MET/VEGFR2 Inhibitor GSK1363089 and Erlotinib Hydrochloride or Erlotinib Hydrochloride Alone in Locally Advanced or Metastatic NSCLC That Has Not Responded to Previous Chemotherapy

Lung Cancer Clinical Trial

Official title:

A Phase I/II Study of Foretinib in Patients With Previously Treated Non-Small Cell Lung Cancer Receiving Standard Erlotinib Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01068587
• Other study ID #: I196
• Secondary ID: CAN-NCIC-IND196G
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: January 21, 2010
• Est. completion date: February 13, 2015

Study information

• Verified date: April 2020
• Source: Canadian Cancer Trials Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: MET/VEGFR2 inhibitor Foretinib and erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

PURPOSE: This randomized phase I/II trial is studying the side effects of erlotinib hydrochloride when given together with or without MET/VEGFR2 inhibitor Foretinib and to see how well it works in treating patients with locally advanced or metastatic non-small cell lung cancer that has not responded to previous chemotherapy.

Description:

OBJECTIVES:

• To determine the recommended phase II dose of MET/VEGFR2 inhibitor Foretinibin combination with standard erlotinib hydrochloride therapy in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) after failure of at least one prior chemotherapy regimen, and whose EGFR-expression status is positive or unknown.

• To determine the safety, tolerability, toxicity profile, dose-limiting toxicities, and pharmacokinetic profile of MET/VEGFR2 inhibitor Foretinib and erlotinib hydrochloride in this schedule.

• To determine the correlation, if any, between the toxicity profile and pharmacokinetics.

• To assess the anti-tumor activity of MET/VEGFR2 inhibitor Foretinib in combination with erlotinib hydrochloride as evidenced by response rates, clinical benefit (complete or partial response or stable disease ≥ 8 weeks duration), and an exploratory endpoint of early assessment of tumor size as a continuous variable (when compared to erlotinib hydrochloride alone).

• To assess one-year survival rate in these patients.

• To investigate the correlation, if any, between response and biomarkers, including EGFR gene mutation, EGFR gene amplification, EGFR gene polymorphisms, c-Met gene mutation, amplification and expression, phospho-c-Met expression, K-Ras gene mutation, and baseline serum HGF levels.

OUTLINE: This is a multicenter, dose-escalation phase I study of MET/VEGFR2 inhibitor Foretinib followed by a randomized, open-label phase II study.

• Phase I (dose-escalation) : Patients receive oral erlotinib hydrochloride once daily on days 1-28. Patients receive oral MET/VEGFR2 inhibitor GSK1363089 once daily on days 15-28 during course 1 and on days 1-28 during all other courses. Courses repeat every 28 days until the maximum-tolerated dose of MET/VEGFR2 inhibitor Foretinib is determined.

Blood samples are collected on days 14 and 28 of course 1 for pharmacokinetics and day 1 of courses 1 and 2 and post treatment for pharmacodynamic studies.

• Phase II: Patients are randomized to 1 of 2 treatment arms:

• Arm I (MET/VEGFR2 inhibitor Foretinib and erlotinib hydrochloride): Patients receive oral MET/VEGFR2 inhibitor Foretinib (at the recommended phase II dose determined in phase I) once daily and oral erlotinib hydrochloride once daily on days 1-28. Courses repeat very 28 days in the absence of disease progression or unacceptable toxicity.

• Arm II (erlotinib hydrochloride only): Patients receive oral erlotinib hydrochloride once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

In both arms, samples are collected for pharmacodynamic studies as in phase I.

After completion of study treatment, patients are followed at week 4 and then every 3 months thereafter.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: February 13, 2015
• Est. primary completion date: March 21, 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed non-small cell lung cancer (NSCLC), meeting all of the following criteria:

• Locally advanced or metastatic disease

• Failed 1-2 prior chemotherapy regimen

• Must be eligible to receive erlotinib therapy (i.e., patients must have received 1-2 prior chemotherapy regimen [combination unless patient is = 70 years]) for advanced or metastatic disease

• No plan to receive further palliative cytotoxic chemotherapy

• EGFR-expression status positive or unknown

• Patients who are known to have tumors that are EGFR negative on IHC are not eligible

• Presence of clinically and/or radiologically documented measurable disease

• At least 1 site of disease must be unidimensionally measurable as follows:

• Chest X-ray = 20 mm

• CT scan (with slice thickness of = 5 mm) = 10 mm (longest diameter)

• Physical exam (using calipers) = 10 mm

• Lymph nodes by CT scan = 15 mm (measured in short axis)

• Measurable lesions must be outside a previous radiotherapy field unless disease progression has been documented

• Must have archival tissue available or undergo a biopsy or FNA prior to registration/ randomization

• No appreciable cavitation in central thoracic lesions

• Patients with overt bleeding from any site (> 30 mL bleeding/episode) within 3 months of study entry are not eligible

• No untreated brain or meningeal metastases (CT scans are not required to rule this out unless there is a clinical suspicion of CNS disease)

• Patients with treated and radiologic or clinical evidence of stable brain metastases, with no evidence of cavitation or hemorrhage in the brain lesion, are eligible providing that they are asymptomatic and do not require corticosteroids (must have discontinued steroids = 1 week prior to entry)

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Patients must have discontinued smoking for = 2 weeks prior to registration, and must be prepared to refrain from cigarette usage until completion of the pharmacokinetic sampling at the end of study course 1 (approximately 6 weeks in total) (Phase I only)

