mFOLFIRINOX Plus Anlotinib and Sintilimab for Advanced Pancreatic Cancer

NCT06761027 | Recruiting Phase 1

• 1 other identifier: IEC-SG-029-3.0
• Study Type: interventional
• Target: 29
• Locations: 1 country
• Sites: 4

Brief Summary

This study is a prospective, single-arm, multicenter, phase Ib/II clinical trial that treats previously untreated patients with locally advanced or metastatic pancreatic cancer using mFOLFIRINOX in combination with anlotinib and sintilimab. The purpose of this trial is to evaluate the efficacy and safety of this treatment regimen and to preliminarily explore the correlation between biomarkers and treatment outcomes.

Conditions

Locally Advanced Pancreatic Cancer; Metastatic Pancreatic Cancer

Keywords

anlotinib; sintilimab

Outcome Measures

Primary Outcomes (1)

• Objective response rate, ORR

  The Objective response rate (ORR) was defined as the complete response (CR) rate or the partial response (PR) rate according to RECIST v1.1.

  Four weeks after the initiation of medication until the day before surgery

Secondary Outcomes (4)

• Overall survival, OS

  From date of enrollment until the date of death from any cause, assessed up to 60 months

• Progression free survival, PFS

  From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months

• Disease control rate, DCR

  Four weeks after the initiation of medication until the day before surgery

• Toxicity Adverse events

  From the initiation of medication, with recordings made whenever an adverse reaction occurs, assessed up to 60 months

Study Arms (1)

mFOLFIRINOX Plus Anlotinib and Sintilimab

EXPERIMENTAL

Phase Ib: 6 patients will receive treatment at dose level-0 and their toxicity will be observed. If 2 or fewer patients experience dose-limiting toxicity, the study will proceed to the phase II part using dose level-0 as the treatment dose. If 3 or more patients have dose-limiting toxicity, another 6 patients will be accrued at a lower dose (dose -1). If two or fewer patients have dose-limiting toxicity, then we proceed with the phase II trial at that dose; otherwise, the trial is discontinued. Dose level - 0: anlotinib at a dose of 10mg per administration, once daily, orally administered on days 1-14, every 3 weeks. Dose level -1: anlotinib at a dose of 8mg per administration, once daily, orally administered on days 1-14, every 3 weeks. Phase II: The efficacy and safety of mFOLFIRINOX combined with anlotinib and sintilimab as first-line treatment for locally advanced or metastatic pancreatic cancer will be conducted at the anlotinib safe dose determined in phase Ib.

Drug: Anlotinib combined with Sintilimab

Interventions

Anlotinib combined with Sintilimab DRUG

Based on the mFOLFIRINOX chemotherapy regimen, combined with the safe dose of anlotinib determined in phase Ib and sintilimab.

mFOLFIRINOX Plus Anlotinib and Sintilimab

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Fully understand this study and voluntarily sign the informed consent form;
• Age between 18 and 75 years inclusive, with no gender restrictions;
• Patients with locally advanced or metastatic pancreatic cancer diagnosed by histology or cytology;
• No prior anti-cancer treatment;
• Patients must have at least one measurable lesion (according to RECIST 1.1 criteria);
• ECOG PS score of 0-1;
• Expected survival of at least 3 months;
• No severe organic diseases of the heart, lungs, brain, liver, kidneys, or other organs;
• Women of childbearing age must agree to use contraceptive measures during the treatment period and for 6 months after the end of treatment; negative serum or urine pregnancy test within 7 days before study enrollment, and must be non-lactating, men must agree to use contraceptive measures during the study period and for 6 months after the study ends.

You may not qualify if:

• Have already received or are currently receiving additional anti-tumor treatment measures such as chemotherapy, radiotherapy, targeted therapy, immunotherapy, or traditional Chinese medicine treatment;
• Known allergies to any of the drugs in the study;
• Symptomatic brain metastases or metastases with symptom control time less than 2 months;
• A large liver metastasis burden, occupying more than 70% of the liver volume;
• Patients with obstructive jaundice whose bilirubin cannot be reduced to the expected level after adequate decompression;
• Presence of any active autoimmune diseases or patients with autoimmune diseases expected to relapse (such as interstitial pneumonia, colitis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases and syndromes);
• History of immunodeficiency; patients currently using immunosuppressants, systemic corticosteroid therapy, or any other form of immunosuppressive treatment;
• Known genetic or acquired bleeding tendencies (such as coagulation disorders) or thrombosis, such as hemophiliacs; currently using or have recently (within 10 days before the start of the study treatment) used full-dose oral or injectable anticoagulants or thrombolytic drugs for therapeutic purposes (preventive use of low-dose aspirin, low molecular weight heparin is allowed);
• Serious infections (CTC AE greater than grade 2) occurred within 4 weeks before the first use of the study drug, such as severe pneumonia requiring hospitalization, bacteremia, infectious complications, etc.; baseline chest imaging suggests active pulmonary inflammation, presence of symptoms and signs of infection within 2 weeks before the first use of the study drug, or requiring oral or intravenous antibiotic treatment (excluding the use of antibiotics for prevention);
• History of other malignant tumors within the past 5 years or concurrently, except for cured basal cell carcinoma of the skin, cervical carcinoma in situ, and papillary thyroid carcinoma;
• Patients with mental illness; history of abuse of psychotropic drugs, alcoholism, and drug addiction;
• Pregnant or lactating women;
• Deemed by the investigator as unsuitable to participate in this trial for other reasons.

Sponsors & Collaborators

• Fujian Provincial Hospital: lead

Study Sites (4)

First Affiliated Hospital of Fujian Medical University

Fuzhou, Fujian, China

NOT YET RECRUITING

Fujian Provincial Hospital

Fuzhou, Fujian, China

RECRUITING

Mengchao Hepatobiliary Hospital of Fujian Medical University

Fuzhou, Fujian, China

NOT YET RECRUITING

Zhangzhou Affiliated Hospital of Fujian Medical University

Zhangzhou, Fujian, China

NOT YET RECRUITING

MeSH Terms

Conditions

Pancreatic Neoplasms

Interventions

sintilimab

Condition Hierarchy (Ancestors)

Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Endocrine Gland Neoplasms; Digestive System Diseases; Pancreatic Diseases; Endocrine System Diseases

Central Study Contacts

Mao-Lin Yan

CONTACT

0591-88217140; yanmaolin74@163.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Department of Hepatobiliary Pancreatic Surgery

Study Record Dates

• First Submitted: December 28, 2024
• First Posted: January 7, 2025
• Study Start: December 23, 2024
• Primary Completion (Estimated): March 1, 2027
• Study Completion (Estimated): May 1, 2027
• Last Updated: January 7, 2025

Record last verified: 2025-01

Locations

CN (4)