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Efficacy and Safety of Neoadjuvant Cadonilimab Plus High-Dose Recombinant Human Interferon α1b in Stage III/IV Melanoma.

7 mai 2026 mis à jour par: Xijing Hospital

Efficacy and Safety of Neoadjuvant Cadonilimab Plus High-Dose Recombinant Human Interferon α1b in Stage III/IV Melanoma: A Single-Center, Open-Label, Phase Ib Trial

  1. Primary Objective

    To evaluate the efficacy and safety of cadonilimab in combination with high-dose recombinant human interferon α1b injection as neoadjuvant therapy in patients with stage III/IV melanoma. Assessments include:

    Target lesion response (complete response [CR], partial response [PR], stable disease [SD], progressive disease [PD]) Objective response rate (ORR) Pathological response rate (pathological complete response [pCR], near pCR, pathological partial response [pPR], pathological non-response [pNR]) Incidence of all adverse events (AEs) and serious adverse events (SAEs) Changes from baseline in physical examinations, vital signs, and laboratory test results.

  2. Exploratory Objectives To investigate the correlation between treatment efficacy/patient outcomes and:PD-L1 expression in tumor tissue CD8+ T-cell infiltration Tumor mutational burden (TMB).
  3. Study Significance To conduct a preliminary exploration in support of future multicenter clinical studies.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

10

Phase

  • Première phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

      • Xi'an, Chine
        • Recrutement
        • Xijing Hospital, Air Force Medical University Xi'an, Shaanxi, China
        • Contact:
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Voluntarily participate in this trial, sign the informed consent form, and be between 18 and 75 years of age, regardless of gender.
  • Patients with histopathologically or cytologically confirmed stage III or resectable stage IV malignant melanoma.

    • Stage III is defined as the presence of at least one clinically accessible lymph node metastasis or in-transit metastasis.
    • Resectable stage IV is defined as a single distant metastasis, excluding brain metastases or any other metastases that cannot be completely surgically resected.
    • Mucosal or ocular melanomas are excluded.
    • Melanomas of unknown primary origin are excluded.
  • Have not received treatment with PD-1, PD-L1, or PD-L2 antibodies, anti-CTLA4 antibodies, interferon (IFN), targeted therapy, radiotherapy, or systemic chemotherapy within the past month.
  • Have an expected survival period of ≥ 6 months.
  • Have at least one measurable lesion according to RECIST version 1.1.
  • Have an ECOG performance status score of 0 or 1.
  • Have adequate organ function, as indicated by the following laboratory values (within 4 weeks prior to the start of study treatment):

    1. Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L
    2. Platelets ≥ 100 × 10⁹/L
    3. Hemoglobin ≥ 90 g/L (no blood transfusion within 14 days prior to enrollment)
    4. Serum creatinine ≤ 1.5 × upper limit of normal (ULN)
    5. Serum total bilirubin ≤ 1.5 × ULN
    6. AST (SGOT) and ALT (SGPT) ≤ 2.5 × ULN or ≤ 5 × ULN (for patients with liver metastases)
    7. Prothrombin time (PT)/International Normalized Ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (unless the subject is receiving anticoagulant therapy, in which case PT or aPTT must be within the therapeutic range intended for the anticoagulant used).

      8.Female patients of childbearing potential must have a negative urine or serum pregnancy test within 7 days prior to receiving the first dose of the study drug.

      9.Female patients enrolled in the study must be willing to use appropriate contraception methods until 12 months after the last dose of the study drug.

      Exclusion Criteria:

  • The patient is currently participating, or has participated within 4 weeks prior to the first dose of the study drug, in another interventional clinical trial of drugs or medical devices.
  • The patient has received any anti-tumor therapy within the past month, including but not limited to chemotherapy, radiotherapy, immunotherapy (e.g., anti-PD-1, anti-PD-L1, or anti-CTLA-4 antibodies, or any other antibody targeting T-cell co-regulatory pathways), etc.
  • The patient has received systemic steroid therapy (>10 mg/kg prednisone or equivalent) within two weeks prior to the first dose, or any other form of immunosuppressive medication.
  • The patient has a known history of hematologic malignancy, primary brain tumor, sarcoma, or another primary solid tumor, unless the patient has been cured and has had no evidence of recurrence for 5 years. Exceptions include cured basal cell carcinoma of the skin and carcinoma in situ of the cervix.
  • The patient has known central nervous system metastases and/or carcinomatous meningitis.
  • The patient has a history of severe hypersensitivity to another monoclonal antibody (mAb) therapy.
  • The patient has had an active autoimmune disease requiring systemic treatment (e.g., with corticosteroids or immunosuppressive drugs) within the past 2 years, and related replacement therapies (e.g., thyroxine, insulin, or physiologic corticosteroid replacement for renal or pituitary insufficiency). Exceptions include patients with vitiligo, type I diabetes, childhood asthma/atopy.
  • Other severe, uncontrolled concomitant diseases that may affect protocol compliance or interpretation of results, including active opportunistic or advanced (severe) infections; uncontrolled diabetes; cardiovascular disease (e.g., Class III or IV heart failure as defined by the New York Heart Association classification, second-degree or greater heart block, myocardial infarction within the past 6 months, unstable arrhythmias or unstable angina, cerebral infarction within 3 months); pulmonary disease (interstitial lung disease, obstructive pulmonary disease, history of symptomatic bronchospasm); HIV positivity; HCV positivity; HBsAg or HBcAb positivity with detectable HBV DNA (quantitative limit ≥500 IU/mL); or a documented history of tuberculosis.
  • The patient has received a live vaccine within 4 weeks prior to the first dose; hematopoietic growth factors (e.g., colony-stimulating factors, erythropoietin) within 2 weeks prior to treatment initiation; or major surgical procedures (excluding diagnostic surgery) within 2 weeks prior to treatment initiation.
  • The patient has a known psychiatric or substance use disorder that would interfere with cooperation with trial requirements.
  • The patient is pregnant or breastfeeding, or plans to become pregnant or father a child during the study period.
  • Any other severe, acute, or chronic medical or laboratory abnormality that, in the investigator's judgment, could increase the risk associated with study participation or could interfere with the interpretation of study results.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Cadonilimab and Recombinant Human Interferon α1b Combination Therapy Arm

