Garden Adam S, Fuller Clifton D, Rosenthal David I, William William N, Gunn Gary B, Beadle Beth M, Johnson Faye M, Morrison William H, Phan Jack, Frank Steven J, Kies Merrill S, Sturgis Erich M
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Thoracic Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2016 Jun 1;122(11):1702-7. doi: 10.1002/cncr.29965. Epub 2016 Mar 28.
Favorable outcomes for human papillomavirus-associated oropharyngeal cancer have led to interest in identifying a subgroup of patients with the lowest risk of disease recurrence after therapy. De-intensification of therapy for this group may result in survival outcomes that are similar to those associated with current therapy but with less toxicity. To advance this effort, this study analyzed the outcomes of oropharyngeal cancer patients treated with or without systemic therapy.
This was a retrospective study of patients with oropharyngeal cancer treated between 1985 and 2012. The criteria for inclusion were ≤10 pack-years of cigarette smoking and stage III/IVA cancer limited to T1-3, N1-N2b, and T3N0 disease. A survival analysis was performed with the primary endpoint of progression-free survival (PFS).
The cohort included 857 patients. Systemic therapy was given to 439 patients (51%). The median survival was 80 months. The 2-year PFS rate was 91%. When the analysis was limited to 324 patients irradiated without systemic therapy, the 2- and 5-year PFS rates were 90% and 85%, respectively. Furthermore, for these 324 patients, the 5-year PFS rates for T1, T2, and T3 disease were 90%, 83%, and 70%, respectively. The 5-year PFS rate for patients treated with systemic therapy for T3 disease was 77% (P = .07).
According to the low-risk definition currently established in cooperative trials, the patients had a 2-year PFS rate approximating 90%. When patients who were treated with radiation alone were evaluated, no compromise was observed in this high rate of PFS, which is higher than the 2-year PFS thresholds used in current cooperative trials. Cancer 2016;122:1702-7. © 2016 American Cancer Society.
人乳头瘤病毒相关口咽癌的良好治疗结果引发了人们对于识别治疗后疾病复发风险最低的患者亚组的兴趣。对于该组患者减少治疗强度可能会带来与当前治疗相似的生存结果,但毒性更低。为推动这一研究,本研究分析了接受或未接受全身治疗的口咽癌患者的治疗结果。
这是一项对1985年至2012年间接受治疗的口咽癌患者的回顾性研究。纳入标准为吸烟史≤10包年且癌症分期为III/IVA期,局限于T1-3、N1-N2b以及T3N0疾病。以无进展生存期(PFS)作为主要终点进行生存分析。
该队列包括857例患者。439例患者(51%)接受了全身治疗。中位生存期为80个月。2年PFS率为91%。当分析仅限于324例未接受全身治疗而接受放疗的患者时,2年和5年PFS率分别为90%和85%。此外,对于这324例患者,T1、T2和T3期疾病的5年PFS率分别为90%、83%和70%。T3期疾病接受全身治疗的患者5年PFS率为77%(P = 0.07)。
根据目前合作试验中确立的低风险定义,这些患者的2年PFS率约为90%。当仅接受放疗的患者被评估时,在这一高PFS率方面未观察到折衷情况,该PFS率高于当前合作试验中使用的2年PFS阈值。《癌症》2016年;122:1702 - 7。©2016美国癌症协会。