Optimization of Immunotherapy Treatment for Advanced Melanoma in the Context of the Public Brazil… (NCT07376317) | Clinical Trial Compass
Active — Not RecruitingPhase 2
Optimization of Immunotherapy Treatment for Advanced Melanoma in the Context of the Public Brazilian Health System (OTIMAS)
Brazil29 participantsStarted 2021-12-10
Plain-language summary
The OTIMAS study is a phase II trial designed to evaluate if the duration of one year of pembrolizumab immunotherapy for advanced metastatic melanoma has equivalent efficacy as the two-year duration of historical controls.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Patients with malignant melanoma (with confirmed histopathological diagnosis) stages III and IV not amenable to locoregional treatment or curative treatment
* Measurable disease by RECIST 1.1
* Eastern Cooperative Oncology Group (ECOG) 0, 1 or 2
* Up to 1 (one) line of prior treatment with palliative chemotherapy (monotherapy), with documented progression and no residual toxicities greater than grade 1 according to CTCAE
* Estimated life expectancy greater than 12 weeks
* Adequate renal function, defined as creatinine clearance estimated by the Cockcroft-Gault equation equal to or greater than 30 mL/min;
* Adequate liver function, defined as alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels equal to or less than 2.0 times the upper limit of normal and total bilirubin less than 2 times the upper limit of normal;
* Hemoglobin greater than or equal to 8 g/dL; neutrophil count equal to or greater than 1,000/mm3; platelet count equal to or greater than 100,000/mm3;
* Ability to understand and adhere to study procedures;
* Age over 18 years;
* Absence of active treatment for the underlying disease, with the exception of the use of bisphosphonates;
Exclusion Criteria:
* Uncontrolled Central Nervous System (CNS) metastases: active symptomatic disease in the central nervous system, requiring doses of corticosteroids greater than the equivalent of 10 mg/day of prednisone. Patients previously submitted to local treatment, such as radioth…
What they're measuring
1
Progression free survival
Timeframe: 24 months
Trial details
NCT IDNCT07376317
SponsorInstituto do Cancer do Estado de São Paulo