Efficacy of platinum agents for stage III non-small-cell lung cancer following platinum-based chemoradiotherapy: a retrospective study.
Cytotoxic chemotherapy
Platinum-based chemotherapy
Second-line setting
Single-agent chemotherapy
Survival
Journal
BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800
Informations de publication
Date de publication:
29 Mar 2022
29 Mar 2022
Historique:
received:
13
05
2021
accepted:
15
03
2022
entrez:
30
3
2022
pubmed:
31
3
2022
medline:
5
4
2022
Statut:
epublish
Résumé
Platinum-based chemoradiotherapy is the standard treatment for unresectable stage III non-small-cell lung cancer (NSCLC). However, few studies have evaluated the efficacy of subsequent chemotherapy for relapsed NSCLC following platinum-based chemoradiotherapy. This study aimed to evaluate the efficacy of platinum-doublet chemotherapy as a second-line treatment for patients with unresectable stage III NSCLC. We retrospectively evaluated patients with unresectable stage III NSCLC treated with cytotoxic chemotherapy following platinum-based chemoradiotherapy who were registered in a nationwide registry NSCLC database. Patients were divided into the platinum-doublet chemotherapy (platinum) group and single-agent chemotherapy (non-platinum) group based on the type of second-line chemotherapy. The platinum group (n = 119) showed significantly better overall survival (OS) than the non-platinum group (n = 201) (median OS: 21.5 vs. 10.5 months, hazard ratio [HR]: 0.54, 95% confidence interval [CI]: 0.40-0.73, p < 0.001). OS from the beginning of chemoradiotherapy was also significantly better in the platinum group than in the non-platinum group (median OS: 34.9 vs. 21.8 months, HR: 0.58, 95% CI: 0.43-0.79, p = 0.001). In the multivariate analysis, platinum-doublet chemotherapy as second-line therapy, female sex, clinical stage IIIA, and duration of ≥ 8.6 months from the beginning of first-line therapy to the beginning of second-line therapy were associated with significantly better OS. Platinum-doublet chemotherapy as a second-line therapy may prolong survival in unresectable stage III NSCLC patients following platinum-based chemoradiotherapy. Thus, re-administration of platinum agents may be a promising treatment for unresectable stage III NSCLC treated with platinum-based chemoradiotherapy.
Sections du résumé
BACKGROUND
BACKGROUND
Platinum-based chemoradiotherapy is the standard treatment for unresectable stage III non-small-cell lung cancer (NSCLC). However, few studies have evaluated the efficacy of subsequent chemotherapy for relapsed NSCLC following platinum-based chemoradiotherapy. This study aimed to evaluate the efficacy of platinum-doublet chemotherapy as a second-line treatment for patients with unresectable stage III NSCLC.
METHODS
METHODS
We retrospectively evaluated patients with unresectable stage III NSCLC treated with cytotoxic chemotherapy following platinum-based chemoradiotherapy who were registered in a nationwide registry NSCLC database. Patients were divided into the platinum-doublet chemotherapy (platinum) group and single-agent chemotherapy (non-platinum) group based on the type of second-line chemotherapy.
RESULTS
RESULTS
The platinum group (n = 119) showed significantly better overall survival (OS) than the non-platinum group (n = 201) (median OS: 21.5 vs. 10.5 months, hazard ratio [HR]: 0.54, 95% confidence interval [CI]: 0.40-0.73, p < 0.001). OS from the beginning of chemoradiotherapy was also significantly better in the platinum group than in the non-platinum group (median OS: 34.9 vs. 21.8 months, HR: 0.58, 95% CI: 0.43-0.79, p = 0.001). In the multivariate analysis, platinum-doublet chemotherapy as second-line therapy, female sex, clinical stage IIIA, and duration of ≥ 8.6 months from the beginning of first-line therapy to the beginning of second-line therapy were associated with significantly better OS.
CONCLUSION
CONCLUSIONS
Platinum-doublet chemotherapy as a second-line therapy may prolong survival in unresectable stage III NSCLC patients following platinum-based chemoradiotherapy. Thus, re-administration of platinum agents may be a promising treatment for unresectable stage III NSCLC treated with platinum-based chemoradiotherapy.
