Prognostic value of host genetic variants determining Bifidobacterium abundance in the lactose metabolism pathway for immunotherapy efficacy.

2651 Background: The potential predicative and therapeutic value of Bifidobacterium in immune checkpoint inhibitors (ICIs) treatment has been widely studied. However, the value of its genetic determinants on the prognosis of ICIs treatment remains unclear. Methods: we examined the associations of 11 single nucleotide polymorphisms (SNPs) located at host genes determining Bifidobacterium abundance with the outcomes of ICIs treatment in 370 eligible cancer patients. Results: Cox regression analysis revealed that rs3739020 TT carriers experienced significantly extended OS ( P -value = 0.003, adjusted HR = 0.46, 95%CI = 0.27-0.77) compared with GG+TG carriers. The LCT haplotype analysis showed that the lactose poor metabolizers exhibited significantly poorer OS ( P -value = 0.002, adjusted HR = 0.45, 95%CI = 0.27-0.74) than the extensive or intermediate metabolizers. In polygenic SNP analysis, the high galactose level carriers exhibited significantly prolonged OS ( P -value = 0.007, adjusted HR = 0.32, 95%CI = 0.14-0.73) and progression-free survival (PFS, P -value = 0.001, adjusted HR = 0.45, 95%CI = 0.29-0.71). All the four SNPs and the LCT metabolic phenotype were not associated with the occurrence of overall immune-related adverse events (irAEs). Genetically predicted Bifidobacterium abundance was significantly associated with an increased abundance of lactose metabolism pathway ( P -value = 0.012, Beta coefficient = 0.549). Conclusions: SNPs determining Bifidobacterium abundance in the lactose metabolism pathway have prognostic value for immunotherapy efficacy, and the lactose extensive and intermediate metabolizers exhibited better immunotherapy efficacy. The details of LCT metabolic phenotypes and the associations of LCT metabolic phenotypes with overall survival. LCT genotypes and their risk allele rs3739020G rs56263017C rs55809728A rs3739022A HR P Lactose extensive metabolizer (EM, no risk allele exist) TT TT GG GG Refernces Lactose inermediate metabolizer (IM, risk alleles exist in 1-3 SNPs) TG or GG TT GG GG 0.58,95%CI=0.33-0.99 0.049 TT TC or CC GG GG TT TT AA or GA GG TG or GG TT GG AA or GA TG or GG TC or CC GG GG TG or GG TT AA or GA GG TT TT GG AA or GA TT TC or CC AA or GA GG TT TC or CC GG AA or GA TG or GG TT AA or GA AA or GA TG or GG TC or CC AA or GA GG TG or GG TC or CC GG AA or GA TT TT AA or GA AA or GA TG or GG TC

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Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.2651
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Prognostic value of host genetic variants determining Bifidobacterium abundance in the lactose metabolism pathway for immunotherapy efficacy.

Ying Jie Zhu, Jun‐Li Luo, Wenhui Liu, Fang Ma et al.
Journal of Clinical Oncology
Immunodeficiency and Autoimmune Disorders
article

Prognostic value of host genetic variants determining Bifidobacterium abundance in the lactose metabolism pathway for immunotherapy efficacy.

Ying Jie Zhu, Jun‐Li Luo, Wenhui Liu, Fang Ma, Gui Yang, Xinyu Jia, Bao Sun
article en

Abstract

2651 Background: The potential predicative and therapeutic value of Bifidobacterium in immune checkpoint inhibitors (ICIs) treatment has been widely studied. However, the value of its genetic determinants on the prognosis of ICIs treatment remains unclear. Methods: we examined the associations of 11 single nucleotide polymorphisms (SNPs) located at host genes determining Bifidobacterium abundance with the outcomes of ICIs treatment in 370 eligible cancer patients. Results: Cox regression analysis revealed that rs3739020 TT carriers experienced significantly extended OS ( P -value = 0.003, adjusted HR = 0.46, 95%CI = 0.27-0.77) compared with GG+TG carriers. The LCT haplotype analysis showed that the lactose poor metabolizers exhibited significantly poorer OS ( P -value = 0.002, adjusted HR = 0.45, 95%CI = 0.27-0.74) than the extensive or intermediate metabolizers. In polygenic SNP analysis, the high galactose level carriers exhibited significantly prolonged OS ( P -value = 0.007, adjusted HR = 0.32, 95%CI = 0.14-0.73) and progression-free survival (PFS, P -value = 0.001, adjusted HR = 0.45, 95%CI = 0.29-0.71). All the four SNPs and the LCT metabolic phenotype were not associated with the occurrence of overall immune-related adverse events (irAEs). Genetically predicted Bifidobacterium abundance was significantly associated with an increased abundance of lactose metabolism pathway ( P -value = 0.012, Beta coefficient = 0.549). Conclusions: SNPs determining Bifidobacterium abundance in the lactose metabolism pathway have prognostic value for immunotherapy efficacy, and the lactose extensive and intermediate metabolizers exhibited better immunotherapy efficacy. The details of LCT metabolic phenotypes and the associations of LCT metabolic phenotypes with overall survival. LCT genotypes and their risk allele rs3739020G rs56263017C rs55809728A rs3739022A HR P Lactose extensive metabolizer (EM, no risk allele exist) TT TT GG GG Refernces Lactose inermediate metabolizer (IM, risk alleles exist in 1-3 SNPs) TG or GG TT GG GG 0.58,95%CI=0.33-0.99 0.049 TT TC or CC GG GG TT TT AA or GA GG TG or GG TT GG AA or GA TG or GG TC or CC GG GG TG or GG TT AA or GA GG TT TT GG AA or GA TT TC or CC AA or GA GG TT TC or CC GG AA or GA TG or GG TT AA or GA AA or GA TG or GG TC or CC AA or GA GG TG or GG TC or CC GG AA or GA TT TT AA or GA AA or GA TG or GG TC

Journal of Clinical OncologyVol. 43(16_suppl)
Central South University (CN), Second Xiangya Hospital of Central South University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 87%
Immunodeficiency and Autoimmune Disorders
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