Rectal arterial infusion chemotherapy combined with anti-PD1 antibody for microsatellite stable locally advanced rectal cancer: The effectiveness and safety of a single-arm, phase II study.
Abstract
e15660 Background: The standard neoadjuvant therapy for locally advanced rectal cancer (LARC) is neoadjuvant chemoradiotherapy (nCRT). Nevertheless, nCRT is linked to an increased risk of peri-operative complications. Neoadjuvant chemotherapy alone demonstrates an objective response rate of approximately 60% and a lower pathological complete response (pCR) rate compared to nCRT.Against this backdrop, we put forward a novel therapeutic strategy, which encompasses arterial infusion chemotherapy and intravenous anti-PD1 antibody, after induction chemotherapy.The objective of this study is to achieve a high pCR rate in patients with microsatellite-stable (MSS) LARC. Methods: Eligible patients with LARC (tumor located 5 - 12 cm from the anal verge, T3/4a or TanyN+) were administered two cycles of CAPOX. Patients who achieved a regression of more than 20% in the maximum tumor diameter received two cycles of rectal arterial infusion chemotherapy with oxaliplatin (50mg, Day 1), intravenous anti-PD1 inhibitor (200mg, Day 2), and capecitabine (1000mg/m2, orally, twice daily, Day 1-14). Total mesorectal excision (TME) was to be performed within six weeks after the last chemotherapy session. Patients with a tumor regression of less than 20% were recommended to receive nCRT. The primary endpoint was pCR rate. A total of 38 patients are planned to be enrolled to receive the arterial infusion chemotherapy combined with intravenous anti-PD1 antibody. Results: Sixty-one patients were enrolled in the study. After induction chemotherapy, 36 out of 61 patients met the 20% regression criterion. One of these 36 patients declined further treatment and withdrew from the study. Subsequently, 35 patients underwent arterial infusion chemotherapy combined with intravenous anti-PD1 antibody.Among them, one patient was deemed to have achieved a clinical complete response and refused operation. Three patients are awaiting surgery and 31 patients had undergone TME operations. The pCR rate was 35.5% (11/31). According to the tumor regression grading(TRG) standard of AJCC, the number of patients in TRG 0, 1, 2, and 3 was 11, 9, 11, and 0, respectively. The rate of major pathological response (MPR) is 77.4% (24/31). Among patients who completed the study protocol, 74.2% (23 of 31) had MRI suspected positive lymph nodes. However, the postoperative pathological results indicated that only 1 lymph node of 1 patient was positive and the remaining 30 patients were diagnosed as pN0. In terms of safety, 8 out of 31 patients had grade 3 adverse event. Conclusions: For MSS LARC patients, rectal arterial infusion chemotherapy of oxaliplatin combined with intravenous anti-PD1 antibody achieved a high pCR rate, demonstrated a favorable therapeutic effect on lymph node metastasis, and exhibited good safety. Clinical trial information: NCT05307198 .
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (11)
Jun Li
Yurong Jiao
Department of Colorectal Surgery and Oncology, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Xiangxing Kong
Department of Colorectal Surgery and Oncology, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Chengcheng Liu
Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering
Shugao Han
Department of Surgery The Second Affiliated Hospital, Zhejiang University School of Medicine Yiwu 322000 China
Liuhong Wang
Department of Radiology,The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China
Yeting Hu
Department of Colorectal Surgery, Second Affiliated Hospital of Zhejiang University School of Medicine & Key Laboratory of Cancer Prevention and Intervention & Center for Medical Research and Innovation in Digestive System Tumors, Ministry of Education, Hangzhou, China
Hanguang Hu
Department of Medical Oncology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Haiting Xie
Department of Colorectal Surgery and Oncology (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), Hangzhou, China
Xinyi Zhou
Kefeng Ding