Publication:
Randomized Phase III Trial of Ibrutinib and Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone in Non–Germinal Center B-Cell Diffuse Large B-Cell Lymphoma

dc.authorscopusid7102505863
dc.authorscopusid6603473744
dc.authorscopusid57212718170
dc.authorscopusid7101791122
dc.authorscopusid7201551831
dc.authorscopusid56256103300
dc.authorscopusid7005103118
dc.contributor.authorYounes, A.
dc.contributor.authorSehn, L.H.
dc.contributor.authorJohnson, P.
dc.contributor.authorZinzani, P.L.
dc.contributor.authorHong, X.
dc.contributor.authorZhu, J.
dc.contributor.authorPatti, C.
dc.date.accessioned2020-06-21T12:26:53Z
dc.date.available2020-06-21T12:26:53Z
dc.date.issued2019
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Younes] Anas, Memorial Sloan-Kettering Cancer Center, New York, NY, United States; [Sehn] Laurie Helen, British Columbia Cancer Agency, Vancouver, BC, Canada; [Johnson] Peter W.M., University of Southampton, Southampton, Hampshire, United Kingdom; [Zinzani] Pier Luigi, Alma Mater Studiorum Università di Bologna, Bologna, BO, Italy; [Hong] Xiaonan, Fudan University, Shanghai, China; [Zhu] Jun, Beijing Cancer Hospital, Beijing, China; [Patti] Caterina, Azienda Ospedaliera Ospedali Riuniti Villa Sofia-Cervello, Palermo, PA, Italy; [Belada] David, Charles University, Prague, Czech Republic, Fakultní Nemocnice Hradec Králové, Hradec Kralove, Czech Republic; [Samoǐlova] Olga S., Semashko Regional Clinical Hospital, Nizhny Novgorod, Russian Federation; [Suh] Cheolwon, University of Ulsan, Ulsan, South Korea; [Leppä] Sirpa M., Helsinki University Hospital, Helsinki, Finland, Helsingin Yliopisto, Helsinki, Uusimaa, Finland; [Rai] Shinya, Kindai University, Higashiosaka, Osaka, Japan; [Turgut] Mehmet, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Jurczak] Wojciech J., Uniwersytet Jagielloński, Krakow, Małopolska, Poland; [Cheung] Matthew C., Odette Cancer Centre, Toronto, ON, Canada; [Gurion] Ronit, Rabin Medical Center Israel, Petah Tiqwa, Israel, Tel Aviv University, Tel Aviv-Yafo, Tel Aviv District, Israel; [Yeh] Su Peng, China Medical University Hospital, Taichung, Taiwan; [López-Hernandez] Andrés, Hospital Universitari Vall d'Hebron, Barcelona, Barcelona, Spain; [Duḧrsen] Ulrich, Universitätsklinikum Essen, Essen, Nordrhein-Westfalen, Germany; [Thièblemont] Catherine, Hôpital Saint-Louis, Paris, France, Diderot University, Paris, France; [Chiattone] Carlos Sérgio, Faculdade de Ciencias Medicas da Santa Casa de Sao Paulo, Sao Paulo, SP, Brazil; [Balasubramanian] Sriram, Janssen Research & Development, Beerse, VAN, Belgium; [Carey] Jodi L., Janssen Research & Development, Beerse, VAN, Belgium; [Liu] Grace, Janssen Pharmaceuticals, Inc., Titusville, NJ, United States; [Martin Shreeve] S., Janssen Research & Development, Beerse, VAN, Belgium; [Sun] Steven, Janssen Pharmaceuticals, Inc., Titusville, NJ, United States; [Zhuang] Senhong, Janssen Pharmaceuticals, Inc., Titusville, NJ, United States; [Vermeulen] Jessica T., Janssen Vaccines & Prevention B.V., Leiden, Zuid-Holland, Netherlands; [Staudt] Louis M., National Cancer Institute (NCI), Rockville, MD, United States; [Wilson] Wyndham H., National Cancer Institute (NCI), Rockville, MD, United Statesen_US
dc.description.abstractPURPOSE Ibrutinib has shown activity in non–germinal center B-cell diffuse large B-cell lymphoma (DLBCL). This double-blind phase III study evaluated ibrutinib and rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in untreated non–germinal center B-cell DLBCL. PATIENTS AND METHODS Patients were randomly assigned at a one-to-one ratio to ibrutinib (560 mg per day orally) plus R-CHOP or placebo plus R-CHOP. The primary end point was event-free survival (EFS) in the intent-to-treat (ITT) population and the activated B-cell (ABC) DLBCL subgroup. Secondary end points included progression-free survival (PFS), overall survival (OS), and safety. RESULTS A total of 838 patients were randomly assigned to ibrutinib plus R-CHOP (n = 419) or placebo plus R-CHOP (n = 419). Median age was 62.0 years; 75.9% of evaluable patients had ABC subtype disease, and baseline characteristics were balanced. Ibrutinib plus R-CHOP did not improve EFS in the ITT (hazard ratio [HR], 0.934) or ABC (HR, 0.949) population. A preplanned analysis showed a significant interaction between treatment and age. In patients age younger than 60 years, ibrutinib plus R-CHOP improved EFS (HR, 0.579), PFS (HR, 0.556), and OS (HR, 0.330) and slightly increased serious adverse events (35.7% v 28.6%), but the proportion of patients receiving at least six cycles of R-CHOP was similar between treatment arms (92.9% v 93.0%). In patients age 60 years or older, ibrutinib plus R-CHOP worsened EFS, PFS, and OS, increased serious adverse events (63.4% v 38.2%), and decreased the proportion of patients receiving at least six cycles of R-CHOP (73.7% v 88.8%). CONCLUSION The study did not meet its primary end point in the ITT or ABC population. However, in patients age younger than 60 years, ibrutinib plus R-CHOP improved EFS, PFS, and OS with manageable safety. In patients age 60 years or older, ibrutinib plus R-CHOP was associated with increased toxicity, leading to compromised R-CHOP administration and worse outcomes. Further investigation is warranted. © © 2019 American Society of Clinical Oncology. All rights reserved.en_US
dc.identifier.doi10.1200/JCO.18.02403
dc.identifier.endpage1295en_US
dc.identifier.issn1527-7755
dc.identifier.issue15en_US
dc.identifier.pmid30901302
dc.identifier.scopus2-s2.0-85065791928
dc.identifier.scopusqualityQ1
dc.identifier.startpage1285en_US
dc.identifier.urihttps://doi.org/10.1200/JCO.18.02403
dc.identifier.volume37en_US
dc.identifier.wosWOS:000468868300004
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherAmerican Society of Clinical Oncology jcoservice@asco.orgen_US
dc.relation.ispartofJournal of Clinical Oncologyen_US
dc.relation.journalJournal of Clinical Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleRandomized Phase III Trial of Ibrutinib and Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone in Non–Germinal Center B-Cell Diffuse Large B-Cell Lymphomaen_US
dc.typeArticleen_US
dspace.entity.typePublication

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