Cargando…

Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer

BACKGROUND: Approximately 30–70% percent of patients with non-small cell lung cancer (NSCLC) still relapse after receiving complete resection and even suffer distant metastasis. Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) have gradually replaced chemotherapy to become the...

Descripción completa

Detalles Bibliográficos
Autores principales: Bao, Yi, Gu, Chang, Xie, Huikang, Zhao, Shengnan, Xie, Dong, Chen, Chang, Jiang, Gening, Dai, Chenyang, Zhu, Yuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039639/
https://www.ncbi.nlm.nih.gov/pubmed/33850890
http://dx.doi.org/10.21037/atm-21-1134
_version_ 1783677637179211776
author Bao, Yi
Gu, Chang
Xie, Huikang
Zhao, Shengnan
Xie, Dong
Chen, Chang
Jiang, Gening
Dai, Chenyang
Zhu, Yuming
author_facet Bao, Yi
Gu, Chang
Xie, Huikang
Zhao, Shengnan
Xie, Dong
Chen, Chang
Jiang, Gening
Dai, Chenyang
Zhu, Yuming
author_sort Bao, Yi
collection PubMed
description BACKGROUND: Approximately 30–70% percent of patients with non-small cell lung cancer (NSCLC) still relapse after receiving complete resection and even suffer distant metastasis. Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) have gradually replaced chemotherapy to become the first-line postoperative NSCLC treatment because they can effectively inhibit the postoperative recurrence of lung cancer. However, the clinical efficacy of neoadjuvant EGFR-TKIs in EGFR mutant NSCLC patients is still unclear. The purpose of this study was to evaluate their clinical efficacy and to further explore factors affecting recurrence in such patients. METHODS: EGFR-mutated patients receiving neoadjuvant EGFR-TKI treatment in our hospital from July 2016 to September 2020 were retrospectively included. These patients underwent radical tumor resection after treatment. The primary endpoint was the objective response rate (ORR). The secondary endpoints were the major pathological response (MPR), disease-free survival (DFS), and overall survival (OS). RESULTS: A total of 42 patients who met the inclusion criteria were included in this study. The ORR was 47.6% (20/42), and the MPR was 23.8% (10/42). The average follow-up time was 23.7 months. As of the final follow-up date, 18 (42.9%, 18/42) patients had experienced tumor recurrence. Of these, there were 11 (61.1%) cases of local recurrence and 7 (38.9%) cases of distant metastasis, including 5 bone metastases and 2 brain metastases. Multivariate Cox regression results showed that the high-risk subtype [P=0.012, hazard ratio (HR) =24.560; 95% confidence interval (CI), 2.016–299.227] was a risk factor for postoperative recurrence. Patients with a high-risk subtype (solid or micropapillary subtype) had significantly worse recurrence-free survival (RFS, log-rank P=0.032). Although patients with pathological remission had a similar RFS as patients who did not achieve pathological remission (log-rank P=0.069), the patients without pathological remission showed a tendency toward a worse prognosis. CONCLUSIONS: Neoadjuvant EGFR-TKIs had good effects on EGFR-mutant NSCLC patients at different stages, especially those with MPR. Patients with high-risk subtypes (solid or micropapillary) should be closely followed up after surgery because of the high risk of recurrence.
format Online
Article
Text
id pubmed-8039639
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-80396392021-04-12 Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer Bao, Yi Gu, Chang Xie, Huikang Zhao, Shengnan Xie, Dong Chen, Chang Jiang, Gening Dai, Chenyang Zhu, Yuming Ann Transl Med Original Article BACKGROUND: Approximately 30–70% percent of patients with non-small cell lung cancer (NSCLC) still relapse after receiving complete resection and even suffer distant metastasis. Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) have gradually replaced chemotherapy to become the first-line postoperative NSCLC treatment because they can effectively inhibit the postoperative recurrence of lung cancer. However, the clinical efficacy of neoadjuvant EGFR-TKIs in EGFR mutant NSCLC patients is still unclear. The purpose of this study was to evaluate their clinical efficacy and to further explore factors affecting recurrence in such patients. METHODS: EGFR-mutated patients receiving neoadjuvant EGFR-TKI treatment in our hospital from July 2016 to September 2020 were retrospectively included. These patients underwent radical tumor resection after treatment. The primary endpoint was the objective response rate (ORR). The secondary endpoints were the major pathological response (MPR), disease-free survival (DFS), and overall survival (OS). RESULTS: A total of 42 patients who met the inclusion criteria were included in this study. The ORR was 47.6% (20/42), and the MPR was 23.8% (10/42). The average follow-up time was 23.7 months. As of the final follow-up date, 18 (42.9%, 18/42) patients had experienced tumor recurrence. Of these, there were 11 (61.1%) cases of local recurrence and 7 (38.9%) cases of distant metastasis, including 5 bone metastases and 2 brain metastases. Multivariate Cox regression results showed that the high-risk subtype [P=0.012, hazard ratio (HR) =24.560; 95% confidence interval (CI), 2.016–299.227] was a risk factor for postoperative recurrence. Patients with a high-risk subtype (solid or micropapillary subtype) had significantly worse recurrence-free survival (RFS, log-rank P=0.032). Although patients with pathological remission had a similar RFS as patients who did not achieve pathological remission (log-rank P=0.069), the patients without pathological remission showed a tendency toward a worse prognosis. CONCLUSIONS: Neoadjuvant EGFR-TKIs had good effects on EGFR-mutant NSCLC patients at different stages, especially those with MPR. Patients with high-risk subtypes (solid or micropapillary) should be closely followed up after surgery because of the high risk of recurrence. AME Publishing Company 2021-03 /pmc/articles/PMC8039639/ /pubmed/33850890 http://dx.doi.org/10.21037/atm-21-1134 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Bao, Yi
Gu, Chang
Xie, Huikang
Zhao, Shengnan
Xie, Dong
Chen, Chang
Jiang, Gening
Dai, Chenyang
Zhu, Yuming
Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title_full Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title_fullStr Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title_full_unstemmed Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title_short Comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
title_sort comprehensive study of neoadjuvant targeted therapy for resectable non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039639/
https://www.ncbi.nlm.nih.gov/pubmed/33850890
http://dx.doi.org/10.21037/atm-21-1134
work_keys_str_mv AT baoyi comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT guchang comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT xiehuikang comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT zhaoshengnan comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT xiedong comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT chenchang comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT jianggening comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT daichenyang comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer
AT zhuyuming comprehensivestudyofneoadjuvanttargetedtherapyforresectablenonsmallcelllungcancer