Mesenchymal–Epithelial Transition Kinase Inhibitor Therapy in Patients with Advanced Papillary Renal-Cell Carcinoma: A Systematic Review and Meta-Analysis

Author:

Moraes Francisco Cezar Aquino de1ORCID,Vilbert Maysa2ORCID,Alves Vinícius Freire Costa3,de Oliveira Almeida Gustavo4,Priantti Jonathan N.5ORCID,Madeira Thiago6ORCID,Stecca Carlos7,Fernandes Marianne Rodrigues1ORCID,dos Santos Ney Pereira Carneiro1

Affiliation:

1. Oncology Research Center, Federal University of Pará, Belem 66075-110, Brazil

2. Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON M5T 2S8, Canada

3. School of Medicine, University of São Paulo—USP, São Paulo 14040-904, Brazil

4. School of Medicine, Federal University of Triângulo Mineiro—UFTM, Uberaba 38280-000, Brazil

5. School of Medicine, Federal University of Amazonas—UFAM, Manaus 69020-160, Brazil

6. School of Medicine, Federal University of Minas Gerais—UFMG, Belo Horizonte 31270-901, Brazil

7. Mackenzie Evangelical University Hospital, Curitiba 80710-390, Brazil

Abstract

Papillary subtypes of renal-cell carcinoma (pRCC) represent 10–15% of the cases and commonly have MET alterations. This systematic review and single-arm meta-analysis evaluated MET inhibitor therapy (METi) efficacy and safety in adults with confirmed advanced pRCC. The search strategy included PubMed, Web-of-science, Cochrane, and Scopus. We used the DerSimonian/Laird random effect model for all analyses; p-value < 5% was considered significant, and heterogeneity was assessed with I2. Three clinical trials and six cohort studies were included with 504 patients; 31% were MET-driven. Our pooled analysis demonstrated an objective response rate (ORR) in MET-driven, MET-independent, and overall patients of: 36% (95%CI: 10–62), 0% (95%CI: 0–3), and 21% (95%CI: 1–41), respectively. One-year disease control and progression-free survival rates were, respectively, 70% (95%CI: 52–88) and 15% (95%CI: 10–20). Twelve- and twenty-four-month survival rates were, respectively, 43% (95%CI: 23–64) and 10% (95%CI: 0–30). The prevalence of adverse events of any grade and grades 3–5 were 96% (95%CI: 91–100) and 44% (95%CI: 37–50), respectively. We suggest METi has anti-tumor activity and is tolerable in patients with advanced pRCC.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Universidade Federal do Pará

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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