Systemic immune-inflammation index as a prognostic biomarker to predict overall survival after primary stereotactic radiosurgery for brain metastases - Scorecard - MDSpire

Systemic immune-inflammation index as a prognostic biomarker to predict overall survival after primary stereotactic radiosurgery for brain metastases

  • By

  • Sukwoo Hong

  • Hirokazu Takami

  • Motoyuki Umekawa

  • Yuki Shinya

  • Hirotaka Hasegawa

  • Mariko Kawashima

  • Yosuke Kitagawa

  • Masashi Nomura

  • Shunsaku Takayanagi

  • Shota Tanaka

  • Nobuhito Saito

  • October 15, 2025

  • 0 min

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Clinical Scorecard: Prognostic Value of the Systemic Immune-Inflammation Index for Overall Survival Following Primary Stereotactic Radiosurgery in Patients with Brain Metastases

At a Glance

CategoryDetail
ConditionBrain metastases treated with primary stereotactic radiosurgery (SRS)
Key MechanismsSystemic immune-inflammation index (SII) and systemic inflammation response index (SIRI) reflect systemic inflammation and immune suppression, impacting tumor-promoting environment and immune surveillance
Target PopulationPatients with brain metastases undergoing primary fractionated SRS without prior whole-brain radiation or surgical resection for the target lesion
Care SettingSpecialized neurosurgical and radiation oncology centers performing SRS

Key Highlights

  • Brain metastases are the most common adult brain tumors with SRS as a primary local control treatment.
  • SII and SIRI, derived from routine CBC with differential, are objective biomarkers linked to prognosis in various cancers but understudied in brain metastases treated with SRS.
  • This study evaluates SII and SIRI as prognostic markers for overall survival and local tumor control after primary SRS.

Guideline-Based Recommendations

Diagnosis

  • Use routine pre-SRS complete blood count with differential to calculate SII and SIRI as adjunct prognostic biomarkers.
  • Apply Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM) criteria for tumor progression assessment.

Management

  • Plan SRS with a 1-mm tumor margin and prescribed dose based on fractionation schemes (e.g., 30 Gy in 3 fractions).
  • Exclude patients with prior whole-brain radiation or surgical resection for the target lesion to maintain prognostic accuracy of SII/SIRI.

Monitoring & Follow-up

  • Follow patients with MRI or enhanced CT post-SRS at regular intervals to assess local control and progression.
  • Monitor overall survival from end of SRS to death or last follow-up, with minimum 24 months follow-up for survivors.

Risks

  • Consider potential variability in subjective measures like Karnofsky Performance Status when using traditional prognostic tools.
  • Recognize that active infection or inflammation at time of CBC measurement can confound SII and SIRI values.

Patient & Prescribing Data

Adults with brain metastases undergoing primary fractionated SRS without prior radiation or surgery to the lesion

Higher pre-treatment SII and SIRI values are associated with worse overall survival, suggesting their utility in risk stratification and prognosis beyond traditional clinical indices.

Clinical Best Practices

  • Incorporate objective blood-based biomarkers such as SII and SIRI alongside clinical prognostic tools to improve survival prediction accuracy.
  • Ensure CBC is obtained prior to initiation of systemic cancer therapy and in absence of active infection or inflammation for reliable biomarker calculation.
  • Use standardized imaging and volumetric assessment methods for tumor measurement and progression evaluation post-SRS.
  • Apply rigorous statistical methods including multivariable Cox regression and validation of proportional hazards assumptions when analyzing prognostic factors.

References

Original Source(s)

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