Development and validation of a pre-chemotherapy nomogram integrating systemic immune-inflammation index and prognostic nutritional index to predict severe adjuvant toxicity in colorectal cancer - Scorecard - MDSpire

Development and validation of a pre-chemotherapy nomogram integrating systemic immune-inflammation index and prognostic nutritional index to predict severe adjuvant toxicity in colorectal cancer

  • By

  • Wenjing Li

  • Hua Zhang

  • Jie Wu

  • Liyan Jin

  • May 11, 2026

  • 0 min

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Clinical Scorecard: Creation and assessment of a pre-chemotherapy nomogram utilizing the systemic immune-inflammation index and prognostic nutritional index to forecast significant adjuvant toxicity in colorectal cancer

At a Glance

CategoryDetail
ConditionColorectal Cancer (Stage II/III)
Key MechanismsSystemic Immune-Inflammation Index (SII) and Prognostic Nutritional Index (PNI) as predictors of chemotherapy-induced toxicity.
Target PopulationPatients with stage II/III colorectal cancer receiving oxaliplatin-based adjuvant chemotherapy.
Care SettingOncology outpatient and inpatient settings.

Key Highlights

  • 25.5% of patients experienced severe chemotherapy-induced toxicity (CIT).
  • High SII and low PNI are independent risk factors for severe CIT.
  • The nomogram showed excellent discrimination and calibration for predicting toxicity.
  • Patients in the high-risk group had significantly shorter therapy duration and lower dose intensity.
  • The nomogram provides a cost-effective tool for risk stratification.

Guideline-Based Recommendations

Diagnosis

  • Utilize SII and PNI as baseline markers for assessing risk of severe CIT.

Management

  • Implement risk-adapted strategies including nutritional prehabilitation and dose adjustments for high-risk patients.

Monitoring & Follow-up

  • Monitor patients with elevated SII and decreased PNI closely for adverse events.

Risks

  • Severe CIT can lead to dose reductions, treatment delays, and compromised long-term outcomes.

Patient & Prescribing Data

306 patients with stage II/III CRC receiving oxaliplatin-based chemotherapy.

High-risk patients experienced a median therapy duration of 4.1 months and lower oxaliplatin relative dose intensity.

Clinical Best Practices

  • Incorporate SII and PNI into routine pre-chemotherapy assessments.
  • Use the nomogram to guide personalized treatment plans.
  • Consider proactive growth factor support for patients identified as high-risk.

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