Post-treatment sarcoma in breast cancer patients.
Identifieur interne : 00B261 ( Ncbi/Merge ); précédent : 00B260; suivant : 00B262Post-treatment sarcoma in breast cancer patients.
Auteurs : M S Brady [États-Unis] ; C F Garfein ; J A Petrek ; M F BrennanSource :
- Annals of surgical oncology [ 1068-9265 ] ; 1994.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Bras, Femelle, Fibrosarcome (mortalité), Fibrosarcome (étiologie), Humains, Lymphangiosarcome (mortalité), Lymphangiosarcome (étiologie), Mâle, Pronostic, Radiothérapie (effets indésirables), Sarcomes (étiologie), Seconde tumeur primitive (), Sujet âgé, Taux de survie, Tumeur du sein de l'homme (radiothérapie), Tumeurs du sein (radiothérapie), Tumeurs radio-induites.
- MESH :
- effets indésirables : Radiothérapie.
- mortalité : Fibrosarcome, Lymphangiosarcome.
- radiothérapie : Tumeur du sein de l'homme, Tumeurs du sein.
- étiologie : Fibrosarcome, Lymphangiosarcome, Sarcomes.
- Adulte, Adulte d'âge moyen, Bras, Femelle, Humains, Mâle, Pronostic, Seconde tumeur primitive, Sujet âgé, Taux de survie, Tumeurs radio-induites.
English descriptors
- KwdEn :
- Adult, Aged, Arm, Breast Neoplasms (radiotherapy), Breast Neoplasms, Male (radiotherapy), Female, Fibrosarcoma (etiology), Fibrosarcoma (mortality), Humans, Lymphangiosarcoma (etiology), Lymphangiosarcoma (mortality), Male, Middle Aged, Neoplasms, Radiation-Induced, Neoplasms, Second Primary (therapy), Prognosis, Radiotherapy (adverse effects), Sarcoma (etiology), Survival Rate.
- MESH :
- adverse effects : Radiotherapy.
- etiology : Fibrosarcoma, Lymphangiosarcoma, Sarcoma.
- mortality : Fibrosarcoma, Lymphangiosarcoma.
- radiotherapy : Breast Neoplasms, Breast Neoplasms, Male.
- therapy : Neoplasms, Second Primary.
- Adult, Aged, Arm, Female, Humans, Male, Middle Aged, Neoplasms, Radiation-Induced, Prognosis, Survival Rate.
Abstract
Many patients treated for breast cancer with radiotherapy will survive their disease and be at risk for treatment-related sarcoma for many years.
PubMed: 7834431
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pubmed:7834431Le document en format XML
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<author><name sortKey="Brady, M S" sort="Brady, M S" uniqKey="Brady M" first="M S" last="Brady">M S Brady</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
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<wicri:cityArea>Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York</wicri:cityArea>
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<author><name sortKey="Petrek, J A" sort="Petrek, J A" uniqKey="Petrek J" first="J A" last="Petrek">J A Petrek</name>
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<affiliation wicri:level="2"><nlm:affiliation>Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Arm</term>
<term>Breast Neoplasms (radiotherapy)</term>
<term>Breast Neoplasms, Male (radiotherapy)</term>
<term>Female</term>
<term>Fibrosarcoma (etiology)</term>
<term>Fibrosarcoma (mortality)</term>
<term>Humans</term>
<term>Lymphangiosarcoma (etiology)</term>
<term>Lymphangiosarcoma (mortality)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neoplasms, Radiation-Induced</term>
<term>Neoplasms, Second Primary (therapy)</term>
<term>Prognosis</term>
<term>Radiotherapy (adverse effects)</term>
<term>Sarcoma (etiology)</term>
<term>Survival Rate</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Bras</term>
<term>Femelle</term>
<term>Fibrosarcome (mortalité)</term>
<term>Fibrosarcome (étiologie)</term>
<term>Humains</term>
<term>Lymphangiosarcome (mortalité)</term>
<term>Lymphangiosarcome (étiologie)</term>
<term>Mâle</term>
<term>Pronostic</term>
<term>Radiothérapie (effets indésirables)</term>
<term>Sarcomes (étiologie)</term>
<term>Seconde tumeur primitive ()</term>
<term>Sujet âgé</term>
<term>Taux de survie</term>
<term>Tumeur du sein de l'homme (radiothérapie)</term>
<term>Tumeurs du sein (radiothérapie)</term>
<term>Tumeurs radio-induites</term>
</keywords>
<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Radiotherapy</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Radiothérapie</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Fibrosarcoma</term>
<term>Lymphangiosarcoma</term>
<term>Sarcoma</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en"><term>Fibrosarcoma</term>
<term>Lymphangiosarcoma</term>
</keywords>
<keywords scheme="MESH" qualifier="mortalité" xml:lang="fr"><term>Fibrosarcome</term>
<term>Lymphangiosarcome</term>
</keywords>
<keywords scheme="MESH" qualifier="radiotherapy" xml:lang="en"><term>Breast Neoplasms</term>
<term>Breast Neoplasms, Male</term>
</keywords>
<keywords scheme="MESH" qualifier="radiothérapie" xml:lang="fr"><term>Tumeur du sein de l'homme</term>
<term>Tumeurs du sein</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Neoplasms, Second Primary</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Fibrosarcome</term>
<term>Lymphangiosarcome</term>
<term>Sarcomes</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Arm</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neoplasms, Radiation-Induced</term>
<term>Prognosis</term>
<term>Survival Rate</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Bras</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Pronostic</term>
<term>Seconde tumeur primitive</term>
<term>Sujet âgé</term>
<term>Taux de survie</term>
<term>Tumeurs radio-induites</term>
</keywords>
