- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01142388
Paclitaxel With or Without Cixutumumab as Second-Line Therapy in Treating Patients With Metastatic Esophageal Cancer or Gastroesophageal Junction Cancer
Randomized Phase II Study of Paclitaxel With or Without the Anti-IGF-IR mAb Cixutumumab (IMC-A12) as Second Line Treatment for Patients With Metastatic Esophageal or GE Junction Cancer
Study Overview
Status
Conditions
- Recurrent Esophageal Carcinoma
- Metastatic Gastroesophageal Junction Adenocarcinoma
- Stage IV Esophageal Cancer AJCC v7
- Metastatic Esophageal Squamous Cell Carcinoma
- Metastatic Esophageal Adenocarcinoma
- Recurrent Gastroesophageal Junction Adenocarcinoma
- Recurrent Esophageal Adenocarcinoma
- Recurrent Esophageal Squamous Cell Carcinoma
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVES:
I. To evaluate the progression-free survival of paclitaxel plus cixutumumab (IMC-A12) versus paclitaxel alone as second-line therapy in patients with metastatic esophagus or gastroesophageal (GE) junction cancer.
SECONDARY OBJECTIVES:
I. To evaluate the overall survival of paclitaxel plus cixutumumab (IMC-A12) versus paclitaxel alone in this patient population.
II. To evaluate the response rate of paclitaxel plus cixutumumab (IMC-A12) versus paclitaxel alone in this patient population.
III. To evaluate the toxicity of cixutumumab (IMC-A12) plus paclitaxel versus paclitaxel alone in this patient population.
IV. Exploratory analyses will assess potentially relevant cixutumumab (IMC-A12) pharmacodynamic biomarkers obtained from serum samples, including but not limited to, insulin-like growth factor (IGF)-I, IGF-II, insulin-like growth factor binding protein (IGFBP)-2, and IGFBP-3.
OUTLINE: Patients are equally randomized to 1 of 2 treatment arms.
ARM I: Patients receive paclitaxel intravenously (IV) over 1 hour at a dose of 80 mg/m^2 on days 1, 8, and 15 of every 28 day cycle.
ARM II: Patients receive cixutumumab IV over 1 hour at a dose of 10 mg/kg on days 1 and 15 of every 28 day cycle and paclitaxel as in Arm I.
In both arms, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 3 months for 2 years.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
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Arizona
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Scottsdale, Arizona, United States, 85259
- Mayo Clinic in Arizona
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California
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Palo Alto, California, United States, 94304
- Stanford Cancer Institute Palo Alto
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Colorado
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Aurora, Colorado, United States, 80012
- The Medical Center of Aurora
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Boulder, Colorado, United States, 80301
- Boulder Community Hospital
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Colorado Springs, Colorado, United States, 80907
- Penrose-Saint Francis Healthcare
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Denver, Colorado, United States, 80210
- Porter Adventist Hospital
-
Denver, Colorado, United States, 80218
- Presbyterian - Saint Lukes Medical Center - Health One
-
Denver, Colorado, United States, 80218
- SCL Health Saint Joseph Hospital
-
Denver, Colorado, United States, 80220
- Rose Medical Center
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Denver, Colorado, United States, 80222
- Western States Cancer Research NCORP
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Englewood, Colorado, United States, 80113
- Swedish Medical Center
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Grand Junction, Colorado, United States, 81501
- Saint Mary's Hospital and Regional Medical Center
-
Greeley, Colorado, United States, 80631
- North Colorado Medical Center
-
Lakewood, Colorado, United States, 80228
- Saint Anthony Hospital
-
Littleton, Colorado, United States, 80122
- Littleton Adventist Hospital
-
Lone Tree, Colorado, United States, 80124
- Sky Ridge Medical Center
-
Longmont, Colorado, United States, 80501
- Longmont United Hospital
-
