Early Assessment of Chemotherapy Response in Advanced Non-Small Cell Lung Cancer with Circulating Tumor DNA

被引:2
|
作者
Yaung, Stephanie J. [1 ]
Woestmann, Corinna [2 ]
Ju, Christine [3 ]
Ma, Xiaoju Max [1 ]
Gattam, Sandeep [3 ]
Zhou, Yiyong [3 ]
Xi, Liu [1 ]
Pal, Subrata [3 ]
Balasubramanyam, Aarthi [3 ]
Tikoo, Nalin [4 ]
Heussel, Claus Peter [5 ,6 ,7 ,8 ]
Thomas, Michael [7 ,8 ,9 ]
Kriegsmann, Mark [10 ]
Meister, Michael [7 ,8 ,9 ]
Schneider, Marc A. [7 ,8 ,9 ]
Herth, Felix J. [7 ,8 ,9 ]
Wehnl, Birgit [11 ]
Diehn, Maximilian [12 ]
Alizadeh, Ash A. [12 ]
Palma, John F. [1 ]
Muley, Thomas [7 ,8 ,9 ]
机构
[1] Roche Sequencing Solut Inc, Pleasanton, CA 94588 USA
[2] Roche Sequencing Solut Inc, D-14473 Potsdam, Germany
[3] Roche Mol Syst Inc, Pleasanton, CA 94588 USA
[4] Alector Inc, San Francisco, CA 94080 USA
[5] Univ Hosp, Thoraxklin, Diagnost & Intervent Radiol Nucl Med, D-69126 Heidelberg, Germany
[6] Univ Hosp, Diagnost & Intervent Radiol, D-69120 Heidelberg, Germany
[7] Translat Lung Res Ctr TLRC Heidelberg, D-69120 Heidelberg, Germany
[8] German Ctr Lung Res DZL, D-69120 Heidelberg, Germany
[9] Thoraxklin Heidelberg Univ Hosp, Translat Res Unit, D-69126 Heidelberg, Germany
[10] Univ Hosp Heidelberg, Inst Pathol, D-69120 Heidelberg, Germany
[11] Roche Diagnost GmbH, D-82377 Penzberg, Germany
[12] Stanford Univ, Stanford Canc Inst, Stanford, CA 94305 USA
关键词
ctDNA; NSCLC; chemotherapy; NGS; early molecular response; THERAPEUTIC RESPONSE; EARLY MARKER; SURVIVAL; PREDICTS;
D O I
10.3390/cancers14102479
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary An early assessment of response to treatment is crucial to informing appropriate therapeutic management. Using a plasma-only strategy, we measured changes in circulating tumor DNA (ctDNA) levels after one or two cycles of chemotherapy in 92 patients with advanced non-small-cell lung cancer (NSCLC) treated with first-line chemo- or chemoradiation therapies. A <= 50% decrease in ctDNA level after one cycle of chemotherapy was associated with shorter progression-free survival and overall survival. A <= 50% decrease in ctDNA level after two cycles of chemotherapy also had shorter survival. Our findings demonstrate that using liquid biopsies to measure early changes in ctDNA levels in response to chemotherapy may help identify non-responders before standard-of-care imaging in advanced NSCLC. Monitoring treatment efficacy earlier and accurately can enable more personalized regimens to improve patient outcomes. Monitoring treatment efficacy early during therapy could enable a change in treatment to improve patient outcomes. We report an early assessment of response to treatment in advanced NSCLC using a plasma-only strategy to measure changes in ctDNA levels after one cycle of chemotherapy. Plasma samples were collected from 92 patients with Stage IIIB-IV NSCLC treated with first-line chemo- or chemoradiation therapies in an observational, prospective study. Retrospective ctDNA analysis was performed using next-generation sequencing with a targeted 198-kb panel designed for lung cancer surveillance and monitoring. We assessed whether changes in ctDNA levels after one or two cycles of treatment were associated with clinical outcomes. Subjects with <= 50% decrease in ctDNA level after one cycle of chemotherapy had a lower 6-month progression-free survival rate (33% vs. 58%, HR 2.3, 95% CI 1.2 to 4.2, log-rank p = 0.009) and a lower 12-month overall survival rate (25% vs. 70%, HR 4.3, 95% CI 2.2 to 9.7, log-rank p < 0.001). Subjects with <= 50% decrease in ctDNA level after two cycles of chemotherapy also had shorter survival. Using non-invasive liquid biopsies to measure early changes in ctDNA levels in response to chemotherapy may help identify non-responders before standard-of-care imaging in advanced NSCLC.
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页数:14
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