P24.09 Association Between Circulating EGFR Mutant Tumor DNA and Tumor Lesion Glycolysis in Patients with EGFR Mutated Metastatic Lung Adenocarcinoma

2021 ◽  
Vol 16 (10) ◽  
pp. S1034
Author(s):  
Z. Mihaylova ◽  
V. Hadjiiska ◽  
S. Bichev
2016 ◽  
Vol 34 (15_suppl) ◽  
pp. e23079-e23079
Author(s):  
Collin M. Blakely ◽  
Kimberly C. Banks ◽  
Richard Burnham Lanman ◽  
Jonathan Riess ◽  
Philip C. Mack ◽  
...  

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 8081-8081 ◽  
Author(s):  
Hatim Husain ◽  
Karena Kosco ◽  
Cecile Rose T. Vibat ◽  
Vlada Melnikova ◽  
Mark G. Erlander ◽  
...  

2016 ◽  
Vol 11 (4) ◽  
pp. 556-565 ◽  
Author(s):  
Jessica J. Lin ◽  
Stephanie Cardarella ◽  
Christine A. Lydon ◽  
Suzanne E. Dahlberg ◽  
David M. Jackman ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e20635-e20635
Author(s):  
Romy Jose Thekkekara ◽  
Rohit Kumar ◽  
Thomas E. Lad

e20635 Background:Metastatic lung cancer with systemic chemotherapy has a median progression-free survival (PFS) of 5-6 months and median overall survival time (OS) of around 12 months. In Epidermal Growth Factor Receptor gene (EGFR) mutated metastatic lung cancer the use of EGFR Tyrosine Kinase Inhibitors (EGFR-TKIs) has increased the median PFS to12 months and the median OS to 30 months. The objective of this study is to evaluate the response to TKIs in EGFR mutated metastatic lung cancer in racially diverse inner city population with high smoking rates. Methods:Consecutive patients diagnosed with EGFR mutant metastatic lung adenocarcinoma and treated with TKIs in John H. Stroger Jr. Hospital of Cook County in Chicago, IL between January 2009 to June 2016 were retrospectively evaluated. Demographic data was collected and PFS and OS were analyzed. Results:35 patients with EGFR mutated metastatic lung cancer received EGFR-TKI during the study period. There was a female preponderance (63%). Hispanics formed the most common racial group (37%), followed by Asians (26%), African Americans (AA) (20%) and Caucasians (17%). Mean age of diagnosis of metastatic disease was 56.5± 11.5 years. 20% of the patients were ever smokers. Stage 4 disease at presentation was seen in 88.6 %. Sites of metastatic disease included lungs/pleura (60%), bone (60%), brain (22.9%) and liver (14.3%). 82.9% had TKI as first line treatment. Median PFS and OS were 9.89 (95% CI: 7.8-11.9) months and 19.3 (95% CI: 1.9-36.8) months respectively. The median PFS and OS were 12.88 and 17 months for Asians, 10.8 and 24.4 months for Caucasians and 9.2 and 33 months for Hispanics respectively. Among AA, PFS at 19 months and OS at 35 months was 0.58%, not reaching the median. Patients who continued to smoke had a median OS of 8.5 months vs 19.3 months in nonsmokers/ex-smokers. Conclusions: In an underserved population, patients treated with EGFR mutated metastatic lung adenocarcinoma with EGFR-TKI have similar survival compared previously known data. Race of the patient does not appear to alter response to EGFR-TKI therapy. Active smokers had a lower OS. Studies in minority populations with larger samples are required to further validate the above findings.


Lung Cancer ◽  
2019 ◽  
Vol 138 ◽  
pp. 52-57
Author(s):  
Chia-I Shen ◽  
Hsu-Ching Huang ◽  
Chi-Lu Chiang ◽  
Yung-Hung Luo ◽  
Tsu-Hui Shiao ◽  
...  

Biomolecules ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 618
Author(s):  
Anna Buder ◽  
Ellen Heitzer ◽  
Julie Waldispühl-Geigl ◽  
Sabrina Weber ◽  
Tina Moser ◽  
...  

Background: To assess the clinical relevance of genome-wide somatic copy-number alterations (SCNAs) in plasma circulating tumor DNA (ctDNA) from advanced epidermal growth factor receptor (EGFR)-mutated lung adenocarcinoma patients. Methods: We included 43 patients with advanced EGFR T790M-positive lung adenocarcinoma who were treated with osimertinib after progression under previous EGFR-TKI therapy. We performed genomic profiling of ctDNA in plasma samples from each patient obtained pre-osimertinib and after patients developed resistance to osimertinib. SCNAs were detected by shallow whole-genome plasma sequencing and EGFR mutations were assessed by droplet digital PCR. Results: SCNAs in resistance-related genes (rrSCNAs) were detected in 10 out of 31 (32%) evaluable patients before start of osimertinib. The presence of rrSCNAs in plasma before the initiation of osimertinib therapy was associated with a lower response rate to osimertinib (50% versus 81%, p = 0.08) and was an independent predictor for shorter progression-free survival (adjusted HR 3.33, 95% CI 1.37–8.10, p = 0.008) and overall survival (adjusted HR 2.54, 95% CI 1.09–5.92, p = 0.03). Conclusions: Genomic profiling of plasma ctDNA is clinically relevant and affects the efficacy and clinical outcome of osimertinib. Our approach enables the comprehensive assessment of SCNAs in plasma samples of lung adenocarcinoma patients and may help to guide genotype-specific therapeutic strategies in the future.


2021 ◽  
Vol 1 (1) ◽  
pp. 51-58
Author(s):  
Daniel Dulf ◽  
Paul Kubelak ◽  
Dana Iancu ◽  
Tudor-Eliade Ciuleanu

"Metastatic non-small cell lung cancer has historically been associated with a poor prognosis. The introduction of targeted agents against certain molecules involved in cellular pathways has shown improved responses, but long-term survivors are still rare. We present the case of a patient with lung adenocarcinoma harboring sensitizing EGFR mutations who showed an impressive survival of more than 9 years following a combination of systemic therapies consisting of cytotoxic drugs and EGFR TKIs that were very well tolerated."


2017 ◽  
Vol 18 (3) ◽  
pp. e219-e222 ◽  
Author(s):  
Justin M. Allen ◽  
Alexa B. Schrock ◽  
Rachel L. Erlich ◽  
Vincent A. Miller ◽  
Philip J. Stephens ◽  
...  

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