Local ablative treatment for oligoprogression during immunotherapy in metastatic non-small-cell lung cancer: a systematic review and meta-analysis.

OncoimmunologyOct 31, 2026 (epub)

Ismaell Massalha, Adham Hijab, Reem Zabit et al.

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In 30 seconds

This PRISMA-compliant systematic review and meta-analysis assessed local ablative treatment (LAT), with continuation of the same immune checkpoint inhibitor, for oligoprogressive or oligo-resistant metastatic NSCLC during active immunotherapy. Twenty-two studies entered the qualitative synthesis; four studies contributed to each primary analysis. LAT-oriented management was associated with longer progression-free survival (pooled HR 0.45, 95% CI 0.33-0.62) and overall survival (pooled HR 0.41, 95% CI 0.27-0.63). The authors characterize the evidence as low certainty and predominantly observational, with no NSCLC-specific randomized trials.

Key findings

  • LAT-oriented management was associated with improved progression-free survival (pooled HR 0.45, 95% CI 0.33-0.62; 95% PI 0.28-0.74; I 2 = 0%).
  • Overall survival was also associated with LAT-oriented management (pooled HR 0.41, 95% CI 0.27-0.63; 95% PI 0.24-0.69; I 2 = 0%).
  • The qualitative synthesis included 22 studies, while four studies contributed to each primary analysis.

Why it matters

Focal progression during otherwise effective immunotherapy may not always indicate systemic treatment failure. The pooled associations suggest that ablating limited progressing disease while continuing the same immunotherapy could help preserve disease control in selected patients. However, the evidence base is low certainty and largely observational, so the findings support consideration rather than a definitive treatment strategy.

What to keep in mind

Evidence was predominantly observational and of low certainty; the abstract notes the absence of NSCLC-specific randomized trials.

Source

Published in Oncoimmunology. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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