Biological relapse in multiple myeloma: Outcome and treatment strategies in a Spanish real-world setting

Altres autors/es

Institut Català de la Salut

[Alegre A] Hospital Universitario de la Princesa, Madrid, Spain. [Gironella M] Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Escalante F] Hospital Universitario de León, León, Spain. [Bergua JM] Hospital San Pedro de Alcántara Cáceres, Spain. [Martínez‐Chamorro C] Hospital Universitario Quirónsalud Madrid, Spain. [López A] Hospital Universitari Arnau de Vilanova, Valencia, Spain

Vall d'Hebron Barcelona Hospital Campus

Data de publicació

2024-07-12T08:16:47Z

2024-07-12T08:16:47Z

2024-07-04



Resum

Relapse; Multiple myeloma; Treatment


Recaída; Mieloma múltiple; Tratamiento


Recaiguda; Mieloma múltiple; Tractament


Recommendations regarding the best time to start treatment in patients with relapsed/refractory multiple myeloma (RRMM) after biological relapse/progression (BR) are unclear. This observational, prospective, multicenter registry aimed to evaluate the impact on time to progression (TTP) of treatment initiation at BR versus at symptomatic clinical relapse (ClinR) based on the Spanish routine practice in adult patients with RRMM. Patients had two or less previous treatment lines and at least one previous partial response. Baseline characteristics and treatment outcomes were recorded, and survival was analyzed. Of 225 patients, 110 were treated at BR (TxBR group) and 115 at ClinR (TxClinR group) according to the investigators' criteria. The proportion of patients with higher ECOG, previous noncomplete remission (CR), and second relapse were significantly higher in the TxBR group compared to the TxClinR group. TheTxClinR group showed improved outcomes, including TTP, compared to the TxBR group. Progression-free survival increased in the TxClinR group (56.2 months) compared to the TxBR group (32.5 months) (p = 0.0137), and median overall survival also increased (p = 0.0897). Median TTP was significantly longer in patients relapsing from a CR (50.4 months) and in their first relapse (38.7 months) compared to those relapsing from a non-CR response (32.9 months) and in their second relapse (25.2 months). Physicians seemed to start treatment earlier in RRMM patients with poor prognosis features. Previous responses to anti-MM treatment and the number of prior treatment lines were identified as prognosis factors, whereby relapse from CR and first relapse were associated with a longer time to progression.


This study was funded by Celgene, a BMS company.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Publicat per

Wiley

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