Panettiere F J, Goodman P J, Costanzi J J, Cruz A B, Vaitkevicius V K, McCracken J D, Brownlee R W, Laufman L, Stephens R L, Bonnet J
University of Arkansas for Medical Sciences, Little Rock.
J Clin Oncol. 1988 Jun;6(6):947-54. doi: 10.1200/JCO.1988.6.6.947.
The Southwest Oncology Group (SWOG) colorectal adjuvant study 7510 went through two phases. From 1975 to 1977, 309 patients were randomized to chemotherapy alone or the same chemotherapy plus immunotherapy. From 1977 until 1980, 317 patients were randomized among the same two therapy programs and a control group. With a minimum follow-up in either phase of greater than 7 years, data are now mature. They show no difference in relapse-free survival (RFS) nor overall survival (OS) in either the two-way phase or in the three-way phase. There is no indication, except possibly in one very small subset, that the addition of immunotherapy to chemotherapy provides an improvement in OS or in RFS. Using data from patients accrued after randomization to the control group, we fail to find evidence that either chemotherapy alone or chemoimmunotherapy improves OS or RFS when contrasted to outcomes obtained by patients on the control arm. In fact, we have significant evidence, at the P = .016 level, that chemotherapy does not improve OS by at least 50%; we also have significant evidence, at the P = .011 level, that chemoimmunotherapy will not improve OS by at least 25%. No evidence of efficacy was demonstrated for either treatment regimen, even though enough therapy was given to result in significant toxicities. Acute toxicity was at least moderate, but not fatal, in 75% of patients. Recognizable delayed toxicity included rare cases of fatal renal failure and acute leukemia.
西南肿瘤协作组(SWOG)的结直肠癌辅助治疗研究7510经历了两个阶段。1975年至1977年,309名患者被随机分为单纯化疗组或相同化疗加免疫治疗组。1977年至1980年,317名患者在相同的两个治疗方案和一个对照组之间进行随机分组。两个阶段的最短随访时间均超过7年,现在数据已经成熟。结果显示,无论是两治疗组阶段还是三治疗组阶段,无复发生存期(RFS)和总生存期(OS)均无差异。除了一个非常小的亚组可能有差异外,没有迹象表明化疗加免疫治疗能改善OS或RFS。利用随机分组到对照组后入组患者的数据,与对照组患者的结局相比,我们未能找到证据表明单纯化疗或化疗免疫治疗能改善OS或RFS。事实上,我们有显著证据(P = 0.016水平)表明化疗至少不能使OS提高50%;我们也有显著证据(P = 0.011水平)表明化疗免疫治疗至少不能使OS提高25%。两种治疗方案均未显示出疗效证据,尽管给予了足够的治疗导致了显著的毒性。75%的患者急性毒性至少为中度,但无致命性。可识别的迟发性毒性包括罕见的致命性肾衰竭和急性白血病病例。