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Multicenter Study
. 2025 May;26(3):253-261.
doi: 10.1016/j.cllc.2024.12.010. Epub 2024 Dec 25.

Surgical and Pathological Results Following Neoadjuvant Nivolumab and Platinum-Based Chemotherapy for Locally Advanced Resectable NSCLC: A Multicentre Real-World Series From England

Affiliations
Multicenter Study

Surgical and Pathological Results Following Neoadjuvant Nivolumab and Platinum-Based Chemotherapy for Locally Advanced Resectable NSCLC: A Multicentre Real-World Series From England

Alessandro Brunelli et al. Clin Lung Cancer. 2025 May.

Abstract

Background: To evaluate the real-world surgical and pathological outcomes following neoadjuvant nivolumab in combination with chemotherapy in a multicentre national cohort of patients.

Methods: Retrospective analysis on consecutive patients treated in three tertiary referral hospitals in UK with neoadjuvant chemotherapy and immunotherapy (nivolumab) for stage II-IIIB nonsmall cell lung cancer (March 2023-May 2024). Surgical and pathological outcomes were assessed.

Results: 130 patients started neoadjuvant treatment. 121 patients (93.1%) were able to proceed to surgery. 62% of patients had surgery more than 6 weeks after completion of the last neoadjuvant cycle. 91 operations (75.2%) were started using a minimally invasive approach with a conversion rate of 18.7%. The most frequent resection was lobectomy in 85% of patients. 30- and 90-days postoperative mortality rates were 3.3% and 5.8%. The pCR occurred in 38 patients (31.4% of the surgical patients), MPR in 57 patients (47.1% of the surgical patients). The incidence of pCR (P = .90) and MPR (P = .66) were similar in patients with clinical stage II and III. pCR rate was higher in patients with PD-L1 ≥50% compared to those with PD-L1 <50% (41.9% vs. 25.6%, P = .066). A higher pCR (44.7% vs. 23%, P = .012) and MPR (66% vs. 35.1%, P = .001) in squamous vs. non-squamous histology tumors.

Conclusions: The use of neoadjuvant chemo-ICI in the real clinical practice is safe and effective. The pathological response rates parallel those reported in trials and appear consistent across stages. Our findings provide real world data from a public healthcare system which will be valuable to inform multidisciplinary treatment selection for locally advanced resectable NSCLC.

Keywords: Chemotherapy; Immunotherapy; Lung cancer; Outcome; Surgery.

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Conflict of interest statement

Disclosure Dr. Alessandro Brunelli received consultancy fees for speaker honoraria and advisory Board roles with Astra Zeneca, BMS, Ethicon, MSD, Medela, Medtronic and Roche. Dr Pooja Bhatnagar received consultancy fees for speaker honoraria and advisory Board roles with Astra Zeneca, MSD, Roche, Pfizer and Takeda. Dr. Katy Clarke received consultancy fees for speaker honoraria with Astra Zeneca, MSD and Takeda Dr. Carles Escriu received consultancy fees for speaker honoraria with BMS. Kevin Franks received consultancy fees for speaker honoraria with Astra Zeneca Dr. Shobhit Baijal received consultancy fees for speaker honoraria and advisory Board roles with Abbvie, Agilent, Amgen, AstraZeneca, Boehringer Ingleheim, Bristol Myers-Squibb, Chugai, Daiichi Sankyo, FoundationOne, Gilead, GlaxoSmithKline, Janssen, Lilly, Merck Serono, Merck Sharp & Dohme, Novartis, PierreFabre, Pfizer, Regeneron, Roche, Servier, Sanofi and Takeda Dr. Kevin Franks received consultancy fees for speaker honoraria and advisory Board roles with AstraZeneca, Amgen, Biontech, Boehringer-Ingelheim, Bristol-Meyers-Squibb, ELEKTA, Genesis Cancer Care UK, Lilly, Novartis, Pierre Fabre, Roche and Takeda. Michael Schackcloth received consultancy fees for speaker honoraria and advisory Board roles with AstraZeneca and Roche. The remaining authors have stated that they have no conflicts of interest.

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