Comparison of ibrutinib and idelalisib plus rituximab in real-life relapsed/resistant chronic lymphocytic leukemia cases.
Adenine
/ administration & dosage
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Biomarkers, Tumor
Drug Resistance, Neoplasm
Female
Humans
Immunoglobulins
/ genetics
In Situ Hybridization, Fluorescence
Leukemia, Lymphocytic, Chronic, B-Cell
/ diagnosis
Male
Middle Aged
Mutation
Piperidines
/ administration & dosage
Proportional Hazards Models
Purines
/ administration & dosage
Quinazolinones
/ administration & dosage
Recurrence
Retreatment
Rituximab
/ administration & dosage
Treatment Outcome
chronic lymphocytic leukemia
ibrutinib
idelalisib
therapy
Journal
European journal of haematology
ISSN: 1600-0609
Titre abrégé: Eur J Haematol
Pays: England
ID NLM: 8703985
Informations de publication
Date de publication:
Apr 2021
Apr 2021
Historique:
received:
17
11
2020
accepted:
23
12
2020
pubmed:
31
12
2020
medline:
29
7
2021
entrez:
30
12
2020
Statut:
ppublish
Résumé
To compare the capacity of ibrutinib (IB) and idelalisib-rituximab (IDELA-R) of prolonging overall survival (OS) as in CLL patients, previously treated with chemotherapy only. A real-life cohort of 675 cases has been identified and investigated in the database of the groups participating in the study. At an unadjusted univariate analysis, a significant death risk reduction was observed favoring IB (IDELA-R vs IB HR = 0.5, 95% CI = 0.36-0.71) although with some limitations due to the non-randomized and retrospective nature of the study and to the lower number of patients in the IDELA-R group (112 cases) related to the current prescribing practice. To overcome the potential problem of confounding by indication, we adjusted the association between the type of therapy and mortality for all variables significantly associated with OS at Cox univariate analysis. Furthermore, those variables, differently distributed between the two study groups, were introduced into the multivariate Cox model to improve the effectiveness of the analysis. By introducing all these variables into the multiple Cox regression model, we confirmed the protective effect of IB vs IDELA-R (HR = 0.67, 95% CI = 0.45-0.98, P = .04) independent of potential confounders. Although our analysis presents some constraints, that is, the unavailability of additional potential confounders, and the retrospective nature of the study, this observation may be of help for the daily clinical practice, particularly in the absence of randomized trials comparing the two schedules.
Substances chimiques
Biomarkers, Tumor
0
Immunoglobulins
0
Piperidines
0
Purines
0
Quinazolinones
0
ibrutinib
1X70OSD4VX
Rituximab
4F4X42SYQ6
Adenine
JAC85A2161
idelalisib
YG57I8T5M0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
493-499Subventions
Organisme : Associazione Italiana Ricerca sul Cancro (AIRC)
ID : 9980
Organisme : Associazione Italiana Ricerca sul Cancro (AIRC)
ID : 21198
Organisme : Fondazione CaRiCal co-financed Multi-Unit Regional Grant
ID : 16695
Organisme : Investigator Grant
ID : IG-21687
Organisme : Investigator Grant
ID : IG-5506
Organisme : Progetto Ricerca Finalizzata
ID : PE 2016-02362756
Organisme : Progetto Ricerca Finalizzata
ID : RF-2018-12365790
Organisme : Ministero della Salute, Rome, Italy
Organisme : Compagnia S. Paolo, Turin, Italy
ID : 2017.0526
Organisme : Ministry of Health
Organisme : BEAT Leukemia
Organisme : GILEAD Sciences Srl
ID : ISR-17-10250
Informations de copyright
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
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