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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00003881
Other study ID # CDR0000067048
Secondary ID ECOG-2598
Status Completed
Phase Phase 2
First received November 1, 1999
Last updated June 20, 2013
Start date May 1999
Est. completion date July 2004

Study information

Verified date March 2004
Source National Cancer Institute (NCI)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

RATIONALE: Monoclonal antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining monoclonal antibody therapy with chemotherapy may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of the monoclonal antibody trastuzumab plus carboplatin and paclitaxel in treating patients who have advanced non-small cell lung cancer.


Description:

OBJECTIVES: I. Assess the toxicity of monoclonal antibody HER2 with carboplatin and paclitaxel in patients with HER2 positive non-small cell lung cancer. II. Determine median time to progression and one year freedom from progression in this patient population. III. Evaluate one year survival rate and overall objective response rate in this patient population.

OUTLINE: Patients receive paclitaxel IV over 3 hours immediately followed by carboplatin IV over 30 minutes immediately followed by monoclonal antibody HER2 IV over 30-90 minutes on day 1. Patients also receive monoclonal antibody HER2 on days 8 and 15. Treatment is repeated every 3 weeks for 6 courses. After 6 courses of treatment, patients may receive monoclonal antibody HER2 weekly for up to 1 year in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years, every 6 months for 3 years and once a year thereafter until disease progression or death.

PROJECTED ACCRUAL: A total of 22-44 patients will be accrued for this study.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date July 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility DISEASE CHARACTERISTICS: Histologically confirmed non-small cell lung cancer (NSCLC) Recurrent AND/OR Stage IIIB with pleural or pericardial effusion OR Stage IV Must have at least one bidimensionally measurable lesion Must be HER2 positive (1-3+) Brain metastases allowed, if symptoms controlled and not requiring steroids Prior/Concurrent Therapy-- Biologic therapy: Not specified Chemotherapy: No prior chemotherapy for NSCLC Endocrine therapy: No concurrent steroids Radiotherapy: At least 2 weeks since prior radiotherapy Surgery: Not specified

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-1 Life expectancy: Not specified Hematopoietic: Absolute neutrophil count at least 1,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 mg/dL Transaminases no greater than 5 times upper limit of normal Renal: Creatinine no greater than 2 mg/dL Cardiovascular: No uncontrolled angina pectoris and arrhythmias No myocardial infarction within past 3 months No uncompensated congestive heart failure Ejection fraction at least 45% Other: No active infections Not pregnant or nursing Fertile patients must use effective contraception HIV negative No other active malignancies No evidence of peripheral sensory neuropathy of at least grade 2

