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AK112 Combined With GAP Conversion Therapy for Locally Advanced Gallbladder Cancer (ICORE-GBC)

2026年8月12日 更新者:Geng Zhimin、First Affiliated Hospital Xi'an Jiaotong University

Single-Center, Single-Arm, Two-Stage, Prospective Phase II Clinical Study of AK112 Combined With GAP Regimen as Conversion Therapy for Locally Advanced Gallbladder Cancer

The goal of this clinical trial is to evaluate the efficacy and safety of AK112 combined with the GAP regimen as conversion therapy for patients with locally advanced gallbladder cancer who are initially considered unsuitable for curative surgery.

The main questions this study aims to answer are:

  1. Whether AK112 combined with the GAP regimen can increase the rate of successful R0 radical resection after conversion therapy.
  2. Whether this treatment approach can achieve tumor response and disease control with acceptable safety in patients with locally advanced gallbladder cancer.

Participants will receive AK112 combined with gemcitabine, cisplatin, and albumin-bound paclitaxel (GAP regimen) every 21 days for 4-6 treatment cycles. Tumor response will be evaluated by CT or MRI according to RECIST version 1.1 criteria. Patients who become eligible for surgery after multidisciplinary evaluation will undergo radical resection. All participants will be monitored for treatment-related adverse events, disease progression, and survival outcomes during follow-up.

調査の概要

研究の種類

介入

入学 (推定)

22

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Voluntarily provide written informed consent;
  2. Age ≥18 years and ≤75 years at enrollment;
  3. Histologically or cytologically confirmed gallbladder adenocarcinoma;
  4. Radiological assessment meeting any of the following criteria: a. Hepatic invasion requiring extensive hepatectomy that the patient cannot tolerate; b. Biliary tract invasion extending beyond the bifurcation threshold requiring extensive hepatectomy that the patient cannot tolerate; c. Regional lymph node metastasis with fused bulky lymph nodes (maximum short-axis diameter >2 cm) compressing or invading critical blood vessels/biliary tracts, precluding radical lymphadenectomy; d. Primary tumor vascular invasion: main portal vein or left portal branch invasion without feasible vascular reconstruction; proper hepatic artery/common hepatic artery invasion >180°, or invasion <180% combined with mandatory portal vein reconstruction; right portal vein/right hepatic artery invasion with intolerance to extensive hepatectomy;e. Direct invasion of adjacent organs (pancreas, stomach, duodenum, colon);
  5. MDT consensus confirming initial non-resectability, with anticipated feasibility of radical resection after conversion therapy;
  6. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;
  7. No prior systemic anti-tumor therapy for locally advanced gallbladder cancer;
  8. At least one measurable target lesion per RECIST v1.1 suitable for repeated accurate quantitative measurement;
  9. Adequate organ function to tolerate the conversion regimen;
  10. Estimated survival ≥3 months;
  11. Willing and able to comply with scheduled visits, treatment regimens, laboratory testing, and all other study requirements;
  12. Adequate hematologic, renal, hepatic, coagulation, and cardiac function confirmed by screening laboratory tests (no blood product/growth factor support within 7 days prior to screening lab draws):

    a. Hematology: i. Absolute Neutrophil Count (ANC) ≥1.5 × 10⁹/L (1,500/mm³) ii. Platelet count ≥100 × 10⁹/L (100,000/mm³) iii. Hemoglobin ≥90 g/L; b. Renal function: i. Calculated Creatinine Clearance (CrCl) ≥50 mL/min via the Cockcroft-Gault formula: CrCl (mL/min) = [(140 - Age) × Weight (kg) × F] / [Serum Creatinine (mg/dL) × 72] F = 1 for males, F = 0.85 for females; SCr = serum creatinine. ii. Urine protein ≤1+ or 24-hour urine protein quantification <1.0 g; c. Hepatic function: i. Total bilirubin (TBil) ≤ 2 × the upper limit of normal (ULN); ii. AST and ALT ≤2.5 × ULN; iii. Serum Albumin (ALB) ≥28 g/L; d. Coagulation function: International Normalized Ratio (INR) and Activated Partial Thromboplastin Time (APTT) ≤1.5 × ULN; e. Cardiac function: Left Ventricular Ejection Fraction (LVEF) ≥50% on echocardiogram.

