Open Access
Erlotinib as single agent first line treatment in locally advanced or metastatic activating EGFR mutation-positive lung adenocarcinoma (CEETAC): an open-label, non-randomized, multicenter, phase IV clinical trial
Zsolt Markóczy
1
,
Veronika Sárosi
2
,
Iveta Kudaba
3
,
Gabriella Gálffy
4
,
Ülkü Yilmaz Turay
5
,
Ahmet Demirkazik
6
,
Gunta Purkalne
7
,
Attila Somfay
8
,
Zsolt Pápai Székely
9
,
Erzsebet Raso
10
,
Gyula Ostoros
1
1
National Koranyi Institute of TB and Pulmonology, Budapest, Hungary
|
3
Riga East University Hospital Oncology Center, Riga, Latvia
|
5
Clinic of Chest Diseases, Ataturk Chest Diseases and Chest Surgery Training and Research Hospital, Ankara, Turkey
|
9
St. George Hospital of Fejer County, Szekesfehervar, Hungary
|
Publication type: Journal Article
Publication date: 2018-05-25
scimago Q2
wos Q2
SJR: 1.178
CiteScore: 5.7
Impact factor: 3.4
ISSN: 14712407
PubMed ID:
29801465
Cancer Research
Oncology
Genetics
Abstract
Erlotinib is approved for the first line treatment of epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer. Since the number of prospective studies in Caucasian patients treated in routine clinical setting is limited we conducted a multicenter, phase IV clinical trial to determine the efficacy and safety of erlotinib and to demonstrate the feasibility of the validated standardized companion diagnostic method of EGFR mutation detection. 651 chemonaive, cytologically or histologically verified advanced stage lung adenocarcinoma patients from Hungary, Turkey and Latvia were screened for exon19 microdeletions and exon21 L858R EGFR mutations using the companion diagnostic EGFR test. EGFR mutation-positive, locally advanced or metastatic lung adenocarcinoma patients received as first line treatment erlotinib at 150 mg/day. The primary endpoint was progression-free survival (PFS). 62 EGFR mutation-positive patients (9.5% of screened) were included in the safety/intent-to-treat cohort. Median PFS was 12.8 months (95%CI, 9.9–15.8), objective response rate and one-year survival was 66.1% and 82.5%, respectively. Most frequent treatment related adverse events were diarrhoea and rash. Eastern Oncology Cooperative Group Performance Status (ECOG PS), smoking status and M1a/M1b disease stage were significant prognosticators of PFS (p = 0.017, p = 0.045 and p = 0.002, respectively). There was no significant difference in PFS between the subgroups stratified by gender, age or exon19 vs exon21 mutation. Our study confirmed the efficacy and safety of first line erlotinib monotherapy in Caucasian patients with locally advanced or metastatic lung adenocarcinoma carrying activating EGFR mutations based on the screening with the approved companion diagnostic procedure. ClinicalTrials.gov Identifier: NCT01609543.
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Markóczy Z. et al. Erlotinib as single agent first line treatment in locally advanced or metastatic activating EGFR mutation-positive lung adenocarcinoma (CEETAC): an open-label, non-randomized, multicenter, phase IV clinical trial // BMC Cancer. 2018. Vol. 18. No. 1. 598
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Markóczy Z., Sárosi V., Kudaba I., Gálffy G., Turay Ü. Y., Demirkazik A., Purkalne G., Somfay A., Pápai Székely Z., Raso E., Ostoros G. Erlotinib as single agent first line treatment in locally advanced or metastatic activating EGFR mutation-positive lung adenocarcinoma (CEETAC): an open-label, non-randomized, multicenter, phase IV clinical trial // BMC Cancer. 2018. Vol. 18. No. 1. 598
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TY - JOUR
DO - 10.1186/s12885-018-4283-z
UR - https://doi.org/10.1186/s12885-018-4283-z
TI - Erlotinib as single agent first line treatment in locally advanced or metastatic activating EGFR mutation-positive lung adenocarcinoma (CEETAC): an open-label, non-randomized, multicenter, phase IV clinical trial
T2 - BMC Cancer
AU - Markóczy, Zsolt
AU - Sárosi, Veronika
AU - Kudaba, Iveta
AU - Gálffy, Gabriella
AU - Turay, Ülkü Yilmaz
AU - Demirkazik, Ahmet
AU - Purkalne, Gunta
AU - Somfay, Attila
AU - Pápai Székely, Zsolt
AU - Raso, Erzsebet
AU - Ostoros, Gyula
PY - 2018
DA - 2018/05/25
PB - Springer Nature
IS - 1
VL - 18
PMID - 29801465
SN - 1471-2407
ER -
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@article{2018_Markóczy,
author = {Zsolt Markóczy and Veronika Sárosi and Iveta Kudaba and Gabriella Gálffy and Ülkü Yilmaz Turay and Ahmet Demirkazik and Gunta Purkalne and Attila Somfay and Zsolt Pápai Székely and Erzsebet Raso and Gyula Ostoros},
title = {Erlotinib as single agent first line treatment in locally advanced or metastatic activating EGFR mutation-positive lung adenocarcinoma (CEETAC): an open-label, non-randomized, multicenter, phase IV clinical trial},
journal = {BMC Cancer},
year = {2018},
volume = {18},
publisher = {Springer Nature},
month = {may},
url = {https://doi.org/10.1186/s12885-018-4283-z},
number = {1},
pages = {598},
doi = {10.1186/s12885-018-4283-z}
}