Literature DB >> 25896973

Precision Medicine for Advanced Pancreas Cancer: The Individualized Molecular Pancreatic Cancer Therapy (IMPaCT) Trial.

Lorraine A Chantrill1, Adnan M Nagrial2, Clare Watson3, Amber L Johns3, Mona Martyn-Smith3, Skye Simpson3, Scott Mead4, Marc D Jones5, Jaswinder S Samra6, Anthony J Gill7, Nicole Watson7, Venessa T Chin8, Jeremy L Humphris3, Angela Chou9, Belinda Brown10, Adrienne Morey10, Marina Pajic3, Sean M Grimmond5, David K Chang11, David Thomas8, Lucille Sebastian12, Katrin Sjoquist13, Sonia Yip13, Nick Pavlakis14, Ray Asghari15, Sandra Harvey15, Peter Grimison16, John Simes17, Andrew V Biankin18.   

Abstract

PURPOSE: Personalized medicine strategies using genomic profiling are particularly pertinent for pancreas cancer. The Individualized Molecular Pancreatic Cancer Therapy (IMPaCT) trial was initially designed to exploit results from genome sequencing of pancreatic cancer under the auspices of the International Cancer Genome Consortium (ICGC) in Australia. Sequencing revealed small subsets of patients with aberrations in their tumor genome that could be targeted with currently available therapies. EXPERIMENTAL
DESIGN: The pilot stage of the IMPaCT trial assessed the feasibility of acquiring suitable tumor specimens for molecular analysis and returning high-quality actionable genomic data within a clinically acceptable timeframe. We screened for three molecular targets: HER2 amplification; KRAS wild-type; and mutations in DNA damage repair pathways (BRCA1, BRCA2, PALB2, ATM).
RESULTS: Tumor biopsy and archived tumor samples were collected from 93 patients and 76 were screened. To date 22 candidate cases have been identified: 14 KRAS wild-type, 5 cases of HER2 amplification, 2 mutations in BRCA2, and 1 ATM mutation. Median time from consent to the return of validated results was 21.5 days. An inability to obtain a biopsy or insufficient tumor content in the available specimen were common reasons for patient exclusion from molecular analysis while deteriorating performance status prohibited a number of patients from proceeding in the study.
CONCLUSIONS: Documenting the feasibility of acquiring and screening biospecimens for actionable molecular targets in real time will aid other groups embarking on similar trials. Key elements include the need to better prescreen patients, screen more patients, and offer more attractive clinical trial options. ©2015 American Association for Cancer Research.

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Year:  2015        PMID: 25896973     DOI: 10.1158/1078-0432.CCR-15-0426

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  83 in total

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