Comparative Efficacy of Neoadjuvant Nivolumab Plus Chemotherapy versus Conventional Comparator Treatments in Resectable Non-Small-Cell Lung Cancer: A Systematic Literature Review and Network Meta-Analysis

Author:

Girard Nicolas12,Besada Mariam3,Rogula Basia3,Lucherini Stefano4,Vo Lien5,Chaudhary Mohammad A.5,Goring Sarah3ORCID,Lozano-Ortega Greta3ORCID,Tran Mia5,Varol Nebibe4,Waser Nathalie6ORCID,Lee Jay M.7,Spicer Jonathan8ORCID

Affiliation:

1. Department of Medical Oncology, Institut Curie, 75005 Paris, France

2. Paris Saclay University, University of Versailles Saint-Quentin-en-Yvelines (UVSQ), 78000 Versailles, France

3. Broadstreet HEOR, Vancouver, BC V6A 1A4, Canada

4. Bristol Myers Squibb, Uxbridge UB8 1DH, UK

5. Bristol Myers Squibb, Lawrenceville, NJ 08648, USA

6. ICON Plc, Burlington, ON L7N 3G2, Canada

7. UCLA Health, Los Angeles, CA 90095, USA

8. Department of Thoracic Surgery, McGill University Health Center, Montreal, QC H3G 1A4, Canada

Abstract

Background: This study aimed to estimate the relative efficacy of neoadjuvant nivolumab in combination with chemotherapy (neoNIVO + CT) compared to relevant treatments amongst resectable non-metastatic non-small-cell lung cancer (rNSCLC) patients. Methods: Treatment comparisons were based on a network meta-analysis (NMA) using randomized clinical trial data identified via systematic literature review (SLR). The outcomes of interest were event-free survival (EFS) and pathological complete response (pCR). NeoNIVO + CT was compared to neoadjuvant chemotherapy (neoCT), neoadjuvant chemoradiotherapy (neoCRT), adjuvant chemotherapy (adjCT), and surgery alone (S). Due to the potential for effect modification by stage, all-stage and stage-specific networks were considered. Fixed-effect (FE) and random-effects Bayesian NMA models were run (EFS = hazard ratios [HR]; pCR = odds ratios [OR]; 95% credible intervals [CrI]). Results: Sixty-one RCTs were identified (base case = 9 RCTs [n = 1978 patients]). In the all-stages FE model, neoNIVO + CT had statistically significant EFS improvements relative to neoCT (HR = 0.68 [95% CrI: 0.49, 0.94]), S (0.59 [0.42, 0.82]), adjCT (0.66 [0.45, 0.96]), but not relative to neoCRT (HR = 0.77 [0.52, 1.16]). NeoNIVO + CT (5 RCTs) had statistically significant higher odds of pCR relative to neoCT (OR = 12.53 [5.60, 33.82]) and neoCRT (7.15 [2.31, 24.34]). Stage-specific model findings were consistent. CONCLUSIONS: This NMA signals improved EFS and/or pCR of neoNIVO + CT relative to comparators among patients with rNSCLC.

Funder

Bristol Myers Squibb

Publisher

MDPI AG

Reference73 articles.

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2. NCC Network (2023). NCCN Clinical Practice Guidelines in Oncology: Non-Small Cell Lung Cancer, NCC. Version 3.

3. Early and locally advanced non-small-cell lung cancer (NSCLC): ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up;Postmus;Ann. Oncol.,2017

4. PDQ Adult Treatment Editorial Board (2021, December 02). PDQ Non-Small Cell Lung Cancer Treatment, Available online: https://www.cancer.gov/types/lung/patient/non-small-cell-lung-treatment-pdq.

5. Tumor recurrence after complete resection for non-small cell lung cancer;Taylor;Ann. Thorac. Surg.,2012

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