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Impact of Circulating Tumor DNA-Based Detection of Molecular Residual Disease on the Conduct and Design of Clinical Trials for Solid Tumors.
Kasi, Pashtoon M; Fehringer, Gordon; Taniguchi, Hiroya; Starling, Naureen; Nakamura, Yoshiaki; Kotani, Daisuke; Powles, Thomas; Li, Bob T; Pusztai, Lajos; Aushev, Vasily N; Kalashnikova, Ekaterina; Sharma, Shruti; Malhotra, Meenakshi; Demko, Zachary P; Aleshin, Alexey; Rodriguez, Angel; Billings, Paul R; Grothey, Axel; Taieb, Julien; Cunningham, David; Yoshino, Takayuki; Kopetz, Scott.
Afiliação
  • Kasi PM; Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA.
  • Fehringer G; Natera, Inc., Austin, TX.
  • Taniguchi H; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, Japan.
  • Starling N; The Royal Marsden Hospital NHS Foundation Trust, London, United Kingdom.
  • Nakamura Y; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, Japan.
  • Kotani D; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, Japan.
  • Powles T; Barts Cancer Institute, Queen Mary University of London ECMC, Barts Health, London, United Kingdom.
  • Li BT; Memorial Sloan Kettering Cancer Center and Weill Cornell Medicine, New York, NY.
  • Pusztai L; Yale Cancer Center, Yale School of Medicine, New Haven, CT.
  • Aushev VN; Natera, Inc., Austin, TX.
  • Kalashnikova E; Natera, Inc., Austin, TX.
  • Sharma S; Natera, Inc., Austin, TX.
  • Malhotra M; Natera, Inc., Austin, TX.
  • Demko ZP; Natera, Inc., Austin, TX.
  • Aleshin A; Natera, Inc., Austin, TX.
  • Rodriguez A; Natera, Inc., Austin, TX.
  • Billings PR; Natera, Inc., Austin, TX.
  • Grothey A; West Cancer Center and Research Institute, Germantown, TN.
  • Taieb J; Georges Pompidou European Hospital, SIRIC-CARPEM, Université de Paris, Paris, France.
  • Cunningham D; The Royal Marsden Hospital NHS Foundation Trust, London, United Kingdom.
  • Yoshino T; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, Japan.
  • Kopetz S; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
JCO Precis Oncol ; 6: e2100181, 2022 03.
Article em En | MEDLINE | ID: mdl-35263168
PURPOSE: Earlier detection of cancer recurrence using circulating tumor DNA (ctDNA) to detect molecular residual disease (MRD) has the potential to dramatically affect cancer management. We review evidence supporting the use of ctDNA as a biomarker for detection of MRD and highlight the potential impact that ctDNA testing could have on the conduct of clinical trials. METHODS: We searched the literature using MEDLINE (via PubMed) for articles from January 1, 2000, focusing on studies that assessed ctDNA as a predictor of cancer recurrence. Broadly focused searches on ctDNA and cancer were also performed to provide additional background information. www.clinialtrials.gov was searched to identify trials that incorporate ctDNA testing. RESULTS: Numerous studies across different cancer types indicate that ctDNA-based MRD detection predicts recurrence with high sensitivity and specificity, and with lead times that precede standard imaging by up to 12 months. Recently, ctDNA testing has started being used to enroll MRD-positive patients at high risk of recurrence into trials, promising gains in statistical power that allow clinical utility to be demonstrated with smaller cohorts. Trials where ctDNA testing based-MRD detection is used to stratify patients into low or high-risk categories for treatment assignment are also ongoing. In addition, there is increasing evidence supporting the use of ctDNA dynamics or clearance as a surrogate end point, which could significantly reduce trial duration. CONCLUSION: ctDNA-based trial enrichment across many cancers seems likely to become increasingly common for cost- and time-reduction benefits. Trial efficiency could also benefit from using ctDNA as a surrogate end point, leading to accelerated approval of new therapeutics. A clear demonstration of efficacy from trials that use ctDNA-based MRD detection to assign treatment could transform clinical practice.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Tumoral Circulante Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Tumoral Circulante Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2022 Tipo de documento: Article