Oligoprogression in NSCLC with Other Actionable Oncogenic Drivers Beyond EGFR and ALK: An Emerging Entity

Ilaria Mariangela Scaglione1, Adele Bonato1, Alessandra Dodi2,3

  • 1Section of Innovation Biomedicine-Oncology Area, Department of Engineering for Innovation Medicine (DIMI), University of Verona School of Medicine and Verona University Hospital Trust, 37134 Verona, Italy.

Insights

Oligoprogressive disease (OPD) in non-small-cell lung cancer (NSCLC) patients may benefit from local ablative treatment (LAT). Evidence for LAT in NSCLC with drivers other than EGFR/ALK is limited, highlighting a need for more research.

Area of Science:

  • Oncology
  • Medical Oncology
  • Lung Cancer Research

Background:

  • Oligoprogressive disease (OPD) presents unique challenges in non-small-cell lung cancer (NSCLC) management.
  • Local ablative treatment (LAT) shows survival benefits for OPD patients during systemic therapy.
  • The role of LAT in OPD is well-studied for EGFR-mutant and ALK-rearranged NSCLC but underexplored for other oncogenic drivers.

Purpose of the Study:

  • To review current data on standard treatments for NSCLC with OPD and drivers other than EGFR/ALK.
  • To specifically assess the role and evidence for LAT in this patient population during systemic treatment.
  • To identify gaps in knowledge and future research directions.

Main Methods:

  • Comprehensive literature search of PubMed and ClinicalTrials.gov.
  • Inclusion of data from case reports, retrospective series, and ongoing clinical trials.
  • Focus on NSCLC with actionable oncogenic drivers excluding EGFR and ALK.

Main Results:

  • Limited evidence currently supports the use of LAT in OPD for NSCLC with drivers other than EGFR/ALK.
  • Existing data primarily consists of case reports and small retrospective studies.
  • Several clinical trials are ongoing, indicating active research in this area.

Conclusions:

  • There is a significant unmet clinical need for robust evidence regarding LAT in OPD for NSCLC with non-EGFR/ALK drivers.
  • Systematic and multicentric data collection is crucial to generate stronger evidence.
  • Further research is warranted to optimize treatment strategies for these patients.

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