Outcomes in Patients with Classic Hodgkin Lymphoma Treated with ABVD: A Single-center Retrospective Study.
ABVD
classic Hodgkin lymphoma
older patients
Journal
Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241
Informations de publication
Date de publication:
01 Mar 2021
01 Mar 2021
Historique:
pubmed:
23
10
2020
medline:
15
4
2021
entrez:
22
10
2020
Statut:
ppublish
Résumé
Objective Classic Hodgkin lymphoma (CHL) has been regarded as a curable disease when treated appropriately, especially in younger patients, and ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) has been regarded as the standard regimen. However, a relatively poor prognosis has been reported in older patients with CHL, and the efficacy and tolerability of the ABVD regimen has not been fully elucidated. We retrospectively investigated the outcomes in patients with CHL treated with ABVD at our institute. Methods Twenty-five patients were evaluated; 14 were ≤60 years of age, and 11 were >60 years of age (older group). Results The ABVD doses were reduced in all patients in the older group; the median average relative dose intensity was 0.58. In the older group, the 5-year overall survival (OS) and median OS were 100% and not reached, respectively, for patients with early-stage CHL and 66.7% and not reached, respectively, for those with advanced-stage CHL. No patients died of CHL, and only one treatment-related death was observed in the older group. Conclusion ABVD with dose attenuation may represent a feasible and effective strategy for the treatment of older patients with CHL in clinical practice, particularly in those with early-stage disease, although the optimal degree of attenuation remains unclear.
Identifiants
pubmed: 33087662
doi: 10.2169/internalmedicine.5004-20
pmc: PMC7990646
doi:
Substances chimiques
Bleomycin
11056-06-7
Vinblastine
5V9KLZ54CY
Dacarbazine
7GR28W0FJI
Doxorubicin
80168379AG
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
709-718Références
Eur J Cancer. 2005 May;41(7):1051-7
pubmed: 15862755
Int J Hematol. 2016 Aug;104(2):236-44
pubmed: 27086350
J Clin Oncol. 2003 Oct 1;21(19):3601-8
pubmed: 12913100
J Clin Oncol. 1999 Apr;17(4):1244
pubmed: 10561185
N Engl J Med. 1992 Nov 19;327(21):1478-84
pubmed: 1383821
Ann Intern Med. 1984 May;100(5):651-6
pubmed: 6370065
Br J Cancer. 2015 Apr 28;112(9):1575-84
pubmed: 25867256
Bone Marrow Transplant. 2013 Mar;48(3):452-8
pubmed: 23208313
Blood. 2012 Jan 26;119(4):990-6
pubmed: 22147892
J Support Oncol. 2003 Nov-Dec;1(4 Suppl 2):18-24
pubmed: 15346996
J Clin Oncol. 2005 Aug 1;23(22):5052-60
pubmed: 15955904
J Clin Oncol. 2013 Apr 20;31(12):1522-9
pubmed: 23509310
N Engl J Med. 1998 Nov 19;339(21):1506-14
pubmed: 9819449
Eur J Cancer. 2000 Feb;36(3):384-9
pubmed: 10708941
Br J Haematol. 2002 Nov;119(2):432-40
pubmed: 12406082
J Clin Oncol. 2006 Jul 1;24(19):3128-35
pubmed: 16754934
J Clin Oncol. 2002 Feb 15;20(4):1087-93
pubmed: 11844834
Blood. 2012 Jan 19;119(3):692-5
pubmed: 22117038
Br J Haematol. 2013 Apr;161(1):76-86
pubmed: 23356491
Blood. 2010 Sep 23;116(12):2026-32
pubmed: 20551376
J Clin Oncol. 1990 Dec;8(12):1935-7
pubmed: 2230885
Crit Rev Oncol Hematol. 2009 Sep;71(3):222-32
pubmed: 19179093
Blood. 2011 Dec 8;118(24):6292-8
pubmed: 21917759
Br J Haematol. 2015 Jul;170(2):179-84
pubmed: 25891777
Curr Hematol Malig Rep. 2011 Sep;6(3):164-71
pubmed: 21553348
Int J Hematol. 2020 Feb;111(2):166-179
pubmed: 31784937
Blood. 2012 Jun 21;119(25):6005-15
pubmed: 22577177
Pathol Int. 2000 Sep;50(9):696-702
pubmed: 11012982