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Abstract Background and Objectives The role of cell‐free DNA (cfDNA) in operable nonsmall cell lung cancer (NSCLC) is unclear. This study was aimed to evaluate the feasibility for identification of cfDNA in pleural lavage fluid and its correlation with plasma in resectable NSCLCs. Methods Consecutively resected NSCLCs were evaluated for cfDNA levels in preoperative plasma (PLS1), intraoperative pleural‐lavage (PLV) and postoperative (at 1 month) plasma sample (PLS2). CfDNA was isolated and measured quantitatively by qPCR in a TaqMan probe‐detection approach using the human β‐actin gene as the amplifying target. Results All ( n = 34) except one were negative for malignant cells in PLV cytology. CfDNA could be isolated from all the three samples (PLS1, PLV, and PLS2) successfully in each patient. The median cfDNA levels in PLS1, PLV and PLS2 were 118 ng/mL (IQR 61−158), 167 ng/mL (IQR 59.9−179.9) and 103 ng/mL (IQR 66.5−125.4) respectively. The median follow‐up was 34.1 months (IQR 25.2−41.6). A significant overall‐survival (OS) and disease‐free survival (DFS) were recorded for patients with cfDNA level cut‐offs at 125, 170, and 100 ng/mL, respectively for PLS1, PLV, and PLS2. Patients with raised cfDNA in PLS1 (>125 ng/mL) and PLV (>170 ng/mL) had significantly poorer 2‐year OS, p = 0.005 and p = 0.012, respectively. The hazards (OS) were also higher for those with raised cfDNA in PLV (HR = 5.779, 95% CI = 1.162−28.745, p = 0.032). PLV (>170 ng/mL) had increased pleural recurrences ( p = 0.021) and correlated significantly with poorer DFS at 2‐years ( p = 0.001) with increased hazards (HR = 9.767, 95% CI = 2.098−45.451, p = 0.004). Multivariable analysis suggested higher cfDNA in PLV as a poor prognostic factor for both OS and DFS. Conclusions Among patients with operable NSCLC, it is feasible to identify cfDNA in pleural lavage and correlate PLV cfDNA with pleural recurrences and outcomes.
Saikia et al. (Mon,) studied this question.