Loveland, Colorado, United States, 80539
- McKee Medical Center
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Parker, Colorado, United States, 80138
- Parker Adventist Hospital
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Pueblo, Colorado, United States, 81004
- Saint Mary Corwin Medical Center
-
Thornton, Colorado, United States, 80229
- North Suburban Medical Center
-
Wheat Ridge, Colorado, United States, 80033
- SCL Health Lutheran Medical Center
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Connecticut
-
Hartford, Connecticut, United States, 06105
- Smilow Cancer Hospital Care Center at Saint Francis
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Delaware
-
Lewes, Delaware, United States, 19958
- Beebe Medical Center
-
Newark, Delaware, United States, 19718
- Christiana Care Health System-Christiana Hospital
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Florida
-
Jacksonville, Florida, United States, 32224-9980
- Mayo Clinic in Florida
-
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Georgia
-
Atlanta, Georgia, United States, 30322
- Emory University Hospital/Winship Cancer Institute
-
Savannah, Georgia, United States, 31405
- Lewis Cancer and Research Pavilion at Saint Joseph's/Candler
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Idaho
-
Boise, Idaho, United States, 83706
- Saint Alphonsus Cancer Care Center-Boise
-
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Illinois
-
Aurora, Illinois, United States, 60504
- Rush - Copley Medical Center
-
Berwyn, Illinois, United States, 60402
- MacNeal Hospital and Cancer Center
-
Bloomington, Illinois, United States, 61701
- Saint Joseph Medical Center
-
Canton, Illinois, United States, 61520
- Graham Hospital Association
-
Carthage, Illinois, United States, 62321
- Memorial Hospital
-
Chicago, Illinois, United States, 60611
- Northwestern University
-
Chicago, Illinois, United States, 60611
- Hematology and Oncology Associates
-
Decatur, Illinois, United States, 62526
- Decatur Memorial Hospital
-
Decatur, Illinois, United States, 62526
- Heartland Cancer Research NCORP
-
Eureka, Illinois, United States, 61530
- Eureka Hospital
-
Galesburg, Illinois, United States, 61401
- Illinois CancerCare-Galesburg
-
Harvey, Illinois, United States, 60426
- Ingalls Memorial Hospital
-
Havana, Illinois, United States, 62644
- Mason District Hospital
-
Highland Park, Illinois, United States, 60035
- Hematology Oncology Associates of Illinois-Highland Park
-
Hinsdale, Illinois, United States, 60521
- Hinsdale Hematology Oncology Associates Incorporated
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Joliet, Illinois, United States, 60435
- Duly Health and Care Joliet
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Kankakee, Illinois, United States, 60901
- Presence Saint Mary's Hospital
-
Libertyville, Illinois, United States, 60048
- AMG Libertyville - Oncology
-
Macomb, Illinois, United States, 61455
- Mcdonough District Hospital
-
Moline, Illinois, United States, 61265
- Trinity Medical Center
-
Naperville, Illinois, United States, 60563
- DuPage Medical Group-Ogden
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Niles, Illinois, United States, 60714
- Illinois Cancer Specialists-Niles
-
Normal, Illinois, United States, 61761
- Carle Cancer Institute Normal
-
Normal, Illinois, United States, 61761
- Bromenn Regional Medical Center
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Ottawa, Illinois, United States, 61350
- Ottawa Regional Hospital and Healthcare Center
-
Pekin, Illinois, United States, 61554
- OSF Saint Francis Radiation Oncology at Pekin Cancer Treatment Center
-
Peoria, Illinois, United States, 61636
- Methodist Medical Center of Illinois
-
Peoria, Illinois, United States, 61637
- OSF Saint Francis Medical Center
-
Peoria, Illinois, United States, 61615
- Illinois CancerCare-Peoria
-
Peoria, Illinois, United States, 61614
- Proctor Hospital
-
Peru, Illinois, United States, 61354
- Illinois Valley Hospital
-
Princeton, Illinois, United States, 61356
- Perry Memorial Hospital
-
River Forest, Illinois, United States, 60305
- West Suburban Medical Center
-
Rockford, Illinois, United States, 61104
