Literature DB >> 32220893

Disease Monitoring Using Post-induction Circulating Tumor DNA Analysis Following First-Line Therapy in Patients with Metastatic Colorectal Cancer.

Xiaoju Max Ma1, Johanna C Bendell2, Herbert I Hurwitz3, Christine Ju4, John J Lee5, Alex Lovejoy6, Christoph Mancao7, Alan Nicholas8, Richard Price7, Nicolas Sommer9, Nalin Tikoo4, Lijing Yao10, Stephanie J Yaung11, John F Palma1.   

Abstract

PURPOSE: We assessed plasma circulating tumor DNA (ctDNA) level as a prognostic marker for progression-free survival (PFS) following first-line metastatic colorectal cancer (mCRC) therapy. EXPERIMENTAL
DESIGN: The Sequencing Triplet With Avastin and Maintenance (STEAM) was a randomized, phase II trial investigating efficacy of bevacizumab (BEV) plus 5-fluorouracil/leucovorin/oxaliplatin (FOLFOX) and 5-fluorouracil/leucovorin/irinotecan (FOLFIRI), administered concurrently or sequentially, versus FOLFOX-BEV in first-line mCRC. Evaluation of biomarkers associated with treatment outcomes was an exploratory endpoint. Patients in the biomarker-evaluable population (BEP) had 1 tissue sample, 1 pre-induction plasma sample, and 1 post-induction plasma sample collected ≤60 days of induction from last drug date.
RESULTS: Among the 280 patients enrolled in STEAM, 183 had sequenced and evaluable tumor tissue, 118 had matched pre-induction plasma, and 54 (BEP) had ctDNA-evaluable sequencing data for pre- and post-induction plasma. The most common somatic variants in tumor tissue and pre-induction plasma were TP53, APC, and KRAS. Patients with lower-than-median versus higher-than-median post-induction mean allele fraction (mAF) levels had longer median PFS (17.7 vs. 7.5 months, HR, 0.33; 95% confidence interval, 0.17-0.63). Higher levels of post-induction mAF and post-induction mean mutant molecules per milliliter (mMMPM), and changes in ctDNA (stratified by a 10-fold or 100-fold reduction in mAF between pre- and post-induction plasma), were associated with shorter PFS. Post-induction mAF and mMMPM generally correlated with each other (ρ = 0.987, P < 0.0001).
CONCLUSIONS: ctDNA quantification in post-induction plasma may serve as a prognostic biomarker for mCRC post-treatment outcomes. ©2020 American Association for Cancer Research.

Entities:  

Year:  2020        PMID: 32220893     DOI: 10.1158/1078-0432.CCR-19-1209

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  5 in total

1.  Circulating tumor DNA as a therapy response marker in metastatic colorectal cancer.

Authors:  Xiaoju Max Ma; Stephanie J Yaung
Journal:  Oncoscience       Date:  2022-06-24

2.  Circulating tumour DNA and its clinical utility in predicting treatment response or survival in patients with metastatic colorectal cancer: a systematic review and meta-analysis.

Authors:  Louise B Callesen; Julian Hamfjord; Anders K Boysen; Niels Pallisgaard; Tormod K Guren; Elin H Kure; Karen-Lise G Spindler
Journal:  Br J Cancer       Date:  2022-04-19       Impact factor: 9.075

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

Authors:  Stephanie J Yaung; Corinna Woestmann; Christine Ju; Xiaoju Max Ma; Sandeep Gattam; Yiyong Zhou; Liu Xi; Subrata Pal; Aarthi Balasubramanyam; Nalin Tikoo; Claus Peter Heussel; Michael Thomas; Mark Kriegsmann; Michael Meister; Marc A Schneider; Felix J Herth; Birgit Wehnl; Maximilian Diehn; Ash A Alizadeh; John F Palma; Thomas Muley
Journal:  Cancers (Basel)       Date:  2022-05-18       Impact factor: 6.575

4.  Mutational landscape of circulating tumor DNA identifies distinct molecular features associated with therapeutic response in patients with metastatic colorectal cancer.

Authors:  Min Shi; Hong Yuan; Jun Ji; Shouwei Zhang; Qingyuan Li; Yawei Chen; Xiaoli Gong; Zhenggang Zhu; Jun Zhang
Journal:  Ther Adv Med Oncol       Date:  2022-01-24       Impact factor: 8.168

Review 5.  Clinical Applications of Minimal Residual Disease Assessments by Tumor-Informed and Tumor-Uninformed Circulating Tumor DNA in Colorectal Cancer.

Authors:  Jun Gong; Andrew Hendifar; Alexandra Gangi; Karen Zaghiyan; Katelyn Atkins; Yosef Nasseri; Zuri Murrell; Jane C Figueiredo; Sarah Salvy; Robert Haile; Megan Hitchins
Journal:  Cancers (Basel)       Date:  2021-09-10       Impact factor: 6.639

  5 in total

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