TY - JOUR
T1 - Determining risk of severe gastrointestinal toxicity based on pretreatment gut microbial community in patients receiving cancer treatment
T2 - a new predictive strategy in the quest for personalized cancer medicine
AU - Wardill, Hannah R
AU - Tissing, Wim J E
N1 - Publisher Copyright:
© 2017 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2017/6
Y1 - 2017/6
N2 - PURPOSE OF REVIEW: Currently, our ability to accurately predict a patient's risk of developing severe gastrointestinal toxicity from their cancer treatment is limited. Risk stratification continues to rely on traditional patient-related and treatment-related factors including age, ethnicity, sex, comorbidities, genetics, agent, dose and schedule. Although informative, these crude measures continue to underestimate toxicity risk, and hence alternative methods of risk prediction must be investigated. Given the increasing focus on the gut microbiome in driving disease, this review will provide an overview of the current literature proposing the gut microbiome as a novel predictive tool for treatment-induced gastrointestinal toxicity.RECENT FINDINGS: Predictive gut microbial phenotypes have been identified for gastrointestinal toxicity induced by radiation and the checkpoint blocker, Ipilimumab. Each study employed slightly different methods of gut microbiome assessment; however, in all cases, separation of toxic versus nontoxic patients was achieved. No studies have investigated chemotherapy-induced gastrointestinal toxicity.SUMMARY: The gut microbiome offers an exciting new method of risk stratification for gastrointestinal toxicity. This would enable identification of high-risk patients prior to treatment, enabling tailored treatment regimens based on personalized risk assessment and the proactive provision of supportive care measures. Based on the plasticity of the gut microbiome, methods of risk mitigation may be investigated.
AB - PURPOSE OF REVIEW: Currently, our ability to accurately predict a patient's risk of developing severe gastrointestinal toxicity from their cancer treatment is limited. Risk stratification continues to rely on traditional patient-related and treatment-related factors including age, ethnicity, sex, comorbidities, genetics, agent, dose and schedule. Although informative, these crude measures continue to underestimate toxicity risk, and hence alternative methods of risk prediction must be investigated. Given the increasing focus on the gut microbiome in driving disease, this review will provide an overview of the current literature proposing the gut microbiome as a novel predictive tool for treatment-induced gastrointestinal toxicity.RECENT FINDINGS: Predictive gut microbial phenotypes have been identified for gastrointestinal toxicity induced by radiation and the checkpoint blocker, Ipilimumab. Each study employed slightly different methods of gut microbiome assessment; however, in all cases, separation of toxic versus nontoxic patients was achieved. No studies have investigated chemotherapy-induced gastrointestinal toxicity.SUMMARY: The gut microbiome offers an exciting new method of risk stratification for gastrointestinal toxicity. This would enable identification of high-risk patients prior to treatment, enabling tailored treatment regimens based on personalized risk assessment and the proactive provision of supportive care measures. Based on the plasticity of the gut microbiome, methods of risk mitigation may be investigated.
KW - Age Factors
KW - Antineoplastic Agents/adverse effects
KW - Comorbidity
KW - Dose-Response Relationship, Drug
KW - Drug Administration Schedule
KW - Dysbiosis/immunology
KW - Ethnicity
KW - Gastrointestinal Microbiome/drug effects
KW - Humans
KW - Nausea/chemically induced
KW - Neoplasms/drug therapy
KW - Predictive Value of Tests
KW - Risk Factors
KW - Sex Factors
KW - Vomiting/chemically induced
UR - http://www.scopus.com/inward/record.url?scp=85019418733&partnerID=8YFLogxK
U2 - 10.1097/SPC.0000000000000265
DO - 10.1097/SPC.0000000000000265
M3 - Review article
C2 - 28333867
SN - 1751-4258
VL - 11
SP - 125
EP - 132
JO - Current opinion in supportive and palliative care
JF - Current opinion in supportive and palliative care
IS - 2
ER -