- Swedish American Hospital
-
Skokie, Illinois, United States, 60076
- Hematology Oncology Associates of Illinois - Skokie
-
Springfield, Illinois, United States, 62781
- Memorial Medical Center
-
Urbana, Illinois, United States, 61801
- Carle Cancer Center
-
-
Indiana
-
Elkhart, Indiana, United States, 46515
- Elkhart General Hospital
-
Indianapolis, Indiana, United States, 46202
- Indiana University/Melvin and Bren Simon Cancer Center
-
Indianapolis, Indiana, United States, 46202
- Sidney and Lois Eskenazi Hospital
-
Indianapolis, Indiana, United States, 46202
- Richard L. Roudebush Veterans Affairs Medical Center
-
Indianapolis, Indiana, United States, 46219
- IU Health Central Indiana Cancer Centers-East
-
Kokomo, Indiana, United States, 46904
- Community Howard Regional Health
-
La Porte, Indiana, United States, 46350
- IU Health La Porte Hospital
-
Michigan City, Indiana, United States, 46360
- Franciscan Saint Anthony Health-Michigan City
-
Mishawaka, Indiana, United States, 46545
- Saint Joseph Regional Medical Center-Mishawaka
-
Muncie, Indiana, United States, 47303
- IU Health Ball Memorial Hospital
-
South Bend, Indiana, United States, 46601
- Memorial Hospital of South Bend
-
South Bend, Indiana, United States, 46628
- Northern Indiana Cancer Research Consortium
-
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Iowa
-
Ames, Iowa, United States, 50010
- McFarland Clinic - Ames
-
Cedar Rapids, Iowa, United States, 52403
- Mercy Hospital
-
Cedar Rapids, Iowa, United States, 52403
- Oncology Associates at Mercy Medical Center
-
Clive, Iowa, United States, 50325
- Medical Oncology and Hematology Associates-West Des Moines
-
Des Moines, Iowa, United States, 50309
- Iowa Methodist Medical Center
-
Des Moines, Iowa, United States, 50314
- Mercy Medical Center - Des Moines
-
Des Moines, Iowa, United States, 50309
- Medical Oncology and Hematology Associates-Des Moines
-
Des Moines, Iowa, United States, 50314
- Mission Cancer and Blood - Laurel
-
Des Moines, Iowa, United States, 50316
- Iowa Lutheran Hospital
-
Des Moines, Iowa, United States, 50309
- Iowa-Wide Oncology Research Coalition NCORP
-
Mason City, Iowa, United States, 50401
- Mercy Medical Center - North Iowa
-
Sioux City, Iowa, United States, 51101
- Siouxland Regional Cancer Center
-
Sioux City, Iowa, United States, 51102
- Mercy Medical Center-Sioux City
-
Sioux City, Iowa, United States, 51104
- Saint Luke's Regional Medical Center
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Kansas
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Chanute, Kansas, United States, 66720
- Cancer Center of Kansas - Chanute
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Dodge City, Kansas, United States, 67801
- Cancer Center of Kansas - Dodge City
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El Dorado, Kansas, United States, 67042
- Cancer Center of Kansas - El Dorado
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Fort Scott, Kansas, United States, 66701
- Cancer Center of Kansas - Fort Scott
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Independence, Kansas, United States, 67301
- Cancer Center of Kansas-Independence
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Kingman, Kansas, United States, 67068
- Cancer Center of Kansas-Kingman
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Lawrence, Kansas, United States, 66044
- Lawrence Memorial Hospital
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Liberal, Kansas, United States, 67905
- Cancer Center of Kansas-Liberal
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McPherson, Kansas, United States, 67460
- Cancer Center of Kansas - McPherson
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Newton, Kansas, United States, 67114
- Cancer Center of Kansas - Newton
-
Parsons, Kansas, United States, 67357
- Cancer Center of Kansas - Parsons
-
Pratt, Kansas, United States, 67124
- Cancer Center of Kansas - Pratt
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Salina, Kansas, United States, 67401
- Cancer Center of Kansas - Salina
-
Wellington, Kansas, United States, 67152
- Cancer Center of Kansas - Wellington
