Heart V5 predicts cardiac events in unresectable lung cancer patients undergoing chemoradiation.

Cardiac toxicity chemoradiation unresectable lung cancer

Journal

Journal of thoracic disease
ISSN: 2072-1439
Titre abrégé: J Thorac Dis
Pays: China
ID NLM: 101533916

Informations de publication

Date de publication:
Jun 2019
Historique:
entrez: 3 8 2019
pubmed: 3 8 2019
medline: 3 8 2019
Statut: ppublish

Résumé

Recent studies incorporating dose escalated radiation identified heart dose as a predictor of cardiac toxicity in unresectable lung cancer patients. Whether conventionally dosed radiation impacts cardiac events remains unclear. Stage III lung cancer patients undergoing definitive chemoradiation to 60-70 Gy were analyzed. Clinical and dosimetric factors (mean heart dose, heart V5-60 in 5 Gy increments) were analyzed against freedom from ≥ grade 3 cardiac events and overall survival (OS) by log-rank test. Multivariable analysis (MVA) for factors significant on univariate analysis was performed by Cox proportional hazards. A total of 108 patients were identified. Median follow-up was 18.0 months. One- and two-year OS were 79% and 61%, respectively. On MVA, gross tumor volume (GTV) ≥98.6 cm Heart V5 ≥49% predicted for cardiac events after chemoradiation. However, cardiac dosimetry was not associated with survival. Rather, female gender and GTV ≥98.6 cm

Sections du résumé

BACKGROUND BACKGROUND
Recent studies incorporating dose escalated radiation identified heart dose as a predictor of cardiac toxicity in unresectable lung cancer patients. Whether conventionally dosed radiation impacts cardiac events remains unclear.
METHODS METHODS
Stage III lung cancer patients undergoing definitive chemoradiation to 60-70 Gy were analyzed. Clinical and dosimetric factors (mean heart dose, heart V5-60 in 5 Gy increments) were analyzed against freedom from ≥ grade 3 cardiac events and overall survival (OS) by log-rank test. Multivariable analysis (MVA) for factors significant on univariate analysis was performed by Cox proportional hazards.
RESULTS RESULTS
A total of 108 patients were identified. Median follow-up was 18.0 months. One- and two-year OS were 79% and 61%, respectively. On MVA, gross tumor volume (GTV) ≥98.6 cm
CONCLUSIONS CONCLUSIONS
Heart V5 ≥49% predicted for cardiac events after chemoradiation. However, cardiac dosimetry was not associated with survival. Rather, female gender and GTV ≥98.6 cm

Identifiants

pubmed: 31372260
doi: 10.21037/jtd.2019.06.29
pii: jtd-11-06-2229
pmc: PMC6626817
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2229-2239

Déclaration de conflit d'intérêts

Conflicts of Interest: The authors have no conflicts of interest to declare.

Références

Int J Radiat Oncol Biol Phys. 2001 Mar 1;49(3):649-55
pubmed: 11172945
Int J Radiat Oncol Biol Phys. 2002 Jan 1;52(1):49-57
pubmed: 11777621
Int J Radiat Oncol Biol Phys. 2002 Nov 1;54(3):735-41
pubmed: 12377325
JAMA. 2003 Dec 3;290(21):2831-7
pubmed: 14657067
Radiother Oncol. 2012 Jul;104(1):72-7
pubmed: 22682539
Cancer Res. 1990 Apr 1;50(7):2027-30
pubmed: 2317792
N Engl J Med. 2013 Mar 14;368(11):987-98
pubmed: 23484825
Radiother Oncol. 2015 Jan;114(1):85-90
pubmed: 25554226
Lancet Oncol. 2015 Feb;16(2):187-99
pubmed: 25601342
Front Oncol. 2015 Feb 18;5:39
pubmed: 25741474
Int J Radiat Oncol Biol Phys. 2016 Mar 1;94(3):612-20
pubmed: 26867890
Radiother Oncol. 2016 Jun;119(3):495-500
pubmed: 27189523
Oncol Lett. 2016 Aug;12(2):1144-1148
pubmed: 27446409
Lancet Oncol. 2016 Sep;17(9):1325-34
pubmed: 27470081
J Thorac Oncol. 2017 Feb;12(2):293-301
pubmed: 27743888
J Clin Oncol. 2017 Jan;35(1):56-62
pubmed: 28034064
J Clin Oncol. 2017 Apr 10;35(11):1171-1178
pubmed: 28095159
J Clin Oncol. 2017 May 1;35(13):1387-1394
pubmed: 28113017
Blood. 2017 Apr 20;129(16):2257-2265
pubmed: 28143884
J Clin Oncol. 2017 May 1;35(13):1395-1402
pubmed: 28301264
Ann Oncol. 2017 May 1;28(5):1084-1089
pubmed: 28453703
Lancet Oncol. 2017 Aug;18(8):1116-1125
pubmed: 28642008
Int J Radiat Oncol Biol Phys. 2017 Aug 1;98(5):1116-1123
pubmed: 28721895
Int J Radiat Oncol Biol Phys. 2017 Sep 1;99(1):70-79
pubmed: 28816165
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
N Engl J Med. 1995 Jun 29;332(26):1738-43
pubmed: 7760889
Med Pediatr Oncol. 1993;21(7):477-9
pubmed: 8341214
N Engl J Med. 1999 Jan 28;340(4):265-71
pubmed: 9920950

Auteurs

Lisa Ni (L)

University of Chicago Pritzker School of Medicine, Chicago, IL, USA.

Matthew Koshy (M)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Philip Connell (P)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Sean Pitroda (S)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Daniel W Golden (DW)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Hania Al-Hallaq (H)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Greg Hubert (G)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Greg Kauffman (G)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Anne McCall (A)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Renuka Malik (R)

University of Chicago Department of Radiation and Cellular Oncology, Chicago, IL, USA.

Classifications MeSH