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Cost-Effectiveness of Pembrolizumab as First-Line Treatment for PD-L1 Positive NSCLC: A Systematic Review Muhammad Akbar Ramadhan Munandar; Hendra Priatna Munandar; Liana Herlina
The International Journal of Medical Science and Health Research Vol. 23 No. 2 (2025): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/h3zdy035

Abstract

Introduction: For patients with advanced non-small cell lung cancer (NSCLC) without actionable driver mutations, first-line treatment has been revolutionized by immune checkpoint inhibitors (ICIs), particularly pembrolizumab. While pivotal trials demonstrate superior efficacy of pembrolizumab monotherapy in high PD-L1 expressors (TPS ≥50%) and pembrolizumab-chemotherapy combinations in broader populations, real-world effectiveness, long-term outcomes, and economic sustainability require comprehensive evaluation (Addeo et al., 2019; Rodríguez-Abreu et al., 2021). Methods: This systematic review synthesizes evidence from randomized controlled trials (RCTs), real-world observational studies, and economic evaluations. Literature was sourced from databases including PubMed, Google Scholar, Semantic Scholar, Springer, Wiley Online Library up to 2025. Analyses encompass efficacy (overall survival [OS], progression-free survival [PFS]), safety (immune-related adverse events [irAEs]), and cost-effectiveness (incremental cost-effectiveness ratios [ICERs]). Results: Pembrolizumab-based regimens consistently demonstrate superior OS and PFS compared to chemotherapy alone. In KEYNOTE-024, pembrolizumab monotherapy in PD-L1 TPS ≥50% significantly improved median OS (30.0 vs 14.2 months) (Lisberg et al., 2017). KEYNOTE-189 established pembrolizumab-pemetrexed-platinum as standard for non-squamous NSCLC, showing a 51% reduction in risk of death (Rodríguez-Abreu et al., 2021). Real-world studies confirm this efficacy but note variable outcomes in underrepresented subgroups (Verschueren et al., 2023; Yang et al., 2023). Safety profiles are manageable but distinct, with increased irAEs. Economic analyses show pembrolizumab is cost-effective in the US and several European countries at specific willingness-to-pay thresholds, though results are sensitive to drug costs and healthcare system context (Huang et al., 2017; Chouaid et al., 2019; Kuznik et al., 2021). Discussion: The transformative benefit of pembrolizumab is unequivocal, establishing a new therapeutic paradigm. However, challenges remain in optimizing patient selection beyond PD-L1, managing long-term toxicity and financial toxicity, and integrating novel combinations. The discussion delves into efficacy nuances, safety management, economic implications, and future directions including biomarker refinement and dosing strategies. Conclusion: Pembrolizumab, alone or with chemotherapy, is a cornerstone of first-line advanced NSCLC treatment, offering sustained survival benefits. To maximize its value, future efforts must focus on predictive biomarker development, personalized treatment algorithms, cost-containment strategies, and equitable access.
Peripheral Neuropathy Associated with Linezolid Dosage in MDR-TB: A Systematic Review Muhammad Akbar Ramadhan Munandar; Abdurrachman Machfudz; Hendra Priatna Munandar; Liana Herlina
The International Journal of Medical Science and Health Research Vol. 25 No. 2 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/8fm3z016

Abstract

Introduction: Linezolid is a critical component of modern regimens for multidrug-resistant tuberculosis (MDR-TB) and extensively drug-resistant tuberculosis (XDR-TB). However, its use is limited by significant adverse effects, particularly peripheral neuropathy (PN). The precise relationship between linezolid dosage, treatment duration, and the incidence of PN remains inadequately characterized, posing challenges for optimizing the risk-benefit balance in clinical practice (G. Maartens and C. Benson, 2015). Methods: This comprehensive systematic review analyzed 80 studies, including randomized controlled trials, prospective and retrospective cohorts, systematic reviews with meta-analyses, and case series. Studies were screened and included based on criteria focusing on MDR-TB populations, linezolid use for TB treatment, assessment of PN, provision of dosing details, human subjects, and appropriate study designs. Data were extracted on study characteristics, linezolid dosing regimens, PN incidence and characteristics, other neurological and non-neurological adverse effects, dose-response relationships, patient risk factors, and treatment outcomes (C. Padmapriyadarsini et al., 2022; N. Ahmad et al., 2018). Results: The evidence revealed substantial heterogeneity in linezolid dosing, ranging from 300 mg to 1200 mg daily for durations from weeks to over two years. A clear dose- and duration-dependent relationship with PN was observed. The highest incidence (81%) was reported with 1200 mg/day for 26 weeks, while shorter durations and lower doses (e.g., 600 mg/9 weeks) showed significantly lower rates (13-24%) (F. Conradie et al., 2020; F. Conradie et al., 2022). Structured dose-reduction strategies (e.g., 600 mg to 300 mg) achieved comparable treatment success rates (88-94%) with reduced PN incidence. Other dose-dependent toxicities included myelosuppression and optic neuropathy. Patient risk factors such as diabetes, malnutrition, and alcohol use appeared to modify PN risk (C. Padmapriyadarsini et al., 2024; Yanjun Li et al., 2025). Discussion: The findings underscore that PN risk is influenced by both daily dose and cumulative exposure. The delayed onset (typically after 3 months) suggests a mechanism of cumulative mitochondrial toxicity. While 600 mg daily for 26 weeks offers a favorable balance of efficacy (91% success) and manageable toxicity (24% PN), protocolized dose reduction after an initial intensive phase presents a viable strategy to minimize neurotoxicity while preserving therapeutic effectiveness. The variability in reported PN rates highlights the impact of population-specific risk factors and differences in adverse event monitoring intensity (Xin Zhang et al., 2015; N. Kwak et al., 2025). Conclusion: Peripheral neuropathy is a major, dose- and duration-dependent toxicity of linezolid in MDR-TB treatment. An initial dose of 600 mg daily, with consideration for structured reduction to 300 mg after 9-16 weeks, is supported by evidence as an optimal strategy to maximize efficacy while mitigating neurotoxicity. Active monitoring for PN, especially in patients with underlying risk factors, is essential from 8 weeks of treatment onwards. Future research should focus on therapeutic drug monitoring and personalized dosing strategies to further individualize therapy.