Phase II trial of anti-PD-1 monoclonal antibody and FOLFOXIRI combined with long-course radiotherapy as the total neoadjuvant treatment for proficient, mismatch repair, locally advanced low rectal cancer (PANFORTE).

J Jianhong Peng C Chi Zhou (State Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry) M Miaozhen Qiu (Sun Yat-sen University Cancer Center, Guangzhou, China) W Weihao Li Q Qiaoxuan Wang (MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering Zhejiang University Hangzhou 310058 China) M Min Liu T Ting-Ting Quan Z Zhen-Hai Lu (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China) X Xiao Jun Wu (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China) L Li-Ren Li (Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou, China) D Da Kang (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China) Y Yuanbin Liao (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China) S Song Wang P Pei-Rong Ding (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China) Z Zhizhong Pan J Jun-Zhong Lin (Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China)

Abstract

3621 Background: The current standard treatment for locally advanced low rectal cancer (LALRC) achieves a complete response (CR) rate of only 20–30%. Consequently, radical surgery frequently results in the loss of anal organs, severely affecting patients’ quality of life. Therefore, there is an urgent clinical need to identify novel strategies that can maximize tumor regression and preserve anal function. Recent trials have demonstrated radiotherapy showed a distinctive synergistic anti-tumor effect with immune checkpoint inhibitors. Therefore, this study aims to assess the efficacy and safety of an immunotherapy-based total neoadjuvant therapy (TNT) in patients with proficient mismatch repair (pMMR) LALRC. Methods: Eligible patients (pts) on this investigator-initiated phase II study had pMMR LALRC with ECOG performance status ≤ 1 and an inferior tumor margin distance from the anal verge (DAV) ≤ 5 cm. Eligible patients receive 4 cycles of FOLFOXIRI plus serplulimab (200 mg). Subsequently, they undergo long-course radiotherapy combination with capecitabine and 2 cycles of serplulimab (200 mg), followed by another 4 cycles of FOLFOXIRI and serplulimab (200 mg). The primary endpoint is CR rate with the sum of clinical complete response (cCR) and pathological complete response (pCR). Secondary endpoints include sphincter preservation rate and safety. Results: Between November 2023 and April 2025, 53 patients were enrolled with male percentage 62.3%, median age of 55 years (Range, 28–72) and median DAV of 3 cm (Range, 0.4–5.0). 92.5% (49/53) of patients completed the full TNT regimen. Among the 51 patients eligible for endpoint assessments, the overall CR rate was 68.6% (35/51), and the sphincter preservation rate was 94.1% (48/51). 31 (60.8%) patients achieving cCR opted for a watch-and-wait approach, whereas 20 patients underwent surgery. 20% (4/20) achieved pCR and 70% (17/20) had a tumor regression grade (TRG) of 2. The most common AEs was neutropenia (grade 3-4, 66.0% [35/53]). Other grade 3-4 AEs included leukopenia (32.1%, 17/53), lymphopenia (20.8%, 11/53), and thrombocytopenia (18.9%, 10/53). Immune-related 3-4 AEs comprised myocarditis (1.9%,1/53) and elevated transaminases (1.9%,1/53). Conclusions: Our study indicates that this TNT regimen significantly enhances CR rates and anal preservation in pMMR LALRC compared to historical benchmarks, with an acceptable safety profile. These findings suggest that this new approach may be an alternative treatment option for LALRC patients who strongly desire anal preservation. Clinical trial information: NCT06099951 .

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 3621-3621
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (16)

J

Jianhong Peng

C

Chi Zhou

State Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry

M

Miaozhen Qiu

Sun Yat-sen University Cancer Center, Guangzhou, China

W

Weihao Li

Q

Qiaoxuan Wang

MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering Zhejiang University Hangzhou 310058 China

M

Min Liu

T

Ting-Ting Quan

Z

Zhen-Hai Lu

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China

X

Xiao Jun Wu

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China

L

Li-Ren Li

Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou, China

D

Da Kang

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China

Y

Yuanbin Liao

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China

S

Song Wang

P

Pei-Rong Ding

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China

Z

Zhizhong Pan

J

Jun-Zhong Lin

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, China