Prolonged lenalidomide maintenance therapy improves the depth of response in multiple myeloma.
Journal
Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425
Informations de publication
Date de publication:
26 05 2020
26 05 2020
Historique:
received:
21
01
2020
accepted:
01
04
2020
entrez:
21
5
2020
pubmed:
21
5
2020
medline:
15
5
2021
Statut:
ppublish
Résumé
Lenalidomide is an immunomodulatory drug approved for maintenance treatment in newly diagnosed multiple myeloma, and it has been shown to improve progression-free survival (PFS) and, in several studies, overall survival. Nevertheless, the impact of prolonged treatment with lenalidomide on the kinetics of minimal residual disease (MRD) and its prognostic impact have not been studied in depth. To obtain better knowledge in this regard, we retrospectively analyzed 139 patients who received lenalidomide maintenance in real-world clinical practice and whose MRD levels were observed during the treatment period by multiparametric flow cytometry or next-generation sequencing with a sensitivity of at least 10-4. Lenalidomide maintenance correlated with an increased depth of the disease response, with 38.1% of patients achieving maximal response during maintenance. Moreover, 34.3% of patients who were MRD positive after induction treatment achieved MRD-negative status during maintenance and ultimately had improved PFS. Sequential MRD assessments identified patients with progressively decreasing MRD levels who also had better PFS outcomes, compared with patients not showing a decreasing pattern of MRD. These results support the role of maintenance therapy, not only to sustain, but also to increase the depth of disease response with a PFS benefit. In addition, MRD monitoring during maintenance identifies patients with better prognosis and may help in their clinical management.
Identifiants
pubmed: 32433744
pii: S2473-9529(20)31292-1
doi: 10.1182/bloodadvances.2020001508
pmc: PMC7252556
doi:
Substances chimiques
Lenalidomide
F0P408N6V4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2163-2171Informations de copyright
© 2020 by The American Society of Hematology.
Références
Blood. 2019 Oct 17;134(16):1337-1345
pubmed: 31484647
Leukemia. 2014 Feb;28(2):269-77
pubmed: 23974982
Clin Ther. 2018 Jul;40(7):1193-1202.e1
pubmed: 30007443
J Clin Oncol. 2017 Oct 10;35(29):3279-3289
pubmed: 28742454
N Engl J Med. 2012 May 10;366(19):1770-81
pubmed: 22571201
J Cancer Res Clin Oncol. 2018 Jul;144(7):1357-1366
pubmed: 29675792
Ann Hematol. 2018 Dec;97(12):2425-2436
pubmed: 30056582
Oncotarget. 2017 Jan 24;8(4):5924-5935
pubmed: 27779105
J Clin Oncol. 2011 Apr 20;29(12):1627-33
pubmed: 21402611
J Clin Oncol. 2017 Sep 1;35(25):2911-2918
pubmed: 28686535
Blood. 2014 May 15;123(20):3073-9
pubmed: 24646471
N Engl J Med. 2012 May 10;366(19):1782-91
pubmed: 22571202
Biol Blood Marrow Transplant. 2017 Feb;23(2):262-268
pubmed: 27856369
N Engl J Med. 2014 Sep 4;371(10):906-17
pubmed: 25184863
Leukemia. 2019 Jul;33(7):1713-1722
pubmed: 30573775
Leukemia. 2017 Jun;31(6):1446-1449
pubmed: 28210002
Lancet Oncol. 2019 Jan;20(1):57-73
pubmed: 30559051
N Engl J Med. 2014 Sep 4;371(10):895-905
pubmed: 25184862
Cancer. 2016 Dec 15;122(24):3831-3837
pubmed: 27680710
Lancet Haematol. 2017 Sep;4(9):e431-e442
pubmed: 28826616
Cancer. 2019 Mar 1;125(5):750-760
pubmed: 30561775
Haematologica. 2019 Jul;104(7):1440-1450
pubmed: 30733268
Blood. 2016 Jun 16;127(24):2955-62
pubmed: 27002115
Am J Hematol. 2019 Aug;94(8):853-861
pubmed: 31074033
N Engl J Med. 2012 May 10;366(19):1759-69
pubmed: 22571200
Blood Adv. 2018 Jul 10;2(13):1608-1615
pubmed: 29986853
Lancet Oncol. 2016 Aug;17(8):e328-e346
pubmed: 27511158
JAMA Oncol. 2018 Oct 1;4(10):1389-1397
pubmed: 30098165
Leukemia. 2018 Mar;32(3):712-718
pubmed: 28848227
Blood Cancer J. 2016 Dec 9;6(12):e506
pubmed: 27935580
Blood. 2018 Jan 18;131(3):301-310
pubmed: 29150421
Blood. 2018 Dec 6;132(23):2456-2464
pubmed: 30249784
Leuk Lymphoma. 2019 Feb;60(2):511-514
pubmed: 30616438