Combination Chemotherapy and Computer-Planned Radiation Therapy in Treating Patients With Unresectable Stage III Non-Small Cell Lung Cancer
Induction/Concurrent Chemotherapy and Dose-Escalated Three Dimensional Thoracic Radiation for Patients With Stage III Non Small Cell Lung Cancer: A Randomized Phase II Study
3 other identifiers
interventional
69
1 country
74
Brief Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Computer systems that allow doctors to create a 3-dimensional picture of the tumor to plan treatment may result in more effective radiation therapy. It is not yet known which chemotherapy and/or radiation therapy regimen is more effective in treating non-small cell lung cancer. PURPOSE: Randomized phase II trial to compare the effectiveness of different combination chemotherapy regimens and 3-dimensional radiation therapy in treating patients who have unresectable stage III non-small cell lung cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_2 lung-cancer
Started Mar 2002
Longer than P75 for phase_2 lung-cancer
74 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2002
CompletedFirst Submitted
Initial submission to the registry
April 9, 2002
CompletedFirst Posted
Study publicly available on registry
January 27, 2003
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedJuly 19, 2016
July 1, 2016
4.5 years
April 9, 2002
July 15, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Response
Response is assessed as failure free survival
18 months post treatment
Secondary Outcomes (2)
Overall Survival
6 years post treatment
Toxicity
13 weeks
Study Arms (2)
Paclitaxel + Carboplatin
EXPERIMENTALPaclitaxel and carboplatin induction (2 cycles)followed by chemotherapy with the addition of radiotherapy for 7 cycles
Gemcitabine + Carboplatin
EXPERIMENTALGemcitabine and carboplatin induction (2cycles) followed by chemotherapy with the addition of radiotherapy for 7 cycles
Interventions
Arm A: AUC=6 IV over 30 min for 2 cycles then AUC=2 IV over 30 min q wk for 7 wks Arm B: AUC=5 IV over 30 min for 2 cycles
1000 mg/sq m IV over 30 min days 1 \& 8 repeat q 21 days for 2 cycles; then 35 mg/sq m IV over 30 min 2X wk for 7 wks
225 mg/sq m IV over 3 hrs q 21 days for 2 cycles, then 45 mg/sq m IV over 1 hr q wk for 7 wks
3-D XRT 7400 cGy total after induction (during cycles 3-9)
Eligibility Criteria
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
Study Sites (74)
Northeast Alabama Regional Medical Center
Anniston, Alabama, 36207, United States
Rebecca and John Moores UCSD Cancer Center
La Jolla, California, 92093-0658, United States
Cedars-Sinai Comprehensive Cancer Center at Cedars-Sinai Medical Center
Los Angeles, California, 90048, United States
Naval Medical Center - San Diego
San Diego, California, 92134-3202, United States
Veterans Affairs Medical Center - San Diego
San Diego, California, 92161, United States
UCSF Comprehensive Cancer Center
San Francisco, California, 94115, United States
Veterans Affairs Medical Center - San Francisco
San Francisco, California, 94121, United States
CCOP - Christiana Care Health Services
Newark, Delaware, 19713, United States
Lombardi Cancer Center at Georgetown University Medical Center
Washington D.C., District of Columbia, 20007, United States
Walter Reed Army Medical Center
Washington D.C., District of Columbia, 20307-5001, United States
Veterans Affairs Medical Center - Washington, DC
Washington D.C., District of Columbia, 20422, United States
Broward General Medical Center
Fort Lauderdale, Florida, 33316, United States
Memorial Regional Cancer Center at Memorial Regional Hospital
Hollywood, Florida, 33021, United States
CCOP - Mount Sinai Medical Center
Miami Beach, Florida, 33140, United States
Florida Hospital Cancer Institute
Orlando, Florida, 32804, United States
Veterans Affairs Medical Center - Chicago (Westside Hospital)
Chicago, Illinois, 60612, United States
University of Chicago Cancer Research Center
Chicago, Illinois, 60637-1470, United States
Louis A. Weiss Memorial Hospital
Chicago, Illinois, 60640, United States
CCOP - Illinois Oncology Research Association
Peoria, Illinois, 61615-7828, United States
West Suburban Center for Cancer Care
River Forest, Illinois, 60305, United States
Fort Wayne Medical Oncology and Hematology, Incorporated
Fort Wayne, Indiana, 46885-5099, United States
CCOP - Northern Indiana CR Consortium
South Bend, Indiana, 46601, United States
Holden Comprehensive Cancer Center at University of Iowa
Iowa City, Iowa, 52242-1009, United States
Baptist Hospital East - Louisville
Louisville, Kentucky, 40207, United States
Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute
Boston, Massachusetts, 02115, United States
UMASS Memorial Cancer Center - University Campus
Worcester, Massachusetts, 01655, United States
Lakeland Cancer Care Center at Lakeland Hospital - St. Joseph
Saint Joseph, Michigan, 49085, United States
Veterans Affairs Medical Center - Minneapolis
Minneapolis, Minnesota, 55417, United States
University of Minnesota Cancer Center
Minneapolis, Minnesota, 55455, United States
Veterans Affairs Medical Center - Columbia (Truman Memorial)
Columbia, Missouri, 65201, United States
Ellis Fischel Cancer Center at University of Missouri - Columbia
Columbia, Missouri, 65203, United States
CCOP - Kansas City
Kansas City, Missouri, 64131, United States
Siteman Cancer Center at Barnes-Jewish Hospital
St Louis, Missouri, 63110, United States
Missouri Baptist Cancer Center
St Louis, Missouri, 63131, United States
UNMC Eppley Cancer Center at the University of Nebraska Medical Center
Omaha, Nebraska, 68198-7680, United States
CCOP - Southern Nevada Cancer Research Foundation
Las Vegas, Nevada, 89106, United States
Veterans Affairs Medical Center - Las Vegas
Las Vegas, Nevada, 89106, United States
New Hampshire Oncology-Hematology, PA - Hooksett
Hooksett, New Hampshire, 03106, United States
Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, 03756-0002, United States
Cancer Institute of New Jersey at the Cooper University Hospital
Camden, New Jersey, 08103, United States
Veterans Affairs Medical Center - Buffalo
Buffalo, New York, 14215, United States
Roswell Park Cancer Institute
Buffalo, New York, 14263-0001, United States
CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C.
