新辅助放化疗联合中等分割调强放疗治疗可切除胰腺癌的安全性和有效性:一项前瞻性、开放标签的II期研究。

Safety and efficacy of neoadjuvant chemoradiotherapy with moderately hypofractionated intensity-modulated radiotherapy for resectable pancreatic cancer: A prospective, open-label, phase II study.

作者信息

Masui Toshihiko, Nagai Kazuyuki, Anazawa Takayuki, Kasai Yosuke, Yogo Akitada, Yoshimura Michio, Mizowaki Takashi, Uza Norimitsu, Fukuda Akihisa, Matsumoto Shigemi, Kanai Masashi, Isoda Hiroyoshi, Kawaguchi Yoshiya, Uemoto Shinji, Hatano Etsuro

机构信息

Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Cancer Med. 2023 Sep;12(18):18611-18621. doi: 10.1002/cam4.6470. Epub 2023 Aug 30.

Abstract

BACKGROUND

Resectable pancreatic cancer (RPC) is potentially resectable on admission, and the impact of neoadjuvant therapy on these tumors is controversial. Moreover, the safety and efficacy of neoadjuvant chemoradiotherapy with moderately hypofractionated intensity-modulated radiation therapy (NACIMRT) for RPC have not been studied. Here, we conducted a phase II study to evaluate the safety and efficacy of hypofractionated NACIMRT for RPC.

METHODS

A total of 54 RPC patients were enrolled and treated according to the study protocol. We used moderately hypofractionated (45 Gy in 15 fractions) IMRT with gemcitabine to shorten the duration of radiotherapy and reduce gastrointestinal toxicity. The primary endpoint was overall survival (OS), and we subsequently analyzed the microscopically margin-negative resection (R0) rate, disease-free survival (DFS), and histologic effects and safety of NACIMRT.

RESULTS

Median OS for the cohort was 40.0 months. Forty-two patients (77.8%) underwent pancreatectomy after NACIMRT. Median DFS was 20.3 months. The R0 resection rate was 95.2% (40/42) per protocol and 85.2% (46/54) for the cohort. There were no intervention-related deaths during the study period. Local treatment response, as assessed by the CAP classification, showed no residual tumor in 4.8% of patients. Overall, 23.9% of patients experienced CTCAE grade 3 or 4 during NACIMRT. Adjuvant therapy was initiated in 88% of patients undergoing resection. Postoperative complications grade ≥3b on the Clavien-Dindo scale occurred in 4.8% of patients. CA19-9 level at enrollment was an independent prognostic factor for OS and DFS.

CONCLUSIONS

This is the first prospective study of hypofractionated IMRT as neoadjuvant therapy for RPC. Hypofractionated NACIMRT for RPC could be safely introduced with a high induction rate of adjuvant chemotherapy, with an overall survival of 40.0 months.

摘要

背景

可切除胰腺癌(RPC)入院时可能可切除,新辅助治疗对这些肿瘤的影响存在争议。此外,新辅助放化疗联合中等分割调强放疗(NACIMRT)治疗RPC的安全性和有效性尚未得到研究。在此,我们开展了一项II期研究,以评估分割剂量NACIMRT治疗RPC的安全性和有效性。

方法

共纳入54例RPC患者,并根据研究方案进行治疗。我们采用中等分割(15次分割,共45 Gy)调强放疗联合吉西他滨,以缩短放疗疗程并降低胃肠道毒性。主要终点为总生存期(OS),随后我们分析了镜下切缘阴性切除(R0)率、无病生存期(DFS)以及NACIMRT的组织学效果和安全性。

结果

该队列的中位OS为40.0个月。42例患者(77.8%)在NACIMRT后接受了胰腺切除术。中位DFS为20.3个月。按照方案,R0切除率为95.2%(40/42),该队列的R0切除率为85.2%(46/54)。研究期间无干预相关死亡。根据CAP分类评估的局部治疗反应显示,4.8%的患者无残留肿瘤。总体而言,23.9%的患者在NACIMRT期间出现3级或4级CTCAE。88%接受切除的患者开始了辅助治疗。Clavien-Dindo分级≥3b级的术后并发症发生在4.8%的患者中。入组时的CA19-9水平是OS和DFS的独立预后因素。

结论

这是第一项关于分割剂量调强放疗作为RPC新辅助治疗的前瞻性研究。分割剂量NACIMRT治疗RPC可安全引入,辅助化疗诱导率高,总生存期为40.0个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/10557863/cb4bf4b40314/CAM4-12-18611-g002.jpg

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