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Results from a Real-World Multicenter Analysis of 482 Patients with Chronic Lymphocytic Leukemia Treated with Ibrutinib: A Look at Racial Differences.
Barrientos, Jacqueline C; Ayed, Ayed O; Cha, Agnes; Du, Senxi; Fang, Bruno; Hall, Ryan; Marks, Stanley M; Peng, Eileen; Rhodes, Joanna M; Ryan, Kellie; Winters, Sharon B; Yeung, Percy L; Hou, Jing-Zhou.
Affiliation
  • Barrientos JC; Zucker School of Medicine at Hofstra/Northwell, Lake Success, NY and Mount Sinai Comprehensive Cancer Center, Miami, FL, USA.
  • Ayed AO; Cancer Specialists of North Florida, Jacksonville, FL, USA.
  • Cha A; Northwell Health, New Hyde Park, NY, USA.
  • Du S; Department of Medicine, University of California, Los Angeles, CA, USA.
  • Fang B; Astera Cancer Care, East Brunswick, NJ, USA.
  • Hall R; CARTI Cancer Center, Little Rock, AR, USA.
  • Marks SM; University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, 5115 Centre Ave, Pittsburgh, PA, 15232, USA.
  • Peng E; Astera Cancer Care, East Brunswick, NJ, USA.
  • Rhodes JM; Northwell Health, New Hyde Park, NY, USA.
  • Ryan K; AstraZeneca, Gaithersburg, MD, USA.
  • Winters SB; University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, 5115 Centre Ave, Pittsburgh, PA, 15232, USA.
  • Yeung PL; Astera Cancer Care, East Brunswick, NJ, USA.
  • Hou JZ; University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, 5115 Centre Ave, Pittsburgh, PA, 15232, USA. houj@upmc.edu.
Target Oncol ; 18(5): 727-734, 2023 09.
Article in En | MEDLINE | ID: mdl-37728835
Ibrutinib, a Bruton tyrosine kinase inhibitor, is an approved oral targeted therapy for the treatment of chronic lymphocytic leukemia (CLL). Patients treated with ibrutinib can experience side effects (referred to as adverse events) and may need to reduce the drug dose (referred to as dose reductions) or stop treatment (referred to as discontinuations) for a variety of reasons. A previous study showed that patients who were treated with ibrutinib experienced frequent dose reductions and discontinuations. This study described dose reductions and discontinuations in a larger patient population treated with ibrutinib and also described outcomes in Black patients. Patients with CLL treated with ibrutinib were identified from five medical centers and were followed for a minimum of 6 months. Patients experienced frequent dose reductions and discontinuations in routine clinical practice. The most common cause of discontinuations was adverse events in the overall patient population and disease progression in the Black patient population. Black patients treated with ibrutinib had similar rates of dose reductions and discontinuations as the overall patient population. Rates of dose reductions and discontinuations for patients with CLL treated with ibrutinib were higher in this real-world study than in clinical trials.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Lymphocytic, Chronic, B-Cell Type of study: Observational_studies / Prognostic_studies Limits: Adult / Humans Language: En Journal: Target Oncol Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Lymphocytic, Chronic, B-Cell Type of study: Observational_studies / Prognostic_studies Limits: Adult / Humans Language: En Journal: Target Oncol Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country: