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A Study of QL1706 Combined With OH2 Injection in Perioperative Treatment of Stage III Resectable Acral Melanoma

Efficacy and Safety of Iparomlimab and Tuvonralimab Injection(Anti-PD-1/CTLA-4 Bispecific Antibody) Combined With Recombinant Human GM-CSF Oncolytic HSV-2 (OH2) Injection (Vero Cells) for Perioperative Treatment of Stage III Resectable Acral Melanoma: A Prospective, Randomized, Controlled, Multicenter Clinical Study

This is a prospective, multicenter, open-label, 1:1 randomized phase II trial enrolling 76 patients with AJCC stage III surgically resectable acral melanoma. Arm A receives neoadjuvant combination of intratumoral OH2 oncolytic HSV2 plus IV QL1706 (Iparomlimab and Tuvonralimab Injection) for 6 q2w cycles before radical surgery, followed by stratified QL1706 adjuvant therapy. Arm B undergoes upfront radical surgery followed by single-agent QL1706 adjuvant therapy for up to 1 year. The primary endpoint is 2-year EFS rate. Secondary endpoints include pathologic response, RFS, OS, and overall safety profile. All patients receive regular imaging follow-up up to 5 years post-surgery.

調査の概要

状態

まだ募集していません

条件

介入・治療

研究の種類

介入

入学 (推定)

76

段階

  • フェーズ 4

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:

  1. Voluntarily sign the written informed consent form.
  2. Male or female patients aged ≥18 years and ≤75 years at the time of enrollment.
  3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  4. Histologically and/or cytologically confirmed resectable Stage III acral melanoma (according to the AJCC 8th edition staging system for cutaneous malignant melanoma) with at least one measurable lesion.
  5. Expected survival ≥4 months.
  6. Adequate organ function: a) Hematology (without any blood component or growth factor support within 7 days before the start of study treatment): i. Absolute neutrophil count (ANC) ≥1.5×10⁹/L (1,500/mm³); ii. White blood cell count ≥3.0×10⁹/L; iii. Platelet count >100×10⁹/L (100,000/mm³); iv. Hemoglobin ≥90 g/L. b) Renal: i. Serum creatinine ≤1.5×ULN, or 24-hour creatinine clearance ≥50 mL/min (calculated according to the Cockcroft-Gault formula); ii. Urine protein <2+ or 24-hour urine protein quantification <1.0 g. c) Hepatic: i. Serum total bilirubin (TBil) ≤1.5×ULN; ii. AST and ALT ≤2.5×ULN; iii. Serum albumin (ALB) ≥28 g/L. d) Coagulation: i. International normalized ratio (INR) and activated partial thromboplastin time (APTT) ≤1.5×ULN (if the subject is receiving anticoagulant therapy, the subject must be on a stable dose of anticoagulant, and the coagulation parameters [PT/INR and APTT] at screening should be within the expected therapeutic range for the anticoagulant used). e) Cardiac function: i. Left ventricular ejection fraction (LVEF) ≥50%.

6、Female patients of childbearing potential (including those with premature menopause, menopause <2 years, and those who have not undergone surgical sterilization), male patients, and their partners must agree to use effective contraception during the study period, including surgical sterilization, oral contraceptives, intrauterine devices, abstinence, or barrier contraception combined with spermicide. All patients must continue contraception for 6 months after the last treatment.

8、Subjects with a history of genital herpes must have a 3-month interval after the herpes has resolved.

9、Subjects must be willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study requirements.

Exclusion Criteria:

  1. Patients who have previously received treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 agents.
  2. Patients whose lesions do not meet the volume requirements for intratumoral injection or are unsuitable for intratumoral injection.
  3. Patients who have received anti-herpes simplex virus therapy (e.g., acyclovir, ganciclovir, valacyclovir, vidarabine) within 4 weeks prior to randomization, except for patients with hepatitis B who are receiving ongoing treatment with entecavir, tenofovir disoproxil fumarate, or adefovir dipivoxil.
  4. Receipt of a live attenuated vaccine within 4 weeks prior to randomization.
  5. Use of an investigational drug within 4 weeks prior to randomization.
  6. Lesions that cannot accommodate an intratumoral injection volume of 1 mL.
  7. Receipt of another anti-tumor monoclonal antibody (mAb) therapy within 4 weeks prior to randomization, or failure of adverse events from prior therapy (occurring more than 4 weeks earlier) to recover to ≤ Grade 1.
  8. Patients with a history of other malignancy (including unknown primary site) within 5 years prior to randomization. Note: Patients with curatively treated Stage 1 or 2 basal/squamous cell carcinoma of the skin, superficial bladder cancer, or carcinoma in situ are excluded.
  9. Patients with known hypersensitivity to the investigational drug, its active ingredients, or excipients.
  10. Patients who are positive for hepatitis B surface antigen (HBsAg) with a hepatitis B virus DNA copy number >1×10³ copies/mL; patients who test positive for hepatitis C virus (HCV) antibody or human immunodeficiency virus (HIV) antibody.
  11. Patients with any unstable systemic disease, including but not limited to: severe infection, uncontrolled diabetes, unstable angina, cerebrovascular accident or transient ischemic attack, myocardial infarction, congestive heart failure, severe arrhythmia requiring medication, liver, kidney, or metabolic disease.
  12. Patients with active central nervous system (CNS) metastases. Patients with adequately treated CNS metastases whose neurological symptoms have recovered to ≤ Grade 1 (CTCAE criteria) for at least 2 weeks prior to randomization (excluding residual signs or symptoms related to CNS treatment) may participate in the study. In addition, patients must not be using corticosteroids, or must be on a stable dose of ≤10 mg prednisone/day (or equivalent), or must have tapered to ≤10 mg prednisone/day.
  13. Patients with autoimmune disease, history of liver or other organ transplantation, active tuberculosis; or patients who have undergone major surgery, live vaccination, or immunotherapy within 4 weeks prior to randomization.
  14. Tumor invasion of major blood vessels such as iliac or femoral vessels.
  15. Patients with diseases (e.g., mental illness) or conditions (e.g., alcoholism or drug abuse) that may increase the risk of study drug administration, affect study compliance, or interfere with the interpretation of study results.
  16. Patients who have received any other investigational product or participated in another interventional clinical trial within 30 days prior to the screening period.
  17. Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study; male or female patients unwilling to use effective contraception. Other conditions deemed unsuitable for enrollment by the investigator.

