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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Transl Res. 2020 Apr 5;220:167–181. doi: 10.1016/j.trsl.2020.03.011

Table II.

Summary of microbiota-oriented approaches to mitigate infectious complications in acute leukemia patients treated with intensive chemotherapy

Approach Concept Advantages Challenges
Antibiotic stewardship Minimize antibiotic exposure by rapid de-escalation and/or discontinuation
  • Simple intervention

  • Numerous supportive clinical trials in patient setting

  • Unknown best timing

  • Lack of reliable biomarkers to assure safety

  • Unclear best clinical endpoint

  • Possible reluctance amongst clinicians

Nonselective luminal adsorbents Adsorb the luminal fraction of antibiotics and prevent exposure of microbiota
  • Simple intervention

  • Adsorption of critical nonantibiotic drugs

  • Difficult to implement during chemotherapy

  • No published data in patient setting

Selective luminal antibiotic degraders Degrade the luminal fraction of antibiotics and prevent exposure of microbiota
  • Simple intervention

  • Encouraging efficacy in patient setting (respiratory tract infection)

  • Degraders of most antibiotic classes are not available

Prebiotics Help the beneficial microbes by stimulating their growth
  • Simple intervention

  • High likelihood of safety

  • Questionable history of efficacy

  • May not fix large microbiota injuries

  • No published data supporting efficacy in patient setting

Probiotics Restore a critical component of the microbiota
  • Simple intervention

  • Commercial products available

  • Safety data in patient setting

  • May not fix large microbiota injuries

  • Risk of microbial translocation

  • Minimal published data supporting efficacy in patient setting

Fecal microbiota transplantation Restore entire microbial community
  • Comprehensive microbiota restoration

  • Strong clinical efficacy (C. difficile infection)

  • Risk of microbial translocation

  • Unknown effects of a new microbial community in a new host (ie, microbiota-host “mismatch”)

  • Donor involvement in allogeneic products

  • Technical challenges in production, storage, and administration

  • Limitation of autologous products in patient settings because of possible baseline alterations