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Wichita, Kansas, United States, 67214
- Ascension Via Christi Hospitals Wichita
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Wichita, Kansas, United States, 67208
- Cancer Center of Kansas-Wichita Medical Arts Tower
-
Wichita, Kansas, United States, 67214
- Cancer Center of Kansas - Wichita
-
Wichita, Kansas, United States, 67208
- Associates In Womens Health
-
Wichita, Kansas, United States, 67214
- Wichita NCI Community Oncology Research Program
-
Winfield, Kansas, United States, 67156
- Cancer Center of Kansas - Winfield
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Louisiana
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Baton Rouge, Louisiana, United States, 70809
- Mary Bird Perkins Cancer Center
-
New Orleans, Louisiana, United States, 70112
- University Medical Center New Orleans
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New Orleans, Louisiana, United States, 70112
- Louisiana State University Health Science Center
-
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Maryland
-
Baltimore, Maryland, United States, 21287
- Johns Hopkins University/Sidney Kimmel Cancer Center
-
Elkton, Maryland, United States, 21921
- Christiana Care - Union Hospital
-
-
Michigan
-
Adrian, Michigan, United States, 49221
- Bixby Medical Center
-
Adrian, Michigan, United States, 49221
- Hickman Cancer Center
-
Ann Arbor, Michigan, United States, 48106
- Saint Joseph Mercy Hospital
-
Ann Arbor, Michigan, United States, 48106
- Michigan Cancer Research Consortium NCORP
-
Dearborn, Michigan, United States, 48124
- Beaumont Hospital - Dearborn
-
Detroit, Michigan, United States, 48236
- Ascension Saint John Hospital
-
Flint, Michigan, United States, 48532
- Genesys Regional Medical Center-West Flint Campus
-
Flint, Michigan, United States, 48503
- Hurley Medical Center
-
Jackson, Michigan, United States, 49201
- Allegiance Health
-
Kalamazoo, Michigan, United States, 49007
- West Michigan Cancer Center
-
Kalamazoo, Michigan, United States, 49007
- Bronson Methodist Hospital
-
Kalamazoo, Michigan, United States, 49048
- Borgess Medical Center
-
Lansing, Michigan, United States, 48912
- University of Michigan Health - Sparrow Lansing
-
Livonia, Michigan, United States, 48154
- Trinity Health Saint Mary Mercy Livonia Hospital
-
Monroe, Michigan, United States, 48162
- Mercy Memorial Hospital
-
Monroe, Michigan, United States, 48162
- Toledo Clinic Cancer Centers-Monroe
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Pontiac, Michigan, United States, 48341
- Saint Joseph Mercy Oakland
-
Port Huron, Michigan, United States, 48060
- Lake Huron Medical Center
-
Saginaw, Michigan, United States, 48601
- Ascension Saint Mary's Hospital
-
Saint Joseph, Michigan, United States, 49085
- Lakeland Medical Center Saint Joseph
-
Saint Joseph, Michigan, United States, 49085
- Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center
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Warren, Michigan, United States, 48093
- Saint John Macomb-Oakland Hospital
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Minnesota
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Brainerd, Minnesota, United States, 56401
- Essentia Health Saint Joseph's Medical Center
-
Burnsville, Minnesota, United States, 55337
- Fairview Ridges Hospital
-
Coon Rapids, Minnesota, United States, 55433
- Mercy Hospital
-
Duluth, Minnesota, United States, 55805
- Essentia Health Cancer Center
-
Duluth, Minnesota, United States, 55805
- Essentia Health Saint Mary's Medical Center
-
Duluth, Minnesota, United States, 55805
- Miller-Dwan Hospital
-
Edina, Minnesota, United States, 55435
- Fairview Southdale Hospital
-
Fridley, Minnesota, United States, 55432
- Unity Hospital
-
Hutchinson, Minnesota, United States, 55350
- Hutchinson Area Health Care
-
Maplewood, Minnesota, United States, 55109
- Saint John's Hospital - Healtheast
-
Maplewood, Minnesota, United States, 55109
- Minnesota Oncology Hematology PA-Maplewood
-
Minneapolis, Minnesota, United States, 55415
- Hennepin County Medical Center
-
Minneapolis, Minnesota, United States, 55407
- Abbott-Northwestern Hospital
-
