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Radiotherapy Plus Putelimab and Vibostolimab for Advanced Anal Squamous Cell Carcinoma

11. November 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

33

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 75 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.

Andere Namen:
  • Strahlentherapie

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Objective Response Rate (ORR)
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
3-year Overall survival rate
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Ermittler

  • Hauptermittler: Zhen Zhang, MD, Fudan University

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

31. Oktober 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2028

Studienabschluss (Geschätzt)

31. Dezember 2028

Studienanmeldedaten

Zuerst eingereicht

28. Oktober 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. November 2026

Zuerst gepostet (Tatsächlich)

13. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

13. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • FDRT-2026-177-5029

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .