此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Radiotherapy Plus Putelimab and Vibostolimab for Advanced Anal Squamous Cell Carcinoma

2026年11月11日 更新者:Zhen Zhang、Fudan University

A Single-Arm, Multicenter, Phase II Clinical Study to Evaluate the Efficacy and Safety of Radiotherapy Combined With Putelimab and Vibostolimab as Second-Line Therapy in Patients With Advanced Anal Squamous Cell Carcinoma

Anal squamous cell carcinoma (ASCC) is a rare malignancy, accounting for only 2.5% of gastrointestinal tumours. For patients with early-stage disease , concurrent chemoradiotherapy (fluorouracil/mitomycin combined with radiotherapy) achieves a 5-year survival rate of 60%-80%, whereas the prognosis deteriorates markedly for patients with advanced and metastatic disease. More effective therapeutic regimens are therefore urgently needed for advanced patients to prolong survival. EGFR positivity is frequently observed in head and neck squamous cell carcinoma, and anti-EGFR targeted therapy as well as immunotherapy have demonstrated favourable efficacy in advanced head and neck squamous cell carcinoma. This study aims to explore the efficacy of the PD-1 inhibitor putelimab in combination with the EGFR-targeted ADC MRG003 as second-line treatment for patients with advanced anal squamous cell carcinoma.

研究概览

地位

尚未招聘

条件

研究类型

介入性

注册 (估计的)

33

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

研究联系人备份

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

18年 至 75年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Has provided written informed consent for the clinical study and biobank informed consent prior to initiation of any study-related procedures;

  • Male or female patients aged between 18 and 75 years inclusive;

  • Histologically confirmed squamous cell carcinoma of the anal canal (SCCAC);

  • Patients with unresectable or metastatic disease who have experienced disease progression during or after first-line systemic therapy. For patients with locally limited disease, curative-intent radiotherapy combined with radiosensitising chemotherapy is considered first-line therapy; patients with disease progression during treatment or within 6 months after completion of such treatment are also eligible;

  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1;

  • Expected survival of ≥ 12 months;

  • Adequate organ function, with participants meeting all of the following laboratory criteria:

    1. Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L, without granulocyte colony-stimulating factor (G-CSF) administration in the preceding 14 days;
    2. Platelet count ≥ 100 × 10⁹/L, without blood transfusion in the preceding 14 days;
    3. Haemoglobin > 9 g/dL, without blood transfusion or erythropoietin administration in the preceding 14 days;
    4. Total bilirubin ≤ 1.5 × upper limit of normal (ULN). Participants with total bilirubin > 1.5 × ULN but direct bilirubin ≤ ULN are also eligible;
    5. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN;
    6. Serum creatinine ≤ 1.5 × ULN, or creatinine clearance (calculated using the Cockcroft-Gault formula) ≥ 60 mL/min;
    7. Adequate coagulation function, defined as international normalised ratio (INR) or prothrombin time (PT) ≤ 1.5 × ULN;
    8. No clinically significant thyroid dysfunction as assessed by the investigator;
    9. Cardiac function: New York Heart Association (NYHA) functional class < III; left ventricular ejection fraction (LVEF) ≥ 50%;
  • Agrees to provide adequate archived tumour tissue specimens from prior sampling or agrees to undergo biopsy to collect tumour tissue for correlative biomarker testing;

  • Has at least one lesion at baseline that has not been previously irradiated and qualifies as a target lesion (TL) per RECIST version 1.1. Tumour assessment by imaging must be performed within 28 days prior to study treatment initiation;

  • For female participants of childbearing potential: a negative urine or serum pregnancy test obtained within 3 days before the first dose of study drug (Cycle 1 Day 1). If the urine pregnancy test cannot be confirmed negative, a serum pregnancy test is required. Non-childbearing potential is defined as post-menopausal status for at least 1 year, or status following surgical sterilisation or hysterectomy;

  • All participants (male and female) with reproductive potential must use contraceptive methods with an annual failure rate of <1% throughout the treatment period and for 120 days after the last dose of study drug (or 180 days after the last dose of chemotherapy, as applicable).

Exclusion Criteria:

  • Diagnosis of another malignancy other than squamous cell carcinoma of the anal canal within 5 years prior to the first dose (excluding radically treated basal cell carcinoma of the skin, cutaneous squamous cell carcinoma, and/or radically resected carcinoma in situ);
  • Known high risk of tumour obstruction, bleeding and/or perforation demonstrated endoscopically, requiring urgent surgery or stent placement;
  • Currently receiving treatment in an interventional clinical study, or having received other medicinal therapies for gastrointestinal malignancies within 4 weeks before the first dose;
  • Having received systemic treatment with Chinese patent medicines with anti-tumour indications or immunomodulatory agents (including thymopeptides, interferons, interleukins, excluding local administration for control of pleural effusion) within 2 weeks prior to the first dose;
  • History of active autoimmune disease requiring systemic therapy (e.g., disease-modifying agents, glucocorticoids or immunosuppressants) within 2 years before the first dose of study treatment. Replacement therapy (e.g., thyroxine, insulin, or physiological glucocorticoids for adrenal or pituitary insufficiency) is not considered systemic therapy;
  • Receiving systemic glucocorticoid therapy (excluding intranasal, inhaled or other locally administered glucocorticoids) or any other form of immunosuppressive therapy within 7 days before the first study dose.

Note: Physiological doses of glucocorticoids (≤10 mg prednisone per day or equivalent) are permitted.

