Study in Patients With Unresectable And Metastatic Melanoma: The Optimize Study
NCT ID: NCT02780089
Last Updated: 2022-05-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
408 participants
OBSERVATIONAL
2015-10-23
2020-09-08
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Prospective Patients
There will be 1,600 prospective patients recruited over a period of two years and followed-up for a planned minimum of three years. For the prospective cohort, patients will be recruited after the course of treatment has been decided by the physician and prior to the start of treatment.Prior advanced melanoma treatment information will be collected from patient charts for pre-treated patients. Patients will be followed for a minimum of 3 years from their study index date until death, withdrawal of consent, lost to follow-up/record, or end of study, whichever comes first. Study index date will be the date when first study therapy is initiated.
No interventions assigned to this group
Treatment Group No. 1
Immune checkpoint inhibitor patients who remain on an immune checkpoint inhibitor therapy. Defined as immune checkpoint inhibitor therapy patients who either remained on their initial (index) immune checkpoint inhibitor therapy or switched to another immune checkpoint inhibitor therapy during the study period. Patients in this group remained on an immune checkpoint inhibitor therapy and did not switch to a non-immune checkpoint inhibitor therapy anytime during the study period.
No interventions assigned to this group
Treatment Group No. 2
Immune checkpoint inhibitor patients who switched to a non-immune checkpoint inhibitor therapy. Defined as patients who switched from their index immune checkpoint inhibitor therapy to a non-immune checkpoint inhibitor therapy anytime during the study period.
No interventions assigned to this group
Treatment Group No. 3
Targeted therapy patients who remain on a targeted therapy. Defined as targeted therapy patients who either remained on their initial (index) targeted therapy or switched to another targeted therapy during the study period. Patients in this group remained on a targeted therapy and did not switch to a non-targeted therapy anytime during the study period.
No interventions assigned to this group
Treatment Group No. 4
Targeted therapy patients who switched to a non-targeted therapy. Defined as patients who switched from their index targeted therapy to a non-targeted therapy anytime during the study period.
No interventions assigned to this group
Treatment Group No. 5
Chemotherapy/other therapy patients who remain on a chemotherapy/other therapy. Defined as chemotherapy/other therapy patients who either remained on their initial (index) chemotherapy/other therapy or switched to another chemotherapy/other therapy during the study period. Patients in this group remained on a chemotherapy/other therapy and did not switch to an immune checkpoint inhibitor therapy or targeted therapy anytime during the study period.
No interventions assigned to this group
Treatment Group No. 6
Chemotherapy/other patients who switched to an immune checkpoint inhibitor therapy or targeted therapy. Defined as patients who switched from their index chemotherapy/other therapy to an immune checkpoint inhibitor therapy or targeted therapy anytime during the study period.
No interventions assigned to this group
Retrospective Patients
Retrospective cohort of 600 patients with unresectable or metastatic melanoma, receiving therapies other than immune checkpoint inhibitor or targeted therapies during the four year period prior to the release of ipilimumab (March 25, 2007 -March 24, 2011), will be identified. The data for these 600 retrospective patients will be used as a benchmark for treatment patterns and outcomes prior to the marketed availability of immune checkpoint inhibitors or targeted therapies.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Diagnosis date must occur on or after March 24, 2011 (date of ipilimumab approval in US)
* Diagnosis of stage III (unresectable) or stage IV melanoma (includes mucosal, uveal acral-lentiginous, leptomeningeal disease)
* Age ≥ 18 years at time of entry into study
* Patients must be actively receiving or scheduled to receive systemic treatment (any line, eg, first, second, third line \[including investigational drugs\]).
* For patients initiating new treatment, treatment must be started within 28 days after signing informed consent.
* For patients currently receiving treatment, patients must enroll within the first 21 days of starting new treatment
Retrospective cohort patients:
* Patients with diagnosis of confirmed unresectable stage III or stage IV melanoma (including mucosal, uveal, acral-lentiginous, leptomeningeal disease)
* Age ≥ 18 years at time of unresectable or metastatic melanoma diagnosis
* Initiated therapy for unresectable or metastatic melanoma within 4 years prior to approval of ipilimumab (first immune checkpoint inhibitor therapy approved in US)
* March 25, 2007 - March 24, 2011
* One year of follow-up data is required from date of therapy initiation, if a patient passed away within the one year of follow-up; such patients are still eligible and the date of death will be collected.
1. If retrospective patients have at least one year of follow-up data and are then treated with immuno-oncology, immune checkpoint inhibitor therapy, or targeted therapy, these patients will be analyzed separately.