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:ランダム化
  • 介入モデル:並列代入
  • 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:Experimental:(Neoadjuvant Therapy + Radical Surgery + Postoperative Adjuvant Therapy)

Patients receive 6 cycles of neoadjuvant therapy (QL1706 3 mg/kg IV Q2W + OH2 intratumoral injection up to 8 mL Q2W), followed by radical surgery within 2 weeks after the last neoadjuvant dose. Postoperatively, patients with pCR or near pCR receive observation and follow-up; patients with pPR or NR receive adjuvant QL1706 5 mg/kg IV Q3W for up to 1 year (calculated from the first neoadjuvant dose). BRAF-mutant recurrent patients receive dabrafenib + trametinib instead of QL1706 during adjuvant phase.

A PD-1/CTLA-4 combination antibody produced using MabPair® technology. It contains two engineered monoclonal antibodies (anti-PD-1 IgG4 and anti-CTLA-4 IgG1) expressed at a fixed ratio from a single cell line. Administered intravenously. In the neoadjuvant phase: 3 mg/kg Q2W for 6 cycles. In the adjuvant phase: 5 mg/kg Q3W for up to 1 year. Manufactured by Qilu Pharmaceutical Co., Ltd. Supplied as 50 mg/2 mL vial. Store at 2-8°C, protect from light, do not freeze.

A genetically modified oncolytic type II herpes simplex virus (HSV2) strain HG52, with ICP34.5 and ICP47 genes deleted to enable selective replication in tumor cells and enhance antitumor immunity, and engineered to express human GM-CSF. Administered via intratumoral injection. Planned dose: 10^7 CCID50/mL, Q2W for up to 6 cycles. Maximum single-visit volume: 8 mL, adjusted based on lesion diameter. Dose may be reduced to 10^6 CCID50/mL in case of ≥ Grade 3 related AEs. Manufactured by Wuhan Binhui Bio-technology Co., Ltd. Supplied as 1 mL/vial. Store at -70°C or below.

アクティブコンパレータ:Active Comparator: (Radical Surgery + Postoperative Adjuvant Therapy)

Patients undergo radical surgery directly after enrollment. Postoperatively, all patients receive adjuvant QL1706 5 mg/kg IV Q3W for up to 1 year (calculated from the first adjuvant dose), unless contraindicated. BRAF-mutant recurrent patients receive dabrafenib + trametinib instead of QL1706 during adjuvant phase.

A PD-1/CTLA-4 combination antibody produced using MabPair® technology. It contains two engineered monoclonal antibodies (anti-PD-1 IgG4 and anti-CTLA-4 IgG1) expressed at a fixed ratio from a single cell line. Administered intravenously. In the neoadjuvant phase: 3 mg/kg Q2W for 6 cycles. In the adjuvant phase: 5 mg/kg Q3W for up to 1 year. Manufactured by Qilu Pharmaceutical Co., Ltd. Supplied as 50 mg/2 mL vial. Store at 2-8°C, protect from light, do not freeze.

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
2-Year Event-Free Survival Rate
時間枠:From randomization up to 2 years

Event-free survival (EFS) is defined as the time from randomization to the occurrence of any of the following events: disease progression leading to inoperability (development of locally unresectable disease or distant metastasis), local or distant recurrence, melanoma-related or treatment-related death. The occurrence of a new primary melanoma during treatment or follow-up will also be considered an event.

From randomization up to 2 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Pathologic Response Rate (pCR, Near pCR, pPR)
時間枠:At the time of surgery (approximately 12 weeks after enrollment)

Assessment is performed according to the International Neoadjuvant Melanoma Consortium (INMC) scoring system. Partial pathological response (pPR) is defined as viable tumor cells ≥10% and ≤50%. Near pathological complete response (near pCR) is defined as viable tumor cells >0% and <10%. Pathological complete response (pCR) is defined as the absence of viable tumor cells. The aim is to evaluate pathological response rates, including the partial pathological response rate, major pathological response/near pathological complete response rate, and pathological complete response rate.

At the time of surgery (approximately 12 weeks after enrollment)
Relapse-Free Survival (RFS)
時間枠:5 years

The time from randomization to the first occurrence of any of the following events: disease recurrence (local, regional, or distant metastasis) or death from any cause, whichever occurs first.

5 years
Overall Survival (OS)
時間枠:5 years

The time from randomization to death from any cause.

5 years
The incidence and severity of adverse events (AEs)
時間枠:5 years

Safety

5 years

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

協力者

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1日

一次修了 (推定)

2029年9月1日

研究の完了 (推定)

2030年6月1日

試験登録日

最初に提出

2026年9月28日

QC基準を満たした最初の提出物

2026年10月1日

最初の投稿 (実際)

2026年10月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月2日

QC基準を満たした最後の更新が送信されました

2026年10月1日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • QL-MLM-QIBA-1001

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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