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Different-Dose SCRT Plus CAPOX, PD-1 Blockade and IL-2 in LARC (PRIDE-02)

Different-Dose Short-Course Radiotherapy Plus CAPOX, Anti-PD-1 Antibody and Interleukin-2 for Locally Advanced Rectal Cancer: A Single-Centre, Prospective, Randomised Phase II Trial

This prospective, randomized phase II trial is designed to evaluate whether low-dose short-course radiotherapy differs from common-dose short-course radiotherapy in terms of efficacy when both regimens are sequentially combined with CAPOX, a PD-1 monoclonal antibody, and interleukin-2 (IL-2) in patients with locally advanced rectal cancer. The study is based on findings from our previous single-center, single-arm PRIDE01 study, in which neoadjuvant short-course radiotherapy followed by systemic chemoimmunotherapy and IL-2 demonstrated encouraging antitumor activity relative to historical short-course radiotherapy-based approaches. The current trial aims to provide more robust clinical evidence regarding the potential role of low-dose radiotherapy combined with IL-2 as a sensitization strategy in multimodal neoadjuvant therapy. By comparing complete response rates between the two radiotherapy dose levels, this study may help define an optimized neoadjuvant approach and support future organ-preservation strategies for patients with locally advanced rectal cancer.

研究概览

详细说明

Standard multimodality treatment, including neoadjuvant chemoradiotherapy or total neoadjuvant therapy followed by total mesorectal excision, has improved LARC control and radical resection rates. However, several important clinical challenges remain, including suboptimal complete response rates, impaired sphincter and organ preservation, treatment-related toxicity, distant metastasis, and limited improvement in long-term survival for some patients. Although total neoadjuvant therapy has further improved systemic disease control by delivering chemotherapy and radiation therapy before surgery, the optimal intensity and sequencing of radiation therapy, chemotherapy, and immunotherapy remain to be defined.

Immune checkpoint blockade (ICB) has transformed the treatment landscape of colorectal cancer with deficient mismatch repair or microsatellite instability-high disease. However, this subgroup accounts for only a small proportion of rectal cancers, while the majority of patients have proficient mismatch repair or microsatellite-stable tumors and derive limited benefit from single-agent PD-1 or PD-L1 inhibition. Immune resistance in microsatellite-stable colorectal cancer is closely associated with insufficient effector T-cell infiltration, T-cell dysfunction or exhaustion, and an immunosuppressive tumor microenvironment. Therefore, strategies that enhance tumor antigen release, promote immune-cell infiltration, reverse local immunosuppression, and restore cytotoxic T-cell function may improve the efficacy of immunotherapy in locally advanced rectal cancer.

Radiation therapy can induce immunogenic tumor-cell death, increase antigen presentation, remodel the tumor microenvironment, and promote immune-cell recruitment. Short-course radiation therapy is an established neoadjuvant radiation strategy for locally advanced rectal cancer and offers advantages including a shorter treatment duration and greater feasibility for integration with systemic therapy. In addition, oxaliplatin-based chemotherapy such as CAPOX may contribute to tumor-cell killing and immune modulation. Early clinical studies combining neoadjuvant chemoradiotherapy or short-course radiation therapy with PD-1 blockade have shown encouraging pathological complete response rates in patients with proficient mismatch repair or microsatellite-stable locally advanced rectal cancer, supporting further investigation of radiation-based immunomodulatory strategies.

Interleukin-2 is a key cytokine involved in T-cell proliferation, cytotoxic T-lymphocyte activation, natural killer cell function, and antitumor immunity. Although high-dose IL-2 has historically been limited by substantial toxicity, low-dose or modified IL-2-based approaches may enhance antitumor immune responses with improved tolerability. Preclinical and translational evidence suggests that IL-2 may synergize with PD-1 blockade by expanding activated effector T cells and supporting reinvigoration of exhausted T-cell populations. When integrated with radiation therapy, IL-2 may further amplify antitumor immunity by promoting immune-cell activation in the context of increased antigen release and local inflammatory priming.

Our previous single-center, single-arm PRIDE-01 study evaluated neoadjuvant short-course radiation therapy followed by CAPOX, PD-1 blockade, and IL-2 in patients with locally advanced rectal cancer and showed encouraging antitumor activity and complete response outcomes compared with historical short-course radiation therapy-based approaches. These findings provide the clinical rationale for further evaluation of this multimodal neoadjuvant strategy in a prospective randomized setting.

This single-center, prospective, randomized, open-label phase II trial is designed to compare low-dose versus standard-dose short-course radiation therapy, each followed by CAPOX, a PD-1 monoclonal antibody, and IL-2, in patients with locally advanced rectal cancer. Eligible patients will be randomly assigned to receive either low-dose short-course radiation therapy or standard-dose short-course radiation therapy, followed by sequential systemic therapy consisting of CAPOX, PD-1 blockade, and IL-2. The study aims to determine whether low-dose short-course radiation therapy combined with IL-2-containing chemoimmunotherapy can achieve comparable or favorable complete response outcomes while potentially reducing radiation-related toxicity.

