as a percentage of the pretreatment value.</p><p>The results of the bone marrow (full bone marrow and nucleated cell fraction) radioactivity were corrected for physical decay in order to compare the interindividual values of the samples drawn at different time-points. Similarly, calculated absorbed dose to the bone marrow (self-dose and cross-dose) were correlated with the decrease in platelet counts.</p></sec><sec id="Sec8"><title>Statistics</title><p>Pearson’s correlation coefficient was calculated. A <italic>p</italic> value ≤0.05 was considered significant.</p></sec></sec><sec id="Sec9" sec-type="results"><title>Results</title><p>The treatment with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate was well tolerated by all patients and no serious adverse events occurred. The injected radioactivity ranged from 7.26 to 7.75 GBq (7.47±0.10 GBq, mean±SD). On the posttreatment scans all patients showed the expected distribution of the radiopharmaceutical with specific uptake in all known tumours. No patient had known or visible bone metastases.</p><p>The bone marrow aspirations were uneventful. One patient had a dry tap. The volume of bone marrow aspirated in the other patients ranged from 1 to 9.2 g (5.3±2.9 g). Simultaneously a tube of blood of 2.8 to 7.3 g (5.8±1.3 g) was drawn. Smears were made from the bone marrow aspirates. A differential count was performed to establish the numbers of immature (bone marrow) and mature nucleated cells. The fraction of immature cells ranged from 25% to 80% (51±15%) indicating that the purified aspirates consisted of a considerable amount of bone marrow and that the contamination with blood was moderate. A typical example of a purified bone marrow smear is shown in Fig. <xref rid="Fig1" ref-type="fig">1</xref>.
<fig id="Fig1"><label>Fig. 1</label><caption><p>Typical example of a smear of a bone marrow aspirate. It shows a mixture of immature nucleated cells originating from the bone marrow as well as red blood cells and mature nucleated cells originating from the peripheral blood</p></caption><graphic position="anchor" xlink:href="259_2009_1072_Fig1_HTML" id="MO1"></graphic></fig></p><p>The radioactivity in the full bone marrow samples ranged from 850 to 4,473 Bq/ml (2,216±899 Bq/ml). The radioactivity in the blood ranged from 1,077 to 6,451 Bq/ml (2,437±1,324 Bq/ml). Fitting the correlation line through the origin (0,0) as seems right from a theoretical point of view, showed a strong, significant, linear correlation between the radioactivity determined in the blood and in the bone marrow aspirate (<italic>y</italic>=1.13<italic>x</italic>, <italic>r</italic>=0.90, <italic>p</italic><0.001; Fig. <xref rid="Fig2" ref-type="fig">2</xref>). This results in a mean red marrow over blood ratio of 0.88 (value not significantly different from 1). Both qualitatively and quantitatively the results showed strong agreement over a whole range of activities at the three different time-points.
<fig id="Fig2"><label>Fig. 2</label><caption><p>Correlation between the activities measured in the bone marrow aspirate and the activities measured in the blood at the same time-points. The straight line is the linear regression line: <italic>r</italic>=0.914, <italic>p</italic><0.001. The slope of the regression line is 1.35 indicating that the absolute values of the measured activities are also comparable</p></caption><graphic position="anchor" xlink:href="259_2009_1072_Fig2_HTML" id="MO2"></graphic></fig></p><p>The self-absorbed doses to the bone marrow calculated from the accumulated activity in the blood (Eq. <xref rid="Equ2" ref-type="">2</xref>), calculated according to the MIRD scheme, and the changes in platelet counts after 6 weeks are presented in Table <xref rid="Tab1" ref-type="table">1</xref>. The contribution of the cross-dose to the red marrow dose was substantial in relation to the contribution of the self-dose (Table <xref rid="Tab1" ref-type="table">1</xref>).
