Gem+Nab-P+LEN+TIS for Advanced Unresectable BTC (GALENT-BT)

NCT ID: NCT06963060

Last Updated: 2025-05-08

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Clinical Phase: PHASE2
• Total Enrollment: 44 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-06-01
• Study Completion Date: 2027-06-30

Brief Summary

The goal of this clinical trial is to evaluate the efficacy and safety of combining Gemcitabine, nab-Paclitaxel, Lenvatinib, and Tislelizumab in adults aged 18-75 years with advanced unresectable biliary tract malignancies (including gallbladder cancer, intrahepatic cholangiocarcinoma, and extrahepatic cholangiocarcinoma). The main questions it aims to answer are:

What is the objective response rate (ORR) of this quadruplet regimen as first-line therapy?

What are the secondary outcomes, including disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety profile?

This is a single-arm, open-label, phase II study with no comparison group.

Participants will:

Receive Gemcitabine (1000 mg/m² IV on Days 1 and 8) and nab-Paclitaxel (125 mg/m² IV on Days 1 and 8) every 3 weeks.

Take Lenvatinib (4-8 mg orally daily on Days 1-21).

Receive Tislelizumab (200 mg IV on Day 1) every 3 weeks.

Undergo 6-8 treatment cycles (adjusted for tolerability) with regular imaging, laboratory tests, and safety assessments.

Be followed for 3 years to monitor survival and long-term outcomes.

The study plans to enroll 29 participants and will be conducted at a single center over 36 months.

Detailed Description

1. Study Background Biliary tract malignancies (BTCs), including gallbladder cancer (GBC), intrahepatic cholangiocarcinoma (ICC), and extrahepatic cholangiocarcinoma (ECC), are aggressive cancers with a 5-year survival rate <5%. Current first-line systemic therapies (e.g., gemcitabine/cisplatin) yield limited efficacy (ORR <30%, median OS ~11.7 months). Preclinical and clinical evidence suggests synergistic effects of combining chemotherapy, anti-angiogenic agents, and immune checkpoint inhibitors. The GALENT-BT trial evaluates a novel quadruplet regimen-Gemcitabine + nab-Paclitaxel + Lenvatinib + Tislelizumab-to improve outcomes in advanced unresectable BTCs.

2. Study Objectives

Primary Objective: Assess the safety and tolerability of the quadruplet regimen over 8 treatment cycles.

Secondary Objectives:

Evaluate objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and surgical conversion rate.

Monitor adverse events (AEs), serious adverse events (SAEs), and quality of life (QoL).

Exploratory Objectives: Investigate biomarkers (e.g., PD-L1 expression, genetic mutations) and radiomic/pathologic features associated with treatment response.

3. Study Design

Design: Prospective, single-arm, open-label, single-center, phase II trial.

Sample Size: Two-stage enrollment:

Stage 1 (Lead-in): 9 participants for initial safety evaluation. If ≤3/9 experience grade ≥3 AEs, proceed to Stage 2.

Stage 2 (Expansion): 20 additional participants (total 29 evaluable patients).

Duration: 36 months (June 2024-June 2027).

4. Study Population

Inclusion Criteria:

Adults aged 18-75 years with histologically confirmed, untreated, advanced unresectable BTC (GBC/ICC/ECC) or recurrent BTC (≥3 months post-adjuvant therapy).

ECOG PS 0-1, measurable disease per RECIST 1.1, adequate organ function.

Exclusion Criteria: Prior systemic therapy for advanced BTC, severe comorbidities, pregnancy, or intolerance to study drugs.

5. Intervention

Regimen:

Gemcitabine: 1000 mg/m² IV on Days 1 and 8 of each 21-day cycle.

nab-Paclitaxel: 125 mg/m² IV on Days 1 and 8.

Lenvatinib: 4-8 mg orally daily (weight-based dosing) on Days 1-21.

Tislelizumab: 200 mg IV on Day 1.

Treatment Duration: 6-8 cycles (adjustable for tolerability), followed by 3-year survival follow-up.

6. Assessments

Efficacy:

Tumor response evaluated by CT/MRI every 6 weeks using RECIST 1.1.

