TY - JOUR
T1 - Real-world utility of an amplicon-based next-generation sequencing liquid biopsy for broad molecular profiling in patients with advanced non-small-cell lung cancer
AU - Remon, Jordi
AU - Lacroix, Ludovic
AU - Jovelet, Cecile
AU - Caramella, Caroline
AU - Howarth, Karen
AU - Plagnol, Vincent
AU - Rosenfeld, Nitzan
AU - Morris, Clive
AU - Mezquita, Laura
AU - Pannet, Chloe
AU - Ngocamus, Maud
AU - Le Pechoux, Cecile
AU - Adam, Julien
AU - Grecea, Alina Miruna
AU - Planchard, David
AU - Vassal, Gilles
AU - Benitez, Jose Carlos
AU - Gazzah, Anas
AU - Green, Emma
AU - Soria, Jean Charles
AU - Besse, Benjamin
N1 - Publisher Copyright:
© 2019 American Society of Clinical Oncology.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - PURPOSE To assess the feasibility and utility of circulating tumor DNA (ctDNA) by amplicon-based nextgeneration sequencing (NGS) analysis in the daily clinical setting in a cohort of patients with advanced non-small-cell lung cancer (NSCLC), as an alternative approach to tissue molecular profiling. PATIENTS AND METHODS In this single-center prospective study, treatment-naïve and previously treated patients with advanced NSCLC were enrolled. Clinical validation of ctDNA using amplicon-based NGS analysis (with a 36-gene panel) was performed against standard-of-care tissue molecular analysis in treatment-naïve patients. The feasibility, utility, and prognostic value of ctDNA as a dynamic marker of treatment efficacy was evaluated. Results of tissue molecular profile were blinded during ctDNA analysis. RESULTS Of 214 patients with advanced NSCLC who were recruited, 156 were treatment-naïve patients and 58 were pretreated patients with unknown tissue molecular profile. ctDNA screening was successfully performed for 91% (n = 194) of all patients, and mutations were detected in 77% of these patients. Tissue molecular analysis was available for 111 patients (52%), and tissue somatic mutations were found for 78% (n = 87) of patients. For clinically relevant variants, concordance agreement between ctDNA and tumor tissue analysis was 95% among 94 treatment-naïve patients who had concurrent liquid and tumor biopsy molecular profiles. Sensitivity and specificity were 81% and 97%, respectively. Of the 103 patients with no tissue available, ctDNA detected potential actionable mutations in 17% of patients; of these, 10% received personalized treatment. ctDNA kinetics correlated with response rate and progression-free survival in 31 patients treated with first-line platinum-based chemotherapy. CONCLUSION These real-world data from a prospective study endorse ctDNA molecular profile by ampliconbased NGS as an accurate and reliable tool to detect and monitor clinically relevant molecular alterations in patients with advanced NSCLC.
AB - PURPOSE To assess the feasibility and utility of circulating tumor DNA (ctDNA) by amplicon-based nextgeneration sequencing (NGS) analysis in the daily clinical setting in a cohort of patients with advanced non-small-cell lung cancer (NSCLC), as an alternative approach to tissue molecular profiling. PATIENTS AND METHODS In this single-center prospective study, treatment-naïve and previously treated patients with advanced NSCLC were enrolled. Clinical validation of ctDNA using amplicon-based NGS analysis (with a 36-gene panel) was performed against standard-of-care tissue molecular analysis in treatment-naïve patients. The feasibility, utility, and prognostic value of ctDNA as a dynamic marker of treatment efficacy was evaluated. Results of tissue molecular profile were blinded during ctDNA analysis. RESULTS Of 214 patients with advanced NSCLC who were recruited, 156 were treatment-naïve patients and 58 were pretreated patients with unknown tissue molecular profile. ctDNA screening was successfully performed for 91% (n = 194) of all patients, and mutations were detected in 77% of these patients. Tissue molecular analysis was available for 111 patients (52%), and tissue somatic mutations were found for 78% (n = 87) of patients. For clinically relevant variants, concordance agreement between ctDNA and tumor tissue analysis was 95% among 94 treatment-naïve patients who had concurrent liquid and tumor biopsy molecular profiles. Sensitivity and specificity were 81% and 97%, respectively. Of the 103 patients with no tissue available, ctDNA detected potential actionable mutations in 17% of patients; of these, 10% received personalized treatment. ctDNA kinetics correlated with response rate and progression-free survival in 31 patients treated with first-line platinum-based chemotherapy. CONCLUSION These real-world data from a prospective study endorse ctDNA molecular profile by ampliconbased NGS as an accurate and reliable tool to detect and monitor clinically relevant molecular alterations in patients with advanced NSCLC.
UR - http://www.scopus.com/inward/record.url?scp=85074358986&partnerID=8YFLogxK
U2 - 10.1200/PO.18.00211
DO - 10.1200/PO.18.00211
M3 - Article
AN - SCOPUS:85074358986
SN - 2473-4284
VL - 3
SP - 1
EP - 14
JO - JCO Precision Oncology
JF - JCO Precision Oncology
ER -