Cadonilimab: 10 mg/kg administered via intravenous infusion every 3 weeks. The neoadjuvant treatment course consists of 4 cycles, totaling 3 months.

Recombinant Human Interferon α1b Injection: 600 μg administered subcutaneously every other day. The neoadjuvant treatment course is 3 months. If intolerable (e.g., occurrence of Grade 3 or 4 adverse reactions or other qualifying events), the dose should be reduced to 300 μg subcutaneously every other day.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Systolic blood pressure
Délai: through study completion, an average of 3 months
Systolic blood pressure
through study completion, an average of 3 months
respiratory rate
Délai: through study completion, an average of 3 months
respiratory rate
through study completion, an average of 3 months
body temperature
Délai: through study completion, an average of 3 months
body temperature
through study completion, an average of 3 months
heart rate
Délai: through study completion, an average of 3 months
heart rate
through study completion, an average of 3 months
Hemoglobin concentration
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
Hemoglobin concentration assessed by complete blood count
Baseline and every 3 weeks through study completion (up to 3 months)
Left ventricular ejection fraction (LVEF)
Délai: Baseline and every 8 weeks through study completion (up to 3 months)
LVEF assessed by echocardiography
Baseline and every 8 weeks through study completion (up to 3 months)
White blood cell count
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
White blood cell count assessed by complete blood count
Baseline and every 3 weeks through study completion (up to 3 months)
Platelet count
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
Platelet count assessed by complete blood count
Baseline and every 3 weeks through study completion (up to 3 months)
Alanine aminotransferase (ALT) level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
ALT level measured from clinical biochemistry panel
Baseline and every 3 weeks through study completion (up to 3 months)
Aspartate aminotransferase (AST) level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
AST level measured from clinical biochemistry panel
Baseline and every 3 weeks through study completion (up to 3 months)
Creatinine level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
Creatinine level measured from clinical biochemistry panel
Baseline and every 3 weeks through study completion (up to 3 months)
Blood glucose level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
Blood glucose level measured from clinical biochemistry panel (fasting or as specified in protocol)
Baseline and every 3 weeks through study completion (up to 3 months)
Lactate dehydrogenase (LDH) level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
LDH measured from clinical biochemistry panel
Baseline and every 3 weeks through study completion (up to 3 months)
Triiodothyronine (T3) level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
T3 level measured from blood sample.
Baseline and every 3 weeks through study completion (up to 3 months)
Thyroid-stimulating hormone (TSH) level
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
TSH levell measured from blood sample.
Baseline and every 3 weeks through study completion (up to 3 months)
Left ventricular end-diastolic diameter (LVEDD)
Délai: Baseline and every 8 weeks through study completion (up to 3 months)
LVEDD assessed by echocardiography
Baseline and every 8 weeks through study completion (up to 3 months)
Cardiac output
Délai: Baseline and every 8 weeks through study completion (up to 3 months)
Cardiac output estimated by echocardiography
Baseline and every 8 weeks through study completion (up to 3 months)
PR interval
Délai: Baseline and every 8 weeks through study completion (up to 3 months)
PR interval assessed by 12-lead electrocardiography
Baseline and every 8 weeks through study completion (up to 3 months)
QRS duration
Délai: Baseline and every 8 weeks through study completion (up to 3 months)
QRS duration assessed by 12-lead electrocardiography
Baseline and every 8 weeks through study completion (up to 3 months)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Lymph node target lesion short-axis diameter
Délai: Baseline and every 3 weeks through study completion (up to 3 months)
Short axis diameter of target lesions in lymph nodes, assessed by imaging (e. g., utrasonography, CT,or MRI per schedule of assessments
Baseline and every 3 weeks through study completion (up to 3 months)
Percentage of residual viable tumor cells in lymph nodes
Délai: Perioperative (after 3 months of treatment)
Proportion of viable tumor cells in lymph node tissue assessed by histopathological analysis.
Perioperative (after 3 months of treatment)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 mai 2025

Achèvement primaire (Estimé)

1 décembre 2026

Achèvement de l'étude (Estimé)

1 juin 2027

Dates d'inscription aux études

Première soumission

18 novembre 2025

Première soumission répondant aux critères de contrôle qualité

7 mai 2026

Première publication (Réel)

14 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

14 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 mai 2026

Dernière vérification

1 octobre 2025

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

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