<table-wrap id="Tab1"><label>Table 1</label><caption><p>Doses to the bone marrow after injection of 3,700 MBq [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, and decrease in platelet counts 6 weeks after treatment</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2">Patient</th><th rowspan="2">Total absorbed dose to the red marrow (mGy)<sup>a</sup></th><th rowspan="2">Absorbed self-dose (mGy)<sup>b</sup></th><th colspan="2">Cross-dose (mGy)<sup>c</sup></th><th rowspan="2">Decrease in platelet count 6 weeks after treatment (%)</th></tr><tr><th>From the remainder of the body</th><th>From organs<sup>d</sup></th></tr></thead><tbody><tr><td>1</td><td>40</td><td>16 (41%)</td><td>12 (31%)</td><td>11 (29%)</td><td>40</td></tr><tr><td>2</td><td>82</td><td>37 (46%)</td><td>26 (32%)</td><td>19 (23%)</td><td>8</td></tr><tr><td>3</td><td>212</td><td>49 (23%)</td><td>152 (72%)</td><td>11 (5%)</td><td>40</td></tr><tr><td>4</td><td>108</td><td>17 (16%)</td><td>83 (77%)</td><td>8 (8%)</td><td>16</td></tr><tr><td>5</td><td>64</td><td>23 (36%)</td><td>26 (41%)</td><td>15 (23%)</td><td>4</td></tr><tr><td>6</td><td>129</td><td>37 (28%)</td><td>78 (61%)</td><td>14 (11%)</td><td>–</td></tr><tr><td>7</td><td>73</td><td>28 (39%)</td><td>0 (0%)</td><td>45 (61%)</td><td>−9</td></tr><tr><td>8</td><td>74</td><td>39 (53%)</td><td>28 (39%)</td><td>6 (9%)</td><td>−9</td></tr><tr><td>9</td><td></td><td>29</td><td>–</td><td>–</td><td>47</td></tr><tr><td>10</td><td>466</td><td>26 (5%)</td><td>429 (92%)</td><td>11 (2%)</td><td>8</td></tr><tr><td>11</td><td>147</td><td>56 (38%)</td><td>84 (58%)</td><td>7 (5%)</td><td>27</td></tr><tr><td>12</td><td>78</td><td>23 (30%)</td><td>39 (50%)</td><td>16 (20%)</td><td>32</td></tr><tr><td>13</td><td>86</td><td>29 (34%)</td><td>39 (45%)</td><td>18 (21%)</td><td>28</td></tr><tr><td>14</td><td>83</td><td>24 (29%)</td><td>48 (57%)</td><td>12 (14%)</td><td>21</td></tr><tr><td>Median</td><td>83</td><td>29 (34%)</td><td>39 (50%)</td><td>12 (14%)</td><td>21</td></tr><tr><td>Mean</td><td>126</td><td>31 (32%)</td><td>80 (50%)</td><td>15 (18%)</td><td>19</td></tr><tr><td>SD</td><td>111</td><td>12 (12%)</td><td>112 (24%)</td><td>10 (16%)</td><td>18</td></tr></tbody></table><table-wrap-foot><p><sup>a</sup>Taking into account the absorbed self-dose, the cross-dose from the remainder of the body and the absorbed dose of organs and tumour.</p><p><sup>b</sup>From the red marrow to the red marrow.</p><p><sup>c</sup>To the red marrow.</p><p><sup>d</sup>Liver, spleen, kidneys and tumour.</p></table-wrap-foot></table-wrap></p><p>No or only very faint uptake in the bone marrow could be seen on the SPECT scans of the thorax. The bone marrow to background (ROI placed into the lungs) ratios were between 1 and 1.8. Therefore it was not possible to place a ROI reliably, and consequently no absorbed dose to the bone marrow was calculated from SPECT scans. An example of transaxial SPECT slices in one patient is shown in Fig. <xref rid="Fig3" ref-type="fig">3</xref>.
