Quality over quantity: biopsy-anchored CT radiogenomics models outperform all-lesion training in a multi-tumour cohort despite a smaller sample size - Scorecard - MDSpire

Quality over quantity: biopsy-anchored CT radiogenomics models outperform all-lesion training in a multi-tumour cohort despite a smaller sample size

  • By

  • Diana Ivonne Rodríguez Sánchez

  • Julian Middelkoop

  • Thera Vanneste

  • Olga Maxouri

  • Stephan Ursprung

  • Sajjad Rostami

  • Nino Bogveradze

  • Kalina Chupetlovska

  • Francesca Castagnoli

  • Federica Landolfi

  • Eun Kyoung Hong

  • Andrea Delli Pizzi

  • Nicolo Gennaro

  • Warissara Jutidamrongphan

  • Liliana Petrychenko

  • Petur Snaebjornsson

  • Zuhir Bodalal

  • Regina Beets-Tan

  • May 16, 2026

  • 0 min

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Clinical Scorecard: Prioritizing Quality: Biopsy-Based CT Radiogenomics Models Surpass All-Lesion Training in a Multi-Tumor Analysis Despite Reduced Sample Size

At a Glance

CategoryDetail
ConditionSolid Tumors with EGFR Mutations
Key MechanismsIntra- and inter-tumoral heterogeneity affecting mutation concordance
Target PopulationPatients with solid tumors undergoing biopsy for next-generation sequencing
Care SettingOncology, specifically within institutions conducting precision oncology

Key Highlights

  • Single tissue samples may not represent the genomic complexity of malignancies.
  • EGFR mutations show significant discordance rates, especially in treatment-exposed patients.
  • Radiogenomics can non-invasively capture tumor biology across visible disease.
  • Training models on biopsy-confirmed lesions improves generalizability.
  • The study establishes a framework for integrating radiogenomics with tissue testing.

Guideline-Based Recommendations

Diagnosis

  • Utilize comprehensive imaging to assess tumor heterogeneity.
  • Confirm EGFR mutation status through biopsy and consider lesion-specific testing.

Management

  • Incorporate radiogenomic data to guide targeted therapy decisions.
  • Consider lesion-level molecular heterogeneity when planning treatment.

Monitoring & Follow-up

  • Regularly assess imaging features to track tumor response and evolution.
  • Monitor for discordance in mutation status across lesions.

Risks

  • Assuming molecular homogeneity can lead to misinformed treatment decisions.
  • Label noise from biopsy-derived mutation status may affect model accuracy.

Patient & Prescribing Data

Patients with solid tumors, particularly those with EGFR mutations.

Targeted therapies should be informed by comprehensive molecular profiling.

Clinical Best Practices

  • Use biopsy-confirmed lesions for training radiogenomic models.
  • Integrate imaging and genomic data to enhance precision oncology outcomes.
  • Adhere to CLEAR criteria for radiomics research reporting.

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