이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

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.

연구 개요

상태

모병

정황

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (추정된)

122

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Jiangsu
      • Nanjing, Jiangsu, 중국, 210000
        • 모병
        • Jiangsu Province Hospital
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: Short-course standard-dose radiotherapy, IL-2 and Sintilimab Combined with CAPOX
Enhanced immuno-chemotherapy cocktail.
A short-course radiotherapy (SCRT, 25Gy/5f)
실험적: Short-course low-dose radiotherapy, IL-2 and Sintilimab Combined with CAPOX
Enhanced immuno-chemotherapy cocktail.
A short-course radiotherapy (SCRT, 10Gy/5f)

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Complete remission
기간: Two years
Complete remission rate defined as the sum of pathological complete remission (pCR) and clinical complete remission (cCR)
Two years

2차 결과 측정

결과 측정
측정값 설명
기간
Event-free survival (EFS)
기간: 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
기간: 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
기간: Three years
Overall survival (OS), defined as the time from treatment initiation to death from any cause
Three years
Locoregional recurrence rate
기간: Three years
Locoregional recurrence rate assessed by clinical, radiologic, and/or pathologic evaluation
Three years
Distant metastasis rate
기간: 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
기간: 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)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 20일

기본 완료 (추정된)

2028년 12월 31일

연구 완료 (추정된)

2030년 12월 31일

연구 등록 날짜

최초 제출

2025년 9월 15일

QC 기준을 충족하는 최초 제출

2026년 6월 9일

처음 게시됨 (실제)

2026년 6월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 9일

마지막으로 확인됨

2026년 3월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • PRSYM20260325

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .