Kim Jun Won, Cho Yeona, Kim Hyung Sun, Choi Won Hoon, Park Joon Seong, Lee Ik Jae
Department of Radiation Oncology, Gangnam Severance Hospital, Yonsei University College of Medicine, 211 Eonju-ro, Gangnam-gu, Seoul, 06273, Republic of Korea.
Department of Pancreatobiliary Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, 211 Eonju-ro, Gangnam-gu, Seoul, 06273, Republic of Korea.
BMC Surg. 2019 Mar 7;19(1):31. doi: 10.1186/s12893-019-0492-x.
The current standard treatment for resectable pancreatic cancer is surgical resection followed by adjuvant chemotherapy. Local recurrence rates are high even after curative resection; thus, the long-term outcome of locally advanced pancreatic cancer remains poor. Intraoperative radiotherapy (IORT) uses a low-energy x-ray source to deliver a single fraction of high-dose radiation to the tumor bed during a surgical procedure, while effectively sparing the surrounding normal tissues. IORT has the potential to improve the efficacy of radiation therapy for pancreatic cancer.
METHODS/DESIGN: This prospective, one-armed, phase II study will investigate the role of IORT in improving local control in patients with resectable pancreatic adenocarcinoma. The patients will receive surgery and IORT of 10 Gy prescribed at a 5-mm depth of the tumor bed, followed by adjuvant gemcitabine chemotherapy according to the current standard of care. The aim is to enroll 42 patients.
The primary endpoint of this trial is to evaluate the feasibility of IORT and the local recurrence rate after one year. The secondary endpoints include the acute and late toxicities, and disease-free survival and overall survival rates.
The trial was prospectively registered at Clinicaltrials.gov NCT03273374 on September 6, 2017.
可切除胰腺癌的当前标准治疗方法是手术切除后进行辅助化疗。即使在根治性切除后,局部复发率仍很高;因此,局部晚期胰腺癌的长期预后仍然很差。术中放疗(IORT)使用低能X射线源在手术过程中向肿瘤床单次给予高剂量辐射,同时有效地保护周围正常组织。IORT有可能提高胰腺癌放疗的疗效。
方法/设计:这项前瞻性、单臂、II期研究将调查IORT在改善可切除胰腺腺癌患者局部控制方面的作用。患者将接受手术和在肿瘤床5毫米深度处给予10 Gy的IORT,然后根据当前护理标准进行辅助吉西他滨化疗。目标是招募42名患者。
该试验的主要终点是评估IORT的可行性和一年后的局部复发率。次要终点包括急性和晚期毒性、无病生存率和总生存率。
该试验于2017年9月6日在Clinicaltrials.gov上进行了前瞻性注册,注册号为NCT03273374。