Real-world treatment patterns and outcomes in relapsed/refractory multiple myeloma (1-3 prior lines): Flatiron database.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
07 Aug 2024
Historique:
accepted: 11 07 2024
received: 12 01 2024
revised: 24 05 2024
medline: 7 8 2024
pubmed: 7 8 2024
entrez: 7 8 2024
Statut: aheadofprint

Résumé

In multiple myeloma (MM), early use of the immunomodulatory drug lenalidomide has led to an increased population of patients with lenalidomide-refractory MM in early-line settings, but their outcomes are not well characterized. Here, we report treatment patterns, survival outcomes, prognostic variables, and attrition rates for patients with proteasome inhibitor-exposed, lenalidomide-refractory MM, treated with 1-3 prior lines of therapy (LOT). From 12 767 patients with MM in the Flatiron Health database between January 2016 and April 2022, 1455 met the inclusion criteria. The most common subsequent treatments were triplet combinations (41.6% of patients); daratumumab/pomalidomide/dexamethasone was the most common treatment regimen (13.2%). Median real-world progression-free survival (RW-PFS) and overall survival (OS) were 6.5 months and 44.4 months, respectively. RW-PFS was similar in patients with 1, 2, or 3 prior LOT. International Staging System stage III, Eastern Cooperative Oncology Group performance status of 1, hemoglobin <12 g/dL, high-risk cytogenetics, and refractoriness to anti-CD38 antibody at baseline were associated with worse RW-PFS and OS. Outcomes remained similar for patients who received National Comprehensive Cancer Network-preferred treatments and those who received treatments after 2020. In 561 patients with 1 prior LOT at inclusion, cumulative attrition rate from LOT 2-5 was 85%, which included 25% patients who died and 60% with no further treatment. Patients with lenalidomide-refractory MM who have received 1-3 prior LOT have poor outcomes and progress rapidly through available therapies, highlighting the need for more effective treatments early in the disease course, before patients are lost to attrition.

Identifiants

pubmed: 39110988
pii: 517296
doi: 10.1182/bloodadvances.2024012640
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Binod Dhakal (B)

Medical College of Wisconsin, Wauwatosa, Wisconsin, United States.

Hermann Einsele (H)

Universitätsklinikum Würzburg, Würzburg, Germany.

Jordan M Schecter (JM)

Janssen Research & Development, LLC, Raritan, New Jersey, United States.

William Deraedt (W)

Janssen R&D, Beerse, Belgium, Beerse, Belgium.

Nikoletta Lendvai (N)

Janssen Research & Development, United States.

Ana Slaughter (A)

Cilag GmbH International, Zug, Switzerland.

Carolina Lonardi (C)

(Janssen Research & Development, LLC, Buenos Aires, Argentina.

Sandhya Nair (S)

Janssen Pharmaceutica, Belgium.

Jianming He (J)

Janssen Global Services LLC, Raritan, New Jersey, United States.

Akshay Kharat (A)

Janssen Scientific Affairs, LLC, Horsham, Pennsylvania, United States.

Patricia Cost (P)

Janssen Global Services, LLC, Raritan, New Jersey, United States.

Satish Valluri (S)

Janssen Global Services, LLC, Raritan, New Jersey, United States.

Kwee L Yong (KL)

Unviersity College London, London, United Kingdom.

Classifications MeSH