Are PD-L1 and molecular markers from pleural fluid specimens reliable enough to guide decision making in metastatic NSCLC?
Do you use pleural fluid cytology for molecular testing in newly diagnosed NSCLC?
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There is some good data to support the adequacy of malignant pleural effusion specimens as a source of tissue to detect actionable molecular and genetic alterations, if the cellularity of the cell block made from the fluid is adequate (Yang S-R, et al., J Mol Diagn 2018 is one such example). Many la...
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In terms of molecular markers – pleural fluid is probably fine, though again, I am sending ctDNA on almost all newly diagnosed patients regardless. Regarding PD-L1: testing is not perfect, and I try to take this into account with all therapeutic decision-making. PD-L1 score can vary a lot by site of...
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Agree that NGS testing can be done if the specimen (cell block) is adequate. PDL-1 testing is a bit more complex given known interobserver and tumor site heterogeneity. However, a recent review article showed good correlation between cytology vs tissue-based PDL-1 testing (Mansour et al., PMID 34233...
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Depending on how the specimen is prepared and the number of cells, often PD-L1 and moleculars are able to be performed based on pleural fluid specimens. If I am worried the sample will be insufficient, I will send a liquid biopsy (which unless the molecular results are complete, I typically send any...
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