Identifiants
pubmed: 35351059
doi: 10.1186/s12885-022-09441-3
pii: 10.1186/s12885-022-09441-3
pmc: PMC8962203
doi:
Substances chimiques
Platinum
49DFR088MY
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
342Informations de copyright
© 2022. The Author(s).
Références
N Engl J Med. 2018 Jun 14;378(24):2288-2301
pubmed: 29863955
J Thorac Oncol. 2007 Aug;2(8):706-14
pubmed: 17762336
Lancet Oncol. 2016 Aug;17(8):1147-1157
pubmed: 27312053
Int J Clin Oncol. 2004 Oct;9(5):378-82
pubmed: 15549588
N Engl J Med. 2018 Nov 22;379(21):2040-2051
pubmed: 30280635
J Clin Oncol. 2016 Mar 20;34(9):953-62
pubmed: 26811519
World J Clin Oncol. 2017 Feb 10;8(1):1-20
pubmed: 28246582
Springerplus. 2015 Mar 31;4:152
pubmed: 25897409
Lancet. 2003 Jun 21;361(9375):2099-106
pubmed: 12826431
Eur J Cancer. 2014 Sep;50(13):2211-8
pubmed: 24981975
J Exp Clin Cancer Res. 2010 Apr 27;29:38
pubmed: 20423465
N Engl J Med. 2018 Dec 13;379(24):2342-2350
pubmed: 30280658
J Clin Oncol. 2000 Jun;18(12):2354-62
pubmed: 10856094
Ann Oncol. 2017 Nov 1;28(suppl_8):viii51-viii56
pubmed: 29232464
Lung Cancer. 2007 Oct;58(1):73-9
pubmed: 17548127
Cancer Med. 2020 Sep;9(18):6597-6608
pubmed: 32730697
Cancer Med. 2013 Dec;2(6):916-24
pubmed: 24403265
N Engl J Med. 2017 Nov 16;377(20):1919-1929
pubmed: 28885881
Cancer Sci. 2020 May;111(5):1685-1691
pubmed: 32103551
Cancer Chemother Pharmacol. 2011 Dec;68(6):1405-12
pubmed: 21468755
Oncol Rep. 1999 Jul-Aug;6(4):797-800
pubmed: 10373659
J Clin Oncol. 2000 May;18(10):2095-103
pubmed: 10811675
Lung Cancer. 2013 Sep;81(3):337-342
pubmed: 23891507
Lancet. 2014 Aug 23;384(9944):665-73
pubmed: 24933332
J Clin Oncol. 2015 Feb 20;33(6):532-3
pubmed: 25559800
J Clin Oncol. 2010 May 1;28(13):2181-90
pubmed: 20351327
N Engl J Med. 2018 May 31;378(22):2078-2092
pubmed: 29658856
Lung Cancer. 2010 Oct;70(1):71-6
pubmed: 20096475
Lancet Oncol. 2014 Feb;15(2):143-55
pubmed: 24411639
Lancet Oncol. 2019 Jul;20(7):924-937
pubmed: 31122901
BMC Cancer. 2010 Nov 19;10:633
pubmed: 21092076
J Natl Cancer Inst. 2000 Feb 2;92(3):205-16
pubmed: 10655437
Anticancer Res. 2005 May-Jun;25(3c):2555-9
pubmed: 16080492
Clin Transl Oncol. 2020 Jan;22(1):21-36
pubmed: 31172444
Int J Gynecol Cancer. 2011 May;21(4):771-5
pubmed: 21543939
J Clin Oncol. 2012 Dec 20;30(36):4501-7
pubmed: 23109689
J Clin Oncol. 2004 May 1;22(9):1589-97
pubmed: 15117980
J Clin Oncol. 2006 Oct 10;24(29):4699-707
pubmed: 16966687
Tumour Biol. 2016 Jul;37(7):8901-7
pubmed: 26753955
Med Oncol. 2011 Mar;28(1):300-6
pubmed: 20049560