Neoadjuvant chemoimmunotherapy has shown a good therapeutic effect on non-small cell lung cancer, which also opens up the possibility of applying organ preservation strategies. This study investigated the feasibility of modified surgery after potent neoadjuvant chemoimmunotherapy in central type non-small cell lung cancer. In this multi-center retrospective cohort study, patients with central type non-small cell lung cancer who received 2-4 cycles of neoadjuvant chemoimmunotherapy between January 2019 and June 2022 at XXX Hospital and XXX Hospital were eligible. Patients were divided into modified and non-modified groups according to the extent of surgery, after which, safety and long-term prognosis of surgery were investigated. A total of 84 patients were enrolled. Of 36 (42.9%) patients who underwent modified surgery, 21 patients underwent lobectomy, 12 patients underwent lobectomy with bronchoplasty, 2 patients underwent sleeve lobectomy, and 1 patient underwent bilobectomy. The modification rate for the initially estimated pneumonectomy, sleeve lobectomy, and bilobectomy was 48.6%, 44.8%, and 30%, respectively. Grade II-V postoperative complications were found in 5 (13.9%) patients in the modified group and 17 (35.4%) patients in the non-modified group (relative risk, 0.393; 95% CI, 0.016 to 0.963; P=0.026). No significant difference was observed regarding the surgical approach, operative duration, blood loss, or R0 resection rate. The 2-year local recurrence rate was 3.7% (95% CI, 0.004-0.175) and 5.2% (95% CI, 0.012-0.168) in the modified group and non-modified group, respectively. The one-year PFS rate of modified and non-modified groups was 97.1% (95% CI, 83.7-99.8) and 86.9% (95% CI, 73.4-94.4), respectively, while two-year PFS were 89.8% (95% CI, 74.1-96.9) and 71.8% (95% CI, 56.7-83.4), respectively. Applying organ preservation strategies, i.e., undergoing modified surgery after neoadjuvant chemoimmunotherapy, is feasible for selected central-type NSCLC patients with favorable safety and long-term survival.