Abstract 1305P
Background
For patients who show downstaging of lung cancer following targeted therapy, salvage surgery can be considered. Resection of regrowing pulmonary masses can also be performed to acquire a tumor specimen. The aim of this study is to evaluate the prognosis of patients who have undergone prior tyrosine kinase inhibitor (TKI) treatment and later lung surgery.
Methods
The deidentified data of NSCLC patients admitted to eight university hospitals affiliated with the Catholic University of Korea were obtained from the Clinical Data Warehouse (CDW) database. Forty patients who had prior targeted therapies and later received surgical resection were evaluated for the study. The primary endpoint was overall survival, defined as the time between surgical resection and death or censoring. The secondary endpoint was postoperative progression-free survival.
Results
Of 40 patients diagnosed with adenocarcinoma. 36 (87.8%) received prior EGFR TKI treatment, while 4 (9.8%) received ALK TKI treatment. At the time of TKI initiation, 31 (77.5%) were staged as IV, and 9 (22.5%) were staged as III. Salvage surgery was performed in 18 patients (45.0%), and 22 (55.0%) underwent resection for biopsy purposes. At the time of resection, tumor burden was unchanged in 7 patients (17.5%), significantly regressing in 12 patients (30.0%), and increasing in 21 patients (52.5%). Among the 28 patients with EGFR mutations from resected tumor specimens, 9 (32.1%) exhibited the T790M mutation. Next-generation sequencing of the resected samples identified mutations such as MET amplification and TP53. Only one postoperative complication, atrial fibrillation, was observed. Patients with poor preoperative ECOG (Eastern Cooperative Oncology Group) scores had significantly worse 1-year and 2-year survival rates (P=0.014 and P=0.011, respectively). There was a significant difference in 6-month PFS rates between groups stratified by pleural invasion levels (PL0-3) (P=0.029). Furthermore, patients with T790M mutation showed a trend towards improved PFS (P=0.052).
Conclusions
Lung surgery following targeted therapies is safe and can be used to predict the prognosis of patients with initially unresectable NSCLC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
488P - Comprehensive genomic profiling to identify actionable alterations for breast cancer brain metastases in the Chinese population
Presenter: Qianyi Lu
Session: Poster session 04
489P - Liquid biopsy with combination of cell & cell-free analysis identifies HER2-expression in patients with metastatic breast cancer
Presenter: Fengting Yan
Session: Poster session 04
491P - Comparison of ctDNA profiles from HR+/HER2-low and HR+/HER2-0 advanced breast cancer patients
Presenter: Nina Dobrić
Session: Poster session 04
492P - Wound stress stimulation promotes lung metastasis of breast cancer by regulating CXCL12/CXCR4 axis through MDSC exosome miR-126a-5p
Presenter: Xiaomeng Yin
Session: Poster session 04
493P - Identifying genomic changes in breast tumours that metastasise to the brain
Presenter: Ivonne Olivares
Session: Poster session 04
494P - Proviral insertion in murine 1 (PIM1) kinase expression and clinical outcomes in advanced breast cancer (ABC)
Presenter: Stephanie Graff
Session: Poster session 04
495P - Prognostic value of PIK3CA mutational status in tissue & plasma in HR+/HER2- breast cancer (BC)
Presenter: Rebeca Lozano Mejorada
Session: Poster session 04
496P - Comprehensive genomic profiling of advanced HR+/HER2- breast cancer patients using liquid biopsy
Presenter: Bin Shao
Session: Poster session 04
497P - Metastatic potential of the somatic alteration associated with TCA-cycle in breast cancer
Presenter: Narumi Harada
Session: Poster session 04