Idelalisib addition has neutral to beneficial effects on quality of life in bendamustine/rituximab-treated patients: results of a phase 3, randomized, controlled trial.


Journal

Health and quality of life outcomes
ISSN: 1477-7525
Titre abrégé: Health Qual Life Outcomes
Pays: England
ID NLM: 101153626

Informations de publication

Date de publication:
15 Nov 2019
Historique:
received: 28 06 2019
accepted: 11 10 2019
entrez: 16 11 2019
pubmed: 16 11 2019
medline: 4 3 2020
Statut: epublish

Résumé

In a phase 3 randomized, double-blind, placebo-controlled trial, treatment with idelalisib, a phosphoinositol-3 kinase δ inhibitor, + bendamustine/rituximab improved progression-free survival (PFS) and overall survival (OS) in adult patients with relapsed/refractory chronic lymphocytic leukemia (R/R CLL). Here we report the results of health-related quality of life (HRQL) analyses from this study. From June 15, 2012 to August 21, 2014, 416 patients with R/R CLL were enrolled; 207 patients were randomized to the idelalisib arm and 209 to the placebo arm. In the 416 patients randomized to receive bendamustine/rituximab and either oral idelalisib 150 mg twice-daily or placebo, HRQL was assessed at baseline and throughout the blinded part of the study using the Functional Assessment of Cancer Therapy-Leukemia (FACT-Leu) and EuroQoL Five-Dimension (EQ-5D) visual analogue scale (VAS) questionnaires. The assessments were performed at scheduled patient visits; every 4 weeks for the first 6 months from the initiation of treatment, then every 8 weeks for the next 6 months, and every 12 weeks thereafter until end of study. Least-squares mean changes from baseline were estimated using a mixed-effects model by including treatment, time, and treatment-by-time interaction, and stratification factors as fixed effects. Time to first symptom improvement was assessed by Kaplan-Meier analysis. In mixed-effects model analysis, idelalisib + bendamustine/rituximab treatment led to clinically meaningful improvements from baseline in leukemia-associated symptoms. Moreover, per Kaplan-Meier analysis, the proportion of patients with symptom improvement was higher and time to improvement was shorter among patients in the idelalisib-containing arm compared with those who did not receive idelalisib. The physical and social/family FACT-Leu subscale scores, along with the self-rated health assessed by EQ-VAS, showed improvement with idelalisib over placebo, but the difference did not reach statistical significance. The functional and emotional FACT-Leu subscale scores remained similar to placebo. Addition of idelalisib to bendamustine/rituximab, apart from improving PFS and OS, had a neutral to beneficial impact on HRQL in patients with R/R CLL, particularly by reducing leukemia-specific disease symptoms. Clinicaltrials.gov NCT01569295. Registered April 3, 2012.

Sections du résumé

BACKGROUND BACKGROUND
In a phase 3 randomized, double-blind, placebo-controlled trial, treatment with idelalisib, a phosphoinositol-3 kinase δ inhibitor, + bendamustine/rituximab improved progression-free survival (PFS) and overall survival (OS) in adult patients with relapsed/refractory chronic lymphocytic leukemia (R/R CLL). Here we report the results of health-related quality of life (HRQL) analyses from this study.
METHODS METHODS
From June 15, 2012 to August 21, 2014, 416 patients with R/R CLL were enrolled; 207 patients were randomized to the idelalisib arm and 209 to the placebo arm. In the 416 patients randomized to receive bendamustine/rituximab and either oral idelalisib 150 mg twice-daily or placebo, HRQL was assessed at baseline and throughout the blinded part of the study using the Functional Assessment of Cancer Therapy-Leukemia (FACT-Leu) and EuroQoL Five-Dimension (EQ-5D) visual analogue scale (VAS) questionnaires. The assessments were performed at scheduled patient visits; every 4 weeks for the first 6 months from the initiation of treatment, then every 8 weeks for the next 6 months, and every 12 weeks thereafter until end of study. Least-squares mean changes from baseline were estimated using a mixed-effects model by including treatment, time, and treatment-by-time interaction, and stratification factors as fixed effects. Time to first symptom improvement was assessed by Kaplan-Meier analysis.
RESULTS RESULTS
In mixed-effects model analysis, idelalisib + bendamustine/rituximab treatment led to clinically meaningful improvements from baseline in leukemia-associated symptoms. Moreover, per Kaplan-Meier analysis, the proportion of patients with symptom improvement was higher and time to improvement was shorter among patients in the idelalisib-containing arm compared with those who did not receive idelalisib. The physical and social/family FACT-Leu subscale scores, along with the self-rated health assessed by EQ-VAS, showed improvement with idelalisib over placebo, but the difference did not reach statistical significance. The functional and emotional FACT-Leu subscale scores remained similar to placebo.
CONCLUSIONS CONCLUSIONS
Addition of idelalisib to bendamustine/rituximab, apart from improving PFS and OS, had a neutral to beneficial impact on HRQL in patients with R/R CLL, particularly by reducing leukemia-specific disease symptoms.
TRIAL REGISTRATION BACKGROUND
Clinicaltrials.gov NCT01569295. Registered April 3, 2012.