<fig id="Fig3"><label>Fig. 3</label><caption><p>Typical example of transverse SPECT slices through the thorax obtained 24 h after treatment with 7.4 GBq [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate. Note that there is no clear uptake over the spine area</p></caption><graphic position="anchor" xlink:href="259_2009_1072_Fig3_HTML" id="MO3"></graphic></fig></p><p>No correlation was found between the calculated absorbed doses to the bone marrow and the decrease in platelet counts, expressed as a percentage of the pretreatment value.</p><p>The correlation between the radioactivity in the full bone marrow aspirate and the decrease in platelet counts was poor (<italic>r</italic>=0.35, <italic>p</italic>=0.24; Fig. <xref rid="Fig4" ref-type="fig">4</xref>). However, the correlation between the calculated absorbed doses and the decrease in platelet counts was even less significant.
<fig id="Fig4"><label>Fig. 4</label><caption><p>Plot of the radioactivity in the bone marrow aspirate versus the percentage decrease in platelet count. The activities measured in the bone marrow were decay-corrected to the theoretical value on day 8. Linear regression coefficient: <italic>r</italic>=0.35 (<italic>p</italic>=0.24)</p></caption><graphic position="anchor" xlink:href="259_2009_1072_Fig4_HTML" id="MO4"></graphic></fig></p><p>The ratios of the radioactivity in the isolated mononuclear cell fraction of the bone marrow to the isolated mononuclear cell fraction of the blood obtained on the same day were highly variable. We found ratios ranging from 0.29 to 536 (59.3±143.6). In three patients a higher radioactivity was found in the mononuclear cells isolated from the blood whereas 11 patients showed a higher radioactivity in the mononuclear cells isolated from the bone marrow.</p><p>In 11 patients the radioactivity in the isolated mononuclear cell fraction, microscopically containing a mixture of immature and mature cells, could be weight-corrected. In the other three patients, the isolated fraction could not be weighted reliably because of the small number of isolated cells. Weight-corrected ratios of the radioactivity in the isolated cell fraction of the bone marrow to the isolated cell fraction of the blood ranged from 0.54 to 133.41 (19.4±38.6). Only one patient showed a higher radioactivity in the isolated cell fraction per gram of blood. The correlation coefficient between the radioactivity per gram in the nucleated cell fraction of the bone marrow aspirate and the decrease in platelet count after treatment was <italic>r</italic>=0.51 (<italic>p</italic>=0.13; Fig. <xref rid="Fig5" ref-type="fig">5</xref>). From our study this was the best relationship that could be obtained.
<fig id="Fig5"><label>Fig. 5</label><caption><p>Correlation between the radioactivity per gram measured in the isolated mononuclear cell fraction of the bone marrow aspirate with the decrease in platelet count after treatment. Linear regression coefficient: <italic>r</italic>=0.51 (<italic>p</italic>=0.13)</p></caption><graphic position="anchor" xlink:href="259_2009_1072_Fig5_HTML" id="MO5"></graphic></fig></p></sec><sec id="Sec10" sec-type="discussion"><title>Discussion</title><p>Accurate bone marrow dosimetry is mandatory for safe PRRT. All methods available have certain disadvantages: aspiration of bone marrow is costly and time consuming, and it is an invasive procedure associated with a high level of discomfort for the patients. Calculating the dose to the red marrow from the accumulated activity concentration in the blood deals with the assumption that no specific binding of the radiolabelled somatostatin analogue occurs in the bone marrow. Also, it neglects the contribution of other radiation sources in the body, such as organs and tumours, thereby underestimating the true radiation absorbed dose to the bone marrow. Alternatively, the determination of the radioactivity in the remainder of the body (needed for the MIRD scheme) depends on accuracy in urine collection, which is subject to errors. Apart from these considerations, it should be realized that at present none of the diverse models to estimate the dose to the bone marrow has been actually confirmed with toxicity data, be it the incidence of thrombocytopenia or the occurrence of MDS. Apart from the risk of patients developing MDS, the essential issue of bone marrow dosimetry is to predict, or better to avoid, severe haematological toxicity caused by PRRT.