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<front><div type="abstract" xml:lang="en">Many patients treated for breast cancer with radiotherapy will survive their disease and be at risk for treatment-related sarcoma for many years.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7834431</PMID>
<DateCreated><Year>1995</Year>
<Month>03</Month>
<Day>02</Day>
</DateCreated>
<DateCompleted><Year>1995</Year>
<Month>03</Month>
<Day>02</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>08</Month>
<Day>19</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">1068-9265</ISSN>
<JournalIssue CitedMedium="Print"><Volume>1</Volume>
<Issue>1</Issue>
<PubDate><Year>1994</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Annals of surgical oncology</Title>
<ISOAbbreviation>Ann. Surg. Oncol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Post-treatment sarcoma in breast cancer patients.</ArticleTitle>
<Pagination><MedlinePgn>66-72</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Many patients treated for breast cancer with radiotherapy will survive their disease and be at risk for treatment-related sarcoma for many years.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">In order to identify patients with post-treatment sarcoma and define this disease, we examined the records of 99 patients treated for sarcoma with a history of antecedent breast carcinoma. Of these patients, 51 were felt to have a sarcoma unrelated to breast cancer treatment and 48 were felt to have a treatment-related sarcoma (secondary to lymphedema and/or radiation).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Lymphangiosarcoma of the extremity was the most common histologic subtype of post-treatment sarcoma, accounting for 22 of 48 cases (46%). Twenty-six patients (54%) developed nonlymphangiosarcoma post-treatment sarcoma; all of these were radiation-associated sarcomas. The median latency interval between the diagnosis of breast cancer and the development of sarcoma was 11 years (range 4-44) and was not different between the two groups. However, patients with nonlymphangiosarcoma were significantly younger when diagnosed with breast cancer than were those with lymphangiosarcoma of the extremity (median 43 vs. 51 years, p < 0.001). The survival of all 48 patients was poor: 5-year survival was 29%. Five-year survival of patients with other types of post-treatment sarcoma was just as poor as those with lymphangiosarcoma of the extremity (30% vs. 28%, p = 0.98).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Patients who develop sarcoma after treatment for breast cancer have a poor prognosis whether it occurs as Stewart-Treves syndrome or other types of post-treatment sarcoma. Younger patients may be at higher risk than are older patients for the development of nonlymphangiosarcoma post-treatment sarcoma.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Brady</LastName>
<ForeName>M S</ForeName>
<Initials>MS</Initials>
<AffiliationInfo><Affiliation>Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Garfein</LastName>
<ForeName>C F</ForeName>
<Initials>CF</Initials>
</Author>
<Author ValidYN="Y"><LastName>Petrek</LastName>
<ForeName>J A</ForeName>
<Initials>JA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Brennan</LastName>
<ForeName>M F</ForeName>
<Initials>MF</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>CA 47179</GrantID>
<Acronym>CA</Acronym>
<Agency>NCI NIH HHS</Agency>
<Country>United States</Country>
</Grant>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
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<MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001132" MajorTopicYN="N">Arm</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001943" MajorTopicYN="N">Breast Neoplasms</DescriptorName>
<QualifierName UI="Q000532" MajorTopicYN="Y">radiotherapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018567" MajorTopicYN="N">Breast Neoplasms, Male</DescriptorName>
<QualifierName UI="Q000532" MajorTopicYN="N">radiotherapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005354" MajorTopicYN="N">Fibrosarcoma</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName>
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<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
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<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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<MeshHeading><DescriptorName UI="D009381" MajorTopicYN="Y">Neoplasms, Radiation-Induced</DescriptorName>
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<MeshHeading><DescriptorName UI="D016609" MajorTopicYN="Y">Neoplasms, Second Primary</DescriptorName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
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<MeshHeading><DescriptorName UI="D011379" MajorTopicYN="N">Prognosis</DescriptorName>
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<MeshHeading><DescriptorName UI="D011878" MajorTopicYN="N">Radiotherapy</DescriptorName>
<QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName>
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<MeshHeading><DescriptorName UI="D012509" MajorTopicYN="N">Sarcoma</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName>
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<MeshHeading><DescriptorName UI="D015996" MajorTopicYN="N">Survival Rate</DescriptorName>
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