Whole-genome DNA and RNA sequencing in patients with metastatic colorectal cancer (mCRC).

2014 ◽  
Vol 32 (15_suppl) ◽  
pp. e22078-e22078
Author(s):  
Simon Daniel Baxter ◽  
Howard John Lim ◽  
Yaoqing Shen ◽  
Janessa J. Laskin ◽  
Daniel John Renouf ◽  
...  
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Steven A. Buechler ◽  
Melissa T. Stephens ◽  
Amanda B. Hummon ◽  
Katelyn Ludwig ◽  
Emily Cannon ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Vijayalakshmi Shanmugam ◽  
Ramesh K Ramanathan ◽  
Nicole A Lavender ◽  
Shripad Sinari ◽  
Manpreet Chadha ◽  
...  

2021 ◽  
Vol 13 ◽  
pp. 175883592110090
Author(s):  
Pilar García-Alfonso ◽  
Andrés Jesús Muñoz Martín ◽  
Laura Ortega Morán ◽  
Javier Soto Alsar ◽  
Gabriela Torres Pérez-Solero ◽  
...  

Colorectal cancer (CRC) is one of the most common forms of cancer, with an estimated 1.36 million new cases and almost 700,000 deaths annually. Approximately 21% of patients with CRC have metastatic disease at diagnosis. The objective of this article is to review the literature on the efficacy and safety of oral drugs available for the treatment of metastatic colorectal cancer (mCRC). Several such drugs have been developed, and fluoropyrimidines are the backbone of chemotherapy in this indication. They exert their antitumour activity by disrupting the synthesis and function of DNA and RNA. Oral fluoropyrimidines include prodrugs capecitabine, tegafur, eniluracil/5-fluorouracil, tegafur/uracil, tegafur/gimeracil/oteracil and trifluridine/tipiracil (FTD/TPI). Oral drugs offer several advantages over injectable formulations, including convenience, flexibility, avoidance of injection-related adverse events (AEs) and, in some circumstances, lower costs. However, oral drugs may not be suitable for patients with gastrointestinal obstruction or malabsorption, they may result in reduced treatment adherence and should not be co-administered with drugs that interfere with absorption or hepatic metabolism. Oral fluoropyrimidines such as capecitabine, as monotherapy or in combination with oxaliplatin, irinotecan or bevacizumab, are as effective as intravenous 5-fluorouracil (5-FU) in first-line treatment of mCRC. Other oral fluoropyrimidines, such as FTD/TPI, are effective in patients with mCRC who are refractory, intolerant or ineligible for 5-FU. In addition, oral fluoropyrimidines are used in adjuvant treatment of mCRC. Regorafenib is an oral multikinase inhibitor used in patients in whom several previous lines of therapy have failed. Frequent AEs associated with oral drugs used in the treatment of CRC include hand-foot syndrome and gastrointestinal and haematological toxicities.


2016 ◽  
Vol 13 (11) ◽  
pp. 953-958 ◽  
Author(s):  
Jason A Reuter ◽  
Damek V Spacek ◽  
Reetesh K Pai ◽  
Michael P Snyder

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e20563-e20563 ◽  
Author(s):  
Erica S Tsang ◽  
Yaoqing Shen ◽  
Negar Chooback ◽  
Cheryl Ho ◽  
Martin Jones ◽  
...  

e20563 Background: The Personalized OncoGenomics (POG) program at the BC Cancer Agency integrates whole genome (DNA) and RNA sequencing into practice for metastatic malignancies. We examine patients with metastatic NSCLC and report the prevalence of actionable targets, treatments, and outcomes. Methods: Between 2012-2016, 217 patients had a tumor biopsy and blood sample with comprehensive DNA (80X; 40X normal) and RNA sequencing followed by in-depth bioinformatics to identify potential cancer “drivers” and/or actionable/treatable targets. In NSCLC cases, we compared the progression-free survival (PFS) of “POG-informed therapies” with the PFS of the last regimen prior to POG (PFS ratio). Results: In 29 NSCLC cases, median age was 60.2 years (range 39.4-72.6), 11 were male (38%), and histologies were: adenocarcinoma (93%); squamous cell carcinoma (7%). Potential molecular targets (i.e. cancer “drivers”) were identified in 26 (90%), and 21 (72%) had actionable targets. 13 received POG-informed therapies, of which 3 had no therapy before POG. Of 10 patients with POG-informed therapy, median PFS ratio was 0.94 (IQR 0.2-3.4). 3 (30%) had a PFS ratio ≥1.3, and 3 (30%) had a PFS ratio ≥0.8 and <1.3. Conclusions: In this NSCLC cohort, 30% demonstrated longer PFS with POG-informed therapies. Larger studies will help clarify the role of whole genome analysis in clinical practice. [Table: see text]


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