Your browser doesn't support javascript.
loading
Overall survival of patients with CLL treated with ibrutinib in the first line compared to second-line ibrutinib after chemotherapy/chemoimmunotherapy.
Robak, Tadeusz; Doubek, Michael; Ferrant, Emmanuelle; Diels, Joris; Andersone, Liva; Wilbertz, Sabine; Healy, Nollaig C; Neumayr, Lynne; van Sanden, Suzy.
Afiliação
  • Robak T; Department of Hematology, Medical University of Lodz, Copernicus Memorial Hospital, Lodz, Poland.
  • Doubek M; Internal Medicine - Hematology and Oncology Department, University Hospital Brno, Brno, Czech Republic.
  • Ferrant E; Department of Hematology, Hôpital Lyon-Sud, Lyon, France.
  • Diels J; Janssen Pharmaceutica NV, Beerse, Belgium.
  • Andersone L; UAB "JOHNSON & JOHNSON" filiale Latvija, Riga, Latvia.
  • Wilbertz S; Janssen-Cilag GmbH, Neuss, Germany.
  • Healy NC; Janssen Sciences Ireland UC, Cork, Ireland.
  • Neumayr L; Pharmacyclics, an AbbVie Company, Sunnyvale, California, USA.
  • van Sanden S; Janssen Pharmaceutica NV, Beerse, Belgium.
Curr Med Res Opin ; 40(8): 1369-1378, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38885086
ABSTRACT

OBJECTIVE:

To evaluate the overall survival (OS) of patients with chronic lymphocytic leukemia (CLL) receiving either ibrutinib monotherapy as a first-line (1L) treatment or chemotherapy/chemoimmunotherapy-based (CT/CIT) regimens in 1L followed by ibrutinib in the second line (1L CT/CIT-2L ibrutinib) after disease progression by emulating a randomized trial comparing both treatment sequences.

METHODS:

Patient-level data from the RESONATE-2 trial (NCT01722487) and real-world PHEDRA databases were analyzed. Three scenarios were considered using the following data sources (1) RESONATE-2, (2) combined RESONATE-2/PHEDRA, (3) combined RESONATE-2/PHEDRA for 1L ibrutinib and PHEDRA for 1L CT/CIT-2L ibrutinib. Propensity score-based weights and inverse probability of censoring weighting were used to adjust for baseline (Scenarios 2 and 3) and time-dependent confounding (all scenarios), and to address potential biases. A weighted Cox proportional hazards model was used to estimate the OS hazard ratio (HR) and 95% confidence interval (CI) for 1L ibrutinib versus 1L CT/CIT-2L ibrutinib.

RESULTS:

Results from Scenario 1 showed a significantly lower risk of death with 1L ibrutinib compared with 1L chlorambucil followed by 2L ibrutinib (HR 0.35 [95% CI 0.20-0.62]). Results from Scenarios 2 and 3 demonstrated a reduced risk of death with 1L ibrutinib compared with 1L CT/CIT-2L ibrutinib (HR 0.35 [0.21-0.61] and 0.64 [0.39-1.04], respectively).

CONCLUSION:

The analyses consistently showed a reduced risk of death when ibrutinib was used as a 1L treatment in CLL compared with delaying its use until 2L after CT/CIT regimens, which suggests that initiating ibrutinib in 1L is advantageous for improving survival outcomes.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piperidinas / Pirazóis / Pirimidinas / Adenina / Leucemia Linfocítica Crônica de Células B Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piperidinas / Pirazóis / Pirimidinas / Adenina / Leucemia Linfocítica Crônica de Células B Idioma: En Ano de publicação: 2024 Tipo de documento: Article