Microbiota modification in hematology: still at the bench or ready for the bedside?

CJ Severyn, R Brewster, TM Andermann - Blood Advances, 2019 - ashpublications.org
Blood Advances, 2019ashpublications.org
Growing evidence suggests that human microbiota likely influence diverse processes
including hematopoiesis, chemotherapy metabolism, and efficacy, as well as overall survival
in patients with hematologic malignancies and other cancers. Both host genetic
susceptibility and host-microbiota interactions may impact cancer risk and response to
treatment; however, microbiota have the potential to be uniquely modifiable and accessible
targets for treatment. Here, we focus on strategies to modify microbiota composition and …
Abstract
Growing evidence suggests that human microbiota likely influence diverse processes including hematopoiesis, chemotherapy metabolism, and efficacy, as well as overall survival in patients with hematologic malignancies and other cancers. Both host genetic susceptibility and host-microbiota interactions may impact cancer risk and response to treatment; however, microbiota have the potential to be uniquely modifiable and accessible targets for treatment. Here, we focus on strategies to modify microbiota composition and function in patients with cancer. First, we evaluate the use of fecal microbiota transplant to restore microbial equilibrium following perturbation by antibiotics and chemotherapy, and as a treatment of complications of hematopoietic stem cell transplantation (HSCT), such as graft-versus-host disease and colonization with multidrug-resistant organisms. We then address the potential use of both probiotics and dietary prebiotic compounds in targeted modulation of the microbiota intended to improve outcomes in hematologic diseases. With each type of therapy, we highlight the role that abnormal, or dysbiotic, microbiota play in disease, treatment efficacy, and toxicity and evaluate their potential promise as emerging strategies for microbiota manipulation in patients with hematologic malignancies and in those undergoing HSCT.
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