Treatment patterns and outcomes in real-world transplant-ineligible patients newly diagnosed with multiple myeloma

Despite the significant proportion of older patients with newly diagnosed multiple myeloma (MM), most clinical trials driving therapeutic decisions in routine practice include younger and presumably healthier patients than those in the real world. Furthermore, longitudinal studies suggest that elder...

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Veröffentlicht in:Annals of hematology 2021-07, Vol.100 (7), p.1769-1778
Hauptverfasser: Cejalvo, María José, Bustamante, Gabriela, González, Esther, Vázquez-Álvarez, Judith, García, Ricarda, Ramírez-Payer, Ángel, Pérez-Persona, Ernesto, Abella, Eugenia, Garzón, Sebastián, García, Antoni, Jarque, Isidro, González, Marta Sonia, Sampol, Antonia, Motlló, Cristina, Martí, Josep María, Alcalá, Magdalena, Duro, Rafael, González, Yolanda, Sastre, José Luis, Sarrà, Josep, Lostaunau, Giselle, López, Rocío, de la Rubia, Javier
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Sprache:eng
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Zusammenfassung:Despite the significant proportion of older patients with newly diagnosed multiple myeloma (MM), most clinical trials driving therapeutic decisions in routine practice include younger and presumably healthier patients than those in the real world. Furthermore, longitudinal studies suggest that elderly, transplant-ineligible patients with MM are not benefitting enough from new anti-MM agents. We retrospectively analyzed the profile of and treatment patterns and outcomes in 675 transplant-ineligible patients with MM who started frontline therapy in routine practice. The mean (SD) age was 75.6 (6.7) years; 152 (47.4%) had Eastern Cooperative Oncology Group performance status (ECOG PS) 2–4, and 73 (25.1%) had high cytogenetic risk. The most frequent frontline therapy was non-VMP bortezomib-based regimens ( n =207; 30.7%), which were more frequent among patients with ECOG PS 0/1 and higher risk (e.g., international staging system (ISS) stage III, severely impaired glomerular filtrate rate (GFR), high lactate dehydrogenase (LDH), and high-risk cytogenetics); 185 patients (27.4%) started an attenuated ( lite ) VMP regimen, and 159 (23.6%) a VMP (VISTA) regimen. Median progression-free survival and overall survival (OS) were 15.3 months (95%CI 14.0–16.9) and 33.5 months (95%CI 29.1–37.2), respectively; 405 patients (78.2%) achieved partial response or better. Age, ECOG PS, ISS stage, serum LDH, GFR, cytogenetic risk, and treatment regimen significantly influenced OS. In this study, a remarkable proportion of transplant-ineligible patients with MM were older, frontline regimens were highly heterogeneous, and patients at higher risk often received less efficacious combinations. These findings suggest that clinicians have limited objective criteria for therapeutic decisions for this patient group.
ISSN:0939-5555
1432-0584
DOI:10.1007/s00277-021-04529-5