Ofatumumab maintenance prolongs progression-free survival in relapsed chronic lymphocytic leukemia: final analysis of the PROLONG study.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
04 12 2019
Historique:
received: 10 07 2019
accepted: 07 11 2019
revised: 18 10 2019
entrez: 6 12 2019
pubmed: 6 12 2019
medline: 16 5 2020
Statut: epublish

Résumé

We report the final analysis of the PROLONG study on ofatumumab maintenance in relapsed chronic lymphocytic leukemia (CLL). In all, 480 patients with CLL in complete or partial remission after second- or third-line treatment were randomized 1:1 to ofatumumab (300 mg first week, followed by 1000 mg every 8 weeks for up to 2 years) or observation. Median follow-up duration was 40.9 months. Median progression-free survival was 34.2 and 16.9 months for ofatumumab and observation arms, respectively, (hazard ratio, 0.55 [95% confidence interval, 0.43-0.70]; P < 0.0001). Median time to next treatment for ofatumumab and observation arms, respectively, was 37.4 and 27.6 months (0.72 [0.57-0.91]; P = 0.0044). Overall survival was similar in both arms; median was not reached (0.99 [0.72-1.37]). Grade ≥ 3 adverse events occurred in 62% and 51% of patients in ofatumumab and observation arms, respectively, the most common being neutropenia (23% and 10%), pneumonia (13% and 12%) and febrile neutropenia (6% and 4%). Up to 60 days after the last treatment, four deaths were reported in the ofatumumab arm versus six in the observation arm, none considered related to ofatumumab. Ofatumumab maintenance significantly prolonged progression-free survival in patients with relapsed CLL and was well tolerated.

Identifiants

pubmed: 31801940
doi: 10.1038/s41408-019-0260-2
pii: 10.1038/s41408-019-0260-2
pmc: PMC6893027
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
ofatumumab M95KG522R0

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

98

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Auteurs

Marinus van Oers (M)

Academisch Medisch Centrum and HOVON, Amsterdam, The Netherlands. m.h.vanoers@amc.uva.nl.

Lukas Smolej (L)

University Hospital and Faculty of Medicine, Hradec Kralove, Czech Republic.

Mario Petrini (M)

Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.

Fritz Offner (F)

Universitair Ziekenhuis Gent, Gent, Belgium.

Sebastian Grosicki (S)

Department of Hematology and Cancer Prevention, Silesian Medical University, Katowice, Poland.

Mark-David Levin (MD)

Albert Schweitzer Ziekenhuis Dordrecht and HOVON, Dordrecht, The Netherlands.

Jaclyn Davis (J)

Novartis Oncology, East Hanover, NJ, USA.

Hiya Banerjee (H)

Novartis Oncology, East Hanover, NJ, USA.

Tommaso Stefanelli (T)

Novartis Pharma AG, Basel, Switzerland.

Petra Hoever (P)

Novartis Pharma AG, Basel, Switzerland.

Christian Geisler (C)

Rigshospitalet-Koebenhavn, Copenhagen, Denmark.

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Classifications MeSH