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Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

In the phase III study RESONATE, ibrutinib reduced the risk of progression and improved overall survival versus ofatumumab in previously treated patients with CLL/SLL. In this novel analysis of patient well-being including patient-reported outcomes, ibrutinib reduced disease burden while preserving...

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Autores principales: Barrientos, Jacqueline C., O’Brien, Susan, Brown, Jennifer R., Kay, Neil E., Reddy, Nishitha M., Coutre, Steven, Tam, Constantine, Mulligan, Stephen, Jaeger, Ulrich, Devereux, Stephen, Pocock, Christopher, Robak, Tadeusz, Schuster, Stephen J., Schuh, Anna, Gill, Devinder, Bloor, Adrian, Dearden, Claire, Moreno, Carol, Cull, Gavin, Hamblin, Mike, Jones, Jeffrey A., Eckert, Karl, Solman, Isabelle G., Suzuki, Samuel, Hsu, Emily, James, Danelle F., Byrd, John C., Hillmen, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527106/
https://www.ncbi.nlm.nih.gov/pubmed/30249389
http://dx.doi.org/10.1016/j.clml.2018.08.007
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author Barrientos, Jacqueline C.
O’Brien, Susan
Brown, Jennifer R.
Kay, Neil E.
Reddy, Nishitha M.
Coutre, Steven
Tam, Constantine
Mulligan, Stephen
Jaeger, Ulrich
Devereux, Stephen
Pocock, Christopher
Robak, Tadeusz
Schuster, Stephen J.
Schuh, Anna
Gill, Devinder
Bloor, Adrian
Dearden, Claire
Moreno, Carol
Cull, Gavin
Hamblin, Mike
Jones, Jeffrey A.
Eckert, Karl
Solman, Isabelle G.
Suzuki, Samuel
Hsu, Emily
James, Danelle F.
Byrd, John C.
Hillmen, Peter
author_facet Barrientos, Jacqueline C.
O’Brien, Susan
Brown, Jennifer R.
Kay, Neil E.
Reddy, Nishitha M.
Coutre, Steven
Tam, Constantine
Mulligan, Stephen
Jaeger, Ulrich
Devereux, Stephen
Pocock, Christopher
Robak, Tadeusz
Schuster, Stephen J.
Schuh, Anna
Gill, Devinder
Bloor, Adrian
Dearden, Claire
Moreno, Carol
Cull, Gavin
Hamblin, Mike
Jones, Jeffrey A.
Eckert, Karl
Solman, Isabelle G.
Suzuki, Samuel
Hsu, Emily
James, Danelle F.
Byrd, John C.
Hillmen, Peter
author_sort Barrientos, Jacqueline C.
collection PubMed
description In the phase III study RESONATE, ibrutinib reduced the risk of progression and improved overall survival versus ofatumumab in previously treated patients with CLL/SLL. In this novel analysis of patient well-being including patient-reported outcomes, ibrutinib reduced disease burden while preserving parameters of hematologic and immunologic function in RESONATE. These results suggest that ibrutinib can improve quality of life while prolonging survival. BACKGROUND: Ibrutinib compared with ofatumumab significantly improves progression-free and overall survival in patients with previously treated chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). PATIENTS AND METHODS: Measures of well-being were assessed in RESONATE, where previously treated patients with CLL/SLL were randomized to receive ibrutinib 420 mg/day (n = 195) or ofatumumab (n = 196) for up to 24 weeks. Endpoints included hematologic function, Functional Assessment of Chronic Illness Therapy—Fatigue (FACIT-F), disease-related symptoms, European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Core 30 (EORTC QLQ-C30), and medical resource utilization. RESULTS: With up to 24 months’ follow-up (median, 16.4 months), 79% of cytopenic patients showed sustained hematologic improvement (82% with improved platelet count, 69% with improved hemoglobin) on ibrutinib versus 43% on ofatumumab (P < .0001). Higher rates of clinically meaningful improvement were demonstrated with ibrutinib versus ofatumumab for FACIT-F and EORTC global health. Greater improvement was observed in disease-related weight loss, fatigue, night sweats, and abdominal discomfort with ibrutinib versus ofatumumab. Hospitalizations in the first 30 days occurred less frequently with ibrutinib than ofatumumab (0.087 vs. 0.184 events/patient; P = .0198). New-onset diarrhea was infrequent with ibrutinib after the first 6 months (47% at ≤6 months vs. 5% at 12-18 months). With ibrutinib, grade ≥ 3 hypertension occurred in 6%, grade ≥ 3 atrial fibrillation in 4%, major hemorrhage in 2%, and tumor lysis syndrome in 1% of patients. CONCLUSION: Ibrutinib led to significant improvements in hematologic function and disease symptomatology versus ofatumumab, and can restore quality of life while prolonging survival in relapsed/refractory CLL/SLL.
