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ARTÍCULO

Cilta-cel or standard care in lenalidomide-refractory multiple myeloma

Autores: San Miguel Izquierdo, Jesús (Autor de correspondencia); Dhakal, B.; Yong, K.; Spencer, A.; Anguille, S.; Mateos, M. V.; Fernández de Larrea, C.; Martínez-López, J.; Moreau, P.; Touzeau, C.; Leleu, X.; Avivi, I.; Cavo, M.; Ishida, T.; Kim, S. J.; Roeloffzen, W.; van de Donk, N. W. C. J.; Dytfeld, D.; Sidana, S.; Costa, L. J.; Oriol, A.; Popat, R.; Khan, A. M.; Cohen, Y. C.; Ho, P. J.; Griffin, J.; Lendvai, N.; Lonardi, C.; Slaughter, A.; Schecter, J. M.; Jackson, C. C.; Connors, K.; Li, K.; Zudaire, E.; Chen, D.; Gilbert, J.; Yeh, T. M.; Nagle, S.; Florendo, E.; Pacaud, L.; Patel, N.; Harrison, S. J.; Einsele, H.
Título de la revista: NEW ENGLAND JOURNAL OF MEDICINE
ISSN: 0028-4793
Volumen: 389
Número: 4
Páginas: 335 - 347
Fecha de publicación: 2023
Resumen:
BACKGROUND Ciltacabtagene autoleucel (cilta-cel), a B-cell maturation antigen (BCMA)-directed CAR-T cell therapy, is effective in heavily pretreated patients with relapsed or refractory multiple myeloma. We investigated cilta-cel in earlier treatment lines in patients with lenalidomide-refractory disease. METHODS In this phase 3, randomized, open-label trial, we assigned patients with lenalidomide-refractory multiple myeloma to receive cilta-cel or the physician's choice of effective standard care. All the patients had received one to three previous lines of treatment. The primary outcome was progression-free survival. RESULTS A total of 419 patients underwent randomization (208 to receive cilta-cel and 211 to receive standard care). At a median follow-up of 15.9 months (range, 0.1 to 27.3), the median progression-free survival was not reached in the cilta-cel group and was 11.8 months in the standard-care group (hazard ratio, 0.26; 95% confidence interval [CI], 0.18 to 0.38; P<0.001). Progression-free survival at 12 months was 75.9% (95% CI, 69.4 to 81.1) in the cilta-cel group and 48.6% (95% CI, 41.5 to 55.3) in the standard-care group. More patients in the cilta-cel group than in the standard-care group had an overall response (84.6% vs. 67.3%), a complete response or better (73.1% vs. 21.8%), and an absence of minimal residual disease (60.6% vs. 15.6%). Death from any cause was reported in 39 patients and 46 patients, respectively (hazard ratio, 0.78; 95% CI, 0.5 to 1.2). Most patients reported grade 3 or 4 adverse events during treatment. Among the 176 patients who received cilta-cel in the as-treated population, 134 (76.1%) had cytokine release syndrome (grade 3 or 4, 1.1%; no grade 5), 8 (4.5%) had immune effector cell-associated neurotoxicity syndrome (all grade 1 or 2), 1 had movement and neurocognitive symptoms (grade 1), 16 (9.1%) had cranial nerve palsy (grade 2, 8.0%; grade 3, 1.1%), and 5 (2.8%) had CAR-T-related peripheral neuropathy (grade 1 or 2, 2.3%; grade 3, 0.6%). CONCLUSIONS A single cilta-cel infusion resulted in a lower risk of disease progression or death than standard care in lenalidomide-refractory patients with multiple myeloma who had received one to three previous therapies.
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