Predictive value of NRI, NLR, PLR and LMR for therapeutic efficacy and prognosis in advanced rectal cancer patients treated with PD-1/PD-L1 immunotherapy - Scorecard - MDSpire

Predictive value of NRI, NLR, PLR and LMR for therapeutic efficacy and prognosis in advanced rectal cancer patients treated with PD-1/PD-L1 immunotherapy

  • By

  • Mengli Gao

  • Zhe Gao

  • Yanan Wang

  • Wenguang Song

  • May 28, 2026

  • 0 min

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Clinical Scorecard: Evaluating the Predictive Significance of NRI, NLR, PLR, and LMR for Treatment Outcomes and Prognosis in Advanced Rectal Cancer Patients Undergoing PD-1/PD-L1 Immunotherapy

At a Glance

CategoryDetail
Condition
Key MechanismsNutritional Risk Index (NRI), Neutrophil-to-Lymphocyte Ratio (NLR), Platelet-to-Lymphocyte Ratio (PLR), Lymphocyte-to-Monocyte Ratio (LMR)
Target Population
Care Setting

Key Highlights

  • Retrospective analysis of 172 advanced rectal cancer patients
  • Optimal cut-off values: NLR 2.50, PLR 142.23, LMR 3.92, NRI 50.45
  • High NLR and PLR associated with shorter median progression-free survival (PFS) and overall survival (OS)
  • NLR≥2.50 identified as an independent biomarker for poor efficacy and prognosis
  • Correlation between nutritional and inflammatory indicators and immunotherapy outcomes

Guideline-Based Recommendations

Diagnosis

  • Histopathological confirmation of rectal adenocarcinoma
  • Staging according to AJCC Rectal Cancer Staging System

Management

  • Consider PD-1/PD-L1 inhibitors for eligible patients
  • Evaluate nutritional and inflammatory biomarkers for treatment planning

Monitoring & Follow-up

  • Regular assessment of NRI, NLR, PLR, and LMR during treatment

Risks

  • High NLR and PLR are independent risk factors for shortened PFS and OS

Patient & Prescribing Data

Patients aged > 18 years with advanced rectal cancer, staged III to IV

Patients received at least 2 cycles of PD-1/PD-L1 inhibitor therapy, with or without combination therapies

Clinical Best Practices

  • Utilize NRI, NLR, PLR, and LMR as predictive biomarkers for immunotherapy efficacy
  • Incorporate multidisciplinary team assessments for treatment eligibility
  • Monitor for potential complications and treatment responses regularly

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