Optimization of Immunotherapy Treatment for Advanced Melanoma in the Context of the Public Brazilian Health System (OTIMAS)

Instituto do Cancer do Estado de São Paulo

Status and phase

Active, not recruiting

Phase 2

Conditions

Melanoma Recurrent

Melanoma Metastatic

Stage IV Melanoma

Cutaneous Melanoma

Treatments

Drug: Pembrolizumab

Study type

Interventional

Funder types

Other

Identifiers

NCT07376317

NP 1957/2021

Details and patient eligibility

About

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.

Full description

The development of immune checkpoints inhibitors marked a new era in the treatment of melanoma patients. The use these therapies has more than doubled the expected median overall survival of patients with metastatic melanoma compared with chemotherapy At 5-year follow-up, the median overall survival of patients treated with nivolumab, an anti-PD-1 agent, was 37.3 months compared with 11.2 months in the group treated with dacarbazine, a chemotherapy agent, which represented a 50% reduction in the risk of death with a hazard ratio (HR) of 0.5 (95% CI, 0.40 to 0.63; P < .0001). However, these revolutionary therapies are accessible only to a minority of the Brazilian population, as chemotherapy remains the standard of care for patients with advanced melanoma treated by the Brazilian public health system (Sistema Único de Saúde - SUS), which covers more than 70% of the population.

No published study has specifically evaluated the optimal treatment time with immune checkpoint inhibitors. In studies with nivolumab, treatment was administered until progression or limiting toxicities, whereas in studies with another PD-1 inhibitor, pembrolizumab, treatment was administered for two years.

In this study, patients with advanced (metastatic or unresectable) cutaneous melanoma are treated with pembrolizumab 200mg every 3 weeks for a maximum duration of 12 months. Efficacy will be measured according to RECIST v1.1 criteria, with progression-free survival (PSF) in 24 months as the primary endpoint, compared to historical control. Additionally, the study will assess microRNAs as possible biomarkers in the responders. Other secondary analysis include: quality of life by EORTC QLC-C30 and EuroQol-3L and cost-effectiveness (12 versus 24 months) in the context of Brazilian health system.

This trial is being conducted at Institute of Cancer of the State of São Paulo (ICESP), with an estimated duration of four years.

Enrollment

29 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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 radiotherapy, will be eligible if they have demonstrated clinical stability in the 2 weeks prior to the start of treatment;
Diagnosis of uveal or mucosal melanoma;
Diagnosis of acral melanoma;
Leptomeningeal disease
Pregnancy; effective contraceptive methods should be recommended to women of childbearing age;
Uncontrolled associated disease;
Known active hepatitis B and C;
HIV with detectable viral load or CD4<350;
Active autoimmune disease with use of immunosuppressive therapy or history of autoimmune disease whose risk of recurrence is considered high by the investigator;
More than one line of prior systemic therapy in the context of metastatic or advanced disease or prior use of polychemotherapy;
Prior use of anti-PD-1 in the (neo)adjuvant setting;
Concomitant active malignant neoplasia;
History of malignant neoplasia in the last 5 years, with the exception of squamous cell carcinoma, basal cell carcinoma of the skin, in situ tumors, prostate adenocarcinoma gleason <=6;
Infection with systemic involvement in the last 2 weeks;
Use of corticosteroids in a dose equivalent to greater than 10 mg/d of prednisone on a continuous basis.
History of solid organ transplantation under immunosuppression.