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JK5G postbiotics attenuate immune-related adverse events in NSCLC patients by regulating gut microbiota: a randomized
Mengting Chen1, Liling Ma2, Huiqing Yu1,2
1Department of Clinical Nutrition, Chongqing University Cancer Hospital, School of Medicine, Chongqing University, Chongqing, China.
Scope:
This study aimed to evaluate the effects of JK5G postbiotics to regulate imbalanced gut microbiota and its impacts on the efficacy and incidence rate of immune-related adverse events (irAEs) in non-small-cell lung cancer (NSCLC) patients treated with immune checkpoint inhibitors (ICIs).
Methods:
This randomized, double-blind, placebo-controlled trial was conducted in China and included non-squamous or squamous NSCLC patients without EGFR, ROS1, and ALK alteration, treatment-naive, and stage IIIb-IV. Patients were randomly (1:1) divided into two groups to receive four cycles (three weeks for each cycle) of programmed cell death-1 (PD-1) plus chemotherapy plus placebo (control group, n = 30) or to receive PD-1 plus chemotherapy plus JK5G postbiotics (JK5G group, n = 30). The primary endpoint was objective response rate. The secondary endpoints were quality of life (QoL), adverse effects, and the 16S DNA sequencing of gut microbiota, blood inflammatory cytokines, and lymphocyte subsets. This study was registered at www.chictr.org.cn (ChiCTR2200064690).
Results:
Sixty patients were enrolled. The objective response rate was 36.67% (11/30) in the control group and 50.00% (15/30) in the JK5G group (p = 0.297). The JK5G group had better QoL and nutritional levels, as well as lower depression symptoms than the control group (all p < 0.05). Moreover, the JK5G group had a lower incidence of anemia (63.33% vs. 13.33%, p < 0.001), decreased lymphocyte count (20.00% vs. 0%, p = 0.010), decreased appetite (53.33% vs. 16.67%, p = 0.003), nausea (33.33% vs. 6.67%, p = 0.010), and asthenia (30.00% vs. 6.67%, p = 0.017) than the control group. Moreover, JK5G attenuated gut microbiota imbalance, accompanied by increased Faecalibacterium, Ruminococcaceae, and fecal butyrate concentration, and diminished Escherichia-Shigella. Furthermore, JK5G administration significantly decreased the levels of pro-inflammatory markers, including TNF-α, IL-2, and C-reactive protein (CRP) (all p < 0.05). Significant increases in CD3+CD4+ T cells and CD4/CD8 ratio were observed in the peripheral blood of JK5G group patients (all p < 0.05). The enterotype data showed that patients were clustered into Blautia (E1) and Escherichia-Shigella (E2) enterotypes, and JK5G postbiotics intervention might be related to enterotype modulations.
Conclusion:
Our current findings indicated that JK5G postbiotics might attenuate irAEs, and enhance the QoL and nutrition levels of advanced NSCLC patients who received ICIs. JK5G postbiotics could also improve the gut microbiota structures and ameliorate the tumor microenvironment and inflammation.
Clinical Trial Registration:
www.chictr.org.cn, identifier ChiCTR2200064690.
Insights
JK5G postbiotics may reduce immune-related adverse events and improve quality of life in non-small-cell lung cancer patients receiving immune checkpoint inhibitors. This intervention also positively impacts gut microbiota and inflammation.
Area of Science:
- Oncology
- Microbiology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) are vital in treating non-small-cell lung cancer (NSCLC).
- Gut microbiota dysbiosis can influence ICI efficacy and immune-related adverse events (irAEs).
Purpose of the Study:
- To evaluate JK5G postbiotics' effect on gut microbiota regulation.
- To assess JK5G postbiotics' impact on irAEs and treatment efficacy in NSCLC patients receiving ICIs.
Main Methods:
- Randomized, double-blind, placebo-controlled trial in China.
- NSCLC patients (stage IIIb-IV) received PD-1 plus chemotherapy with either placebo or JK5G postbiotics.
- Primary endpoint: objective response rate. Secondary endpoints: quality of life, irAEs, gut microbiota, inflammatory markers, and lymphocyte subsets.
Main Results:
- JK5G group showed improved quality of life, nutrition, and reduced depression.
- Lower incidence of anemia, decreased lymphocyte count, appetite loss, nausea, and asthenia in the JK5G group.
- JK5G attenuated gut microbiota imbalance, increased beneficial bacteria (e.g., Faecalibacterium), and reduced pro-inflammatory markers (TNF-α, IL-2, CRP).
Conclusions:
- JK5G postbiotics may attenuate irAEs and enhance quality of life in advanced NSCLC patients on ICIs.
- JK5G postbiotics improve gut microbiota structure, ameliorate the tumor microenvironment, and reduce inflammation.
- Further research into JK5G's role in modulating gut microbiota and immune responses is warranted.
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