Nandikolla Amara G, Venugopal Sangeetha, Anampa Jesus
Department of Oncology, Montefiore Medical Center, Albert Einstein College of Medicine, Albert Einstein Cancer Center, Bronx, NY, USA.
Breast Cancer (Dove Med Press). 2017 Mar 23;9:207-215. doi: 10.2147/BCTT.S134241. eCollection 2017.
Li-Fraumeni Syndrome (LFS) is a rare disease with autosomal dominant inheritance linked to germline mutations of tumor suppressor gene . These patients are predisposed to malignancies such as sarcoma, breast cancer, leukemia, and other malignancies. Breast cancer, the most common malignancy in adult patients with LFS, has an early-onset presentation and is usually treated as per the guidelines for the general population due to the limited literature about breast cancer in LFS. We aimed to describe our institutional experience treating patients with breast cancer and LFS to contribute to literature about this entity.
Retrospective single-institution case-series study. We searched for cases with LFS and breast cancer from 01/01/2000 to 12/31/2015 with treatment received at our institution.
We identified 4 cases (2 African Americans, 1 Indian, and 1 Hispanic) in 4 different families, who were diagnosed with LFS after presenting with breast cancer. Three cases were triple-negative disease and 1 case was ER+, HER2 positive disease. They were treated with mastectomy and a third-generation breast chemotherapy regimen and/or trastuzumab-containing regimen. Radiation therapy was used in 2 patients. Breast cancer recurrence was seen in 1 patient, while three other malignancies were identified after breast cancer treatment (1 breast sarcoma, 1 leiomyosarcoma, and 1 myelodysplastic syndrome). A patient, who underwent surveillance with a positron emission tomography-computed tomography scan, was found to have a stage I leiomyosarcoma and was treated with surgical resection, but then developed metastatic disease requiring cytotoxic chemotherapy.
Breast cancer among patients with LFS needs a multidisciplinary treatment approach. Surgical management follows the guidelines for the general population. Risk-benefit assessment of chemotherapy and radiotherapy needs to be performed carefully in a case-by-case approach. Patients should undergo multimodality cancer surveillance, preferably in the context of a clinical trial.
李-佛美尼综合征(LFS)是一种罕见的常染色体显性遗传病,与肿瘤抑制基因的种系突变有关。这些患者易患肉瘤、乳腺癌、白血病等恶性肿瘤。乳腺癌是成年LFS患者中最常见的恶性肿瘤,发病较早,由于关于LFS患者乳腺癌的文献有限,通常按照普通人群的指南进行治疗。我们旨在描述我们机构治疗LFS合并乳腺癌患者的经验,为有关该疾病的文献提供参考。
回顾性单机构病例系列研究。我们检索了2000年1月1日至2015年12月31日在我们机构接受治疗的LFS合并乳腺癌病例。
我们在4个不同家庭中确定了4例患者(2名非裔美国人、1名印度人和1名西班牙裔),他们在患乳腺癌后被诊断为LFS。3例为三阴性疾病,1例为雌激素受体阳性、人表皮生长因子受体2阳性疾病。他们接受了乳房切除术和第三代乳腺癌化疗方案和/或含曲妥珠单抗的方案治疗。2例患者接受了放射治疗。1例患者出现乳腺癌复发,而在乳腺癌治疗后发现另外3例恶性肿瘤(1例乳腺肉瘤、1例平滑肌肉瘤和1例骨髓增生异常综合征)。1例接受正电子发射断层扫描-计算机断层扫描监测的患者被发现患有I期平滑肌肉瘤,并接受了手术切除,但随后出现转移性疾病,需要细胞毒性化疗。
LFS患者的乳腺癌需要多学科治疗方法。手术管理遵循普通人群的指南。化疗和放疗的风险效益评估需要逐案仔细进行。患者应接受多模式癌症监测,最好是在临床试验的背景下。