Frontiers in Immunology (Nov 2022)

Proposed new prognostic model using the systemic immune-inflammation index for primary central nervous system lymphoma: A prospective-retrospective multicohort analysis

  • Shengjie Li,
  • Shengjie Li,
  • Shengjie Li,
  • Shengjie Li,
  • Shengjie Li,
  • Shengjie Li,
  • Zuguang Xia,
  • Zuguang Xia,
  • Jiazhen Cao,
  • Jiazhen Cao,
  • Jinsen Zhang,
  • Jinsen Zhang,
  • Jinsen Zhang,
  • Jinsen Zhang,
  • Jinsen Zhang,
  • Bobin Chen,
  • Tong Chen,
  • Xin Zhang,
  • Xin Zhang,
  • Xin Zhang,
  • Xin Zhang,
  • Xin Zhang,
  • Wei Zhu,
  • Wei Zhu,
  • Wei Zhu,
  • Wei Zhu,
  • Wei Zhu,
  • Danhui Li,
  • Wei Hua,
  • Wei Hua,
  • Wei Hua,
  • Wei Hua,
  • Wei Hua,
  • Ying Mao,
  • Ying Mao,
  • Ying Mao,
  • Ying Mao,
  • Ying Mao

DOI
https://doi.org/10.3389/fimmu.2022.1039862
Journal volume & issue
Vol. 13

Abstract

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PurposeThe systemic immune-inflammation index (SII) has been considered a novel prognostic biomarker in several types of lymphoma. Our aims were to determine the best statistical relationship between pretreatment SII and survival and to combination of SII and the Memorial Sloan Kettering Cancer Center model (MSKCC) to derive the best prognostic mode in primary central nervous system lymphoma (PCNSL).MethodsPretreatment SII and clinical data in 174 newly diagnosed PCNSL patients were included from two retrospective discovery cohorts (n = 128) and one prospective validation cohort (n = 46). A generalized additive model, Kaplan-Meier curve, and Cox analysis were performed. The high risk versus low risk of SII-MSKCC for the PCNSL cutoff point (0–1 vs. 2–4) was determined by the minimum P-value approach.ResultsThe SII showed a U-shaped relationship with the risk of overall survival (OS; P = 0.006). The patients with low SII or high SII had poorer OS and progression-free survival (PFS) than those with median SII. For PFS and OS, SII-MSKCC was a better predictor than MSKCC alone. The area under the receiver operating characteristic curve of the SII-MSKCC score was 0.84 for OS and 0.78 for PFS in the discovery cohorts. The predictive value of the SII-MSKCC score (OS, 0.88; PFS, 0.95) was verified through the validation cohort. Multivariable Cox analysis and Kaplan-Meier curve showed excellent performance for SII-MSKCC, with significant separation of two groups and better performance than MSKCC alone.ConclusionsWe propose a new prognostic model using SII, age, and Karnofsky score that outperforms MSKCC alone and enables individualized estimates of patient outcome.

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