Huang Fleur, Kushner Yael B, Langleben Adrian, Foulkes William D
Radiation Oncology Program, Department of Oncology, McGill University, Montreal, QC, Canada.
Nat Rev Clin Oncol. 2009 Aug;6(8):488-92. doi: 10.1038/nrclinonc.2009.90.
Infiltrating ductal carcinoma of the breast, staged as pT1N3, was diagnosed in a 41-year-old premenopausal French-Canadian woman. Rapid nodal recurrence progressed to diffuse bone metastases, despite tamoxifen and megestrol. Following enrollment in an in-house study protocol, she received high-dose anthracycline-based induction chemotherapy followed by tandem autologous bone marrow transplantation with high-dose alkylator and platinum-based conditioning regimens. Upon full remission, protocol-mandated locoregional breast and prophylactic cranial radiation was delivered. Complete clinical and radiologic remission has been maintained in the 11 years since study enrolment, which prompted further investigation.
Pedigree construction and BRCA1/2 mutation analysis.
A BRCA2 8765delAG mutation was identified, in the context of unusual and sustained complete remission from widely metastatic breast cancer.
The patient is now followed at a multidisciplinary high-risk prevention clinic because BRCA2 mutations are associated with increased risk of ovarian and breast cancers. This case supports the possibility of differential treatment response in BRCA2-positive breast cancer, although this remains to be conclusively demonstrated.
一名41岁的绝经前法裔加拿大女性被诊断为浸润性乳腺导管癌,分期为pT1N3。尽管接受了他莫昔芬和甲地孕酮治疗,但淋巴结迅速复发并进展为弥漫性骨转移。在参加一项内部研究方案后,她接受了以蒽环类药物为基础的大剂量诱导化疗,随后进行了自体骨髓串联移植,并采用了大剂量烷化剂和铂类预处理方案。完全缓解后,按照方案要求进行了局部乳腺和预防性颅脑放疗。自参加研究以来的11年里,患者一直保持着完全的临床和影像学缓解,这促使了进一步的研究。
构建家系图谱并进行BRCA1/2突变分析。
在广泛转移性乳腺癌出现异常且持续的完全缓解的情况下,发现了BRCA2基因8765delAG突变。
由于BRCA2突变与卵巢癌和乳腺癌风险增加相关,该患者目前在多学科高危预防诊所接受随访。尽管这一点仍有待最终证实,但该病例支持BRCA2阳性乳腺癌可能存在不同治疗反应的可能性。