Literature DB >> 27471619

Efficacy of antineoplastic treatment is associated with the use of antibiotics that modulate intestinal microbiota.

Natali Pflug1, Sandra Kluth1, Jörg J Vehreschild2, Jasmin Bahlo1, Daniela Tacke2, Lena Biehl2, Barbara Eichhorst1, Kirsten Fischer1, Paula Cramer1, Anna-Maria Fink1, Michael von Bergwelt-Baildon3, Stephan Stilgenbauer4, Michael Hallek1, Oliver A Cornely5, Maria J G T Vehreschild2.   

Abstract

Reduced anticancer efficacy of cyclophosphamide and platinum salts has been reported in animals treated with anti-Gram-positive antibiotics. These effects were related to translocation of Gram-positive bacteria during mucositis with subsequent induction of cytotoxic oxygen reactive species and tumor invasion by pathogenic Th17 cells. To assess these hypotheses in a clinical setting, we identified patients receiving cyclophosphamide for chronic lymphocytic leukemia (CLL) and cisplatin for relapsed lymphoma. Data originated from the CLL8 trial (NCT00281918) and the Cologne Cohort of Neutropenic Patients (NCT01821456). Relevant antibiotics were defined as compounds with primary activity against Gram-positive bacteria. We evaluated their impact on response, progression-free survival (PFS) and overall survival (OS) by Kaplan-Meier methodology and Cox proportional hazards regression analysis. Among 800 available CLL patients, those receiving anti-Gram-positive antibiotics (n = 45/800) achieved a significantly lower overall response rate (OR 74.3% vs. 90.2%, p = 0.007). Patients with anti-Gram-positive antibiotics progressed significantly earlier, had a reduced OS (median PFS 14.1 vs. 44.1 mo, p < 0.001; median OS 56.1 vs. 91.7 mo, p < 0.001) and multivariate analysis showed that administration of anti-Gram-positive antibiotic treatment was independently associated with reduced PFS (Hazard ratio (HR) 2.090, p = 0.001) and OS (HR 2.966, p < 0.001). Of 122 patients with relapsed lymphoma, those treated with anti-Gram-positive antibiotics (n = 21/122) achieved a significantly lower OR rate (70.3% vs. 42.9%, p = 0.016). Patients with anti-Gram-positive antibiotics progressed significantly earlier than others (median PFS 2.3 vs. 11.5 mo, p = 0.001). As for multivariate analysis, the use of anti-Gram-positive antibiotics was independently associated with reduced PFS (HR 2.237, p = 0.012) and OS (HR 7.831, p < 0.001). Our data supports a potential negative impact of anti-Gram-positive antibiotics on the anticancer activity of cyclophosphamide and cisplatin in a clinical setting.

Entities:  

Keywords:  Antibiotics; chemotherapy; cisplatin; cyclophosphamide; microbiota

Year:  2016        PMID: 27471619      PMCID: PMC4938364          DOI: 10.1080/2162402X.2016.1150399

Source DB:  PubMed          Journal:  Oncoimmunology        ISSN: 2162-4011            Impact factor:   8.110


  14 in total

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2.  Intestinal Blautia Is Associated with Reduced Death from Graft-versus-Host Disease.

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3.  The effects of intestinal tract bacterial diversity on mortality following allogeneic hematopoietic stem cell transplantation.

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4.  Revised response criteria for malignant lymphoma.

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5.  Low urinary indoxyl sulfate levels early after transplantation reflect a disrupted microbiome and are associated with poor outcome.

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Journal:  Blood       Date:  2015-07-24       Impact factor: 22.113

Review 6.  Empirical antibiotics targeting Gram-positive bacteria for the treatment of febrile neutropenic patients with cancer.

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Journal:  Cochrane Database Syst Rev       Date:  2014-01-14

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Journal:  Science       Date:  2013-11-22       Impact factor: 47.728

9.  Regulation of intestinal inflammation by microbiota following allogeneic bone marrow transplantation.

Authors:  Robert R Jenq; Carles Ubeda; Ying Taur; Clarissa C Menezes; Raya Khanin; Jarrod A Dudakov; Chen Liu; Mallory L West; Natalie V Singer; Michele J Equinda; Asia Gobourne; Lauren Lipuma; Lauren F Young; Odette M Smith; Arnab Ghosh; Alan M Hanash; Jenna D Goldberg; Kazutoshi Aoyama; Bruce R Blazar; Eric G Pamer; Marcel R M van den Brink
Journal:  J Exp Med       Date:  2012-04-30       Impact factor: 14.307

10.  Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile.

Authors:  Charlie G Buffie; Vanni Bucci; Richard R Stein; Peter T McKenney; Lilan Ling; Asia Gobourne; Daniel No; Hui Liu; Melissa Kinnebrew; Agnes Viale; Eric Littmann; Marcel R M van den Brink; Robert R Jenq; Ying Taur; Chris Sander; Justin R Cross; Nora C Toussaint; Joao B Xavier; Eric G Pamer
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2.  The Microbiota: A New Variable Impacting Cancer Treatment Outcomes.

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Review 5.  Targeting the gut and tumor microbiota in cancer.

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6.  Fecal microbiota diversity disruption and clinical outcomes after auto-HCT: a multicenter observational study.

Authors:  Niloufer Khan; Sarah Lindner; Antonio L C Gomes; Sean M Devlin; Gunjan L Shah; Anthony D Sung; Craig S Sauter; Heather J Landau; Parastoo B Dahi; Miguel-Angel Perales; David J Chung; Alexander M Lesokhin; Anqi Dai; Annelie Clurman; John B Slingerland; Ann E Slingerland; Daniel G Brereton; Paul A Giardina; Molly Maloy; Gabriel K Armijo; Carlos Rondon-Clavo; Emily Fontana; Lauren Bohannon; Sendhilnathan Ramalingam; Amy T Bush; Meagan V Lew; Julia A Messina; Eric Littmann; Ying Taur; Robert R Jenq; Nelson J Chao; Sergio Giralt; Kate A Markey; Eric G Pamer; Marcel R M van den Brink; Jonathan U Peled
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Authors:  N Tinsley; C Zhou; S Nahm; S Rack; G C L Tan; P Lorigan; F Blackhall; N Cook
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Review 9.  The Microbiome and Gynecologic Cancer: Current Evidence and Future Opportunities.

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10.  The impact of antibiotic usage on the efficacy of chemoimmunotherapy is contingent on the source of tumor-reactive T cells.

Authors:  Michal P Kuczma; Zhi-Chun Ding; Tao Li; Tsadik Habtetsion; Tingting Chen; Zhonglin Hao; Locke Bryan; Nagendra Singh; James N Kochenderfer; Gang Zhou
Journal:  Oncotarget       Date:  2017-12-05
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