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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.

調査の概要

状態

まだ募集していません

条件

研究の種類

介入

入学 (推定)

33

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~75年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

他の名前:
  • 放射線治療

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate (ORR)
時間枠: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.

二次結果の測定

結果測定
メジャーの説明
時間枠
3-year Overall survival rate
時間枠: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
時間枠: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)
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Zhen Zhang, MD、Fudan University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月31日

一次修了 (推定)

2028年12月31日

研究の完了 (推定)

2028年12月31日

試験登録日

最初に提出

2026年10月28日

QC基準を満たした最初の提出物

2026年11月11日

最初の投稿 (実際)

2026年11月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月13日

QC基準を満たした最後の更新が送信されました

2026年11月11日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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