The critical role of PD-L1 expression in immunotherapy for advanced non-small cell lung cancer
Recently, we were highly intrigued by the study published in this journal by Xu et al. (1), which examines the maintenance immunotherapy following microwave ablation (MWA) combined with drug-eluting bead bronchial arterial chemoembolization (DEB-BACE) in patients with advanced non-small cell lung cancer (NSCLC). We are extremely grateful for the valuable insights offered by the authors. Although this study offers significant reference points for future clinical practice, it is important to acknowledge several limitations that, if resolved, could strengthen the reliability and validity of the findings.
First, the article is deficient in data on the baseline expression levels of programmed cell death-ligand 1 (PD-L1) among the patients. Although the authors noted that patients in Group A had high PD-L1 expression, specific details regarding PD-L1 expression should be provided. Furthermore, a prospective study indicated that in the immunochemotherapy group, The pathological complete remission (pCR) rates varied with PD-L1 expression levels: 9.0% for <1%, 16.3% for 1–49%, and 27.5% for ≥50% (2). There was a positive correlation between the short-term efficacy of immunochemotherapy and PD-L1 expression. Besides, in studies of perioperative immunotherapy, the decrease in the likelihood of disease progression, recurrence, and demise in the immunotherapy group with PD-L1 positivity (PD-L1 expression ≥1%) was greater than that in the negative group (PD-L1 expression <1%), suggesting that it could be used as a biomarker to predict the short-term efficacy and survival benefit of perioperative immunotherapy in resectable NSCLC (2-4).
Additionally, in observational trials, what matters more than the P value is the size of differences between groups, or the expert opinion on the importance of a predictor (5). Moreover, in Tab. 1 (1), the numbers of patients in Groups A, B, and C under the indications for interventional therapy—resistance to standard treatments—were incorrect, and the P value needs revision.
To summarize, this study offers valuable perspectives on the maintenance immunotherapy following MWA combined with DEB-BACE in the treatment of advanced NSCLC. Nevertheless, tackling the previously mentioned challenges in subsequent research endeavors could strengthen the study’s findings and provide a more effective direction for clinical applications.
Appendix 1: Response to “The critical role of PD-L1 expression in immunotherapy for advanced non-small cell lung cancer”
Acknowledgments
None.
Footnote
Funding: This study was supported by
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://qims.amegroups.com/article/view/10.21037/qims-2025-209/coif). The authors have no conflicts of interest to declare.
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