Helicobacter pylori serology is associated with worse overall survival in patients with melanoma treated with immune checkpoint inhibitors
Saved in:
| Title: | Helicobacter pylori serology is associated with worse overall survival in patients with melanoma treated with immune checkpoint inhibitors |
|---|---|
| Authors: | Tonneau, M., Nolin-Lapalme, A., Kazandjian, S., Auclin, E., Panasci, J., Benlaifaoui, M., Ponce, M., Al-Saleh, A., Belkaid, W., Naimi, S., Mihalcioiu, C., Watson, I., Bouin, M., Miller, W., Hudson, M., Wong, M.K., Pezo, R.C., Turcotte, S., Bélanger, K., Jamal, R., Oster, P., Velin, D., Richard, C., Messaoudene, M., Elkrief, A., Routy, B. |
| Source: | Oncoimmunology OncoImmunology, Vol 11, Iss 1 (2022) Oncoimmunology, vol. 11, no. 1, pp. 2096535 |
| Publisher Information: | Informa UK Limited, 2022. |
| Publication Year: | 2022 |
| Subject Terms: | 0301 basic medicine, immune checkpoint inhibitor therapy, Lung Neoplasms, Helicobacter pylori, microbiome, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Syndrome, Metastatic melanoma, RC581-607, Helicobacter Infections, 3. Good health, 03 medical and health sciences, Carcinoma, Non-Small-Cell Lung/drug therapy, Helicobacter Infections/drug therapy, Helicobacter Infections/microbiology, Helicobacter pylori/physiology, Humans, Immune Checkpoint Inhibitors/therapeutic use, Lung Neoplasms/drug therapy, Melanoma/drug therapy, helicobacter pylori, non-small cell lung cancer, onco-immunology, Carcinoma, Non-Small-Cell Lung, Immunologic diseases. Allergy, Immune Checkpoint Inhibitors, Melanoma, RC254-282, Original Research |
| Description: | The microbiome is now regarded as one of the hallmarks of cancer and several strategies to modify the gut microbiota to improve immune checkpoint inhibitor (ICI) activity are being evaluated in clinical trials. Preliminary data regarding the upper gastro-intestinal microbiota indicated that Helicobacter pylori seropositivity was associated with a negative prognosis in patients amenable to ICI. In 97 patients with advanced melanoma treated with ICI, we assessed the impact of H. pylori on outcomes and microbiome composition. We performed H. pylori serology and profiled the fecal microbiome with metagenomics sequencing. Among the 97 patients, 22% were H. pylori positive (Pos). H. pylori Pos patients had a significantly shorter overall survival (p = .02) compared to H. pylori negative (Neg) patients. In addition, objective response rate and progression-free survival were decreased in H. pylori Pos patients. Metagenomics sequencing did not reveal any difference in diversity indexes between the H. pylori groups. At the taxa level, Eubacterium ventriosum, Mediterraneibacter (Ruminococcus) torques, and Dorea formicigenerans were increased in the H. pylori Pos group, while Alistipes finegoldii, Hungatella hathewayi and Blautia producta were over-represented in the H. pylori Neg group. In a second independent cohort of patients with NSCLC, diversity indexes were similar in both groups and Bacteroides xylanisolvens was increased in H. pylori Neg patients. Our results demonstrated that the negative impact of H. pylori on outcomes seem to be independent from the fecal microbiome composition. These findings warrant further validation and development of therapeutic strategies to eradicate H. pylori in immuno-oncology arena. |
| Document Type: | Article Other literature type |
| File Description: | application/pdf |
| Language: | English |
| ISSN: | 2162-402X |
| DOI: | 10.1080/2162402x.2022.2096535 |
| Access URL: | https://pubmed.ncbi.nlm.nih.gov/35832043 https://doaj.org/article/adb7b6925dfe48898a2dcd6d9e30f8ad https://serval.unil.ch/notice/serval:BIB_D970B474B020 http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_D970B474B0209 https://serval.unil.ch/resource/serval:BIB_D970B474B020.P001/REF.pdf |
| Rights: | CC BY NC URL: http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (http://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| Accession Number: | edsair.doi.dedup.....4b97dd345c6a550c54ebc0486ffd42af |
| Database: | OpenAIRE |
| Abstract: | The microbiome is now regarded as one of the hallmarks of cancer and several strategies to modify the gut microbiota to improve immune checkpoint inhibitor (ICI) activity are being evaluated in clinical trials. Preliminary data regarding the upper gastro-intestinal microbiota indicated that Helicobacter pylori seropositivity was associated with a negative prognosis in patients amenable to ICI. In 97 patients with advanced melanoma treated with ICI, we assessed the impact of H. pylori on outcomes and microbiome composition. We performed H. pylori serology and profiled the fecal microbiome with metagenomics sequencing. Among the 97 patients, 22% were H. pylori positive (Pos). H. pylori Pos patients had a significantly shorter overall survival (p = .02) compared to H. pylori negative (Neg) patients. In addition, objective response rate and progression-free survival were decreased in H. pylori Pos patients. Metagenomics sequencing did not reveal any difference in diversity indexes between the H. pylori groups. At the taxa level, Eubacterium ventriosum, Mediterraneibacter (Ruminococcus) torques, and Dorea formicigenerans were increased in the H. pylori Pos group, while Alistipes finegoldii, Hungatella hathewayi and Blautia producta were over-represented in the H. pylori Neg group. In a second independent cohort of patients with NSCLC, diversity indexes were similar in both groups and Bacteroides xylanisolvens was increased in H. pylori Neg patients. Our results demonstrated that the negative impact of H. pylori on outcomes seem to be independent from the fecal microbiome composition. These findings warrant further validation and development of therapeutic strategies to eradicate H. pylori in immuno-oncology arena. |
|---|---|
| ISSN: | 2162402X |
| DOI: | 10.1080/2162402x.2022.2096535 |
Full Text Finder
Nájsť tento článok vo Web of Science