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Teclistamab versus real-world physician’s choice of therapy in triple-class exposed relapsed/refractory multiple myeloma

AIMS: We compared the effectiveness of teclistamab versus real-world physician’s choice of therapy (RWPC) in triple-class exposed relapsed/refractory multiple myeloma. MATERIALS & METHODS: MajesTEC-1 eligibility criteria were applied to the RWPC cohort. Baseline covariate imbalances were adjuste...

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Detalles Bibliográficos
Autores principales: Krishnan, Amrita, Nooka, Ajay K, Chari, Ajai, Garfall, Alfred L, Martin, Thomas G, Nair, Sandhya, Lin, Xiwu, Qi, Keqin, Londhe, Anil, Pei, Lixia, Ammann, Eric, Kobos, Rachel, Smit, Jennifer, Parekh, Trilok, Marshall, Alexander, Slavcev, Mary, Usmani, Saad Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Becaris Publishing Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402759/
https://www.ncbi.nlm.nih.gov/pubmed/37114426
http://dx.doi.org/10.57264/cer-2022-0186
Descripción
Sumario:AIMS: We compared the effectiveness of teclistamab versus real-world physician’s choice of therapy (RWPC) in triple-class exposed relapsed/refractory multiple myeloma. MATERIALS & METHODS: MajesTEC-1 eligibility criteria were applied to the RWPC cohort. Baseline covariate imbalances were adjusted using inverse probability of treatment weighting. Overall survival, progression-free survival and time to next treatment were compared. RESULTS: After inverse probability of treatment weighting, baseline characteristics were similar between cohorts (teclistamab, n = 165; RWPC, n = 364 [766 observations]). Teclistamab treated patients had numerically better overall survival (hazard ratio [HR]: 0.82 [95% CI: 0.59–1.14]; p = 0.233) and significantly greater progression-free survival (HR: 0.43 [0.33–0.56]; p < 0.0001) and time to next treatment (HR: 0.36 [0.27–0.49]; p < 0.0001) versus the RWPC cohort. CONCLUSION: Teclistamab offered clinical benefit over RWPC in triple-class exposed relapsed/refractory multiple myeloma.