Plain Language Summary of the iNNOVATE study: ibrutinib plus rituximab is well-tolerated and effective in people with Waldenström's macroglobulinemia.


Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Feb 2023
Historique:
medline: 2 5 2023
pubmed: 24 2 2023
entrez: 23 2 2023
Statut: ppublish

Résumé

This article provides a short summary of 5-year results from the iNNOVATE trial. The original paper was published in the During the 5 years of monitoring, more people who took ibrutinib plus rituximab experienced an improvement in their disease and lived longer without their disease getting worse compared to those who took placebo plus rituximab. Side effects from ibrutinib and rituximab were manageable and generally decreased over time. Participants in both study groups reported improvements in quality of life, but those who took ibrutinib plus rituximab reported significantly greater improvement in their quality of life (as measured by FACT-An score) compared to those who took placebo plus rituximab. These results show that ibrutinib plus rituximab is better than rituximab alone in people with WM and that ibrutinib plus rituximab is safe and effective in the long term. This information confirms the role of ibrutinib plus rituximab as a standard of care for WM.

Identifiants

pubmed: 36815271
doi: 10.2217/fon-2022-1015
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
ibrutinib 1X70OSD4VX
Adenine JAC85A2161

Banques de données

ClinicalTrials.gov
['NCT02165397']

Types de publication

Journal Article Review Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

345-353

Commentaires et corrections

Type : CommentOn
https://ascopubs.org/doi/full/10.1200/JCO.21.00838

Auteurs

Christian Buske (C)

Institute of Experimental Cancer Research, Comprehensive Cancer Center Ulm, University Hospital of Ulm, Ulm, Germany.

Alessandra Tedeschi (A)

ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Judith Trotman (J)

Concord Hospital, University of Sydney, Sydney, Australia.

Ramón García-Sanz (R)

Department of Hematology, University Hospital of Salamanca (HUS/IBSAL), CIBERONC & Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), Salamanca, Spain.

David MacDonald (D)

The Ottawa Hospital, University of Ottawa, Ottawa, Canada.

Veronique Leblond (V)

Département d'Hématologie Hôpital Pitié-Salpêtrière AP-HP, Sorbonne Université, Paris, France.

Beatrice Mahe (B)

Centre Hospitalier Universitaire de Nantes, Hôtel Dieu Hematologie Clinique, Nantes, France.

Charles Herbaux (C)

Centre Hospitalier Régional Universitaire de Lille, Institute of Hematology-Transfusion, Lille, France.

Jeffrey V Matous (JV)

Colorado Blood Cancer Institute, Denver, CO, USA.

Constantine S Tam (CS)

The Alfred Hospital & the University of Melbourne, Melbourne, Australia.

Leonard T Heffner (LT)

Winship Cancer Institute of Emory University, Atlanta, GA, USA.

Marzia Varettoni (M)

Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

M Lia Palomba (ML)

Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Chaim Shustik (C)

Royal Victoria Hospital at McGill University Health Centre, Montreal, Canada.

Efstathios Kastritis (E)

National & Kapodistrian University of Athens School of Medicine, Athens, Greece.

Steven P Treon (SP)

Dana-Farber Cancer Institute, Boston, MA, USA.

Jerry Ping (J)

Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA, USA.

Bernhard Hauns (B)

Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA, USA.

Israel Arango-Hisijara (I)

Janssen Pharmaceuticals, Raritan, NJ, USA.

Meletios A Dimopoulos (MA)

National & Kapodistrian University of Athens School of Medicine, Athens, Greece.

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Classifications MeSH