Pemigatinib and Immune Checkpoint Inhibitor Treated FGFR1/2/3 Alteration Advanced Solid Tumor

Official title

Pemigatinib and Immune Checkpoint Inhibitor Treated FGFR1/2/3 Alteration Advanced Solid Tumor: a Single Arm, Multiple Center, Phase II Study (Pigeon Study)

Overview

This prospective phase Il study is aim to evaluate the efficacy and safety of FGFR inhibitor combined with immune checkpoint inhibitors in FGFR1/2/3 variant advanced solid tumors.

Interventions

• Drug Pemigatinib
  Pemigatinib and immune checkpoint inhibitors

Primary outcome measures

• Objective response rate (ORR) [Time frame: every 8 weeks during treatment]

Secondary outcome measures (3)

• Disease control rate（DCR） [Time frame: every 8 weeks during during treatment]
• Progression-free survival （PFS） [Time frame: every 8 weeks during treatment]
• Overall survival（OS） [Time frame: every 8 weeks during treatment]

Eligibility criteria

Inclusion criteria

• Age ≥ 18 years;
• Histologically or cytologically confirmed unresectable advanced solid tumors with failure or intolerance to standard treatments;
• At least one measurable lesion per RECIST v1.1 criteria;
• Gene testing confirms FGFR1/2/3 variants, including but not limited to mutations, fusions/rearrangements in solid tumors;
• Patients have not previously used specific small molecule multi-target inhibitors of the FGFR pathway, as assessed by investigators, and have been treated with immune checkpoint inhibitors;
• ECOG performance status of 0-1;
• Expected survival time > 3 months;
• Laboratory criteria:

• Absolute neutrophil count (ANC) ≥ 1.5 x 10⁹/L in the past 14 days without granulocyte colony-stimulating factor;
• Platelets ≥ 100 x 10⁹/L without transfusion in the past 14 days;
• Hemoglobin > 9 g/dL in the last 14 days without transfusion or erythropoietin;
• Total bilirubin ≤ 1.5 x upper limit of normal (ULN), or total bilirubin > ULN but direct bilirubin ≤ ULN;
• AST, ALT ≤ 2.5 x ULN (≤ 5 x ULN in patients with liver metastasis);
• Serum creatinine ≤ 1.5 x ULN and creatinine clearance (Cockcroft-Gault) ≥ 50 ml/min;
• Good coagulation function, defined as INR or PT ≤ 1.5 x ULN. If on anticoagulant therapy, PT should be within the therapeutic range of anticoagulants;
• Female subjects of reproductive age must have a negative urine or serum pregnancy test within 3 days prior to the first dose (Cycle 1, Day 1). If the urine test is inconclusive, a blood test is required. Non-reproductive females are defined as post-menopausal for at least one year or surgically sterile;
• Subjects with reproductive potential must use contraception with an annual failure rate of less than 1% during treatment and for 120 days after the last study drug dose (or 180 days after the last chemotherapy dose).

Exclusion criteria

• Diagnosis of other malignancies within 3 years before the first dose, except for certain treated skin carcinomas and in-situ carcinomas;
• Previous treatment with selective FGFR inhibitors;
• Receipt of other investigational drugs within 21 days or antitumor drugs within 14 days before the first dose;
• Unresolved toxicity from prior treatments unless ≤ Grade 1 or related to alopecia or fatigue;
• Known symptomatic CNS metastasis or carcinomatous meningitis. Stable patients post-treatment with no evidence of progression may be eligible if steroid-free for at least 14 days;
• History of allogeneic organ or hematopoietic stem cell transplantation;
• Abnormal laboratory parameters:

• Serum phosphate > 1.5 x ULN;
• Elevated serum calcium or albumin-adjusted calcium outside the reference range;
• Known HIV infection or positive HIV test;
• Active or poorly controlled serious infection;
• Need for drainage treatment for pleural effusion, ascites, or pericardial effusion;
• Active hepatitis B or C infection with high viral load, or positive HBsAg or anti-HCV antibodies. Patients on antiviral therapy must meet lower thresholds;
• Significant uncontrolled heart disease, including recent MI, severe heart failure, or uncontrolled arrhythmias;
• Clinically significant ECG changes or history of significant cardiac issues; Screening QTcF interval > 480 ms, or JTc interval if applicable, must be ≤ 340 ms;
• Uncontrolled hypertension despite treatment;
• Hepatic encephalopathy, hepatorenal syndrome, or Child-Pugh grade B or higher cirrhosis;
• Major surgery within 4 weeks before the first dose or planned major surgery during the study;
• Unresolved complications from prior surgery;
• Pregnant or breastfeeding women, or those planning to become pregnant during the study period and for safety follow-up;
• Radiotherapy within 4 weeks before the first dose, except for non-CNS palliative radiotherapy with a 2-week washout period;
• History of systemic electrolyte imbalance or ectopic soft tissue calcification;
• Clinically significant corneal or retinal disease;
• Use of potent CYP3A4 inhibitors or inducers within 14 days or 5 half-lives before the first dose;

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06551896 · SYSKY-2024-546-01

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