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

2026년 5월 7일 업데이트: 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.

연구 개요

연구 유형

중재적

등록 (추정된)

10

단계

  • 초기 1단계

연락처 및 위치

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연구 연락처

연구 장소

      • Xi'an, 중국
        • 모병
        • Xijing Hospital, Air Force Medical University Xi'an, Shaanxi, China
        • 연락하다:
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Systolic blood pressure
기간: through study completion, an average of 3 months
Systolic blood pressure
through study completion, an average of 3 months
respiratory rate
기간: through study completion, an average of 3 months
respiratory rate
through study completion, an average of 3 months
body temperature
기간: through study completion, an average of 3 months
body temperature
through study completion, an average of 3 months
heart rate
기간: through study completion, an average of 3 months
heart rate
through study completion, an average of 3 months
Hemoglobin concentration
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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)

2차 결과 측정

결과 측정
측정값 설명
기간
Lymph node target lesion short-axis diameter
기간: 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
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 5월 1일

기본 완료 (추정된)

2026년 12월 1일

연구 완료 (추정된)

2027년 6월 1일

연구 등록 날짜

최초 제출

2025년 11월 18일

QC 기준을 충족하는 최초 제출

2026년 5월 7일

처음 게시됨 (실제)

2026년 5월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 7일

마지막으로 확인됨

2025년 10월 1일

추가 정보

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아니요

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아니

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