Pemigatinib in the Advanced Gastrointestinal Cancer With FGFR 1-3 Alterations

Phase 2

Recruiting

• Conditions: Gastrointestinal Cancer
• Interventions: Drug: Pemigatinib

• Registration Number: NCT05651672
• Lead Sponsor: Tianjin Medical University Cancer Institute and Hospital

Brief Summary

This study is a prospective single-arm phase II study to evaluate the efficacy and safety of Pemigatinib in the advanced gastrointestinal cancer with FGFR 1-3 alterations and failed standard therapy.

Detailed Description

Not available

Study Timeline

• Status Verified: 2022-12
• Study Start: 2022-12-02
• Study First Submitted: 2022-12-07
• Study First Submitted QC: 2022-12-07
• Last Update Submitted: 2022-12-07
• Study First Posted: 2022-12-15
• Last Update Posted: 2022-12-15
• Primary Completion: 2024-12
• Study Completion: 2026-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• Aged 18 or older
• Histologically or cytologically confirmed unresectable advanced, recurrent or metastatic gastrointestinal cancer
• Have at least one measurable lesion according to RECIST v1.1
• With histologically confirmed FGFR1-3 alterations, including but not limited to amplification, mutation, fusion/rearrangement
• Disease progression after prior standard therapy
• No previous use of small molecule multi-target inhibitors targeting the FGFR pathway (including but not limited to anlotinib, lenvatinib, sorafenib, apatinib)
• ECOG performance status of 0~1
• Expected survival time > 3 months
• Sufficient organ functions
• Negative pregnancy test results of childbearing age women
• Patients at risk of conception (including their partners) need to use contraception

Exclusion Criteria

• Diagnosed with malignant tumors other than gastrointestinal cancer within 5 years before the first dose, excluding radically cured cutaneous basal cell carcinoma, cutaneous squamous cell carcinoma, and/or radically resected carcinoma in situ

• Prior receipt of selective FGFR inhibitors

• Have received any other investigational drug or participated in another interventional clinical trial within 28 days before the first dose, or have received anti-tumor drug treatment within 28 days before the first dose (including Chinese herbal medicine with anti-tumor indications)

• Have not recovered ( ≤ grade 1 or reaching the baseline, excluding asthenia and alopecia) from toxicity and/or complications caused by any intervention before the start of treatment

• Known symptomatic central nervous system metastasis and/or carcinomatous meningitis.

• Known history of allotransplantation or allogeneic hematopoietic stem cell transplantation

• Abnormal laboratory parameters listed below:

  • Serum phosphate > upper limit of normal (ULN)
  • Serum calcium exceeds the normal range, or the calcium concentration corrected for serum albumin exceeds the normal range when serum albumin exceeds the normal range
  • Potassium level < lower limit of normal (LLN)#potassium levels can be corrected by supplements at screening

• Known history of human immunodeficiency virus (HIV) infection or confirmed with positive immune test results

• Presence of severe infection in the active phase or with poor clinical control

• Pleural effusion, ascites, or pericardial effusion with obvious clinical symptoms that require drainage

• Acute or chronic active hepatitis B or C infection

• Clinically significant or uncontrolled heart diseases, including unstable angina, acute myocardial infarction within 6 months before the first dose, grade III/IV congestive heart failure (New York Heart Association), and uncontrolled arrhythmia (patients with pacemakers or with atrial fibrillation but well controlled heart rate are allowed)

• ECG changes or medical history considered clinically significant by the investigator, QTcF interval > 480 ms at screening, JTc interval can be used instead of QTc interval (in such cases, JTc must be ≤ 340 ms) for patients with intraventricular conduction block (QRS interval > 120 ms)

• Uncontrolled hypertension (systolic pressure > 160 mmHg or diastolic pressure > 100 mmHg) after the optimal medical treatment, or a history of hypertensive crisis or hypertensive encephalopathy

• Hepatic encephalopathy, hepatorenal syndrome, or liver cirrhosis with Child-Pugh grade B or C

• Have received a major surgery (craniotomy, thoracotomy, or laparotomy) within 4 weeks prior to the first dose, or will receive a major surgery during the study treatment period

• Not fully recovered from toxicity and/or complications of a major surgery before the study treatment

• Pregnant or lactating women, or patients expected to conceive or give birth during the study period from the screening to the completion of the safety follow-up visit (90 days after the last dose for male subjects)

• Have received radiotherapy within 4 weeks before the first dose.

• History of disorders of calcium and phosphorus metabolism or systemic electrolyte metabolism imbalance with ectopic calcification of soft tissues (excluding calcification of soft tissues such as skin, kidneys, tendon, or blood vessels without systemic electrolyte metabolism imbalance caused by injury, disease, and old age)

• Clinically significant corneal or retinal diseases confirmed by ophthalmological examination

• Prior receipt of any potent CYP3A4 inhibitor or inducer within 14 days or 5 half lives (whichever is shorter) before the first dose. Ketoconazole is allowed for external use

• Known allergic reactions to pemigatinib or excipients of pemigatinib

• Unable or unwilling to swallow pemigatinib or are suffering from significant digestive system diseases that may interfere with absorption, metabolism, or excretion

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
experimental group	Pemigatinib	Pemigatinib

Primary Outcome Measures

Name	Time	Method
Overall response rate (ORR)	up to 2 years	Defined as proportion of patients who have a best response of complete response (CR) + partial response (PR) according to the RECIST 1.1 criteria

Secondary Outcome Measures

Name	Time	Method
Overall Survival (OS)	Up to 4 years	Defined as the time from enrollment to the death
Duration of Response (DOR)	up to 4 years	Defined as the time from the date of CR or PR to PD
Adverse Events (AEs)	Up to 2 years	Defined as the proportion of patients with AE, treatment-related AE (TRAE), immune-related AE (irAE), serious adverse event (SAE), assessed by NCI CTCAE v5.0
Progress Free Survival (PFS)	Up to 4 years	Defined as the time from enrollment to disease progression or death (whichever occurs first)
Disease Control Rate (DCR)	Up to 2 years	Defined as proportion of patients who have a best response of complete response (CR) + partial response (PR) + stable disease (SD) according to the RECIST1.1 criteria

Trial Locations

Locations (1)

Tianjin Medical University Cancer Institute & Hospital; 🇨🇳 Tianjin, Tianjin, China