Short-course radiotherapy followed by sintilimab and CAPOX as total neoadjuvant treatment in locally advanced rectal cancer: A prospective, randomized controlled trial (SPRING-01).

F Feng Tian H Honghai Dai (Tumor Research and Therapy Center, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China) D Dan Sha (Department of Minimally Invasive Treatment of Cancer, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China) H Haiyan Jing (Department of Pathology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China) L Leping Li (State Key Laboratory of Crystal Materials Tianjin Key Laboratory of Functional Crystal Materials School of Integrated Circuit Science and Engineering Tianjin University of Technology Tianjin China) C Changqing Jing

Abstract

3519 Background: Neoadjuvant short-course radiotherapy (SCRT) combined with chemotherapy as total neoadjuvant therapy (TNT) increases the pathological complete response (pCR) rate for locally advanced rectal cancer (LARC). The potential synergistic effects of combining radiotherapy and immunotherapy might benefit patients with LARC. This study aimed to compare the efficacy and safety of SCRT followed by 6 cycles of CAPOX chemotherapy with or without immunotherapy as TNT in LARC patients. Methods: In this randomized controlled trial, patients with T3-4, N+, EMVI(+), MRF(+) or lateral lymph node(+) rectal adenocarcinoma were randomly assigned to receive SCRT followed by 6 cycles of CAPOX chemotherapy with or without sintilimab. Total mesorectal excision (TME) was performed 2-3 weeks after the completion of TNT. The primary study endpoint was the pCR rate. Results: In this randomized controlled trial, patients with T3-4, N+, EMVI(+), MRF(+) or lateral lymph node(+) rectal adenocarcinoma were randomly assigned to receive SCRT followed by 6 cycles of CAPOX chemotherapy with or without sintilimab. Total mesorectal excision (TME) was performed 2-3 weeks after the completion of TNT. The primary study endpoint was the pCR rate. Conclusions: In LARC patients, SCRT combined with sintilimab and CAPOX as a TNT significantly increases the pCR rate while maintaining manageable safety in patients with LARC. SCRT followed by sintilimab and CAPOX can be recommended as a superior neoadjuvant treatment option for these patients. Clinical trial information: ChiCTR2100052288 . The efficacy of SIN+CAPOX and surgical and pathological results. Intention-to-treat (ITT) population SIN+CAPOX (N = 49) CAPOX (N = 49) Pathological complete response (ypT0N0, ITT population) — no. (%) 29(59.2) 16(32.7) (% [95% CI]) (45.4, 72.9) (19.5, 45.8) Complete response 30(61.2) 16(32.7) Surgical population SIN+CAPOX (N = 45) CAPOX (N = 44) Tumor regression grading (AJCC 8th edition) — no. (%) 0 29(64.4) 16(36.4) 1 7(15.6) 7(15.9) 2 5(11.1) 13(29.5) 3 4(8.9) 8(18.2) Abbreviations: IQR, interquartile range; N, regional nodal category; T, primary tumor category; yp, pathologic.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 3519-3519
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (6)

F

Feng Tian

H

Honghai Dai

Tumor Research and Therapy Center, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China

D

Dan Sha

Department of Minimally Invasive Treatment of Cancer, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China

H

Haiyan Jing

Department of Pathology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China

L

Leping Li

State Key Laboratory of Crystal Materials Tianjin Key Laboratory of Functional Crystal Materials School of Integrated Circuit Science and Engineering Tianjin University of Technology Tianjin China

C

Changqing Jing