JCO Global Oncology (Aug 2022)

Treatment and Survival Outcomes of Waldenstrom Macroglobulinemia in Latin American Patients: A Multinational Retrospective Cohort Study

  • Eloísa Riva,
  • Patricio José Duarte,
  • Bryan Valcárcel,
  • Guillermina Remaggi,
  • Ivan Murrieta,
  • Ariel Corzo,
  • Daniel del Carpio,
  • Camila Peña,
  • Jule Vásquez,
  • Virginia Bove,
  • Larissa Teixeira,
  • Guilherme Fleury-Perini,
  • Sebastian Yantorno,
  • César Samánez,
  • Sergio Lopresti,
  • Milagros Altamirano,
  • Luis Villela,
  • Guillermo J. Ruiz-Arguelles,
  • Guillermo J. Ruiz-Delgado,
  • Efreen Montaño,
  • Verónica Verri,
  • Elia Zamora Pérez,
  • Fernando Pérez Jacobo,
  • Henry Idrobo,
  • Humberto Martínez-Cordero,
  • Brady E. Beltran,
  • Jhoanna Ramírez,
  • Jorge J. Castillo,
  • Luis E. Malpica Castillo

DOI
https://doi.org/10.1200/GO.21.00380
Journal volume & issue
no. 8

Abstract

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PURPOSEWaldenstrom Macroglobulinemia (WM) is a rare lymphoma with distinct clinical features, and data from Latin American patients are lacking. Therefore, we aim to investigate the clinical, therapy, and outcome patterns of WM in Latin America.METHODSWe retrospectively analyzed patients with WM diagnosed between 1991 and 2019 from 24 centers in seven Latin American countries. The study outcomes were overall survival (OS) and progression-free survival (PFS).RESULTSWe identified 159 cases (median age 67 years, male 62%). Most patients (95%) were symptomatic at diagnosis. The International Prognostic Scoring System for WM (IPSSWM) at diagnosis was available in 141 (89%) patients (high-risk 40%, intermediate-risk 37%, and low-risk 23%). Twenty-seven (17%) patients were tested for MYD88L265P, with 89% (n = 24 of 27) carrying the mutation. First-line and second-line therapies were administered to 142 (89%) and 53 (33%) patients, respectively. Chemoimmunotherapy was the most commonly used first-line (66%) and second-line (45%) approach; only 18 (11%) patients received ibrutinib. With a median follow-up of 69 months, the 5-year OS rate was 81%. In treated patients, the 5-year OS and PFS rates were 78% and 59%, respectively. High-risk IPSSWM at treatment initiation was an independent risk factor for OS (adjusted hazard ratio: 4.73, 95% CI, 1.67 to 13.41, P = .003) and PFS (adjusted hazard ratio: 2.43, 95% CI, 1.31 to 4.50, P = .005).CONCLUSIONIn Latin America, the management of WM is heterogeneous, with limited access to molecular testing and novel agents. However, outcomes were similar to those reported internationally. We validated the IPSSWM score as a prognostic factor for OS and PFS. There is an unmet need to improve access to recommended diagnostic approaches and therapies in Latin America.