TY - JOUR
T1 - Refractory metastatic colorectal cancer
T2 - Current challenges and future prospects
AU - Lam, Marissa
AU - Lum, Caroline
AU - Latham, Sarah
AU - Smith, Sam Tipping
AU - Prenen, Hans
AU - Segelov, Eva
PY - 2020/6/26
Y1 - 2020/6/26
N2 - Despite advances, patients with metastatic colorectal cancer (mCRC) still have poor long-term survival. Identification of molecular subtypes is important to guide therapy through standard treatment pathways and holds promise for the development of new treat-ments. Following standard first-and second-line chemotherapy plus targeted agents, many patients retain a reasonable performance status, and thus are seeking further effective treatment to extend life and maintain symptom control. The challenge lies in selecting the most appropriate therapy in the third-and fourth-line settings, from a range of options including the relatively new oral agents TAS-102 and regorafenib, or rechallenge with previous chemotherapy or anti-epidermal growth factor receptor (anti-EGFR) monoclonal antibodies (mAB). Beyond this, therapy consists of trials involving novel agents and new combinations of treatments with theoretical synergy and/or non-overlapping toxicity. There is a great focus on enhancing immunogenicity in mCRC, to reflect the impressive results of immunotherapy drugs in the small cohort with mismatch repair deficient (dMMR) mCRC. Rare molecular subtypes of mCRC are increasingly being identified, including Her2-positive disease, NTRK fusions and others. Clinical trials exploring the efficacy of immunomodula-tory and precision agents are plentiful and will hopefully yield clinically meaningful results that can be rapidly translated into routine care.
AB - Despite advances, patients with metastatic colorectal cancer (mCRC) still have poor long-term survival. Identification of molecular subtypes is important to guide therapy through standard treatment pathways and holds promise for the development of new treat-ments. Following standard first-and second-line chemotherapy plus targeted agents, many patients retain a reasonable performance status, and thus are seeking further effective treatment to extend life and maintain symptom control. The challenge lies in selecting the most appropriate therapy in the third-and fourth-line settings, from a range of options including the relatively new oral agents TAS-102 and regorafenib, or rechallenge with previous chemotherapy or anti-epidermal growth factor receptor (anti-EGFR) monoclonal antibodies (mAB). Beyond this, therapy consists of trials involving novel agents and new combinations of treatments with theoretical synergy and/or non-overlapping toxicity. There is a great focus on enhancing immunogenicity in mCRC, to reflect the impressive results of immunotherapy drugs in the small cohort with mismatch repair deficient (dMMR) mCRC. Rare molecular subtypes of mCRC are increasingly being identified, including Her2-positive disease, NTRK fusions and others. Clinical trials exploring the efficacy of immunomodula-tory and precision agents are plentiful and will hopefully yield clinically meaningful results that can be rapidly translated into routine care.
KW - Genomic profiling
KW - Immunotherapy
KW - Molecular targets
KW - Precision medicine
UR - http://www.scopus.com/inward/record.url?scp=85087986692&partnerID=8YFLogxK
U2 - 10.2147/CMAR.S213236
DO - 10.2147/CMAR.S213236
M3 - Review Article
AN - SCOPUS:85087986692
SN - 1179-1322
VL - 12
SP - 5819
EP - 5830
JO - Cancer Management and Research
JF - Cancer Management and Research
ER -