Patterns of survival in patients with recurrent mantle cell lymphoma in the modern era: progressive shortening in response duration and survival after each relapse.
Journal
Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469
Informations de publication
Date de publication:
20 05 2019
20 05 2019
Historique:
received:
03
01
2019
accepted:
03
04
2019
revised:
27
02
2019
entrez:
22
5
2019
pubmed:
22
5
2019
medline:
20
2
2020
Statut:
epublish
Résumé
As the survival of patients with mantle cell lymphoma (MCL) continues to improve, patients are increasingly being treated with multiple regimens. However, outcome after each line remains poorly characterized in the modern era. To address this knowledge gap, we retrospectively studied 404 consecutive MCL patients who were managed between 2000 and 2014 at Memorial Sloan Kettering Cancer Center. Histologic diagnosis was centrally confirmed, and patients were followed longitudinally from diagnosis throughout their disease course. Progression-free survival (PFS) and overall survival (OS) were determined by Kaplan-Meier method. The median OS and PFS after first-line treatment were 9.7 and 4.0 years, respectively. After second-line therapy, the median OS and PFS were 41.1 and 14.0 months, third line were 25.2 and 6.5 months, and fourth line were 14.4 and 5.0 months. In patients less than 65 years, stem cell transplant (SCT)-based frontline regimens were associated with improved PFS compared with non-SCT regimens (median PFS: 86.2 versus 40.0 months; P < 0.01), with a trend toward longer OS (median OS: 165.0 versus 120.0 months; P = 0.06). Early treatment failure after first-line regimens was associated with worse OS (5.9 versus 2.5 years; P < 0.01). Our study should facilitate establishing proper endpoints for future clinical trials using novel treatment approaches.
Identifiants
pubmed: 31110172
doi: 10.1038/s41408-019-0209-5
pii: 10.1038/s41408-019-0209-5
pmc: PMC6527702
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
50Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA192937
Pays : United States
Références
Br J Haematol. 2016 Nov;175(3):410-418
pubmed: 27378674
N Engl J Med. 2012 Aug 9;367(6):520-31
pubmed: 22873532
Lancet. 2016 Feb 20;387(10020):770-8
pubmed: 26673811
Br J Haematol. 2018 Apr;181(2):215-228
pubmed: 29532919
J Clin Oncol. 2009 Feb 1;27(4):511-8
pubmed: 19075279
Blood. 2008 Jan 15;111(2):558-65
pubmed: 17962512
Cancer. 2008 Aug 15;113(4):791-8
pubmed: 18615506
N Engl J Med. 2017 Sep 28;377(13):1250-1260
pubmed: 28953447
Blood. 2016 May 19;127(20):2375-90
pubmed: 26980727
Blood. 2010 Nov 11;116(19):3724-34
pubmed: 20664057
Cancer. 2011 May 1;117(9):1901-10
pubmed: 21509767
J Clin Oncol. 2013 Oct 10;31(29):3688-95
pubmed: 24002500
Br J Cancer. 2011 Nov 22;105(11):1684-92
pubmed: 22045184
Lancet. 2018 Feb 17;391(10121):659-667
pubmed: 29241979
N Engl J Med. 2018 Mar 29;378(13):1211-1223
pubmed: 29590547
J Clin Oncol. 2006 Oct 20;24(30):4867-74
pubmed: 17001068
J Clin Oncol. 2014 Feb 1;32(4):273-81
pubmed: 24344210
Blood. 2017 Oct 26;130(17):1903-1910
pubmed: 28819011
Leukemia. 2018 Aug;32(8):1799-1803
pubmed: 29572505