2010
DOI: 10.1007/s10549-010-0894-z
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Local therapy in BRCA1 and BRCA2 mutation carriers with operable breast cancer: comparison of breast conservation and mastectomy

Abstract: Purpose Women with BRCA1 and BRCA2 mutations have an elevated risk of breast cancer and ovarian cancer, but also of developing second primary breast cancer. BRCA1/2 mutation carriers with breast cancer must choose between breast conservation (BCT) and mastectomy (M) yet data on outcomes are limited. The purpose of this study is to compare BCT to M in BRCA1/2 carriers. Methods 655 women with BRCA1/2 mutations diagnosed with breast cancer and treated with BCT (n=302) or M (n=353) were identified and underwent … Show more

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Cited by 176 publications
(145 citation statements)
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“…The risk for local recurrence is obviously greater if conservative treatment rather than radical management was applied, although type of surgery in the latter approach has no correlation with the overall survival [29]. Current data indicate that radiation as an element of conservative management does not elevate the risk for carcinogenesis in BRCA carriers as compared to other BC patients.…”
Section: Management In Brca Carriersmentioning
confidence: 96%
“…The risk for local recurrence is obviously greater if conservative treatment rather than radical management was applied, although type of surgery in the latter approach has no correlation with the overall survival [29]. Current data indicate that radiation as an element of conservative management does not elevate the risk for carcinogenesis in BRCA carriers as compared to other BC patients.…”
Section: Management In Brca Carriersmentioning
confidence: 96%
“…23,24 Furthermore, most BRCA1/2 mutation carriers with breast tissue present at age 60 in our study did not have a history of breast cancer. Older age at onset, also in BRCA1/2 mutation carriers, can be a family trait.…”
Section: Discussionmentioning
confidence: 71%
“…[36,37] Meme kanseri tanısı konulan ve BRCA mutasyonu olan kadınların 15 yıl için kümülatif aynı memede kanser görülme riskleri, konservatif meme cerrahisi sonrası %23.5 iken, mastektomi sonrası bu riskin %5.5'lere düştüğü belirtilmektedir. [38] Herediter Kanser Riskinin Belirlenmesi Kalıtımsal kanser riskinin belirlenmesi, risk altındaki bireylere genetik danışmanlık verilmesi ve genetik test yapılması sonucu elde edilen verilere göre risk azaltıcı stratejilerin uygulanması, kanser mortalite ve morbiditesinin azaltılmasında giderek önem kazanmaktadır. [39] Kademeli genetik tarama (cascade genetic screening), bir ailede ilk olarak genetik danışmana başvuran ve herediter meme-over kanseri, Lynch sendromu gibi herediter kanser tanısı konulan bireylerin (proband) risk altındaki biyolojik akrabalarının tanımlanması ve test edilmesi sürecidir.…”
Section: Herediter Kolon Kanserleriunclassified