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spelling pubmed-65271062019-05-20 Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Barrientos, Jacqueline C. O’Brien, Susan Brown, Jennifer R. Kay, Neil E. Reddy, Nishitha M. Coutre, Steven Tam, Constantine Mulligan, Stephen Jaeger, Ulrich Devereux, Stephen Pocock, Christopher Robak, Tadeusz Schuster, Stephen J. Schuh, Anna Gill, Devinder Bloor, Adrian Dearden, Claire Moreno, Carol Cull, Gavin Hamblin, Mike Jones, Jeffrey A. Eckert, Karl Solman, Isabelle G. Suzuki, Samuel Hsu, Emily James, Danelle F. Byrd, John C. Hillmen, Peter Clin Lymphoma Myeloma Leuk Article In the phase III study RESONATE, ibrutinib reduced the risk of progression and improved overall survival versus ofatumumab in previously treated patients with CLL/SLL. In this novel analysis of patient well-being including patient-reported outcomes, ibrutinib reduced disease burden while preserving parameters of hematologic and immunologic function in RESONATE. These results suggest that ibrutinib can improve quality of life while prolonging survival. BACKGROUND: Ibrutinib compared with ofatumumab significantly improves progression-free and overall survival in patients with previously treated chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). PATIENTS AND METHODS: Measures of well-being were assessed in RESONATE, where previously treated patients with CLL/SLL were randomized to receive ibrutinib 420 mg/day (n = 195) or ofatumumab (n = 196) for up to 24 weeks. Endpoints included hematologic function, Functional Assessment of Chronic Illness Therapy—Fatigue (FACIT-F), disease-related symptoms, European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Core 30 (EORTC QLQ-C30), and medical resource utilization. RESULTS: With up to 24 months’ follow-up (median, 16.4 months), 79% of cytopenic patients showed sustained hematologic improvement (82% with improved platelet count, 69% with improved hemoglobin) on ibrutinib versus 43% on ofatumumab (P < .0001). Higher rates of clinically meaningful improvement were demonstrated with ibrutinib versus ofatumumab for FACIT-F and EORTC global health. Greater improvement was observed in disease-related weight loss, fatigue, night sweats, and abdominal discomfort with ibrutinib versus ofatumumab. Hospitalizations in the first 30 days occurred less frequently with ibrutinib than ofatumumab (0.087 vs. 0.184 events/patient; P = .0198). New-onset diarrhea was infrequent with ibrutinib after the first 6 months (47% at ≤6 months vs. 5% at 12-18 months). With ibrutinib, grade ≥ 3 hypertension occurred in 6%, grade ≥ 3 atrial fibrillation in 4%, major hemorrhage in 2%, and tumor lysis syndrome in 1% of patients. CONCLUSION: Ibrutinib led to significant improvements in hematologic function and disease symptomatology versus ofatumumab, and can restore quality of life while prolonging survival in relapsed/refractory CLL/SLL. 2018-08-18 2018-12 /pmc/articles/PMC6527106/ /pubmed/30249389 http://dx.doi.org/10.1016/j.clml.2018.08.007 Text en This is on open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Barrientos, Jacqueline C.
O’Brien, Susan
Brown, Jennifer R.
Kay, Neil E.
Reddy, Nishitha M.
Coutre, Steven
Tam, Constantine
Mulligan, Stephen
Jaeger, Ulrich
Devereux, Stephen
Pocock, Christopher
Robak, Tadeusz
Schuster, Stephen J.
Schuh, Anna
Gill, Devinder
Bloor, Adrian
Dearden, Claire
Moreno, Carol
Cull, Gavin
Hamblin, Mike
Jones, Jeffrey A.
Eckert, Karl
Solman, Isabelle G.
Suzuki, Samuel
Hsu, Emily
James, Danelle F.
Byrd, John C.
Hillmen, Peter
Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title_full Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title_fullStr Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title_full_unstemmed Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title_short Improvement in Parameters of Hematologic and Immunologic Function and Patient Well-being in the Phase III RESONATE Study of Ibrutinib Versus Ofatumumab in Patients With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
title_sort improvement in parameters of hematologic and immunologic function and patient well-being in the phase iii resonate study of ibrutinib versus ofatumumab in patients with previously treated chronic lymphocytic leukemia/small lymphocytic lymphoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527106/
https://www.ncbi.nlm.nih.gov/pubmed/30249389
http://dx.doi.org/10.1016/j.clml.2018.08.007
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