Wallgren A, Bernier J, Gelber R D, Goldhirsch A, Roncadin M, Joseph D, Castiglione-Gertsch M
Department of General Oncology, Salgrenska University Hospital, Gothenborg, Sweden.
Int J Radiat Oncol Biol Phys. 1996 Jul 1;35(4):649-59. doi: 10.1016/0360-3016(96)00186-1.
A controversy exists regarding whether it is safe to delay radiation therapy until the completion of chemotherapy following breast-conserving surgery for patients with node-positive breast cancer. Within the context of two concurrent randomized clinical trials we had the opportunity to evaluate outcomes for patients who received breast irradiation after completing different durations of chemotherapy.
From July 1986 to April 1993 the International Breast Cancer Study Group (IBCSG) Trial VI randomly assigned 1554 pre/perimenopausal node-positive breast cancer patients to receive cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) for either three consecutive courses on months 1-3, or six consecutive courses on months 1-6, both with or without reintroduction CMF. IBCSG Trial VII randomly assigned 1266 postmenopausal node-positive breast cancer patients to receive tamoxifen for 5 years, or tamoxifen for 5 years with three early cycles of CMF, both with or without three courses of delayed CMF. Both trials allowed a choice of mastectomy, or breast-conserving surgery plus radiation therapy, and both were stratified by type of surgery. Radiotherapy was delayed until the initial block of CMF was completed; 4 or 7 months after surgery for pre/perimenopausal patients, and 2 or 4 months after surgery for postmenopausal patients. Over both trials, 718 eligible patients elected to receive breast-conserving surgery plus radiation therapy: 433 on Trial VI, and 285 on Trial VII. Four-year actuarial total failure rates (failure at any site), risks of developing distant metastases (DM at any time during observation), and overall survival (OS) were estimated using the Kaplan-Meier method. To avoid potential bias due to competing causes of failure, only patients who could be followed for at least 4 years (enrolled prior to July 1, 1990) were used to evaluate the patterns of first relapse site. Crude percents of local failure with or without other sites (LF), distant metastases including regional nodal failure (DM/RNF), or other first events (second primaries/death without recurrence) were estimated for each treatment group. For this report, an intent to treat analysis was performed at a median follow-up of 48 months.
No differences were found in the 4-year actuarial total failure rates, risk of developing distant metastases, and overall survival among the two radiotherapy groups of each study. The cumulative incidence of types of first failure and the 4-year crude rates showed no treatment differences in the patterns of site of first event. Estimates for the 4-year crude percent of local failures were 8 and 9% for pre/perimenopausal patients who had radiation therapy at 4 or 7 months after surgery, and 3 and 6% for postmenopausal patients who had radiation therapy at 2 months or 4 months after surgery.
For node positive patients receiving breast-conserving surgery followed by radiation therapy, the incidence of breast recurrence in the conserved ipsilateral breast within 4 years was between 8 and 9% for pre/perimenopausal patients and between 3 and 6% for postmenopausal patients. After 48 months of median follow-up, administering radiation therapy after three or six cycles of CMF for pre/perimenopausal women, or after no cycles or three cycles of CMF for postmenopausal women does not influence overall efficacy or local control in this series.
对于淋巴结阳性乳腺癌患者,在保乳手术后延迟放疗直至化疗结束是否安全存在争议。在两项同期进行的随机临床试验背景下,我们有机会评估在完成不同疗程化疗后接受乳腺照射的患者的结局。
1986年7月至1993年4月,国际乳腺癌研究组(IBCSG)试验VI将1554例绝经前/围绝经期淋巴结阳性乳腺癌患者随机分为两组,一组在第1 - 3个月连续接受3个疗程的环磷酰胺、甲氨蝶呤和5 - 氟尿嘧啶(CMF),另一组在第1 - 6个月连续接受6个疗程的CMF,两组均可选择是否重新引入CMF。IBCSG试验VII将1266例绝经后淋巴结阳性乳腺癌患者随机分为两组,一组接受5年他莫昔芬治疗,另一组接受5年他莫昔芬治疗并联合3个早期疗程的CMF,两组均可选择是否接受3个疗程的延迟CMF。两项试验均允许选择乳房切除术或保乳手术加放疗,并按手术类型进行分层。放疗延迟至初始CMF疗程结束后进行;绝经前/围绝经期患者在术后4或7个月进行,绝经后患者在术后2或4个月进行。在两项试验中,718例符合条件的患者选择接受保乳手术加放疗:试验VI中有433例,试验VII中有285例。采用Kaplan - Meier方法估计4年精算总失败率(任何部位失败)、发生远处转移的风险(观察期间任何时间的远处转移)和总生存率。为避免因竞争失败原因导致的潜在偏倚,仅对能够随访至少4年(1990年7月1日前入组)的患者进行首次复发部位模式的评估。估计每个治疗组局部失败(无论有无其他部位)、远处转移(包括区域淋巴结失败)或其他首次事件(第二原发性肿瘤/无复发死亡)的粗略百分比。本报告在中位随访48个月时进行意向性分析。
每项研究的两个放疗组在4年精算总失败率、发生远处转移的风险和总生存率方面均未发现差异。首次失败类型的累积发生率和4年粗略率在首次事件部位模式上未显示出治疗差异。绝经前/围绝经期患者在术后4或7个月接受放疗,4年局部失败粗略百分比估计为8%和9%;绝经后患者在术后2个月或4个月接受放疗,4年局部失败粗略百分比估计为3%和6%。
对于接受保乳手术并随后接受放疗的淋巴结阳性患者,绝经前/围绝经期患者4年内患侧保乳乳房的复发率在8%至9%之间,绝经后患者在3%至6%之间。在中位随访48个月后,绝经前女性在3或6个疗程的CMF后进行放疗,绝经后女性在未进行CMF或3个疗程的CMF后进行放疗,在本系列研究中不影响总体疗效或局部控制。