New Ulm, Minnesota, United States, 56073
- New Ulm Medical Center
-
Robbinsdale, Minnesota, United States, 55422
- North Memorial Medical Health Center
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic in Rochester
-
Saint Louis Park, Minnesota, United States, 55416
- Park Nicollet Clinic - Saint Louis Park
-
Saint Louis Park, Minnesota, United States, 55416
- Metro Minnesota Community Oncology Research Consortium
-
Saint Paul, Minnesota, United States, 55101
- Regions Hospital
-
Saint Paul, Minnesota, United States, 55102
- United Hospital
-
Shakopee, Minnesota, United States, 55379
- Saint Francis Regional Medical Center
-
Stillwater, Minnesota, United States, 55082
- Lakeview Hospital
-
Waconia, Minnesota, United States, 55387
- Ridgeview Medical Center
-
Willmar, Minnesota, United States, 56201
- Rice Memorial Hospital
-
Woodbury, Minnesota, United States, 55125
- Minnesota Oncology Hematology PA-Woodbury
-
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Nebraska
-
Lincoln, Nebraska, United States, 68510
- Nebraska Cancer Research Center
-
Omaha, Nebraska, United States, 68124
- Alegent Health Bergan Mercy Medical Center
-
Omaha, Nebraska, United States, 68122
- Alegent Health Immanuel Medical Center
-
Omaha, Nebraska, United States, 68130
- Alegent Health Lakeside Hospital
-
Omaha, Nebraska, United States, 68131
- Creighton University Medical Center
-
Omaha, Nebraska, United States, 68106
- Missouri Valley Cancer Consortium
-
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New Jersey
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Camden, New Jersey, United States, 08103
- Cooper Hospital University Medical Center
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East Orange, New Jersey, United States, 07018-1095
- Veterans Adminstration New Jersey Health Care System
-
Freehold, New Jersey, United States, 07728
- CentraState Medical Center
-
Hamilton, New Jersey, United States, 08690
- The Cancer Institute of New Jersey Hamilton
-
New Brunswick, New Jersey, United States, 08903
- Rutgers Cancer Institute of New Jersey
-
Newark, New Jersey, United States, 07101
- Rutgers New Jersey Medical School
-
Newark, New Jersey, United States, 07112
- Newark Beth Israel Medical Center
-
-
New York
-
Albany, New York, United States, 12208
- New York Oncology Hematology PC - Albany Medical Center
-
-
North Dakota
-
Fargo, North Dakota, United States, 58103
- Essentia Health Cancer Center-South University Clinic
-
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Ohio
-
Akron, Ohio, United States, 44304
- Summa Health System - Akron Campus
-
Bowling Green, Ohio, United States, 43402
- Toledo Clinic Cancer Centers-Bowling Green
-
Canton, Ohio, United States, 44708
- Cleveland Clinic Mercy Hospital
-
Cleveland, Ohio, United States, 44109
- MetroHealth Medical Center
-
Clyde, Ohio, United States, 43410
- North Coast Cancer Care-Clyde
-
Elyria, Ohio, United States, 44035
- Mercy Cancer Center-Elyria
-
Elyria, Ohio, United States, 44035
- Hematology Oncology Center Incorporated
-
Lima, Ohio, United States, 45801
- Saint Rita's Medical Center
-
Lima, Ohio, United States, 45804
- Lima Memorial Hospital
-
Maumee, Ohio, United States, 43537
- Toledo Clinic Cancer Centers-Maumee
-
Maumee, Ohio, United States, 43537
- Saint Luke's Hospital
-
Norwalk, Ohio, United States, 44857
- Fisher-Titus Medical Center
-
Oregon, Ohio, United States, 43616
- Saint Charles Hospital
-
Oregon, Ohio, United States, 43616
- Toledo Clinic Cancer Centers-Oregon
-
Sandusky, Ohio, United States, 44870
- North Coast Cancer Care
-
Sylvania, Ohio, United States, 43560
- ProMedica Flower Hospital
-
Tiffin, Ohio, United States, 44883
- Mercy Hospital of Tiffin
-
Toledo, Ohio, United States, 43606
- ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
-
Toledo, Ohio, United States, 43608
- Saint Vincent Mercy Medical Center
-
Toledo, Ohio, United States, 43623
- Mercy Health - Saint Anne Hospital
-
Toledo, Ohio, United States, 43623
- Toledo Clinic Cancer Centers-Toledo
-
Toledo, Ohio, United States, 43614
- University of Toledo
-
Toledo, Ohio, United States, 43617
- Toledo Community Hospital Oncology Program CCOP
-
Wauseon, Ohio, United States, 43567
