Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Radiation Oncology, The University of Pennsylvania Cancer Center, Perelman School of Medicine, Philadelphia, Pennsylvania.
Int J Radiat Oncol Biol Phys. 2019 Sep 1;105(1):90-95. doi: 10.1016/j.ijrobp.2019.04.040. Epub 2019 May 22.
Definitive chemoradiation with concurrent 5-fluorouracil (5-FU)/mitomycin C (MMC) is an effective treatment for localized anal cancer, but it is associated with significant acute long-term treatment-related toxicity. Pencil beam scanning proton beam (PBS-PT) radiation therapy may potentially reduce this toxicity. This is a multi-institutional pilot study evaluating the feasibility of definitive concurrent chemoradiation with PBS-PT in combination with 5-FU and MMC for carcinoma of the anal canal.
Patients were enrolled on a National Cancer Institute-sponsored, prospective, multi-institutional, single-arm pilot study (NCT01858025). Key eligibility criteria included Eastern Cooperative Oncology Group 0 to 2, age ≥18 years, histologically confirmed invasive squamous cell carcinoma of the anal canal, and clinically staged T1-4, N0-3 disease. Patients were treated with PBS-PT per Radiation Therapy Oncology Group 0529 dose schema and concurrent 5-FU/MMC on day 1 and 29. The primary objective of this study was to determine feasibility of PBS-PT with concurrent 5-FU/MMC, defined as grade 3+ dermatologic toxicity less than 48% (reported grade 3+ dermatologic toxicity from Radiation Therapy Oncology Group 98-11). Secondary objectives were to determine the rates of overall grade 3+ toxicities, clinical complete response rate, and disease outcomes.
Between February 2014 and April 2017, we enrolled 25 patients into our study, all of whom were analyzed. Twenty-three patients (92%) completed treatment per protocol, and 2 patients died on treatment. Median time to completion of treatment was 42 days (range, 38-49). The grade 3+ radiation dermatitis rate was 24%. Median follow-up is 27 months (range, 21-50) among the 21 patients still alive. The overall rate of clinical complete response was 88%. The 2-year local failure, colostomy-free survival, progression-free survival, and overall survival are 12%, 72%, 80%, and 84%, respectively.
In our prospective, multi-institutional pilot study of PBS-PT with concurrent 5-FU/MMC, PBS-PT was found to be feasible. A phase 2 study of proton beam radiation therapy is currently underway.
采用同步氟尿嘧啶(5-FU)/丝裂霉素 C(MMC)的确定性放化疗是治疗局限性肛门癌的有效方法,但它与显著的急性长期治疗相关毒性相关。铅笔束扫描质子束(PBS-PT)放射治疗可能会降低这种毒性。这是一项多机构的试点研究,评估了在联合 5-FU 和 MMC 的情况下,使用 PBS-PT 进行确定性同期放化疗治疗肛管癌的可行性。
患者参加了由美国国家癌症研究所赞助的前瞻性、多机构、单臂试点研究(NCT01858025)。主要入选标准包括东部肿瘤协作组 0 至 2 级、年龄≥18 岁、经组织学证实的侵袭性肛门管鳞状细胞癌和临床分期为 T1-4、N0-3 疾病。患者按照放射治疗肿瘤组 0529 剂量方案接受 PBS-PT 治疗,并在第 1 天和第 29 天接受 5-FU/MMC 治疗。本研究的主要目的是确定 PBS-PT 联合 5-FU/MMC 的可行性,定义为 3+级以上皮肤毒性<48%(根据放射治疗肿瘤组 98-11 报告的 3+级以上皮肤毒性)。次要目标是确定总 3+级毒性、临床完全缓解率和疾病结局的发生率。
2014 年 2 月至 2017 年 4 月,我们共招募了 25 例患者参加我们的研究,所有患者均进行了分析。23 例(92%)患者按方案完成治疗,2 例患者在治疗期间死亡。中位治疗完成时间为 42 天(范围 38-49 天)。3+级放射性皮炎的发生率为 24%。在 21 例仍存活的患者中,中位随访时间为 27 个月(范围 21-50 个月)。总的临床完全缓解率为 88%。2 年局部失败、无结肠造口生存、无进展生存和总生存分别为 12%、72%、80%和 84%。
在我们的前瞻性、多机构 PBS-PT 联合 5-FU/MMC 试点研究中,发现 PBS-PT 是可行的。目前正在进行质子束放射治疗的 2 期研究。