Early Changes in Lymphocyte/Monocyte Ratio on Treatment as a Prognostic Marker to Predict Overall Survival in Patients with Advanced Cancer Treated with Immune Checkpoint Inhibitors.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
1077 patients treated with ICI, including 880 patients with both baseline and on-treatment assessment of LMR.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In multivariable analysis, high on-treatment LMR was most highly associated with fewer deaths compared to low on-treatment LMR, regardless of baseline LMR. [CONCLUSIONS] We observed that baseline LMR, as well as change in LMR from baseline after the first cycle of ICI were associated with OS in cancer patients treated with ICI.
[BACKGROUND] A low absolute lymphocyte/monocyte ratio (LMR) in the peripheral blood is associated with poor prognosis in various cancers; however, its role as a predictive biomarker has not been well
- 95% CI 7.8-10.3
APA
Patel SH, Zhao S, et al. (2025). Early Changes in Lymphocyte/Monocyte Ratio on Treatment as a Prognostic Marker to Predict Overall Survival in Patients with Advanced Cancer Treated with Immune Checkpoint Inhibitors.. Cancer investigation, 43(9), 717-725. https://doi.org/10.1080/07357907.2025.2557004
MLA
Patel SH, et al.. "Early Changes in Lymphocyte/Monocyte Ratio on Treatment as a Prognostic Marker to Predict Overall Survival in Patients with Advanced Cancer Treated with Immune Checkpoint Inhibitors.." Cancer investigation, vol. 43, no. 9, 2025, pp. 717-725.
PMID
41070402 ↗
Abstract 한글 요약
[BACKGROUND] A low absolute lymphocyte/monocyte ratio (LMR) in the peripheral blood is associated with poor prognosis in various cancers; however, its role as a predictive biomarker has not been well defined in the era of treatment with immune checkpoint inhibitors (ICIs).
[METHODS] We queried a database of advanced cancer patients treated with at least 1 dose of ICI from 2011 to 2019 to study the association of LMR with overall survival (OS). We calculated LMR at baseline and a median of 21 days after the first cycle of ICI (on-treatment LMR) and considered it low if < 2 and high if ≥ 2. OS was calculated from the initiation of ICI to the date of death or censored at the last follow-up.
[RESULTS] We identified 1077 patients treated with ICI, including 880 patients with both baseline and on-treatment assessment of LMR. Patients with low baseline LMR had shorter median OS of 8.8 months (95% CI 7.8-10.3) compared to patients with high baseline LMR (19.4 months [95% CI 16.1-21.7], < 0.0001). Patients with low baseline LMR whose on-treatment LMR increased to high had longer median OS compared to those whose on-treatment LMR remained low (16.8 vs 7.8 months, < 0.002). Patients with high baseline LMR whose on-treatment LMR remained high had longer median OS compared to patients with low on-treatment LMR (23.9 vs 9.2 months, < 0.001). In multivariable analysis, high on-treatment LMR was most highly associated with fewer deaths compared to low on-treatment LMR, regardless of baseline LMR.
[CONCLUSIONS] We observed that baseline LMR, as well as change in LMR from baseline after the first cycle of ICI were associated with OS in cancer patients treated with ICI.
[METHODS] We queried a database of advanced cancer patients treated with at least 1 dose of ICI from 2011 to 2019 to study the association of LMR with overall survival (OS). We calculated LMR at baseline and a median of 21 days after the first cycle of ICI (on-treatment LMR) and considered it low if < 2 and high if ≥ 2. OS was calculated from the initiation of ICI to the date of death or censored at the last follow-up.
[RESULTS] We identified 1077 patients treated with ICI, including 880 patients with both baseline and on-treatment assessment of LMR. Patients with low baseline LMR had shorter median OS of 8.8 months (95% CI 7.8-10.3) compared to patients with high baseline LMR (19.4 months [95% CI 16.1-21.7], < 0.0001). Patients with low baseline LMR whose on-treatment LMR increased to high had longer median OS compared to those whose on-treatment LMR remained low (16.8 vs 7.8 months, < 0.002). Patients with high baseline LMR whose on-treatment LMR remained high had longer median OS compared to patients with low on-treatment LMR (23.9 vs 9.2 months, < 0.001). In multivariable analysis, high on-treatment LMR was most highly associated with fewer deaths compared to low on-treatment LMR, regardless of baseline LMR.
[CONCLUSIONS] We observed that baseline LMR, as well as change in LMR from baseline after the first cycle of ICI were associated with OS in cancer patients treated with ICI.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Lymphocyte Count
- Monocytes
- Prognosis
- Biomarkers
- Tumor
- Immune Checkpoint Inhibitors
- Neoplasms
- Follow-Up Studies
- Retrospective Studies
- Neoplasm Staging
- Lymphocytes
- Humans
- Male
- Female
- Middle Aged
- Aged
- Kaplan-Meier Estimate
- Biomarker
- Immune checkpoint inhibitor (ICI)
- Immunotherapy
- Lymphocyte/monocyte ratio (LMR)
- Overall survival
- Tumor microenvironment (TME)
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