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.authorscopusid | 7102505863 | |
| dc.authorscopusid | 6603473744 | |
| dc.authorscopusid | 57212718170 | |
| dc.authorscopusid | 7101791122 | |
| dc.authorscopusid | 7201551831 | |
| dc.authorscopusid | 56256103300 | |
| dc.authorscopusid | 7005103118 | |
| dc.contributor.author | Younes, A. | |
| dc.contributor.author | Sehn, L.H. | |
| dc.contributor.author | Johnson, P. | |
| dc.contributor.author | Zinzani, P.L. | |
| dc.contributor.author | Hong, X. | |
| dc.contributor.author | Zhu, J. | |
| dc.contributor.author | Patti, C. | |
| dc.date.accessioned | 2020-06-21T12:26:53Z | |
| dc.date.available | 2020-06-21T12:26:53Z | |
| dc.date.issued | 2019 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_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 States | en_US |
| dc.description.abstract | PURPOSE 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.doi | 10.1200/JCO.18.02403 | |
| dc.identifier.endpage | 1295 | en_US |
| dc.identifier.issn | 1527-7755 | |
| dc.identifier.issue | 15 | en_US |
| dc.identifier.pmid | 30901302 | |
| dc.identifier.scopus | 2-s2.0-85065791928 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 1285 | en_US |
| dc.identifier.uri | https://doi.org/10.1200/JCO.18.02403 | |
| dc.identifier.volume | 37 | en_US |
| dc.identifier.wos | WOS:000468868300004 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | American Society of Clinical Oncology jcoservice@asco.org | en_US |
| dc.relation.ispartof | Journal of Clinical Oncology | en_US |
| dc.relation.journal | Journal of Clinical Oncology | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | 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 | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