The primary objective is to compare complete response rates between the two treatment groups, including pathological complete response in patients undergoing surgery and clinical complete response in patients managed with a watch-and-wait strategy. Secondary objectives include evaluation of tumor response, organ preservation, sphincter preservation, disease-free survival, event-free survival, overall survival, surgical outcomes, treatment compliance, and safety. Exploratory translational analyses will assess dynamic changes in peripheral immune-cell subsets, cytokine profiles, circulating biomarkers, tumor immune microenvironment features, and their associations with treatment response.

By comparing different doses of short-course radiation therapy within the same CAPOX, PD-1 blockade, and IL-2-containing neoadjuvant framework, this trial seeks to generate higher-level evidence for an optimized immunomodulatory neoadjuvant strategy in locally advanced rectal cancer. The results may help define whether low-dose radiation therapy combined with IL-2 can serve as a sensitizing approach to enhance response while supporting future organ-preserving treatment strategies.

研究类型

介入性

注册 (估计的)

122

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Jiangsu
      • Nanjing、Jiangsu、中国、210000
        • 招聘中
        • Jiangsu Province Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Male and female patients aged 18 to 70 years.
  2. Histologically confirmed rectal adenocarcinoma with the distal margin of the tumor located within 12 cm of the anal verge.
  3. MRI-based clinical stage T3-T4 or any T with lymph node-positive (N+) disease.
  4. Adequate hematologic, hepatic, and renal function defined as: absolute neutrophil count >=1.5 x 10^9/L; platelet count >=75 x 10^9/L; serum total bilirubin <=1.5 x upper normal limit (UNL); aspartate aminotransferase <=2.5 x UNL; alanine aminotransferase <=2.5 x UNL; serum creatinine <=1.5 x UNL.
  5. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.

Exclusion Criteria:

  1. Metastatic disease (Stage IV).
  2. Recurrent rectal cancer.
  3. Concurrent active bleeding, perforation, or other complicated conditions requiring emergency surgery.
  4. Prior systemic anticancer therapy for rectal cancer.
  5. Presence of another non-colorectal neoplastic disease at the same time.
  6. Patients with any active autoimmune disease or a history of autoimmune disease requiring steroids or immunomodulatory therapy.
  7. Patients with interstitial lung disease, non-infectious pneumonitis, or uncontrolled systemic diseases (e.g., diabetes mellitus, hypertension, pulmonary fibrosis, and acute pneumonitis).
  8. Any unresolved grade >=2 toxicity (according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0) resulting from previous treatment, except for anemia, alopecia, and skin hyperpigmentation.
  9. Prior treatment with anti-programmed death-1 (PD-1)/PD-L1 antibody or anti-cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody.
  10. Pregnant or breastfeeding women.
  11. Known or tested positive for human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS).
  12. Known or suspected history of allergy to any of the relevant drugs used in the study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Short-course standard-dose radiotherapy, IL-2 and Sintilimab Combined with CAPOX
Enhanced immuno-chemotherapy cocktail.
A short-course radiotherapy (SCRT, 25Gy/5f)
实验性的:Short-course low-dose radiotherapy, IL-2 and Sintilimab Combined with CAPOX
Enhanced immuno-chemotherapy cocktail.
A short-course radiotherapy (SCRT, 10Gy/5f)

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Complete remission
大体时间:Two years
Complete remission rate defined as the sum of pathological complete remission (pCR) and clinical complete remission (cCR)
Two years

次要结果测量

结果测量
措施说明
大体时间
Event-free survival (EFS)
大体时间:Three years
Event-free survival (EFS), defined as the time from initiation of radiotherapy to the first occurrence of disease progression, locoregional recurrence, distant metastasis, or death from any cause.
Three years
Disease-free survival rate
大体时间:Three years
Disease-free survival (DFS), defined as the time from the date of surgery to the first documented locoregional recurrence, distant metastasis, or death from any cause.
Three years
Overall survival rate
大体时间:Three years
Overall survival (OS), defined as the time from treatment initiation to death from any cause
Three years
Locoregional recurrence rate
大体时间:Three years
Locoregional recurrence rate assessed by clinical, radiologic, and/or pathologic evaluation
Three years
Distant metastasis rate
大体时间:Three years
Distant metastasis rate assessed by imaging and/or pathologic confirmation
Three years
Acute toxicity incidence assessed by CTCAE v5.0 during radiotherapy, chemotherapy, and immunotherapy
大体时间:From enrollment to the end of treatment, up to 6 months
Incidence of acute toxicities during radiotherapy, chemotherapy, and/or immunotherapy assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
From enrollment to the end of treatment, up to 6 months
Quality of life (QoL)
大体时间:Up to 10 years
Quality of life assessed by the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)
Up to 10 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月20日

初级完成 (估计的)

2028年12月31日

研究完成 (估计的)

2030年12月31日

研究注册日期

首次提交

2025年9月15日

首先提交符合 QC 标准的

2026年6月9日

首次发布 (实际的)

2026年6月15日

研究记录更新

最后更新发布 (实际的)

2026年6月15日

上次提交的符合 QC 标准的更新

2026年6月9日

最后验证

2026年3月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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