Cell-Free Circulating (Tumor) DNA before Surgery as a Prognostic Factor in Non-Metastatic Colorectal Cancer: A Systematic Review
Schraa, Suzanna J; van Rooijen, Karlijn L; Koopman, Miriam; Vink, Geraldine R; Fijneman, Remond J A
(2022) Cancers, volume 14, issue 9
(Article)
Abstract
Identification of non-metastatic colorectal cancer (CRC) patients with a high risk of recurrence after tumor resection is important to select patients who might benefit from adjuvant treatment. Cell-free DNA (cfDNA) and circulating tumor DNA (ctDNA) analyses after surgery are promising biomarkers to predict recurrence in these patients. However, these analyses
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face several challenges and do not allow guidance of neoadjuvant treatment, which might become a novel standard option in colon cancer treatment. The prognostic value of cfDNA/ctDNA before surgery is unclear. This systematic review aims to provide an overview of publications in which the prognostic value of presurgery cfDNA/ctDNA in non-metastatic CRC patients was studied and is performed according to PRISMA guidelines. A total of 29 out of 1233 articles were included and categorized into three groups that reflect the type of approach: measurement of cfDNA, ctDNA somatic alterations, and ctDNA methylation. Overall, a clear association between presurgery cfDNA/ctDNA and the outcome was not observed, but large studies that primarily focus on the prognostic value of presurgery cfDNA/ctDNA are lacking. Designing and performing studies that focus on the value of presurgery cfDNA/ctDNA is needed, in addition to standardization in the reporting of cfDNA/ctDNA results according to existing guidelines to improve comparability and interpretation among studies.
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Keywords: circulating cell-free DNA, circulating tumor DNA, colorectal cancer, DNA methylation, liquid biopsy, prognosis, surgery, survival, systematic review, Oncology, Cancer Research, Review, Journal Article
ISSN: 2072-6694
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Note: Funding Information: Conflicts of Interest: S.J.S. and K.L.v.R. declare no conflicts of interest. M.K. reports having an advisory role for Nordic Farma, Merck-Serono, Pierre Fabre, Servier, and institutional scientific grants from Bayer, Bristol Myers Squibb, Merck, Personal Genome Diagnostics (PGDx), Pierre Fabre, Roche, Sirtex, and Servier. G.R.V. reports research grants and financial support to the organization from BMS, Merck, Servier, Personal Genome Diagnostics, Bayer, Sirtex, and Pierre Fabre. R.J.A.F. reports grants and non-financial support from Personal Genome Diagnostics, non-financial support from Delfi Diagnostics, grants from MERCK BV, non-financial support from Pacific Biosciences, grants and non-financial support from Cergentis BV. In addition, R.J.A.F. has several patents pending. Funding Information: Funding: This work was made possible by financial support from the Dutch Digestive Foundation (SK 17-28) and the ZonMw ‘Personalised Medicine’ program (COIN, project number 848101011). Publisher Copyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
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