Exclusion Criteria:

  1. Histological or cytological confirmation of gallbladder non-adenocarcinoma: squamous cell carcinoma, neuroendocrine neoplasm, lymphoma, sarcoma;
  2. Presence of distant metastatic disease at screening;
  3. Prior radiotherapy, chemotherapy, targeted therapy, or immunotherapy for gallbladder cancer;
  4. Concurrent other malignant tumors besides gallbladder cancer;
  5. Severe uncontrolled biliary tract infection or untreated obstructive jaundice;
  6. Major surgery or severe trauma within 30 days prior to first study drug administration:

    1. Definitions:

      Major surgery: All open/laparoscopic procedures requiring general endotracheal anesthesia entering thoracic, abdominal, or pelvic cavities (e.g.,, exploratory laparotomy, gastrointestinal resection, hernia repair, partial hepatectomy); Severe trauma: Deep tissue injury, visceral rupture requiring hospitalization or surgical repair (e.g., fractures, extensive soft-tissue contusion, closed abdominal trauma);

    2. Minimally invasive/interventional procedures permitted with mandatory washout intervals:

    Diagnostic biopsy (lymph node, liver/gallbladder fine needle, EUS biopsy): minimum 7 days between the procedure and the first drug administration, no active hemorrhage/hematoma; Biliary decompression (PTCD, ERCP stent/nasobiliary drainage): a minimum of 14 days between the procedure and the first drug administration, no active hemorrhage, peritonitis, or biliary leakage confirmed by clinical and radiological evaluation;

  7. Active autoimmune disease, active inflammatory bowel disease, congenital or acquired immunodeficiency, active pulmonary tuberculosis, active syphilis infection, prior solid organ or allogeneic hematopoietic stem cell transplantation, or non-infectious interstitial lung disease requiring long-term systemic corticosteroid therapy;
  8. Severe bleeding diathesis or coagulation disorder history:

    1. Screening lab abnormalities: PLT <100 ×10⁹/L; INR >1.5 (without anticoagulation); APTT >1.5 × ULN; Fibrinogen <1.5 g/L;
    2. CTCAE Grade ≥2 active bleeding event within 3 months before enrollment, or uncontrolled major vascular complications;
  9. Confirmed hypersensitivity to any excipient or active component of the study drugs;
  10. Pregnant or lactating female patients;
  11. Severe psychiatric disorder, history of substance dependence, or other medical conditions that may impair trial compliance throughout study participation.

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:なし
  • 介入モデル:単一グループの割り当て
  • 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:AK112 Combined with GAP Regimen
AK112 will be administered intravenously at a dose of 20 mg/kg every 3 weeks in combination with gemcitabine, cisplatin, and albumin-bound paclitaxel as conversion therapy for locally advanced gallbladder cancer.
Gemcitabine is a nucleoside analog chemotherapy agent administered intravenously as part of the GAP regimen. Gemcitabine is administered at the specified dose on days 1 and 8 of each 21-day cycle (Q3W) in combination with AK112, cisplatin, and albumin-bound paclitaxel.
Cisplatin is a platinum-based chemotherapy agent administered intravenously as part of the GAP regimen. Cisplatin is administered at the specified dose on days 1 and 8 of each 21-day cycle (Q3W) in combination with AK112, gemcitabine, and albumin-bound paclitaxel.
Albumin-bound paclitaxel is a taxane-based chemotherapy agent administered intravenously as part of the GAP regimen. Albumin-bound paclitaxel is administered at the specified dose on days 1 and 8 of each 21-day cycle (Q3W) in combination with AK112, gemcitabine, and cisplatin.

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
時間枠
R0 Resection Rate
時間枠:Approximately 6 months after treatment initiation
Approximately 6 months after treatment initiation

二次結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate (ORR)
時間枠:From the first dose of study treatment until documented disease progression, unacceptable toxicity, or radical surgery, whichever occurs first, assessed up to 24 months.
The proportion of participants achieving complete response (CR) or partial response (PR) according to RECIST version 1.1 criteria after treatment.
From the first dose of study treatment until documented disease progression, unacceptable toxicity, or radical surgery, whichever occurs first, assessed up to 24 months.
Disease Control Rate (DCR)
時間枠:From the first dose of study treatment until documented disease progression, unacceptable toxicity, or radical surgery, whichever occurs first, assessed up to 24 months.
The proportion of participants achieving complete response, partial response, or stable disease according to RECIST version 1.1 criteria after treatment.
From the first dose of study treatment until documented disease progression, unacceptable toxicity, or radical surgery, whichever occurs first, assessed up to 24 months.
Major Pathological Response Rate
時間枠:At the time of radical surgery
The proportion of participants achieving major pathological response after conversion therapy among patients undergoing surgical resection.
At the time of radical surgery
Progression-Free Survival (PFS)
時間枠:Up to 3 years after treatment initiation
The time from initiation of treatment to disease progression or death from any cause.
Up to 3 years after treatment initiation
Overall Survival (OS)
時間枠:Up to 3 years after treatment initiation
The time from initiation of treatment to death from any cause.
Up to 3 years after treatment initiation

協力者と研究者

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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8月28日

一次修了 (推定)

2028年6月30日

研究の完了 (推定)

2028年6月30日

試験登録日

最初に提出

2026年8月4日

QC基準を満たした最初の提出物

2026年8月12日

最初の投稿 (実際)

2026年8月17日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月17日

QC基準を満たした最後の更新が送信されました

2026年8月12日

最終確認日

2026年8月1日

詳しくは

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