Feasibility and safety of video-assisted thoracic surgery after neoadjuvant chemoimmunotherapy in non-small cell lung cancer: A single-centre experience


Çetinkaya Ç., Keskin S., Öztürk M. A., Saglam E. K., YAMAN M., Yildizeli B., ...Daha Fazla

Journal of Minimal Access Surgery, cilt.22, sa.2, ss.173-179, 2026 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 22 Sayı: 2
  • Basım Tarihi: 2026
  • Doi Numarası: 10.4103/jmas.jmas_93_25
  • Dergi Adı: Journal of Minimal Access Surgery
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, Directory of Open Access Journals
  • Sayfa Sayıları: ss.173-179
  • Anahtar Kelimeler: Neoadjuvant chemoimmunotherapy, non-small cell lung cancer, video-assisted thoracic surgery
  • İstanbul Yeni Yüzyıl Üniversitesi Adresli: Evet

Özet

Introduction: Neoadjuvant chemoimmunotherapy has emerged as a promising strategy in the multimodal treatment of locally advanced non-small cell lung cancer (NSCLC). However, concerns remain regarding its impact on surgical complexity and the feasibility of video-assisted thoracic surgery (VATS) in this setting. Patients and Methods: Between April 2021 and August 2024, 17 patients who received neoadjuvant chemoimmunotherapy (PD-1 inhibitor plus chemotherapy) underwent lung resection. A significant proportion of cases (58.8%) were managed through VATS (primarily biportal approach), with no conversions to open surgery. The remaining patients underwent thoracotomy or Dartavelle incision due to anatomical complexity. Results: The mean operative time was 135 ± 25 min for VATS and 172.9 ± 30 min for open surgery (P = 0.068). While hospital stay was similar between VATS (5.9 days) and open surgery (6.4 days) (P = 0.449), intensive care unit stay was significantly shorter in the VATS group (0.5 vs. 1.3 days, P = 0.007). Significant tumour downstaging was observed in 88.2% of patients, with four achieving complete pathological response and three demonstrating a major pathological response (P < 0.05). Post-operative complications were observed in 41.2% of patients, but no 90-day mortality occurred. Conclusion: VATS appears to be a feasible and safe approach for selected NSCLC patients after neoadjuvant chemoimmunotherapy, demonstrating favourable short-term outcomes. These findings contribute to the growing evidence supporting minimally invasive surgery as a viable option in complex, locally advanced cases following immunotherapy.