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铅笔束扫描质子束放化疗联合氟尿嘧啶和丝裂霉素 C 治疗肛管癌的多中心可行性研究。

Pencil Beam Scanning Proton Beam Chemoradiation Therapy With 5-Fluorouracil and Mitomycin-C for Definitive Treatment of Carcinoma of the Anal Canal: A Multi-institutional Pilot Feasibility Study.

机构信息

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.

出版信息

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.

Abstract

PURPOSE

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.

METHODS AND MATERIALS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法和材料

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。

结果

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%。

结论

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。

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