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).
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (16)
Jianhong Peng
Chi Zhou
State Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry
Miaozhen Qiu
Sun Yat-sen University Cancer Center, Guangzhou, China
Weihao Li
Qiaoxuan Wang
MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering Zhejiang University Hangzhou 310058 China
Min Liu
Ting-Ting Quan
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
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
Li-Ren Li
Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou, China
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
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
Song Wang
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
Zhizhong Pan
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