East Syracuse, New York, 13057, United States
Elmhurst Hospital Center
Elmhurst, New York, 11373, United States
Queens Cancer Center of Queens Hospital
Jamaica, New York, 11432, United States
CCOP - North Shore University Hospital
Manhasset, New York, 11030, United States
North Shore University Hospital
Manhasset, New York, 11030, United States
Memorial Sloan-Kettering Cancer Center
New York, New York, 10021, United States
New York Weill Cornell Cancer Center at Cornell University
New York, New York, 10021, United States
Mount Sinai Medical Center
New York, New York, 10029, United States
SUNY Upstate Medical University Hospital
Syracuse, New York, 13210, United States
Veterans Affairs Medical Center - Syracuse
Syracuse, New York, 13210, United States
Veterans Affairs Medical Center - Asheville
Asheville, North Carolina, 28805, United States
Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
Chapel Hill, North Carolina, 27599-7295, United States
NorthEast Oncology Associates - Concord
Concord, North Carolina, 28025, United States
Veterans Affairs Medical Center - Durham
Durham, North Carolina, 27705, United States
Duke Comprehensive Cancer Center
Durham, North Carolina, 27710, United States
Cape Fear Valley Health System
Fayetteville, North Carolina, 28302-2000, United States
CCOP - Southeast Cancer Control Consortium
Goldsboro, North Carolina, 27534-9479, United States
Lenoir Memorial Cancer Center
Kinston, North Carolina, 28503-1678, United States
Comprehensive Cancer Center at Moore Regional Hospital
Pinehurst, North Carolina, 28374, United States
Zimmer Cancer Center at New Hanover Regional Medical Center
Wilmington, North Carolina, 28402-9025, United States
Comprehensive Cancer Center at Wake Forest University
Winston-Salem, North Carolina, 27157-1082, United States
Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University
Columbus, Ohio, 43210-1240, United States
Oklahoma University Medical Center
Oklahoma City, Oklahoma, 73104, United States
Western Pennsylvania Hospital
Pittsburgh, Pennsylvania, 15224, United States
Lifespan: The Miriam Hospital
Providence, Rhode Island, 02906, United States
Veterans Affairs Medical Center - Dallas
Dallas, Texas, 75219, United States
Vermont Cancer Center at University of Vermont
Burlington, Vermont, 05401-3498, United States
Martha Jefferson Hospital
Charlottesville, Virginia, 22902, United States
Virginia Oncology Associates - Norfolk
Norfolk, Virginia, 23502, United States
MBCCOP - Massey Cancer Center
Richmond, Virginia, 23298-0037, United States
Oncology and Hematology Associates of Southwest Virginia, Incorporated - Roanoke
Roanoke, Virginia, 24014, United States
St. Mary's Medical Center
Huntington, West Virginia, 25701, United States
Related Publications (3)
Socinski MA, Blackstock AW, Bogart JA, Wang X, Munley M, Rosenman J, Gu L, Masters GA, Ungaro P, Sleeper A, Green M, Miller AA, Vokes EE. Randomized phase II trial of induction chemotherapy followed by concurrent chemotherapy and dose-escalated thoracic conformal radiotherapy (74 Gy) in stage III non-small-cell lung cancer: CALGB 30105. J Clin Oncol. 2008 May 20;26(15):2457-63. doi: 10.1200/JCO.2007.14.7371.
PMID: 18487565RESULTBlackstock AW, Socinski MA, Bogart J, et al.: Induction (Ind) plus concurrent (Con) chemotherapy with high-dose (74 Gy) 3-dimensional (3-D) thoracic radiotherapy (TRT) in stage III non-small cell lung cancer (NSCLC): preliminary report of Cancer and Leukemia Group B (CALGB) 30105. [Abstract] J Clin Oncol 24 (Suppl 18): A-7042, 374s, 2006.
RESULTBlackstock AW, Socinski MA, Gu L, et al.: Initial pulmonary toxicity evaluation of chemoradiotherapy (CRT) utilizing 74 Gy 3-dimensional (3-D) thoracic radiation in stage III non-small cell lung cancer (NSCLC): a Cancer and Leukemia Group B (CALGB) randomized phase II trial. [Abstract] J Clin Oncol 23 (Suppl 16): A-7060, 635s, 2005.
RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Arthur William Blackstock, MD
Wake Forest University Health Sciences
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 9, 2002
First Posted
January 27, 2003
Study Start
March 1, 2002
Primary Completion
September 1, 2006
Study Completion
June 1, 2010
Last Updated
July 19, 2016
Record last verified: 2016-07