Identifiants

pubmed: 31729982
doi: 10.1186/s12955-019-1232-8
pii: 10.1186/s12955-019-1232-8
pmc: PMC6858733
doi:

Substances chimiques

Purines 0
Quinazolinones 0
Rituximab 4F4X42SYQ6
Bendamustine Hydrochloride 981Y8SX18M
idelalisib YG57I8T5M0

Banques de données

ClinicalTrials.gov
['NCT01569295']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

173

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : Gilead Sciences, Inc.
ID : N/A

Références

Br J Haematol. 2007 Oct;139(2):255-64
pubmed: 17897301
Leuk Lymphoma. 2017 Jul;58(7):1598-1606
pubmed: 27830957
Cancer Control. 2012 Jan;19(1):37-53
pubmed: 22143061
Value Health. 2012 Dec;15(8):1051-8
pubmed: 23244807
Qual Life Res. 2015 Dec;24(12):2895-906
pubmed: 26205768
Acta Oncol. 2016 Sep - Oct;55(9-10):1115-1120
pubmed: 27494089
Crit Rev Oncol Hematol. 2015 Dec;96(3):542-54
pubmed: 26324461
N Engl J Med. 2000 Dec 28;343(26):1910-6
pubmed: 11136261
Curr Pharm Des. 2012;18(23):3399-405
pubmed: 22591390
J Clin Oncol. 2007 May 1;25(13):1722-31
pubmed: 17389338
Ann Med. 2001 Jul;33(5):337-43
pubmed: 11491192
Blood. 2008 Jun 15;111(12):5446-56
pubmed: 18216293
Hematology Am Soc Hematol Educ Program. 2013;2013:158-67
pubmed: 24319177
Leukemia. 2009 Jan;23(1):117-24
pubmed: 18843282
Lancet Oncol. 2017 Mar;18(3):297-311
pubmed: 28139405
Med Care. 2005 Mar;43(3):203-20
pubmed: 15725977
Qual Life Res. 2008 Nov;17(9):1137-46
pubmed: 18841493
Acta Medica (Hradec Kralove). 2010;53(4):213-20
pubmed: 21400979
Eval Health Prof. 2005 Jun;28(2):192-211
pubmed: 15851773
N Engl J Med. 2014 Mar 13;370(11):997-1007
pubmed: 24450857
Leuk Lymphoma. 2018 Sep;59(9):2075-2084
pubmed: 29295653
J Clin Oncol. 1993 Mar;11(3):570-9
pubmed: 8445433
Lancet. 2007 Jul 21;370(9583):230-239
pubmed: 17658394
Leuk Lymphoma. 2005 Dec;46(12):1709-14
pubmed: 16263572
Curr Hematol Malig Rep. 2011 Mar;6(1):36-46
pubmed: 21153774
Health Policy. 1990 Dec;16(3):199-208
pubmed: 10109801
Lancet Haematol. 2017 Mar;4(3):e114-e126
pubmed: 28257752
Health Qual Life Outcomes. 2007 Dec 21;5:70
pubmed: 18154669
J Clin Oncol. 2007 Nov 10;25(32):5106-12
pubmed: 17991929
Haematologica. 2007 Sep;92(9):1242-5
pubmed: 17666364
J Clin Oncol. 2012 Dec 1;30(34):4249-55
pubmed: 23071244

Auteurs

Marco Montillo (M)

Department of Hematology, Niguarda Cancer Center, Niguarda Hospital, Piazza Ospedale Maggiore, 3, 20162, Milan, Italy. marco.montillo@ospedaleniguarda.it.

Árpád Illés (Á)

Department of Hematology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Tadeusz Robak (T)

Department of Hematology, Medical University of Lodz and Copernicus Memorial Hospital, Lodz, Poland.

Alexander S Pristupa (AS)

Department of Hematology, Ryazan Regional Clinical Hospital, Ryazan, Russia.

Malgorzata Wach (M)

Department Hemato-Oncology and Bone Marrow Transplantation, Medical University of Lublin, Lublin, Poland.

Miklós Egyed (M)

Department of Hematology, Somogy County Kaposi Mor Hospital, Kaposvar, Hungary.

Julio Delgado (J)

Department of Hematology, Hospital Clínic, Barcelona, Spain.

Wojciech Jurczak (W)

Maria Sklodowska Curie Institute of Oncology, Krakow, Poland.

Franck Morschhauser (F)

CHRU Lille, Unité GRITA, Department of Hematology, Université de Lille, Lille, France.

Anna Schuh (A)

University of Oxford, Oxford Cancer and Haematology Centre, Churchill Hospital, Oxford, UK.

Herbert Eradat (H)

Division of Hematology-Oncology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

Sanatan Shreay (S)

Gilead Sciences, Inc., Foster City, CA, USA.

Jacqueline C Barrientos (JC)

Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.

Andrew D Zelenetz (AD)

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

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH