Concomitant radiotherapy and TKI in metastatic EGFR- or ALK-mutated non-small cell lung cancer: a multicentric analysis on behalf of AIRO lung cancer study group.
Adult
Aged
Aged, 80 and over
Anaplastic Lymphoma Kinase
/ genetics
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Combined Modality Therapy
DNA Mutational Analysis
ErbB Receptors
/ genetics
Female
Humans
Italy
Lung Neoplasms
/ drug therapy
Male
Middle Aged
Mutation
Neoplasm Metastasis
Protein Kinase Inhibitors
/ therapeutic use
Retrospective Studies
Societies, Medical
Survival Rate
Treatment Outcome
ALK mutated
EGFR mutated
Oligometastatic
Oligoprogressive
Radiotherapy
Stage IV NSCLC
Stereotactic radiotherapy
Journal
La Radiologia medica
ISSN: 1826-6983
Titre abrégé: Radiol Med
Pays: Italy
ID NLM: 0177625
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
received:
25
07
2018
accepted:
29
01
2019
pubmed:
17
2
2019
medline:
13
7
2019
entrez:
17
2
2019
Statut:
ppublish
Résumé
To investigate the role of radiotherapy (RT) in the management of EGFR- or ALK-mutated metastatic non-small cell lung cancer (NSCLC) treated with TKI. Clinical data of 106 patients (pts) from five Institutions treated with RT concomitant to TKI were retrospectively revised. Overall survival (OS) and toxicities were analyzed as endpoints of the study. Median age of pts was 65 years. TKIs were given for EGFR (81%)- or ALK (19%)-mutated metastatic NSCLC. Stereotactic RT (SRT) was delivered to 49 pts (46%). Patients with four or less metastasis were defined as oligometastatic/oligoprogressive (OM/OP); sites of RT were brain, bone, lung or others in 46%, 27%, 14% and 13%, respectively. Median OS was 23 months. At univariate analysis SRT, ECOG PS 0-1, OM/OP disease, lung sites and a TKI duration longer than median favorably affected OS (all p < 0.001). Multivariate analysis confirmed SRT (HR 0.355, CI 95% 0.212-0.595; p < 0.001) and median duration of TKI > 14 months (HR 0.17, 95% CI 0.10-0.30; p < 0.001) as independent factors related to better OS. Toxicities were rare. SRT seems to positively affect OS with limited toxicity in selected patients.
Identifiants
pubmed: 30771218
doi: 10.1007/s11547-019-00999-w
pii: 10.1007/s11547-019-00999-w
doi:
Substances chimiques
Protein Kinase Inhibitors
0
ALK protein, human
EC 2.7.10.1
Anaplastic Lymphoma Kinase
EC 2.7.10.1
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
662-670Références
Int J Oncol. 2004 Dec;25(6):1677-83
pubmed: 15547705
Cancer Res. 2005 Apr 15;65(8):3328-35
pubmed: 15833866
Acta Oncol. 2009;48(4):578-83
pubmed: 19373699
Jpn J Clin Oncol. 2010 Feb;40(2):107-11
pubmed: 20047860
Radiat Oncol. 2011 Jun 30;6:80
pubmed: 21718501
Lancet Oncol. 2012 Mar;13(3):239-46
pubmed: 22285168
J Thorac Oncol. 2012 Oct;7(10):1547-55
pubmed: 22982655
J Natl Cancer Inst. 2013 May 1;105(9):595-605
pubmed: 23594426
Int J Cancer. 2013 Nov 15;133(10):2277-83
pubmed: 23720067
Lung Cancer. 2013 Oct;82(1):95-102
pubmed: 23973202
Lung Cancer. 2013 Dec;82(3):431-5
pubmed: 24113550
Int J Radiat Oncol Biol Phys. 2014 Mar 15;88(4):892-8
pubmed: 24462383
Int J Radiat Oncol Biol Phys. 2014 Jul 15;89(4):880-7
pubmed: 24867533
Oncologist. 2015 Apr;20(4):400-10
pubmed: 25795635
J Clin Oncol. 2015 Oct 20;33(30):3488-515
pubmed: 26324367
Ann Oncol. 2016 Sep;27(suppl 5):v1-v27
pubmed: 27664245
Lancet Oncol. 2016 Dec;17(12):1672-1682
pubmed: 27789196
Cancer Treat Rev. 2017 Feb;53:25-37
pubmed: 28056412
Ann Oncol. 2017 Feb 1;28(2):270-277
pubmed: 28426106
Lancet. 2017 Jul 1;390(10089):29-39
pubmed: 28501140