Perez C A, Bauer M, Emami B N, Byhardt R, Brady L W, Doggett R L, Gardner P, Zinninger M
Radiation Oncology Center, Mallinckrodt Institute of Radiology, St. Louis, MO 63108.
Int J Radiat Oncol Biol Phys. 1988 Dec;15(6):1337-46. doi: 10.1016/0360-3016(88)90229-5.
A total of 285 patients with medically inoperable (RTOG Stage T1-2, N0-1) or unresectable (RTOG Stage T3, N0-1) non-small cell carcinoma of the lung were randomized by the Radiation Therapy Oncology Group (RTOG) to receive radiation therapy (6000 cGy total dose/6 weeks) plus levamisole (2.5 mg/kg twice weekly for 2 years or until tumor progression) or a placebo. One hundred twenty-nine evaluable patients were assigned to placebo and 131 to levamisole. This report is based on 260 (91%) eligible patients who started treatment and have adequate follow-up. Fifty percent of the patients in both treatment groups had Karnofsky scores of 90-100; 72% had squamous cell carcinoma, 12% adenocarcinoma, and 16% large cell undifferentiated carcinoma; 60% had RTOG Stage I or II primary tumors and 40% had Stage III (T3, N0-1) tumors. Complete regression of tumor was reported in 20% of the patients treated with levamisole and 36% of those receiving placebo. An additional 33% and 19%, respectively, had a partial response (trend test p = 0.08). Median survival was 9 months for patients treated with levamisole and 12 months for those on placebo (two-sided p less than 0.01); at 2 years, patients treated with levamisole had a 15% survival rate as compared to 24% in those receiving placebo. The cumulative proportion failing within the irradiated field with or without other sites of progression at 2 years was 30% in the levamisole group and 34% in the placebo patients. Median progression-free survival was 6 months for patients on levamisole and 7 months for those on placebo (overall two-sided p = 0.014); the estimated proportions progression-free at 2 years were 11% and 18%, respectively. The study showed no significant prolongation of survival, progression-free survival, or differences in patterns of failure in irradiated patients treated with levamisole compared with a placebo. Toxicity related to this immunoadjuvant was, in general, of moderate clinical importance. This study confirms a report by the Southeastern Cancer Study Group concluding that levamisole combined with definitive irradiation has no benefit in the treatment of unresectable non-small cell carcinoma of the lung.
放射肿瘤学组(RTOG)将总计285例医学上无法手术(RTOG分期T1 - 2,N0 - 1)或不可切除(RTOG分期T3,N0 - 1)的非小细胞肺癌患者随机分组,分别接受放射治疗(总剂量6000 cGy/6周)加左旋咪唑(2.5 mg/kg,每周两次,共2年或直至肿瘤进展)或安慰剂治疗。129例可评估患者被分配至安慰剂组,131例被分配至左旋咪唑组。本报告基于260例(91%)开始治疗并获得充分随访的符合条件患者。两个治疗组中50%的患者卡氏评分在90 - 100;72%为鳞状细胞癌,12%为腺癌,16%为大细胞未分化癌;60%的患者RTOG分期为I期或II期原发性肿瘤,40%为III期(T3,N0 - 1)肿瘤。接受左旋咪唑治疗的患者中20%报告肿瘤完全消退,接受安慰剂治疗的患者中这一比例为36%。另外,分别有33%和19%的患者有部分缓解(趋势检验p = 0.08)。接受左旋咪唑治疗的患者中位生存期为9个月,接受安慰剂治疗的患者为12个月(双侧p小于0.01);2年时,接受左旋咪唑治疗的患者生存率为15%,接受安慰剂治疗的患者为24%。左旋咪唑组2年时在照射野内出现进展(无论有无其他部位进展)的累积比例为30%,安慰剂组患者为34%。接受左旋咪唑治疗的患者中位无进展生存期为6个月,接受安慰剂治疗的患者为7个月(总体双侧p = 0.014);2年时估计的无进展比例分别为11%和18%。该研究表明,与安慰剂相比,接受左旋咪唑治疗的照射患者在生存期、无进展生存期方面未显著延长,在失败模式上也无差异。与这种免疫佐剂相关的毒性一般具有中等临床重要性。本研究证实了东南癌症研究组的一份报告,该报告得出结论,左旋咪唑联合根治性放疗对不可切除的非小细胞肺癌治疗无益处。