  • Known history of allogeneic solid organ transplantation (corneal transplantation excluded) or allogeneic haematopoietic stem cell transplantation;
  • Known hypersensitivity to putelimab, chemotherapy agents, platinum compounds used in this study, or any of their excipients;
  • Has not adequately recovered from toxicities and/or complications caused by prior interventions before treatment initiation (i.e., ≤ Grade 1 or return to baseline, excluding fatigue or alopecia);
  • Known history of human immunodeficiency virus (HIV) infection (i.e., positive HIV-1/2 antibody);
  • Untreated active hepatitis B (defined as positive HBsAg together with HBV-DNA copy number above the upper limit of normal of the local laboratory at the study site).

Note: Participants with hepatitis B meeting the following criteria are eligible:

  1. HBV viral load < 1000 copies/mL (200 IU/mL) before the first dose. Participants shall receive anti-HBV prophylaxis throughout chemotherapy in this study to prevent viral reactivation;

  2. For participants with anti-HBc (+), HBsAg (-), anti-HBs (-) and undetectable HBV viral load, prophylactic anti-HBV therapy is not required, but close monitoring for viral reactivation is mandatory.

    • Participants with active HCV infection (positive HCV antibody and HCV-RNA level above the lower limit of detection);
    • Received a live vaccine within 30 days before the first dose (Cycle 1 Day 1). Note: Inactivated injectable seasonal influenza vaccines administered within 30 days prior to the first dose are permitted; intranasal live attenuated influenza vaccines are not allowed.
    • Pregnant or breastfeeding women;
    • Presence of any severe or uncontrolled systemic disease, such as:

(1) Significant, symptomatic and poorly controlled abnormalities in rhythm, conduction or morphology on resting electrocardiogram, including complete left bundle branch block, second-degree or higher atrioventricular block, ventricular arrhythmia or atrial fibrillation; (2) Unstable angina, congestive heart failure, chronic heart failure with New York Heart Association (NYHA) functional class ≥ II; (3) Any arterial thrombosis, embolism or ischaemic event occurring within 6 months before enrolment, such as myocardial infarction, unstable angina, cerebrovascular accident or transient ischaemic attack; (4) Poorly controlled hypertension despite pharmacological treatment; (5) History of non-infectious pneumonitis requiring glucocorticoid therapy within 1 year before the first dose, or currently clinically active interstitial lung disease; (6) Active pulmonary tuberculosis; (7) Active or uncontrolled infection requiring systemic therapy; (8) Clinically active diverticulitis or intra-abdominal abscess; (9) Hepatic diseases such as decompensated liver disease, acute or chronic active hepatitis; (10) Poorly controlled diabetes mellitus; (11) Psychiatric disorder rendering the participant unable to comply with treatment;

  • Presence of gastrointestinal physiological dysfunction or malabsorption syndrome; Any medical history, disease condition, treatment or abnormal laboratory finding that may interfere with study results, prevent the participant from completing the study, or any other condition deemed by the investigator to confer potential risks or render the participant unsuitable for study participation.

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:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:treatment

Radiotherapy is delivered to recurrent or metastatic lesions. Thereafter, the PD-1 inhibitor putelimab in combination with the EGFR-targeted ADC vibostolimab is administered once every 3 weeks until disease progression or intolerable toxicity.

Radiotherapy is delivered to recurrent or metastatic lesions (short-term radiotherapy). Thereafter, the PD-1 inhibitor putelimab (200 mg per dose, intravenous infusion, once every 3 weeks, administered on Day 1.)in combination with the EGFR-targeted ADC vibostolimab (2.0 mg/kg, intravenous infusion, Q3W, D1.)is administered once every 3 weeks until disease progression or intolerable toxicity.

其他名称:
  • 放疗

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
Objective Response Rate (ORR)
大体时间:From enrolment until first documented disease progression, death, subsequent anti-cancer therapy, or loss to follow-up,assessed up to 24 months. Responses require confirmation ≥4 weeks after first documentation.

the proportion of participants achieving a Complete Response (CR) or Partial Response (PR) among all enrolled participants.

From enrolment until first documented disease progression, death, subsequent anti-cancer therapy, or loss to follow-up,assessed up to 24 months. Responses require confirmation ≥4 weeks after first documentation.

次要结果测量

结果测量
措施说明
大体时间
3-year Overall survival rate
大体时间:From enrolment until death from any cause; participants are followed for up to 36 months (3 years).

the proportion of participants alive at 3 years after enrolment.

From enrolment until death from any cause; participants are followed for up to 36 months (3 years).
3-year Disease-Free Survival (DFS) Rate
大体时间:From enrolment until documented disease recurrence, distant metastasis or death from any cause; follow-up up to 36 months.

the proportion of participants who are alive and free from disease recurrence or metastasis at 3 years after enrolment.

From enrolment until documented disease recurrence, distant metastasis or death from any cause; follow-up up to 36 months.
Adverse Events (AEs)
大体时间:From the start of study treatment until 90 days after the last dose of study treatment.

Any untoward medical occurrence in a participant administered the study intervention, which does not necessarily have a causal relationship with the study treatment.

From the start of study treatment until 90 days after the last dose of study treatment.

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。

调查人员

  • 首席研究员:Zhen Zhang, MD、Fudan University

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 (估计的)

2026年10月31日

初级完成 (估计的)

2028年12月31日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年10月28日

首先提交符合 QC 标准的

2026年11月11日

首次发布 (实际的)

2026年11月13日

研究记录更新

最后更新发布 (实际的)

2026年11月13日

上次提交的符合 QC 标准的更新

2026年11月11日

最后验证

2026年11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)?

未定

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.

订阅