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Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study.
Epperla, Narendranath; Zhao, Qiuhong; Chowdhury, Sayan Mullick; Shea, Lauren; Moyo, Tamara K; Reddy, Nishitha; Sheets, Julia; Weiner, David M; Geethakumari, Praveen Ramakrishnan; Kandarpa, Malathi; Bruno, Ximena Jordan; Thomas, Colin; Churnetski, Michael C; Hsu, Andrew; Zurbriggen, Luke; Tan, Cherie; Lindsey, Kathryn; Maakaron, Joseph; Caimi, Paolo F; Torka, Pallawi; Bello, Celeste; Ayyappan, Sabarish; Karmali, Reem; Kim, Seo-Hyun; Kress, Anna; Kothari, Shalin; Sawalha, Yazeed; Christian, Beth; David, Kevin A; Greenwell, Irl Brian; Janakiram, Murali; Kenkre, Vaishalee P; Olszewski, Adam J; Cohen, Jonathon B; Palmisiano, Neil; Umyarova, Elvira; Wilcox, Ryan A; Awan, Farrukh T; Alderuccio, Juan Pablo; Barta, Stefan K; Grover, Natalie S; Ghosh, Nilanjan; Bartlett, Nancy L; Herrera, Alex F; Shouse, Geoffrey.
Afiliação
  • Epperla N; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH, 43210, USA. Narendranath.Epperla@osumc.edu.
  • Zhao Q; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
  • Chowdhury SM; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
  • Shea L; Washington University, St. Louis, MO, USA.
  • Moyo TK; Levine Cancer Center, Atrium Health, Charlotte, NC, USA.
  • Reddy N; Vanderbilt University Medical Center, Nashville, TN, USA.
  • Sheets J; University of North Carolina, Chapel Hill, NC, USA.
  • Weiner DM; Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Geethakumari PR; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Kandarpa M; Rogel Cancer Center, University of Michigan, Ann Arbor, MI, USA.
  • Bruno XJ; University of Vermont, Burlington, VT, USA.
  • Thomas C; Thomas Jefferson University, Philadelphia, PA, USA.
  • Churnetski MC; Winship Cancer Institute, Emory University Medical Center, Atlanta, GA, USA.
  • Hsu A; Brown University, Providence, RI, USA.
  • Zurbriggen L; University of Wisconsin, Madison, WI, USA.
  • Tan C; Cancer Institute of New Jersey, New Brunswick, NJ, USA.
  • Lindsey K; Medical University of South Carolina, Charleston, SC, USA.
  • Maakaron J; University of Minnesota, Minneapolis, MN, USA.
  • Caimi PF; University Hospitals Seidman Cancer Center, Cleveland, OH, USA.
  • Torka P; Roswell Park Cancer Institute, Buffalo, NY, USA.
  • Bello C; H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Ayyappan S; University of Iowa, Iowa City, IA, USA.
  • Karmali R; Northwestern University, Chicago, IL, USA.
  • Kim SH; Rush University, Chicago, IL, USA.
  • Kress A; Yale University, New Haven, CT, USA.
  • Kothari S; Yale University, New Haven, CT, USA.
  • Sawalha Y; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
  • Christian B; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
  • David KA; Cancer Institute of New Jersey, New Brunswick, NJ, USA.
  • Greenwell IB; Medical University of South Carolina, Charleston, SC, USA.
  • Janakiram M; University of Minnesota, Minneapolis, MN, USA.
  • Kenkre VP; University of Wisconsin, Madison, WI, USA.
  • Olszewski AJ; Brown University, Providence, RI, USA.
  • Cohen JB; Winship Cancer Institute, Emory University Medical Center, Atlanta, GA, USA.
  • Palmisiano N; Thomas Jefferson University, Philadelphia, PA, USA.
  • Umyarova E; University of Vermont, Burlington, VT, USA.
  • Wilcox RA; Rogel Cancer Center, University of Michigan, Ann Arbor, MI, USA.
  • Awan FT; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Alderuccio JP; University of Miami, Miami, FL, USA.
  • Barta SK; Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Grover NS; University of North Carolina, Chapel Hill, NC, USA.
  • Ghosh N; Levine Cancer Center, Atrium Health, Charlotte, NC, USA.
  • Bartlett NL; Washington University, St. Louis, MO, USA.
  • Herrera AF; City of Hope, Duarte, CA, USA.
  • Shouse G; City of Hope, Duarte, CA, USA.
J Hematol Oncol ; 15(1): 96, 2022 07 16.
Article em En | MEDLINE | ID: mdl-35842643
ABSTRACT
Ibrutinib is effective in the treatment of relapsed/refractory (R/R) marginal zone lymphoma (MZL) with an overall response rate (ORR) of 48%. However, factors associated with response (or lack thereof) to ibrutinib in R/R MZL in clinical practice are largely unknown. To answer this question, we performed a multicenter (25 US centers) cohort study and divided the study population into three groups "ibrutinib responders"-patients who achieved complete or partial response (CR/PR) to ibrutinib; "stable disease (SD)"; and "primary progressors (PP)"-patients with progression of disease as their best response to ibrutinib. One hundred and nineteen patients met the eligibility criteria with 58%/17% ORR/CR, 29% with SD, and 13% with PP. The median PFS and OS were 29 and 71.4 months, respectively, with no difference in PFS or OS based on the ibrutinib line of therapy or type of therapy before ibrutinib. Patients with complex cytogenetics had an inferior PFS (HR = 3.08, 95% CI 1.23-7.67, p = 0.02), while those with both complex cytogenetics (HR = 3.00, 95% CI 1.03-8.68, p = 0.04) and PP (HR = 13.94, 95% CI 5.17-37.62, p < 0.001) had inferior OS. Only primary refractory disease to first-line therapy predicted a higher probability of PP to ibrutinib (RR = 3.77, 95% CI 1.15-12.33, p = 0.03). In this largest study to date evaluating outcomes of R/R MZL treated with ibrutinib, we show that patients with primary refractory disease and those with PP on ibrutinib are very high-risk subsets and need to be prioritized for experimental therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma de Zona Marginal Tipo Células B Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma de Zona Marginal Tipo Células B Idioma: En Ano de publicação: 2022 Tipo de documento: Article