Surgery Branch.
Eppley Institute, Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE.
Am J Clin Oncol. 2020 May;43(5):334-339. doi: 10.1097/COC.0000000000000667.
Preoperative chemotherapy is important in the management of women with breast cancer, with the ability to downstage the breast primary tumor and axillary lymph nodes. Long-term studies are needed to identify late toxicities, recurrence patterns, and equivalency with postoperative chemotherapy for recurrence-free survival (RFS) and overall survival (OS).
We conducted a single-institution prospective randomized control trial comparing preoperative or postoperative fluorouracil, leucovorin calcium, doxorubicin, and cyclophosphamides/granulocyte colony-stimulating factor chemotherapy for women with untreated clinical stage II (T1N1, T2N0, and T2N1) breast cancer. Long-term follow-up was conducted to define toxicities, recurrence patterns and RFS and OS.
Fifty-three women with clinical stage II breast cancer were randomized, 26 patients to receive preoperative chemotherapy and 27 to receive postoperative chemotherapy. Long-term follow-up, with a median of 25.3 years, was obtained. Local or systemic recurrence occurred in 8 women in the preoperative group and in 10 women in the postoperative group, and recurrences were predominantly within 10 years of treatment. Late toxicities included local upper extremity paresthesia's, upper extremity edema and congestive heart failure in 1 patient each. Analysis revealed no difference in RFS (20-year RFS probabilities; preoperative: 61.3%, postoperative: 54.7%, P=0.42), or in OS between the 2 treatment groups (20-year probabilities, preoperative: 64.6%, postoperative: 62.2%, P=0.44). Twenty-five of 53 patients (47%) were alive and without disease at this follow-up.
Twenty-five-year follow-up for this prospective randomized trial confirms the equivalency of preoperative versus postoperative chemotherapy with fluorouracil, leucovorin calcium, doxorubicin, and cyclophosphamides/granulocyte colony-stimulating factor for stage II breast cancer for both RFS and OS.
术前化疗在乳腺癌的治疗中很重要,它可以降低乳腺原发肿瘤和腋窝淋巴结的分期。需要进行长期研究来确定晚期毒性、复发模式以及与术后化疗在无复发生存率 (RFS) 和总生存率 (OS) 方面的等效性。
我们进行了一项单机构前瞻性随机对照试验,比较了未经治疗的临床 II 期 (T1N1、T2N0 和 T2N1) 乳腺癌患者接受术前或术后氟尿嘧啶、亚叶酸钙、多柔比星和环磷酰胺/粒细胞集落刺激因子化疗。进行了长期随访以确定毒性、复发模式和 RFS 和 OS。
53 名患有临床 II 期乳腺癌的患者被随机分配,26 名患者接受术前化疗,27 名患者接受术后化疗。中位随访时间为 25.3 年。术前组有 8 名患者和术后组有 10 名患者发生局部或全身复发,复发主要发生在治疗后 10 年内。晚期毒性包括 1 例上肢局部感觉异常、1 例上肢水肿和 1 例充血性心力衰竭。分析显示,RFS(20 年 RFS 概率;术前:61.3%,术后:54.7%,P=0.42)或 2 组治疗之间的 OS(20 年概率,术前:64.6%,术后:62.2%,P=0.44)无差异。53 名患者中有 25 名(47%)在此次随访时仍然存活且无疾病。
这项前瞻性随机试验的 25 年随访结果证实,氟尿嘧啶、亚叶酸钙、多柔比星和环磷酰胺/粒细胞集落刺激因子用于 II 期乳腺癌的术前与术后化疗在 RFS 和 OS 方面具有等效性。