Treatment with Idelalisib in Patients with Relapsed or Refractory Follicular Lymphoma: The Observational Italian Multicenter FolIdela Study.
follicular lymphoma
idelalisib
phosphatidylinositol 3-kinase inhibitor
refractory
relapsed
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
27 Jan 2022
27 Jan 2022
Historique:
received:
26
11
2021
revised:
17
01
2022
accepted:
25
01
2022
entrez:
15
2
2022
pubmed:
16
2
2022
medline:
16
2
2022
Statut:
epublish
Résumé
Follicular lymphoma (FL) is an indolent hematological disease, often responsive to the first line of treatment, but characterized by repeated relapses. The therapeutic algorithm for relapsed/refractory FL patients comprises phosphatidylinositol 3-kinase inhibitors. Idelalisib showed anticancer activity, while inducing a significant rate of toxicities. Since the evidence in the literature on its use in normal clinical practice is scarce, a retrospective multicenter study was conducted to evaluate effectiveness and tolerability in a real-life context. Seventy-two patients with a median age at diagnosis of 57.2 years-mostly with an advanced stage (88.9%) and relapsed to the most recent therapy (79.1%)-were enrolled. The median number of prior therapies was three (20.8% refractory to the last therapy before idelalisib). With a median number of 4 months of treatment, the overall response rate was 41.7% (20.8% complete responses). Median disease-free survival and overall survival were achieved at 8.4 months and at 4 years, respectively. Forty-four percent of patients experienced at least one drug-related toxicity: 6.9% hematological ones and 43% non-hematological. The study confirmed that idelalisib has anticancer effectiveness and an acceptable safety profile in relapsed/refractory FL with unfavorable prognostic characteristics, even in the context of normal clinical practice.
Identifiants
pubmed: 35158922
pii: cancers14030654
doi: 10.3390/cancers14030654
pmc: PMC8833724
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
Lancet Oncol. 2016 Aug;17(8):1081-1093
pubmed: 27345636
Haematologica. 2017 Apr;102(4):e156-e159
pubmed: 27979923
Blood Adv. 2020 Dec 8;4(23):5951-5957
pubmed: 33275769
J Clin Oncol. 2007 Feb 10;25(5):579-86
pubmed: 17242396
Blood. 2011 Jan 13;117(2):591-4
pubmed: 20959606
JAMA Oncol. 2020 Feb 1;6(2):248-254
pubmed: 31855259
J Clin Oncol. 2019 May 10;37(14):1188-1199
pubmed: 30897038
Br J Haematol. 2018 May;181(4):555-559
pubmed: 28342183
Br J Haematol. 2014 May;165(3):334-40
pubmed: 24438080
Expert Rev Anticancer Ther. 2006 Jun;6(6):861-9
pubmed: 16761929
Bone Marrow Transplant. 2020 Dec;55(12):2335-2338
pubmed: 32444863
Nat Rev Mol Cell Biol. 2010 May;11(5):329-41
pubmed: 20379207
J Immunol. 2009 Nov 1;183(9):5673-84
pubmed: 19843950
J Clin Oncol. 2019 Apr 20;37(12):984-991
pubmed: 30811293
Leuk Lymphoma. 2021 May;62(5):1077-1087
pubmed: 33300385
Expert Opin Pharmacother. 2016;17(2):265-74
pubmed: 26818003
N Engl J Med. 2017 Oct 5;377(14):1331-1344
pubmed: 28976863
Blood. 2016 May 19;127(20):2375-90
pubmed: 26980727
N Engl J Med. 2014 Mar 13;370(11):1008-18
pubmed: 24450858
Lancet. 2013 Apr 6;381(9873):1203-10
pubmed: 23433739