- Fulton County Health Center
-
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Pennsylvania
-
Bethlehem, Pennsylvania, United States, 18015
- Saint Luke's University Hospital-Bethlehem Campus
-
Bryn Mawr, Pennsylvania, United States, 19010
- Bryn Mawr Hospital
-
Butler, Pennsylvania, United States, 16001
- Butler Memorial Hospital
-
Danville, Pennsylvania, United States, 17822
- Geisinger Medical Center
-
Hazleton, Pennsylvania, United States, 18201
- Geisinger Medical Center-Cancer Center Hazleton
-
Paoli, Pennsylvania, United States, 19301
- Paoli Memorial Hospital
-
Philadelphia, Pennsylvania, United States, 19111
- Fox Chase Cancer Center
-
Philadelphia, Pennsylvania, United States, 19107
- Thomas Jefferson University Hospital
-
Pittsburgh, Pennsylvania, United States, 15232
- University of Pittsburgh Cancer Institute (UPCI)
-
Pottstown, Pennsylvania, United States, 19464
- Pottstown Hospital
-
Scranton, Pennsylvania, United States, 18508
- Hematology and Oncology Associates of North East Pennsylvania
-
State College, Pennsylvania, United States, 16801
- Geisinger Medical Group
-
West Reading, Pennsylvania, United States, 19611
- Reading Hospital
-
Wilkes-Barre, Pennsylvania, United States, 18711
- Geisinger Wyoming Valley/Henry Cancer Center
-
Wynnewood, Pennsylvania, United States, 19096
- Lankenau Medical Center
-
Wynnewood, Pennsylvania, United States, 19096
- Main Line Health NCORP
-
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Tennessee
-
Jackson, Tennessee, United States, 38301
- Jackson-Madison County General Hospital
-
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Virginia
-
Fredericksburg, Virginia, United States, 22401
- Fredericksburg Oncology Inc
-
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West Virginia
-
Wheeling, West Virginia, United States, 26003
- Wheeling Hospital/Schiffler Cancer Center
-
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Wisconsin
-
Antigo, Wisconsin, United States, 54409
- Langlade Hospital and Cancer Center
-
Green Bay, Wisconsin, United States, 54301
- Saint Vincent Hospital Cancer Center Green Bay
-
Johnson Creek, Wisconsin, United States, 53038
- UW Cancer Center Johnson Creek
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La Crosse, Wisconsin, United States, 54601
- Gundersen Lutheran Medical Center
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Madison, Wisconsin, United States, 53717
- Dean Hematology and Oncology Clinic
-
Madison, Wisconsin, United States, 53792
- University of Wisconsin Carbone Cancer Center
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Manitowoc, Wisconsin, United States, 54221
- Holy Family Memorial Hospital
-
Marinette, Wisconsin, United States, 54143
- Bay Area Medical Center
-
Sheboygan, Wisconsin, United States, 53081
- HSHS Saint Nicholas Hospital
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Wausau, Wisconsin, United States, 54401
- Aspirus Regional Cancer Center
-
Wisconsin Rapids, Wisconsin, United States, 54494
- Aspirus Cancer Care - Wisconsin Rapids
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Life expectancy >= 12 weeks
- Women must not be pregnant or breast-feeding due to potential harm to fetus from cixutumumab (IMC-A12) and paclitaxel; all females of childbearing potential must have a blood test or urine study within 48 hours prior to registration to rule out pregnancy
- Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method or birth control; abstinence) for the duration of study therapy and for 3 months after the last dose of cixutumumab (IMC-A12); should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
- Patients must have measurable disease
Patients must have metastatic disease of the esophagus or gastroesophageal junction
- Histologic, cytologic or radiologic documentation of metastatic squamous cell carcinoma or adenocarcinoma of the esophagus or gastroesophageal junction; radiologic, endoscopic, histologic or cytologic evidence of locally recurrent or locally residual (post-resection) disease is also permitted
