SynthesisJournal of robotic surgery2026
Robotic-assisted versus video-assisted thoracoscopic surgery for non-small cell lung cancer after neoadjuvant immunotherapy: a systematic review and meta-analysis.
Synthesis in Journal of robotic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Administering upfront immunomodulatory agents has completely redefined the clinical pathways for operable non-small cell lung cancer (NSCLC); however, the subsequent inflammatory response and hilar fibrosis have increased the technical complexity of surgical resections. Although robotic-assisted thoracic surgery (RATS) offers theoretical advantages in visualization and precision over video-assisted thoracoscopic surgery (VATS) to address these challenges, comparative evidence between the two platforms in the post-immunotherapy setting remains limited. This investigation sought to juxtapose the operative viability and safety metrics between robotic and video-assisted thoracic platforms following neoadjuvant immunotherapy for NSCLC. A systematic search was conducted across PubMed, Cochrane, and EMBASE databases, identifying five studies involving 984 patients. Analyzed outcomes included conversion to open thoracotomy, operative time, intraoperative bleeding, complete resection rate, blood transfusion, lymph node yield, and explored lymph node stations. RATS was associated with a significantly lower rate of conversion to thoracotomy (OR 0.28, 95% CI 0.13–0.65; P = 0.003), as well as more dissected lymph nodes (MD 4.04, 95% CI 0.93–7.16; P = 0.01) and explored lymph node stations (MD 1.22, 95% CI 0.26–2.18; P = 0.01). There were no major differences in rates of complete resection, length of surgery, blood loss, or the need for transfusions. Both robotic surgery and video-thoracoscopy demonstrated equivalent perioperative and oncological safety. However, RATS was associated with significantly lower rates of conversion to thoracotomy, particularly in cases involving dense hilar fibrosis, and achieved a more comprehensive lymph node assessment compared to VATS.
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Registered trials
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