</p><p>The dose to the red marrow, however, is only one of several factors influencing the haematological toxicity after PRRT. A high interpatient variability in the haematological response after PRRT has been found and also previous therapies can highly influence the results [<xref ref-type="bibr" rid="CR2">2</xref>, <xref ref-type="bibr" rid="CR29">29</xref>]. Using different radiopharmaceuticals, some investigators have found a correlation between haematological toxicity and injected dose of radioactivity [<xref ref-type="bibr" rid="CR32">32</xref>, <xref ref-type="bibr" rid="CR33">33</xref>], whereas others have not found such a correlation [<xref ref-type="bibr" rid="CR34">34</xref>]. It is possible that additional factors such as age and sex of the patients might influence the haematological toxicity as well, although in a trial with radiolabelled antibodies there was only a minor influence of these factors [<xref ref-type="bibr" rid="CR35">35</xref>]. As early as the year 2000, Blumenthal et al reported that plasma levels of FLT3-L help to predict haematological toxicity after radioimmunotherapy [<xref ref-type="bibr" rid="CR36">36</xref>]. In 2003 this was confirmed by Siegel et al. for radioimmunotherapy with iodinated anti-CEA antibodies [<xref ref-type="bibr" rid="CR37">37</xref>]. However, no studies taking this into account have been published for PRRT. Nevertheless, the importance of introducing biological parameters into treatment planning is indisputable [<xref ref-type="bibr" rid="CR38">38</xref>].</p><p>We found a high correlation between the radioactivity concentration in the blood and in the bone marrow aspirate during PRRT with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate. The most probable explanation for the high congruence between the radioactivity measured in the blood and in the bone marrow aspirate is that the amount of stem cells in a bone marrow aspirate is low and that most of the aspirate consists of blood. On the other hand, the high volume of blood in the bone marrow aspirate reflects the fact that the blood contributes most of the self-dose to the bone marrow. Taking into consideration that the path lengths of the common therapeutic radionuclides are in the millimetre range and the structure of the bone marrow it is evident that the radiation from the blood will reach all bone marrow structures.</p><p>Promising results for predicting the haematological response were obtained by using an ROI surrounding a section of the thoracic spine for determining the absorbed dose to the red marrow. In these studies the absorbed dose was calculated with the positron emitter <sup>86</sup>Y before treatment with <sup>90</sup>Y-DOTATOC [<xref ref-type="bibr" rid="CR29">29</xref>, <xref ref-type="bibr" rid="CR39">39</xref>]. <sup>86</sup>Y can be regarded as the ideal surrogate for <sup>90</sup>Y and offers a high resolution when using a PET scanner. However, imaging with <sup>86</sup>Y is currently only available in specialized centres because besides the need for a cyclotron to produce <sup>86</sup>Y, the reconstruction of the PET data requires sophisticated correction algorithms. There is certain evidence in literature that imaging with <sup>86</sup>Y might overestimate doses, particularly if the bone marrow is close to dense tissue such as the spine [<xref ref-type="bibr" rid="CR40">40</xref>, <xref ref-type="bibr" rid="CR41">41</xref>]. Besides, dosimetry using <sup>86</sup>Y will be a gold standard only for treatments with <sup>90</sup>Y because in PRRT the radionuclide used influences the receptor affinity and consequently the biodistribution of the compound [<xref ref-type="bibr" rid="CR42">42</xref>]. Moreover, the relatively short physical half-life of <sup>86</sup>Y (14.7 h) does not allow the radioactivity to be followed over several days which is important for planning of the treatment with <sup>90</sup>Y. However, these results have not yet been confirmed by another group.</p><p>To date one group has found interesting results when calculating the absorbed radiation dose to the bone marrow from scans for radiolabelled antibodies using an integrated SPECT/CT camera [<xref ref-type="bibr" rid="CR30">30</xref>]. The results have also not been confirmed by other groups, and no results using this method with radiopeptides have been published so far. Remarkably no bone marrow dosimetry was feasible on SPECT scans in our setting because no or only very faintly visible uptake in the bone marrow was present on the scans (Fig. <xref rid="Fig3" ref-type="fig">3</xref>).