Sulkes Aaron
Institute of Oncology, Rabin Medical Center Beilinson Campus, Israel.
Harefuah. 2002 Apr;141(4):374-8, 408.
This review summarizes more than 25 years of experience with the use of systemic chemotherapy in the adjuvant setting in patients suffering from stage II breast cancer. The use of the CMF combination in the early 70's marks the onset of the modern era of this modality. Adjuvant chemotherapy must be given at optimal doses and schedule, usually for a period lasting about six months, beginning shortly after the resection of the primary tumor. The incorporation of the anthracyclines, adriamycin and epirubicin represent an important milestone in the developmental history of the adjuvant chemotherapy of breast cancer. The sequential administration of adriamycin followed by CMF in patients with 4 or more involved axillary lymph nodes deserves particular emphasis. Meta-analysis of multiple clinical trials including several tens of thousands of patients with stage II breast cancer indicate that adjuvant chemotherapy results in a significant increase in both recurrence-free and overall survival as compared to locoregional treatment only. This holds true with long-term follow-up of 20 years and more as illustrated by the CMF experience, showing about a 35% decrease in the relative risk of recurrence. Efforts in recent years are investigating the role of newer cytotoxic agents such as the taxanes in the adjuvant setting. Furthermore, clinical trials are now ongoing with the use of the monoclonal antibody herceptin in patients with stage II breast cancer whose tumor over-expresses the oncogene Her2neu. The administration of adjuvant chemotherapy has the potential for undesirable side effects such as an increased risk of osteoporosis and ischemic heart disease in younger patients in whom amenorrhea develops, or cardiotoxicity from anthracyclines. Most clinical trials to date have not shown an increase in the occurrence of second primary tumors among patients receiving adjuvant chemotherapy for breast cancer. Adjuvant chemotherapy has become an integral part of the treatment of stage II breast cancer.
本综述总结了25年多来在II期乳腺癌患者辅助治疗中使用全身化疗的经验。70年代初CMF联合方案的使用标志着这种治疗方式现代时代的开始。辅助化疗必须以最佳剂量和疗程进行,通常持续约六个月,在原发性肿瘤切除后不久开始。蒽环类药物阿霉素和表柔比星的加入是乳腺癌辅助化疗发展史上的一个重要里程碑。对于有4个或更多腋窝淋巴结受累的患者,先给予阿霉素然后序贯CMF尤其值得强调。对包括数万例II期乳腺癌患者在内的多项临床试验的荟萃分析表明,与仅进行局部区域治疗相比,辅助化疗可显著提高无复发生存率和总生存率。正如CMF方案的经验所示,20年及更长时间的长期随访证实了这一点,显示复发相对风险降低约35%。近年来一直在研究新型细胞毒性药物如紫杉烷在辅助治疗中的作用。此外,目前正在对肿瘤过度表达癌基因Her2neu的II期乳腺癌患者使用单克隆抗体赫赛汀进行临床试验。辅助化疗有可能产生不良副作用,如在出现闭经的年轻患者中骨质疏松和缺血性心脏病风险增加,或蒽环类药物引起的心脏毒性。迄今为止,大多数临床试验并未显示接受乳腺癌辅助化疗的患者中第二原发性肿瘤的发生率增加。辅助化疗已成为II期乳腺癌治疗不可或缺的一部分。