Division of Hematology/Oncology, Department of Pediatrics, Lucile Packard Children's Hospital, Stanford, CA.
School of Medicine, Stanford University, Stanford, CA; and.
Blood Adv. 2019 Nov 12;3(21):3461-3472. doi: 10.1182/bloodadvances.2019000365.
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.
越来越多的证据表明,人类微生物群可能会影响多种过程,包括造血、化疗代谢和疗效,以及血液系统恶性肿瘤和其他癌症患者的总生存率。宿主遗传易感性和宿主-微生物群相互作用都可能影响癌症风险和治疗反应;然而,微生物群具有独特的可修饰性和可治疗性靶点。在这里,我们专注于研究改变癌症患者微生物群组成和功能的策略。首先,我们评估了粪便微生物群移植在抗生素和化疗引起的微生态失衡后的应用,以及作为造血干细胞移植(HSCT)并发症的治疗方法,如移植物抗宿主病和耐多药菌定植。然后,我们探讨了益生菌和饮食前体化合物在靶向调节微生物群中的潜在用途,以期改善血液系统疾病的预后。对于每种治疗方法,我们都强调了异常或生态失调的微生物群在疾病、治疗效果和毒性中的作用,并评估了它们作为血液系统恶性肿瘤患者和接受 HSCT 患者微生物群操纵的新兴策略的潜力。