ORR, DCR, PFS, OS, and surgical conversion rate calculated.

Safety:

AEs/SAEs graded per CTCAE v5.0.

Laboratory monitoring (hematology, liver/renal function, thyroid panels).

QoL: Assessed via EORTC QLQ-HCC18 questionnaire at baseline, treatment cycles, and follow-up.

Conditions

Gallbladder Cancer; Cholangiocarcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

Gemcitabine ,nab-Paclitaxel,Lenvatinib and Tislelizumab

Group Type: EXPERIMENTAL

Gemcitabine nab-PaclitaxelLenvatinibTislelizumab

Intervention Type: DRUG

Receive Gemcitabine (1000 mg/m² IV on Days 1 and 8) and nab-Paclitaxel (125 mg/m² IV on Days 1 and 8) every 3 weeks.

Take Lenvatinib (4-8 mg orally daily on Days 1-21).

Receive Tislelizumab (200 mg IV on Day 1) every 3 weeks.

Interventions

Gemcitabine nab-PaclitaxelLenvatinibTislelizumab

Receive Gemcitabine (1000 mg/m² IV on Days 1 and 8) and nab-Paclitaxel (125 mg/m² IV on Days 1 and 8) every 3 weeks.

Take Lenvatinib (4-8 mg orally daily on Days 1-21).

Receive Tislelizumab (200 mg IV on Day 1) every 3 weeks.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Aged 18-75 years, regardless of gender.

2. Histologically or cytologically confirmed, untreated primary advanced unresectable biliary tract malignancies (BTC), including intrahepatic cholangiocarcinoma (ICC), extrahepatic chololiocarcinoma (ECC), and gallbladder cancer (GBC); or untreated recurrent BTC (prior adjuvant/neoadjuvant chemotherapy allowed if completed ≥3 months before recurrence, excluding regimens containing PD-1/L1 inhibitors, gemcitabine, nab-paclitaxel, or lenvatinib).

3. ECOG performance status score 0-1.

4. Expected survival ≥3 months.

5. At least one measurable target lesion per RECIST v1.1 criteria.

6. Adequate organ function:

Hematologic: Hemoglobin ≥90 g/L; WBC ≥lower limit of normal (LLN); ANC ≥1.5×10⁹/L; platelets ≥100×10⁹/L.

Renal: Serum creatinine ≤1.5×ULN; endogenous creatinine clearance rate ≥55 mL/min.

Hepatic: Total bilirubin ≤1.5×ULN; ALT/AST ≤2.5×ULN (≤3×ULN for intrahepatic BTC or liver metastases; ALT/AST ≤5×ULN for liver metastases).

Coagulation: INR ≤1.5×ULN; APTT within normal range.

7. No prior systemic therapy for advanced BTC (chemotherapy, radiotherapy, targeted therapy, immunotherapy, or hormonal therapy). Patients with post-R2 resection are eligible.

8. Negative serum/urine pregnancy test (for women of childbearing potential) and agreement to use contraception during the study and for 6 months post-treatment.

9. Willing and able to provide written informed consent.

Exclusion Criteria

1. Severe systemic infection or uncontrolled comorbidities (e.g., heart failure, thyroid disorders, psychiatric conditions).

2. Known hypersensitivity or intolerance to study drugs or their excipients.

3. Pregnancy, lactation, or refusal to use effective contraception.

4. Participation in other clinical trials within 30 days prior to enrollment.

5. Inability to understand or unwillingness to sign informed consent.

6. Any condition that, in the investigator's judgment, may compromise patient safety or compliance (e.g., severe concurrent illness, abnormal lab results, psychosocial factors).

7. Prior use of PD-1/L1 inhibitors, gemcitabine, nab-paclitaxel, or lenvatinib in adjuvant/neoadjuvant settings.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Wei Gong

OTHER

Sponsor Role: lead

Responsible Party

Wei Gong

Xinhua Hospital A ffiliated to Shanghai Jiaotong University School of Medicine

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

XHEC-C-2024-121-2

Identifier Type: -

Identifier Source: org_study_id