- For the purposes of this study, undifferentiated adenocarcinomas and adenosquamous tumors will be considered as adenocarcinomas; in addition, tumors involving the gastroesophageal junction will be defined by the Siewert classification
Patients with gastroesophageal junction tumors who are eligible:
- Adenocarcinoma of the esophageal junction (AEG) Type I: adenocarcinoma of the distal esophagus which usually arises from an area with specialized intestinal metaplasia of the esophagus, i.e., Barrett's esophagus, and may infiltrate the esophagogastric junction from above
- AEG Type II: true carcinoma of the cardia arising from the cardiac epithelium or short segments with intestinal metaplasia at the esophagogastric junction
Patients with gastroesophageal junction tumors who are NOT eligible:
- AEG Type III: subcardial gastric carcinoma which infiltrates the esophagogastric junction and distal esophagus from below
Patients must have received and progressed on one and only one line of prior systemic therapy for esophagus or esophagogastric cancer; this could have included one regimen for metastatic disease, or one regimen with radiotherapy for initially locally advanced disease; prior radiation therapy is permitted
- If patients progress or recur within 6 months of neoadjuvant/adjuvant therapy, this will be considered one line of therapy; for patients progressing or recurring more than 6 months after neoadjuvant/adjuvant therapy, they will need to receive one line of therapy for recurrent disease to be eligible
- If patients receive one regimen in which a chemotherapy agent is dropped for toxicity without progression, this treatment will be considered one line of therapy; however, substitution or addition of a new agent will be considered a second line of therapy
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Leukocytes > 3,000/mcL
- Absolute neutrophil count >= 1,500/mcL
- Hemoglobin >= 9 g/dL
- Platelets >= 100,000/mcL
- Total bilirubin =< institutional upper limit of normal (ULN)
- Aspartate transaminase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine transaminase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 3 X institutional ULN
- Creatinine =< 1.5 X institutional ULN or creatinine clearance >= 60 mL/min/1.73m^2 for patients with creatinine levels above institutional normal
- Patients must have fasting serum glucose =< 160 mg/dL (8.8 mmol/L) or =< ULN, and hemoglobin A1C =< 7% (0.07 International System of Units [SI units]) within 14 days of registration; if baseline nonfasting glucose =< 160 mg/dL (8.8 mmol/L), fasting glucose measurement is not required
- Registration no fewer than 28 days from last chemotherapy
- A "currently active" second malignancy other than non-melanoma skin cancers are not to be registered; patients are not considered to have a "currently active" malignancy if they have completed therapy and are considered by their physician to be at less than 30% risk of relapse
Exclusion Criteria:
- Patients have received prior taxane or anti-insulin growth factor receptor (IGFR) therapy
Patients must not have any of the following conditions:
- Poorly controlled diabetes mellitus; patients with a history of diabetes mellitus are allowed to participate, provided that their blood glucose is within normal range (fasting glucose =< 160 mg/dL [8.8 mmol/L] or below the ULN and hemoglobin A1C =< 7% [0.07 SI units]) and that they are on a stable dietary or therapeutic regimen for this condition
- Recent major surgery, hormonal therapy (other than replacement) or chemotherapy, within 4 weeks prior to entering the study or those who have not recovered from adverse events
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to cixutumumab (IMC-A12)
- Psychiatric illness that would prevent the patient from giving informed consent
- Medical conditions such as active/uncontrolled infection (including HIV) or cardiac disease that would make this protocol unreasonably hazardous for the patient in the opinion of the treating physician; cardiac disease may include uncontrolled high blood pressure, unstable angina, or serious uncontrolled cardiac arrhythmia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Arm I (paclitaxel)
Patients receive paclitaxel IV over 1 hour on days 1, 8, and 15.
