Your browser doesn't support javascript.
loading
Exceptional Chemotherapy Response in Metastatic Colorectal Cancer Associated With Hyper-Indel-Hypermutated Cancer Genome and Comutation of POLD1 and MLH1.
Sharma, Manish R; Auman, James T; Patel, Nirali M; Grilley-Olson, Juneko E; Zhao, Xiaobei; Moschos, Stergios J; Parker, Joel S; Yin, Xiaoying; Hayward, Michele C; Polite, Blase N; Marangon, Elena; Posocco, Bianca; Toffoli, Giuseppe; Hayes, D Neil; Innocenti, Federico.
Afiliación
  • Sharma MR; University of Chicago Medicine, Chicago, IL.
  • Auman JT; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Patel NM; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Grilley-Olson JE; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Zhao X; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Moschos SJ; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Parker JS; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Yin X; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Hayward MC; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Polite BN; University of Chicago Medicine, Chicago, IL.
  • Marangon E; Centro di Riferimento Oncologico, Aviano, Italy.
  • Posocco B; Centro di Riferimento Oncologico, Aviano, Italy.
  • Toffoli G; Centro di Riferimento Oncologico, Aviano, Italy.
  • Hayes DN; University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Innocenti F; University of North Carolina at Chapel Hill, Chapel Hill, NC.
JCO Precis Oncol ; 20172017.
Article en En | MEDLINE | ID: mdl-30009279
ABSTRACT

PURPOSE:

A73-year-old woman with metastatic colon cancer experienced a complete response to chemotherapy with dose-intensified irinotecan that has been durable for 5 years. We sequenced her tumor and germ line DNA and looked for similar patterns in publicly available genomic data from patients with colorectal cancer. PATIENTS AND

METHODS:

Tumor DNA was obtained from a biopsy before therapy, and germ line DNA was obtained from blood. Tumor and germline DNA were sequenced using a commercial panel with approximately 250 genes. Whole-genome amplification and exome sequencing were performed for POLE and POLD1. A POLD1 mutation was confirmed by Sanger sequencing. The somatic mutation and clinical annotation data files from the colon (n = 461) and rectal (n = 171) adenocarcinoma data sets were downloaded from The Cancer Genome Atlas data portal and analyzed for patterns of mutations and clinical outcomes in patients with POLE- and/or POLD1-mutated tumors.

RESULTS:

The pattern of alterations included APC biallelic inactivation and microsatellite instability high (MSI-H) phenotype, with somatic inactivation of MLH1 and hypermutation (estimated mutation rate > 200 per megabase). The extremely high mutation rate led us to investigate additional mechanisms for hypermutation, including loss of function of POLE. POLE was unaltered, but a related gene not typically associated with somatic mutation in colon cancer, POLD1, had a somatic mutation c.2171G>A[p.Gly724Glu]. Additionally, we noted that the high mutation rate was largely composed of dinucleotide deletions. A similar pattern of hypermutation (dinucleotide deletions, POLD1 mutations, MSI-H) was found in tumors from The Cancer Genome Atlas.

CONCLUSION:

POLD1 mutation with associated MSI-H and hyper-indel-hypermutated cancer genome characterizes a previously unrecognized variant of colon cancer that was found in this patient with an exceptional response to chemotherapy.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: JCO Precis Oncol Año: 2017 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: JCO Precis Oncol Año: 2017 Tipo del documento: Article País de afiliación: Israel