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Whole-genome and transcriptome analysis enhances precision cancer treatment options.
Pleasance, E; Bohm, A; Williamson, L M; Nelson, J M T; Shen, Y; Bonakdar, M; Titmuss, E; Csizmok, V; Wee, K; Hosseinzadeh, S; Grisdale, C J; Reisle, C; Taylor, G A; Lewis, E; Jones, M R; Bleile, D; Sadeghi, S; Zhang, W; Davies, A; Pellegrini, B; Wong, T; Bowlby, R; Chan, S K; Mungall, K L; Chuah, E; Mungall, A J; Moore, R A; Zhao, Y; Deol, B; Fisic, A; Fok, A; Regier, D A; Weymann, D; Schaeffer, D F; Young, S; Yip, S; Schrader, K; Levasseur, N; Taylor, S K; Feng, X; Tinker, A; Savage, K J; Chia, S; Gelmon, K; Sun, S; Lim, H; Renouf, D J; Jones, S J M; Marra, M A; Laskin, J.
Afiliação
  • Pleasance E; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Bohm A; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver; Department of Medicine, University of British Columbia, Vancouver.
  • Williamson LM; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Nelson JMT; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Shen Y; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Bonakdar M; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Titmuss E; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Csizmok V; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Wee K; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Hosseinzadeh S; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver; Department of Medicine, University of British Columbia, Vancouver.
  • Grisdale CJ; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Reisle C; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Taylor GA; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Lewis E; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Jones MR; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Bleile D; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Sadeghi S; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Zhang W; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Davies A; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Pellegrini B; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Wong T; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Bowlby R; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Chan SK; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Mungall KL; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Chuah E; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Mungall AJ; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Moore RA; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Zhao Y; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Deol B; Department of Medical Oncology, BC Cancer, Vancouver.
  • Fisic A; Department of Medical Oncology, BC Cancer, Vancouver.
  • Fok A; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver.
  • Regier DA; Canadian Centre for Applied Research in Cancer Control, Cancer Control Research, BC Cancer, Vancouver.
  • Weymann D; Canadian Centre for Applied Research in Cancer Control, Cancer Control Research, BC Cancer, Vancouver.
  • Schaeffer DF; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver; Pancreas Centre BC, Vancouver.
  • Young S; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver.
  • Yip S; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver.
  • Schrader K; Hereditary Cancer Program, BC Cancer, Vancouver; Department of Medical Genetics, University of British Columbia, Vancouver.
  • Levasseur N; Department of Medical Oncology, BC Cancer, Vancouver.
  • Taylor SK; Department of Medical Oncology, BC Cancer, Kelowna.
  • Feng X; Department of Medical Oncology, BC Cancer, Victoria.
  • Tinker A; Department of Medical Oncology, BC Cancer, Vancouver.
  • Savage KJ; Department of Medical Oncology, BC Cancer, Vancouver.
  • Chia S; Department of Medical Oncology, BC Cancer, Vancouver.
  • Gelmon K; Department of Medical Oncology, BC Cancer, Vancouver.
  • Sun S; Department of Medical Oncology, BC Cancer, Vancouver.
  • Lim H; Department of Medical Oncology, BC Cancer, Vancouver.
  • Renouf DJ; Department of Medical Oncology, BC Cancer, Vancouver; Pancreas Centre BC, Vancouver.
  • Jones SJM; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver; Department of Medical Genetics, University of British Columbia, Vancouver; Department of Molecular Biology and Biochemistry, Simon Fraser University, Vancouver, Canada.
  • Marra MA; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver; Department of Medical Genetics, University of British Columbia, Vancouver.
  • Laskin J; Department of Medical Oncology, BC Cancer, Vancouver. Electronic address: jlaskin@bccancer.bc.ca.
Ann Oncol ; 33(9): 939-949, 2022 09.
Article em En | MEDLINE | ID: mdl-35691590
ABSTRACT

BACKGROUND:

Recent advances are enabling delivery of precision genomic medicine to cancer clinics. While the majority of approaches profile panels of selected genes or hotspot regions, comprehensive data provided by whole-genome and transcriptome sequencing and analysis (WGTA) present an opportunity to align a much larger proportion of patients to therapies. PATIENTS AND

METHODS:

Samples from 570 patients with advanced or metastatic cancer of diverse types enrolled in the Personalized OncoGenomics (POG) program underwent WGTA. DNA-based data, including mutations, copy number and mutation signatures, were combined with RNA-based data, including gene expression and fusions, to generate comprehensive WGTA profiles. A multidisciplinary molecular tumour board used WGTA profiles to identify and prioritize clinically actionable alterations and inform therapy. Patient responses to WGTA-informed therapies were collected.

RESULTS:

Clinically actionable targets were identified for 83% of patients, of which 37% of patients received WGTA-informed treatments. RNA expression data were particularly informative, contributing to 67% of WGTA-informed treatments; 25% of treatments were informed by RNA expression alone. Of a total 248 WGTA-informed treatments, 46% resulted in clinical benefit. RNA expression data were comparable to DNA-based mutation and copy number data in aligning to clinically beneficial treatments. Genome signatures also guided therapeutics including platinum, poly-ADP ribose polymerase inhibitors and immunotherapies. Patients accessed WGTA-informed treatments through clinical trials (19%), off-label use (35%) and as standard therapies (46%) including those which would not otherwise have been the next choice of therapy, demonstrating the utility of genomic information to direct use of chemotherapies as well as targeted therapies.

CONCLUSIONS:

Integrating RNA expression and genome data illuminated treatment options that resulted in 46% of treated patients experiencing positive clinical benefit, supporting the use of comprehensive WGTA profiling in clinical cancer care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article