AI Article Synopsis

  • - Current guidelines suggest that molecular genotyping is essential for patients diagnosed with metastatic nonsquamous non-small-cell lung cancer (mNSq NSCLC), but its effect on overall survival (OS) before first-line therapy was unclear.
  • - A study included 326 patients, finding that 80% had their genotyping results available before treatment, which was linked to a significantly longer OS compared to those without results (adjusted hazard ratio of 0.43).
  • - The research also showed that using both tissue and plasma testing increased the chances of having genotyping results available prior to treatment, indicating the importance of molecular testing in improving patient outcomes.

Article Abstract

Purpose: Current guidelines recommend molecular genotyping for patients newly diagnosed with metastatic nonsquamous (mNSq) non-small-cell lung cancer (NSCLC). The association between availability of molecular genotyping before first line (1L) therapy and overall survival (OS) is not known.

Methods: We conducted a real-world cohort study using electronic health records in patients newly diagnosed with mNSq NSCLC. Cox proportional-hazards multivariable regression models were constructed to examine the association between OS and test result availability before 1L therapy, adjusting for covariates. Additional analyses were conducted to assess the consistency and strength of the relationship. Multivariable logistic regression models were used to examine the association between concurrent tissue and plasma testing ( tissue alone) and result availability.

Results: Three hundred twenty-six patients were included, 80% (261/326) with results available before 1L (available testing group), and 20% (65/326) without results available (unavailable testing group). With 14.2-month median follow-up, patients in the available testing group had significantly longer OS relative to the unavailable testing group (adjusted hazard ratio, 0.43; 95% CI, 0.30 to 0.62; < .0001). The adjusted odds of availability of results before 1L therapy was higher with concurrent tissue and plasma testing ( tissue testing alone; adjusted odds ratio, 2.06; 95% CI, 1.09 to 3.90; = .026).

Conclusion: Among patients with mNSq NSCLC in a real-world cohort, availability of molecular genotyping results before 1L therapy was associated with significantly better OS. Concurrent tissue and plasma testing was associated with a higher odds of availability of results before 1L therapy. These findings warrant renewed attention to the completion of molecular genotyping before 1L therapy.

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Source
http://dx.doi.org/10.1200/PO.23.00191DOI Listing

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