Can Consideration of the Microbiome Improve Antimicrobial Utilization and Treatment Outcomes in the Oncology Patient?

被引:31
作者
Galloway-Pena, Jessica R. [1 ]
Jenq, Robert R. [2 ,3 ]
Shelburne, Samuel A. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77030 USA
关键词
STEM-CELL TRANSPLANTATION; ACUTE MYELOID-LEUKEMIA; VERSUS-HOST-DISEASE; GUT MICROBIOTA; INTESTINAL MICROBIOTA; ANTIBIOTIC-RESISTANCE; T-CELLS; CANCER; INFECTION; CHEMOTHERAPY;
D O I
10.1158/1078-0432.CCR-16-3173
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The need to provide effective and timely antimicrobial treatment to cancer patients with infections is well recognized but tempered by preliminary, but accumulating, evidence that antibiotic-induced microbiome dysbiosis affects cancer therapy response, noninfectious toxicities, and infectious complications. Given only a minority of empirically treated cancer patients are proven to have a true bacterial infection, it is important to consider the potential negative consequences of extensive broad-spectrum antimicrobial use on the commensal microbiota. Herein, we review the literature substantiating the dilemma oncologists face when treating suspected or documented infections with respect to the interaction between the host microbiome, antibiotics, and cancer-related clinical outcomes. We propose microbiome-based explorations that could assist oncologists in optimizing treatment strategies for cancer-related infections as well as the cancer itself. In addition, we discuss knowledge gaps and challenges in this nascent field that must be addressed to deliver medically relevant, translational applications. We anticipate that the emerging knowledge regarding the role of the microbiota in the health of cancer patients maycause a reappraisal of the manner in which antibiotics are used in the oncologic setting and how microorganisms are viewed by oncologists. (C) 2017 AACR.
引用
收藏
页码:3263 / 3268
页数:6
相关论文
共 48 条
[1]   Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation [J].
Arpaia, Nicholas ;
Campbell, Clarissa ;
Fan, Xiying ;
Dikiy, Stanislav ;
van der Veeken, Joris ;
deRoos, Paul ;
Liu, Hui ;
Cross, Justin R. ;
Pfeffer, Klaus ;
Coffer, Paul J. ;
Rudensky, Alexander Y. .
NATURE, 2013, 504 (7480) :451-+
[2]   Human intestinal metagenomics: state of the art and future [J].
Blottiere, Herve M. ;
de Vos, Willem M. ;
Ehrlich, S. Dusko ;
Dore, Joel .
CURRENT OPINION IN MICROBIOLOGY, 2013, 16 (03) :232-239
[3]   Fever and neutropenia: the early years [J].
Bodey, Gerald P. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 63 :I3-I13
[4]   Levofloxacin to prevent bacterial infection in patients with cancer and neutropenia [J].
Bucaneve, G ;
Micozzi, A ;
Menichetti, F ;
Martino, P ;
Dionisi, MS ;
Martinelli, G ;
Allione, B ;
D'Antonio, D ;
Buelli, M ;
Nosari, AM ;
Cilloni, D ;
Zuffa, E ;
Cantaffa, R ;
Specchia, G ;
Amadori, S ;
Fabbiano, F ;
Deliliers, GL ;
Lauria, F ;
Foà, R ;
Del Favero, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (10) :977-987
[5]   Saccharomyces cerevisiae fungemia in a neutropenic patient treated with Saccharomyces boulardii [J].
Cesaro, S ;
Chinello, P ;
Rossi, L ;
Zanesco, L .
SUPPORTIVE CARE IN CANCER, 2000, 8 (06) :504-505
[6]   Fecal Microbiota Transplantation and Successful Resolution of Multidrug-Resistant-Organism Colonization [J].
Crum-Cianflone, Nancy F. ;
Sullivan, Eva ;
Ballon-Landa, Gonzalo .
JOURNAL OF CLINICAL MICROBIOLOGY, 2015, 53 (06) :1986-1989
[7]   Diet rapidly and reproducibly alters the human gut microbiome [J].
David, Lawrence A. ;
Maurice, Corinne F. ;
Carmody, Rachel N. ;
Gootenberg, David B. ;
Button, Julie E. ;
Wolfe, Benjamin E. ;
Ling, Alisha V. ;
Devlin, A. Sloan ;
Varma, Yug ;
Fischbach, Michael A. ;
Biddinger, Sudha B. ;
Dutton, Rachel J. ;
Turnbaugh, Peter J. .
NATURE, 2014, 505 (7484) :559-+
[8]   Intestinal microbiome analyses identify melanoma patients at risk for checkpoint-blockade-induced colitis [J].
Dubin, Krista ;
Callahan, Margaret K. ;
Ren, Boyu ;
Khanin, Raya ;
Viale, Agnes ;
Ling, Lilan ;
No, Daniel ;
Gobourne, Asia ;
Littmann, Eric ;
Huttenhower, Curtis ;
Pamer, Eric G. ;
Wolchok, Jedd D. .
NATURE COMMUNICATIONS, 2016, 7
[9]   Clinical Practice Guideline for the Use of Antimicrobial Agents in Neutropenic Patients with Cancer: 2010 Update by the Infectious Diseases Society of America [J].
Freifeld, Alison G. ;
Bow, Eric J. ;
Sepkowitz, Kent A. ;
Boeckh, Michael J. ;
Ito, James I. ;
Mullen, Craig A. ;
Raad, Issam I. ;
Rolston, Kenneth V. ;
Young, Jo-Anne H. ;
Wingard, John R. .
CLINICAL INFECTIOUS DISEASES, 2011, 52 (04) :E56-E93
[10]   Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells [J].
Furusawa, Yukihiro ;
Obata, Yuuki ;
Fukuda, Shinji ;
Endo, Takaho A. ;
Nakato, Gaku ;
Takahashi, Daisuke ;
Nakanishi, Yumiko ;
Uetake, Chikako ;
Kato, Keiko ;
Kato, Tamotsu ;
Takahashi, Masumi ;
Fukuda, Noriko N. ;
Murakami, Shinnosuke ;
Miyauchi, Eiji ;
Hino, Shingo ;
Atarashi, Koji ;
Onawa, Satoshi ;
Fujimura, Yumiko ;
Lockett, Trevor ;
Clarke, Julie M. ;
Topping, David L. ;
Tomita, Masaru ;
Hori, Shohei ;
Ohara, Osamu ;
Morita, Tatsuya ;
Koseki, Haruhiko ;
Kikuchi, Jun ;
Honda, Kenya ;
Hase, Koji ;
Ohno, Hiroshi .
NATURE, 2013, 504 (7480) :446-+