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Genomic Landscape of Advanced Solid Tumors in Circulating Tumor DNA and Correlation With Tissue Sequencing: A Single Institution's Experience.
Gerratana, Lorenzo; Movarek, Michael; Wehbe, Firas; Katam, Neelima; Mahalingam, Devalingam; Donahue, Jeannine; Shah, Ami; Chae, Young K; Mulcahy, Mary; Tsarwhas, Dean; Villaflor, Victoria; Kalyan, Aparna; Hussein, Maha; Patel, Jyoti; Chandra, Sunandana; Platanias, Leonidas C; Gradishar, William; Cristofanilli, Massimo; Behdad, Amir.
Afiliación
  • Gerratana L; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Movarek M; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Wehbe F; Department of Medicine, University of Udine, Udine, Italy.
  • Katam N; Department of Medical Oncology, Centro di Riferimento Oncologico (CRO), IRCCS, Aviano, Italy.
  • Mahalingam D; Department of Medicine, Division of Hematology-Oncology, Weill Cornell Medicine/New York-Presbyterian Hospital, New York, NY.
  • Donahue J; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Shah A; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Chae YK; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Mulcahy M; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Tsarwhas D; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Villaflor V; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Kalyan A; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Hussein M; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Patel J; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Chandra S; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Platanias LC; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Gradishar W; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Cristofanilli M; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.
  • Behdad A; Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
JCO Precis Oncol ; 6: e2100289, 2022 06.
Article en En | MEDLINE | ID: mdl-35772051
ABSTRACT

PURPOSE:

Circulating tumor DNA (ctDNA) has emerged as a promising noninvasive biomarker for baseline characterization and longitudinal monitoring of a tumor throughout disease management. The aim of this study was to evaluate the utility of ctDNA across a wide spectrum of tumor types.

METHODS:

We retrospectively identified 1,763 patients with advanced cancers who had next-generation sequencing of ctDNA or tumor tissue completed by a designated commercial assay at Northwestern University.

RESULTS:

ctDNA identified at least one gene alteration in 90% of patients. The number of detected alterations (NDA) and mutant allele frequency (MAF) of the most frequently mutated genes varied significantly across tumor types, with the highest MAF observed in gastric, colorectal, and breast cancers and the highest NDA observed in colorectal, lung squamous, and ovarian/endometrial cancers. TP53 was the most mutated gene in all tumor types. PIK3CA, ERBB2, BRCA1, and FGFR1 alterations were associated with breast cancer, and ESR1 mutations were exclusively detected in this tumor type. Colorectal cancer was characterized by alterations in KRAS and APC mutations, whereas KRAS, EGFR, PIK3CA, and BRAF mutations were common in lung adenocarcinoma. Concordance between blood and tissue sequencing was notably observed for truncal gene alterations (eg, APC and KRAS), whereas low concordance was often observed in genes associated with treatment resistance mechanisms (eg, RB1 and NF1). Tumor mutational burden (TMB) varied significantly across tumor types, and patients with high MAF or NDA had a significantly higher TMB score with one of the investigated platforms.

CONCLUSION:

The study provided new insights into the ctDNA mutational landscape across solid tumors, suggesting new hypotheses-generating data and caveats for future histotype-agnostic workflows integrated with tissue-based biomarkers such as TMB.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias de la Mama / Neoplasias Colorrectales / ADN Tumoral Circulante Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: JCO Precis Oncol Año: 2022 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias de la Mama / Neoplasias Colorrectales / ADN Tumoral Circulante Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: JCO Precis Oncol Año: 2022 Tipo del documento: Article País de afiliación: Israel