• Granulocyte count (AGC) = 1.5 times 10^9/L

• Platelet count = 100 x 10^9/L

• Serum creatinine = 1.5 times upper normal limit (UNL) OR calculated creatinine clearance = 50 mL/min (= 0.83 mL/sec)

• Bilirubin = 1.5 times UNL

• ALT and AST = 2 times UNL

• No clinically relevant hemoptysis (> 5 mL fresh blood) within 4 weeks prior to study entry

• Patients with only flecks of blood in sputum are permitted

• No other invasive malignancies, unless curatively treated with no evidence of disease

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 90 days after completion of study therapy

• No untreated and/or uncontrolled cardiovascular conditions and/or have symptomatic cardiac dysfunction, including any of the following:

• Unstable angina, congestive heart failure, or myocardial infarction within the previous year

• Cardiac ventricular arrhythmias requiring medication

• History of 2nd or 3rd degree atrioventricular conduction defects

• Patients with a significant cardiac history (even if controlled) or prior doxorubicin exposure are required to have a LVEF > 50%

• Patients with proliferative diabetic retinopathy, retinal arteritis, or hemorrhage must undergo full ophthalmological examination prior to entry to this study

• Must have resting systolic BP = 150 mm Hg and/or diastolic BP = 100 mm Hg (in the presence or absence of a stable dose of anti-hypertensive medication)

• No poorly controlled hypertension

• No history of labile hypertension or poor compliance with anti-hypertensive medication

• No GI tract disease resulting in an inability to absorb oral medication, including any of the following situations:

• Uncontrolled inflammatory GI disease (e.g., Crohn's disease, ulcerative colitis)

• Post-surgical malabsorption characterized by uncontrolled diarrhea that results in weight loss and vitamin deficiency or requires IV hyperalimentation (use of pancreatic enzyme supplementation is allowed)

• No active or uncontrolled infections

• No serious illnesses or medical conditions that would not permit the patient to be managed according to the protocol

• No known hypersensitivity to the study drugs or their components

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No more than two prior chemotherapy regimens for metastatic NSCLC (excluding adjuvant chemotherapy)

• Recovered from any treatment-related toxicities prior to randomization

• Persistent cisplatin- or taxane-induced sensory neuropathy = grade 2 is acceptable

• No prior therapy with agents acting on the EGFR pathway

• No prior therapy with a c-Met inhibitor

• At least 21 days since the last dose of chemotherapy

• At least 21 days since last fraction of prior radiation therapy

• Exceptions may be made for non-myelosuppressive radiation to peripheral areas

• More than 14 days since prior major surgery, provided that wound healing has occurred

• More than 3 weeks since prior and no other concurrent investigational drugs or anti-cancer therapy

• No concurrent CYP3A4 enzyme inducing or inhibiting drugs known to interact with erlotinib hydrochloride, including any of the following:

• Enzyme-inducing anticonvulsants

• Rifampicin

• Rifabutin

• St. John wort

• Atazanavir

• Ketoconazole

• Patients with a history of pulmonary embolus or a deep vein thrombosis diagnosed and/or treated within 6 months prior to registration will be excluded.

Related Conditions & MeSH terms

• Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• MET/VEGFR2 inhibitor Foretinib
PhaseI and Phase II Arm A: Foretinib PO daily dosing starting cycle 1 day 15 and erlotinib PO daily dosing starting cycle 1 day 1. Recommended Phase II dose to be determine in Phase I.
• erlotinib hydrochloride
erlotinib PO daily dosing starting cycle 1 day 1. Recommended Phase II dose to be determine in Phase I.

Other:
• laboratory biomarker analysis
Tumour markers alone cannot be used to assess objective tumour response. If markers are initially above the upper normal limit, however, they must normalize for a patient to be considered in complete response

Locations

Country	Name	City	State
Canada	Juravinski Cancer Centre at Hamilton Health Sciences	Hamilton	Ontario
Canada	Ottawa Health Research Institute - General Division	Ottawa	Ontario
Canada	Univ. Health Network-Princess Margaret Hospital	Toronto	Ontario
Canada	BCCA - Vancouver Cancer Centre	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
NCIC Clinical Trials Group	GlaxoSmithKline

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Leighl NB, Tsao MS, Liu G, Tu D, Ho C, Shepherd FA, Murray N, Goffin JR, Nicholas G, Sakashita S, Chen Z, Kim L, Powers J, Seymour L, Goss G, Bradbury PA. A phase I study of foretinib plus erlotinib in patients with previously treated advanced non-small c — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The recommended phase II dose of daily oral MET/VEGFR2 inhibitor Foretinib when given in combination with standard erlotinib hydrochloride therapy (phase I)	After completion of Phase I portion of the study	3 years
Primary	Safety, tolerability, dose-limiting toxicities, and pharmacokinetic profile (phase I)	Assessed from the time of first dose. Results will be analyzed at time of final analysis	3 years
Primary	Correlation between toxicity and pharmacokinetics (phase I)	After completion of phase I	3 years
Primary	Objective tumor response rate (partial or complete response) (phase II)		After every second cycle
Secondary	Clinical benefit (complete response, partial response, and stable disease for = 8 weeks) (phase II)	End of every second cycle	8 weeks
Secondary	Tumor size at 8 weeks (phase II)	At end of second cycle.	8 weeks
Secondary	1-year survival rate (phase II)		1 year
Secondary	Response or stable disease duration (phase II)		After progression
Secondary	Progression-free survival (phase II)	After completion of therapy	3 years
Secondary	Toxicity (phase II)	From the time of 1st dose and will be assessed overall at the time of final analysis	3 years