Bronchial Artery Infusion of Gemcitabine in Treating Patients With Recurrent or Progressive Non-Small Cell Lung Cancer

Phase 1

Terminated

• Conditions: Lung Cancer
• Interventions: Drug: gemcitabine hydrochloride

• Registration Number: NCT00619021
• Lead Sponsor: Masonic Cancer Center, University of Minnesota

Brief Summary

RATIONALE: Bronchial artery infusion uses a catheter to deliver antitumor substances directly to the lungs. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Giving gemcitabine in different ways may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of gemcitabine given by bronchial artery infusion and to see how well it works in treating patients with recurrent or progressive non-small cell lung cancer.

Detailed Description

OBJECTIVES:

Primary

* To establish the maximum tolerated dose of gemcitabine hydrochloride delivered via bronchial artery infusion in patients with recurrent or progressive non-small cell lung cancer.

Secondary

* To evaluate local response in patients treated with this therapy.

* To characterize the pharmacokinetics of gemcitabine hydrochloride in patients treated with this therapy.

OUTLINE: This is a dose-escalation study of gemcitabine hydrochloride delivered via bronchial artery infusion.

Patients receive gemcitabine hydrochloride via bronchial artery infusion over 30-60 minutes on day 1 and via IV infusion over 30 minutes on day 8 of course 1. Patients then receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8 of all subsequent courses. Treatment repeats every 21 days in the absence of disease progression and unacceptable toxicity.

After completion of study therapy, patients are followed every 8 weeks to 3 months for up to 2 years.

Study Timeline

• Study Start: 2003-01
• Study First Submitted: 2008-02-19
• Study First Submitted QC: 2008-02-19
• Study First Posted: 2008-02-20
• Primary Completion: 2009-01
• Study Completion: 2009-01
• Status Verified: 2017-11
• Last Update Submitted: 2017-11-27
• Last Update Posted: 2017-11-29

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 4

Inclusion Criteria

• Cytologically or histologically confirmed non-small cell lung cancer meeting the following criteria:

  • No T2 lesions invading the visceral pleura, causing atelectasis, or proximal to an obstructing pneumonia
  • No T3 lesions invading the chest wall (including the parietal pleura, musculature, and/or rib), mediastinal pleura, diaphragm, or pericardium
  • No T4 lesions invading the heart, great vessels, carina, or esophagus

• Must have disease that is incurable by standard treatment, defined as a minimum of first-line therapy with a platinum-containing regimen and second-line therapy with docetaxel, pemetrexed disodium, or erlotinib hydrochloride

• Measurable or nonmeasurable disease as defined by Response Evaluation Criteria In Solid Tumors (RECIST) criteria

• Eastern Cooperative Oncology Group (ECOG) performance status 0-1

• Life expectancy ≥ 12 weeks

• Hemoglobin ≥ 9.0 g/dL

• Absolute neutrophil count (ANC) ≥ 1,500/mm³

• Platelet count ≥ 100,000/mm³

• Serum creatinine ≤ 3.0 mg/dL

• Total bilirubin < 1.5 times upper limit of normal

• International normalized ratio (INR) ≤ 1.3

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective non-hormonal contraception

Exclusion Criteria

• Superior vena cava syndrome or superior sulcus tumors

• Patients with airway obstructing lesions, or patients experiencing hemoptysis, dyspnea, chest pain, and/or copious sputum production may be eligible after careful consideration by the study physicians

• Prior or concurrent malignancy except inactive nonmelanoma skin cancer, carcinoma in situ of the cervix, stage I carcinoma of the prostate with normal PSA, or other cancer from which the patient has been disease free for 3 years

• Medical conditions that would make this protocol unreasonably hazardous, in the opinion of the treating physician, including any of the following:

  • Uncontrolled infection (including HIV)
  • Poorly controlled diabetes mellitus
  • Active cardiac disease (i.e., unstable angina, myocardial infarction within the past 6 months, or congestive heart failure)

• Other serious medical illness that would limit survival to < 3 months, or psychiatric condition that would prevent informed consent, unless a legal guardian is available

• Must consent to participate in the laboratory study, "Population Pharmacokinetics and Pharmacogenetics of Gemcitabine in Adult Patients with Solid Tumors" during course 1

• More than 6 months since prior gemcitabine hydrochloride

  • More than 2 weeks since other prior chemotherapy

• More than 4 weeks since prior radiotherapy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Cohort 1	gemcitabine hydrochloride	Patient receives gemcitabine 600 mg/m\^2.
Cohort 2	gemcitabine hydrochloride	Patient receives gemcitabine 800 mg/m\^2.
Cohort 3	gemcitabine hydrochloride	Patient receives gemcitabine 1000 mg/m\^2.
Cohort 4	gemcitabine hydrochloride	Patient receives gemcitabine 1200 mg/m\^2.

Primary Outcome Measures

Name	Time	Method
Maximum tolerated dose and dose-limiting toxicity of gemcitabine hydrochloride when administered via bronchial artery infusion	At time of dose-limiting toxicity

Secondary Outcome Measures

Name	Time	Method
Local response as measured by RECIST	Week 8

Trial Locations

Locations (1)

Masonic Cancer Center at University of Minnesota; 🇺🇸 Minneapolis, Minnesota, United States