- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07586904
Efficacy and Safety of Neoadjuvant Cadonilimab Plus High-Dose Recombinant Human Interferon α1b in Stage III/IV Melanoma.
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
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.
- 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).
- Study Significance To conduct a preliminary exploration in support of future multicenter clinical studies.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Première phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Weinan Guo
- Numéro de téléphone: + 86-29-84775406
- E-mail: guown@fmmu.edu.cn
Lieux d'étude
-
-
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Xi'an, Chine
- Recrutement
- Xijing Hospital, Air Force Medical University Xi'an, Shaanxi, China
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Contact:
- Weinan Guo
- Numéro de téléphone: +862984775406
- E-mail: guown@fmmu.edu.cn
-
Contact:
- E-mail: guown@fmmu.edu.cn
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
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):
- Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L
- Platelets ≥ 100 × 10⁹/L
- Hemoglobin ≥ 90 g/L (no blood transfusion within 14 days prior to enrollment)
- Serum creatinine ≤ 1.5 × upper limit of normal (ULN)
- Serum total bilirubin ≤ 1.5 × ULN
- AST (SGOT) and ALT (SGPT) ≤ 2.5 × ULN or ≤ 5 × ULN (for patients with liver metastases)
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
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 |
|---|---|
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Expérimental: Cadonilimab and Recombinant Human Interferon α1b Combination Therapy Arm
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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
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- XJPF-LCY-V2025112
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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