Exclusion Criteria
* Patients participating in a clinical study that does not allow enrollment into a non interventional study or clinical studies in which the investigational treatment is blinded
* Patients who started new treatment \> 21 days
* Patients who enrolled in study but did not initiate treatment before 28 days
* Patients with current malignancies (except non-melanoma skin cancer and the following in situ cancers: bladder, gastric, colon, endometrial, cervical/dysplasia, melanoma, or breast) that requires additional systemic therapy
18 Years
ALL
No
Sponsors
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Bristol-Myers Squibb
INDUSTRY
Responsible Party
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Principal Investigators
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Bristol-Myers Squibb
Role: STUDY_DIRECTOR
Bristol-Myers Squibb
Locations
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Northwest Alabama Cancer Center
Muscle Shoals, Alabama, United States
Genesis Cancer Center
Hot Springs, Arkansas, United States
Pacific Shores Medical Group
Long Beach, California, United States
Cancer Care Associates
Redondo Beach, California, United States
University of Colorado
Aurora, Colorado, United States
21st Century Oncology
Jacksonville, Florida, United States
Cancer Specialits, LLC D/B/A
Jacksonville, Florida, United States
Lakeland Regional Health
Lakeland, Florida, United States
Watson Clinical Center for Research, INC
Lakeland, Florida, United States
UF Health Cancer Center at Orlando Health
Longwood, Florida, United States
Mount Sinai Medical Center
Miami Beach, Florida, United States
Mid Florida Hematology and Oncology Centers
Orange City, Florida, United States
Sacred Heart Medical Oncology Group
Pensacola, Florida, United States
Tallahassee Memorial Healthcare
Tallahassee, Florida, United States
H. Lee Moffitt Cancer Center Moffitt Cancer Center
Tampa, Florida, United States
Harbin Clinic
Rome, Georgia, United States
Summit Cancer Care
Savannah, Georgia, United States
The Queen's Medical Center
Honolulu, Hawaii, United States
North Shore University Health System
Evanston, Illinois, United States
Ingalls Cancer Research Center
Harvey, Illinois, United States
Oncology Specialits, S.C.
Niles, Illinois, United States
Orchard Healthcare Research Inc.
Skokie, Illinois, United States
Simmons Cancer Institute at SIU School of Medicine
Springfield, Illinois, United States
Stormont-Vail Cancer Center
Topeka, Kansas, United States
University of Kansas Medical Center
Westwood, Kansas, United States
West Ky Hematology & Oncology
Paducah, Kentucky, United States
Ochsner Clinic Foundation
New Orleans, Louisiana, United States
CHRISTUS Schumpert Cancer Treatment Center
Shreveport, Louisiana, United States
Saint Agnes Hospital
Baltimore, Maryland, United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States
Masonic Cancer Center
Minneapolis, Minnesota, United States
Mayo Clinic Cancer Center (MCCC)
Rochester, Minnesota, United States
Forrest General Cancer Center
Hattiesburg, Mississippi, United States
Central Care Cancer Center
Bolivar, Missouri, United States
Nebraska Hematology-Oncology, P.C.
Lincoln, Nebraska, United States
Oncology Hematology West P.C.
Omaha, Nebraska, United States
John Theurer Cancer Center at Hackensack University Medical Center
Hackensack, New Jersey, United States
Atlantic Health, Morristown Medical Center
Morristown, New Jersey, United States
Meridian Health
Neptune City, New Jersey, United States
Rosewell Park Cancer Institute
Buffalo, New York, United States
Center of Learning Healthcare
Durham, North Carolina, United States
Hematolgoy and Oncology Associates, Inc.
Canton, Ohio, United States
Aultman Hospital
Canton, Ohio, United States
Tri-County Hematology and Oncology Associates, Inc
Massillon, Ohio, United States
Genesis Cancer Care Center
Zanesville, Ohio, United States
St. Charles Medical Center - Cancer Center
Bend, Oregon, United States
Network Office of Research & Innovation / Lehigh Valley Health Network
Allentown, Pennsylvania, United States
St. Luke's Hospital and Health Network
Bethlehem, Pennsylvania, United States
The Regional Cancer Center
Erie, Pennsylvania, United States
Lancaster General Health
Lancaster, Pennsylvania, United States
Jefferson Medical Oncology
Philadelphia, Pennsylvania, United States
Allegheny Health Network
Pittsburgh, Pennsylvania, United States
UPCI - UPMC Cancer Center
Pittsburgh, Pennsylvania, United States
Thompson Cancer Survival Center
Knoxville, Tennessee, United States
Texas Oncology
Austin, Texas, United States
Texas Oncology
El Paso, Texas, United States
Texas Oncology
Paris, Texas, United States
Huntsman Cancer Institute at the University of Utah
Salt Lake City, Utah, United States
Inova Melanoma and Skin Cancer Center
Fairfax, Virginia, United States
Providence Regional Medical Center Everett
Everett, Washington, United States
Cancer Care Northwest
Spokane, Washington, United States
West Virginia University
Bridgeport, West Virginia, United States
West Virginia University
Huntington, West Virginia, United States
West Virginia University Hematolgoy & Oncology
Martinsburg, West Virginia, United States
West Virginia University
Morgantown, West Virginia, United States
Gundersen Lutheran Medical Foundations, Inc.
La Crosse, Wisconsin, United States
Countries
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References
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Kirkwood JM, Kottschade LA, McWilliams RR, Khushalani NI, Jang S, Hallmeyer S, McDermott DF, Tawbi H, Che M, Lee CH, Ritchings C, Le TK, Park B, Ramsey S. Real-world outcomes with immuno-oncology therapies in advanced melanoma: final results of the OPTIMIzE registry study. Immunotherapy. 2024 Jan;16(1):29-42. doi: 10.2217/imt-2022-0292. Epub 2023 Nov 8.
Related Links
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BMS Clinical Trial Information
Investigator Inquiry Form
FDA Safety Alerts and Recalls
BMS Clinical Trial Patient Recruiting
Other Identifiers
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CA209-357
Identifier Type: -
Identifier Source: org_study_id
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