|
Correlative studies
Correlative studies
Given IV
Other Names:
|
Experimental: Arm II (cixutumumab, paclitaxel)
Patients receive cixutumumab IV over 1 hour on days 1 and 15, and paclitaxel as in Arm I.
|
Correlative studies
Correlative studies
Given IV
Other Names:
Given IV
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Progression-free Survival
Time Frame: assessed every 3 months for 2 years after registration
|
Progression-free survival (PFS) is defined as the time from randomization to progression or death without evidence of progression.
For cases without documentation of progression, follow-up was censored at the date of last disease assessment without progression, unless death occurred within a short period of time (4 months) following the date last known progression-free, in which case the death was counted as an event, or in the case of death within 4 months of randomization in the absence of disease evaluation before that time.
PFS was estimated using the Kaplan-Meier method, with 90% confidence intervals calculated using Greenwood's formula, and compared by the log rank test.
|
assessed every 3 months for 2 years after registration
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Overall Survival
Time Frame: assessed every 3 months for 2 years after registration
|
Overall survival (OS) is defined as the time from randomization until death (event), or censored at last date known alive.
OS was estimated using the Kaplan-Meier method, with 90% confidence intervals calculated using Greenwood's formula, and compared by the log rank test.
|
assessed every 3 months for 2 years after registration
|
Objective Response Rate
Time Frame: assessed every 8 weeks while on treatment and every 3 months after treatment for 2 years
|
Objective response rate is defined as number of patients with complete response (CR) or partial response (PR) divided by all eligible patients.
Responses are evaluated using the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline.
CR is defined as disappearance of all target and non-target lesions and normalization of tumor marker level.
PR is defined as disappearance of target lesions or at least a 30% decrease in the sum of the diameters of target lesions (taking as reference the baseline sum diameters), and persistence of one or more non-target lesion(s) and/or maintenance of tumor marker level above the normal limits.
|
assessed every 8 weeks while on treatment and every 3 months after treatment for 2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Steven J Cohen, ECOG-ACRIN Cancer Research Group
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Pathologic Processes
- Neoplasms by Histologic Type
- Neoplasms
- Neoplasms by Site
- Neoplasms, Glandular and Epithelial
- Disease Attributes
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Gastrointestinal Diseases
- Head and Neck Neoplasms
- Esophageal Diseases
- Neoplasms, Squamous Cell
- Carcinoma
- Recurrence
- Adenocarcinoma
- Carcinoma, Squamous Cell
- Esophageal Neoplasms
- Esophageal Squamous Cell Carcinoma
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Antineoplastic Agents
- Immunologic Factors
- Tubulin Modulators
- Antimitotic Agents
- Mitosis Modulators
- Antineoplastic Agents, Phytogenic
- Paclitaxel
- Albumin-Bound Paclitaxel
- Antibodies, Monoclonal
Other Study ID Numbers
- NCI-2011-02045 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- U10CA180820 (U.S. NIH Grant/Contract)
- U10CA021115 (U.S. NIH Grant/Contract)
- ECOG-E2208
- CDR0000674327
- E2208 (Other Identifier: CTEP)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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