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Spots Global Cancer Trial Database for Docetaxel and Cisplatin With or Without Dimesna in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

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Trial Identification

Brief Title: Docetaxel and Cisplatin With or Without Dimesna in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

Official Title: A Phase II Randomized Study Of Dose-Dense Docetaxel And Cisplatin Every Two Weeks With Pegfilgrastim And Darbepoetin Alfa With And Without The Chemoprotector BNP7787 In Patients With Advanced Non-Small Cell Lung Cancer

Study ID: NCT00077311

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as docetaxel and cisplatin, work in different ways to stop tumor cells from dividing so they stop growing or die. Chemoprotective drugs, such as dimesna, may help prevent or decrease the side effects (such as nerve, kidney, and inner ear damage) caused by chemotherapy. PURPOSE: This randomized phase II trial is studying giving docetaxel and cisplatin together with dimesna to see how well it works compared to giving docetaxel and cisplatin alone in treating patients with stage IIIB or stage IV non-small cell lung cancer.

Detailed Description: OBJECTIVES: Primary * Compare the incidence and severity of peripheral neuropathy in patients with stage IIIB or IV non-small cell lung cancer treated with docetaxel and cisplatin with or without dimesna. * Compare the feasibility of these regimens, in terms of febrile neutropenia and treatment delays, in these patients. * Compare the objective response rate in patients treated with these regimens. Secondary * Compare the survival and failure-free survival of patients treated with these regimens. * Compare the toxicity profile of these regimens in these patients. * Compare the incidence and severity of cisplatin-induced nephrotoxicity in patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I\*: Patients receive docetaxel IV over 1 hour and cisplatin IV over 1 hour on day 1 and pegfilgrastim subcutaneously (SC) on day 2. * Arm II\*: Patients receive docetaxel, cisplatin, and pegfilgrastim as in arm I and dimesna IV over 30 minutes on day 1. NOTE: \*In both arms, darbepoetin alfa is administered SC on day 1 of each course for hemoglobin ≤ 11 g/dL. In both arms, treatment repeats every 2 weeks for a total of 6 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 1 year and then every 6 months for 2 years.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

El Camino Hospital, Mountain View, California, United States

Beebe Medical Center, Lewes, Delaware, United States

CCOP - Christiana Care Health Services, Newark, Delaware, United States

St. Francis Hospital, Wilmington, Delaware, United States

St. Joseph Medical Center, Bloomington, Illinois, United States

Graham Hospital, Canton, Illinois, United States

Memorial Hospital, Carthage, Illinois, United States

University of Illinois Cancer Center, Chicago, Illinois, United States

Veterans Affairs Medical Center - Chicago Westside Hospital, Chicago, Illinois, United States

University of Chicago Cancer Research Center, Chicago, Illinois, United States

Louis A. Weiss Memorial Hospital, Chicago, Illinois, United States

Eureka Community Hospital, Eureka, Illinois, United States

Galesburg Clinic, Galesburg, Illinois, United States

Galesburg Cottage Hospital, Galesburg, Illinois, United States

Mason District Hospital, Havana, Illinois, United States

Hopedale Medical Complex, Hopedale, Illinois, United States

Kewanee Hospital, Kewanee, Illinois, United States

McDonough District Hospital, Macomb, Illinois, United States

BroMenn Regional Medical Center, Normal, Illinois, United States

Community Cancer Center, Normal, Illinois, United States

Community Hospital of Ottawa, Ottawa, Illinois, United States

Oncology Hematology Associates of Central Illinois - Ottawa, Ottawa, Illinois, United States

Cancer Treatment Center at Pekin Hospital, Pekin, Illinois, United States

Proctor Hospital, Peoria, Illinois, United States

CCOP - Illinois Oncology Research Association, Peoria, Illinois, United States

Oncology/Hematology Associates of Central Illinois, P.C., Peoria, Illinois, United States

Methodist Medical Center of Illinois, Peoria, Illinois, United States

OSF St. Francis Medical Center, Peoria, Illinois, United States

Illinois Valley Community Hospital, Peru, Illinois, United States

Perry Memorial Hospital, Princeton, Illinois, United States

St. Margaret's Hospital, Spring Valley, Illinois, United States

Hematology Oncology Associates of the Quad Cities, Bettendorf, Iowa, United States

Holden Comprehensive Cancer Center at University of Iowa, Iowa City, Iowa, United States

Greenebaum Cancer Center at University of Maryland Medical Center, Baltimore, Maryland, United States

Veterans Affairs Medical Center - Baltimore, Baltimore, Maryland, United States

Union Hospital Cancer Center at Union Hospital, Elkton MD, Maryland, United States

Arch Medical Services, Incorporated at Center for Cancer Care Research, Saint Louis, Missouri, United States

Missouri Baptist Cancer Center, St. Louis, Missouri, United States

Cancer Resource Center - Lincoln, Lincoln, Nebraska, United States

Methodist Cancer Center at Methodist Hospital - Omaha, Omaha, Nebraska, United States

Creighton University Medical Center, Omaha, Nebraska, United States

University Medical Center of Southern Nevada, Las Vegas, Nevada, United States

CCOP - Nevada Cancer Research Foundation, Las Vegas, Nevada, United States

New Hampshire Oncology-Hematology, PA - Hooksett, Hooksett, New Hampshire, United States

Lakes Region General Hospital, Laconia, New Hampshire, United States

Elliot Regional Cancer Center, Manchester, New Hampshire, United States

Cancer Institute of New Jersey at the Cooper University Hospital - Voorhees, Voorhees, New Jersey, United States

Charles R. Wood Cancer Center at Glens Falls Hospital, Glens Falls, New York, United States

CCOP - Hematology-Oncology Associates of Central New York, Syracuse, New York, United States

SUNY Upstate Medical University Hospital, Syracuse, New York, United States

Community General Hospital of Greater Syracuse, Syracuse, New York, United States

Faxton Regional Cancer Center, Utica, New York, United States

Duke Comprehensive Cancer Center, Durham, North Carolina, United States

Wayne Memorial Hospital, Incorporated, Goldsboro, North Carolina, United States

Lenoir Memorial Cancer Center, Kinston, North Carolina, United States

Zimmer Cancer Center at New Hanover Regional Medical Center, Wilmington, North Carolina, United States

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University, Columbus, Ohio, United States

Cancer Care Associates - Mercy Campus, Oklahoma City, Oklahoma, United States

McLeod Regional Medical Center, Florence, South Carolina, United States

Veterans Affairs Medical Center - Dallas, Dallas, Texas, United States

Parkland Memorial Hospital, Dallas, Texas, United States

Zale Lipshy University Hospital, Dallas, Texas, United States

Simmons Comprehensive Cancer Center at University of Texas Southwestern Medical Center - Dallas, Dallas, Texas, United States

St. Mary's Regional Cancer Center at St. Mary's Medical Center, Huntington, West Virginia, United States

Contact Details

Name: Antonius Miller, MD

Affiliation: Wake Forest University Health Sciences

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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