</p><p>Our results indicate the radioactivity in the blood is a very accurate surrogate for the radioactivity present in the bone marrow. However, we also showed that the radioactivity in the remainder of the body as well as the radioactivity in source organs and tumours significantly contributes to the absorbed radiation dose to the bone marrow. With that, our tacit hope that the cumbersome collection of 24-h urine and time-consuming calculations of cross-radiation from tumours and organs could be circumvented, and that bone marrow absorbed doses could be derived from blood radioactivity levels only, evaporated. Also, the bone marrow absorbed dose after treatment with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate showed considerable variation between patients. This is in contrast with the findings of a previous pilot study in six patients that showed the biodistribution of the radiopharmaceutical [<xref ref-type="bibr" rid="CR43">43</xref>]. These patients, however, all had a very limited tumour load. The present series of patients more truly represented the practice of PRRT in our institution, where the tumour load in patients is highly variable, and so the contribution of the cross-dose to the bone marrow is variable as well. This finding implies that for individual dose optimization, individual calculation of the bone marrow absorbed dose is necessary. The results shown in Table <xref rid="Tab1" ref-type="table">1</xref> indicate that the remainder of the body as well as organs and tumours significantly contribute to the absorbed dose to the bone marrow. Since the contribution to this dose from the remainder of the body, organs and tumours from the β-emission of <sup>177</sup>Lu is virtually negligible, it appears that the γ-radiation from tumours, organs and the remainder of the body contributes to the absorbed bone marrow dose.</p><p>We determined the degree of correlation between the absorbed dose to the red marrow and the decrease in platelet count after 6 weeks. We focused on platelets only since platelets show the most pronounced reaction after PRRT. The degree of correlation between the calculated absorbed doses to the red marrow and the decrease in platelet count was disappointing. A number of reasons may have accounted for this. The absorbed doses were compared with only one posttreatment platelet count. This platelet count, 6 weeks after treatment, may not have reflected the nadir in each patient. Another explanation could have been the relatively small number of patients studied. Moreover, probably the most important reason could have been that the response of an individual patient to PRRT is not only related to the radiation absorbed dose in the bone marrow but also to the pretreatment status of the bone marrow. Especially previous, potentially haemocytotoxic treatments can influence the response after the treatment.</p><p>No conclusions can be drawn concerning the relationship between the calculated radiation absorbed dose in the bone marrow and the risk of developing MDS. However, developing MDS is probably also related to the pretreatment status of the bone marrow and previous treatments.</p><p>Bone marrow dosimetry is a difficult topic. Beside all factors mentioned above that may influence the dosimetry of an individual patient, many other considerations have to be faced. The bone marrow is not a solid organ and simply the determination of the mass is virtually impossible. As for all internal radiotherapy treatments, the dose rate in PRRT is low. Most values that deal with the maximum tolerated dose of healthy organs are derived from external beam radiation with a much higher dose rate. The influence of such physical properties is not well understood and may highly influence the results of internal dosimetry as much as the biological response.</p><p>In conclusion, our results show that: (1) after PRRT with [<sup>177</sup>Lu-DOTA<sup>0</sup>,Tyr<sup>3</sup>]octreotate, the radioactivity concentration in the bone marrow is identical to that in the blood; (2) there is no significant binding of the radiopharmaceutical to bone marrow precursor stem cells; (3) the contribution of the cross-dose from source organs and tumours to the bone marrow dose is significant; (4) there is considerable variation in bone marrow absorbed dose between patients. These findings imply that for individual dose optimization, individual calculation of the bone marrow absorbed dose is necessary.</p></sec></body><back><ack><p>F. Forrer received a personal research grant from the Swiss National Science Foundation and the Novartis Foundation. The authors wish to thank all the supporting personnel of the Department of Nuclear Medicine and the Department of Internal Medicine for their help and effort. 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