Konski Andre, Garcia Miguel, John Madhu, Krieg Richard, Pinover Wayne, Myerson Robert, Willett Christopher
Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Int J Radiat Oncol Biol Phys. 2008 Sep 1;72(1):114-8. doi: 10.1016/j.ijrobp.2007.12.027. Epub 2008 May 9.
Radiation Therapy Oncology Group (RTOG) 92-08 began as a single arm, Phase II trial for patients with anal cancer consisting of radiation (RT) + 5-flourouracil + mitomycin-C with a mandatory 2-week break and was amended after completion to evaluate the same treatment regimen without a treatment break. Long-term efficacy and late toxicity reporting are the specific aims of this study.
Survivals were estimated with the Kaplan-Meier method. Overall survival (OS) was compared with RTOG 87-04 with the log-rank test. Time to local failure, regional failure, locoregional failure (LRF), distant metastases, second primary, and colostomy failure were estimated by the cumulative incidence method. LRF was compared with RTOG 87-04 using the Gray's test.
Forty-seven patients entered in the mandatory treatment break cohort. The study was reopened in 1995 to the no mandatory treatment break cohort completing accrual with 20 patients in 1996. Of 67 total patients, 1 patient in the mandatory treatment break portion of the study did not receive any protocol treatment and is excluded from analyses. After adjusting for tumor size, neither cohort showed a statistically significant difference in OS or LRF compared with the RTOG 87-04 mitomycin-C arm. No patient in either cohort experienced a Grade 3 or higher late toxicity.
No statistically significant differences were seen in OS or LRF when compared to the mitomycin-C arm of RTOG 87-04, but the sample sizes for the mandatory break cohort and the no mandatory break cohort are small. Late toxicity was low and similar for the treatment cohorts.
放射治疗肿瘤学组(RTOG)92 - 08最初是一项针对肛管癌患者的单臂II期试验,治疗方案为放疗(RT)+ 5 - 氟尿嘧啶+丝裂霉素 - C,并强制休息2周,在试验完成后进行了修正,以评估相同治疗方案但不进行治疗中断的情况。本研究的具体目标是报告长期疗效和晚期毒性。
采用Kaplan - Meier方法估计生存率。用对数秩检验将总生存期(OS)与RTOG 87 - 04进行比较。通过累积发病率法估计局部失败、区域失败、局部区域失败(LRF)、远处转移、第二原发肿瘤和结肠造口失败的时间。使用Gray检验将LRF与RTOG 87 - 04进行比较。
47例患者进入强制治疗中断队列。该研究于1995年重新开放至无强制治疗中断队列,1996年有20例患者完成入组。在总共67例患者中,研究中强制治疗中断部分的1例患者未接受任何方案治疗,被排除在分析之外。在调整肿瘤大小后,与RTOG 87 - 04丝裂霉素 - C组相比,两个队列在OS或LRF方面均未显示出统计学上的显著差异。两个队列中均没有患者出现3级或更高等级的晚期毒性。
与RTOG 87 - 04丝裂霉素 - C组相比,在OS或LRF方面未观察到统计学上的显著差异,但强制休息队列和无强制休息队列的样本量较小。治疗队列的晚期毒性较低且相似。