Study Design

Primary Purpose: Treatment


Intervention

Biological:
trastuzumab

Drug:
carboplatin

paclitaxel


Locations

Country Name City State
Puerto Rico MBCCOP - San Juan San Juan
Puerto Rico Veterans Affairs Medical Center - San Juan San Juan
South Africa Pretoria Academic Hospital Pretoria
United States Veterans Affairs Medical Center - Albany Albany New York
United States CCOP - Ann Arbor Regional Ann Arbor Michigan
United States Emory University Hospital - Atlanta Atlanta Georgia
United States Johns Hopkins Oncology Center Baltimore Maryland
United States Beth Israel Deaconess Medical Center Boston Massachusetts
United States New England Medical Center Hospital Boston Massachusetts
United States Albert Einstein Comprehensive Cancer Center Bronx New York
United States Veterans Affairs Medical Center - Brooklyn Brooklyn New York
United States CCOP - Cedar Rapids Oncology Project Cedar Rapids Iowa
United States Robert H. Lurie Comprehensive Cancer Center, Northwestern University Chicago Illinois
United States Veterans Affairs Medical Center - Chicago (Lakeside) Chicago Illinois
United States Ireland Cancer Center Cleveland Ohio
United States Veterans Affairs Medical Center - Cleveland Cleveland Ohio
United States CCOP - Columbus Columbus Ohio
United States CCOP - Geisinger Clinical and Medical Center Danville Pennsylvania
United States CCOP - Central Illinois Decatur Illinois
United States Veterans Affairs Medical Center - Atlanta (Decatur) Decatur Georgia
United States CCOP - Colorado Cancer Research Program, Inc. Denver Colorado
United States CCOP - Iowa Oncology Research Association Des Moines Iowa
United States CCOP - Duluth Duluth Minnesota
United States Veterans Affairs Medical Center - East Orange East Orange New Jersey
United States CCOP - Evanston Evanston Illinois
United States CCOP - Merit Care Hospital Fargo North Dakota
United States Veterans Affairs Medical Center - Gainsville Gainesville Florida
United States CCOP - Northern New Jersey Hackensack New Jersey
United States Indiana University Cancer Center Indianapolis Indiana
United States Veterans Affairs Medical Center - Indianapolis (Roudebush) Indianapolis Indiana
United States CCOP - Kalamazoo Kalamazoo Michigan
United States CCOP - Southern Nevada Cancer Research Foundation Las Vegas Nevada
United States Beckman Research Institute, City of Hope Los Angeles California
United States University of Wisconsin Comprehensive Cancer Center Madison Wisconsin
United States Veterans Affairs Medical Center - Madison Madison Wisconsin
United States CCOP - Marshfield Medical Research and Education Foundation Marshfield Wisconsin
United States Sylvester Cancer Center, University of Miami Miami Florida
United States Medical College of Wisconsin Milwaukee Wisconsin
United States Veterans Affairs Medical Center - Milwaukee (Zablocki) Milwaukee Wisconsin
United States Veterans Affairs Medical Center - Minneapolis Minneapolis Minnesota
United States Vanderbilt Cancer Center Nashville Tennessee
United States Veterans Affairs Medical Center - Nashville Nashville Tennessee
United States Cancer Institute of New Jersey New Brunswick New Jersey
United States CCOP - Ochsner New Orleans Louisiana
United States MBCCOP - LSU Medical Center New Orleans Louisiana
United States Kaplan Cancer Center New York New York
United States Veterans Affairs Medical Center - New York New York New York
United States CCOP - Missouri Valley Cancer Consortium Omaha Nebraska
United States Veterans Affairs Medical Center - Palo Alto Palo Alto California
United States CCOP - Illinois Oncology Research Association Peoria Illinois
United States Allegheny University Hospitals- Hahnemann Philadelphia Pennsylvania
United States Fox Chase Cancer Center Philadelphia Pennsylvania
United States Kimmel Cancer Center of Thomas Jefferson University - Philadelphia Philadelphia Pennsylvania
United States University of Pennsylvania Cancer Center Philadelphia Pennsylvania
United States University of Pittsburgh Cancer Institute Pittsburgh Pennsylvania
United States Veterans Affairs Medical Center - Pittsburgh Pittsburgh Pennsylvania
United States Mayo Clinic Cancer Center Rochester Minnesota
United States University of Rochester Cancer Center Rochester New York
United States CCOP - Metro-Minnesota Saint Louis Park Minnesota
United States CCOP - Scottsdale Oncology Program Scottsdale Arizona
United States CCOP - Sioux Community Cancer Consortium Sioux Falls South Dakota
United States Stanford University Medical Center Stanford California
United States H. Lee Moffitt Cancer Center and Research Institute Tampa Florida
United States Veterans Affairs Medical Center - Tampa (Haley) Tampa Florida
United States CCOP - Toledo Community Hospital Oncology Program Toledo Ohio
United States CCOP - St. Francis Hospital/Natalie Warren Bryant Cancer Center Tulsa Oklahoma
United States CCOP - Carle Cancer Center Urbana Illinois
United States Walter Reed Army Medical Center Washington District of Columbia
United States CCOP - Wichita Wichita Kansas
United States CCOP - Christiana Care Health Services Wilmington Delaware
United States CCOP - MainLine Health Wynnewood Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Eastern Cooperative Oncology Group National Cancer Institute (NCI)

Countries where clinical trial is conducted

United States,  Puerto Rico,  South Africa, 

References & Publications (4)

Huang C, Stephenson P, Langer CJ, et al.: Trastuzumab in combination with paclitaxel/carboplatin in advanced non-small cell lung cancer: final report of ECOG 2598. [Abstract] Lung Cancer 41 (Suppl 2): A-P628, S251, 2003.

Langer CJ, Adak S, Thor A, et al.: Phase II Eastern Cooperative Oncology Group (ECOG) pilot study of paclitaxel (P), carboplatin (C), and trastuzumab (T) in HER-2/neu (+) advanced non-small cell lung cancer (NSCLC): early analysis of E2598. [Abstract] Pro

Langer CJ, Stephenson P, Thor A, Vangel M, Johnson DH; Eastern Cooperative Oncology Group Study 2598. Trastuzumab in the treatment of advanced non-small-cell lung cancer: is there a role? Focus on Eastern Cooperative Oncology Group study 2598. J Clin Onco — View Citation

Schiller J, Langer CJ, Thor A, et al.: Trastuzumab in combination with paclitaxel/carboplatin advanced non-small cell lung cancer: final report of ECOG 2598. [Abstract] Proceedings of the American Society of Clinical Oncology 22: A-2606, 2003.

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