MDT-BRIDGE: Neoadjuvant Durvalumab Plus Chemotherapy Followed by Either Surgery and Adjuvant Durvalumab or Chemoradiotherapy and Consolidation Durvalumab in Resectable or Borderline-resectable Stage IIB-IIIB NSCLC

被引:1
|
作者
Reck, Martin [1 ]
Nadal, Ernest [2 ]
Girard, Nicolas [3 ,4 ]
Filippi, Andrea R. [5 ,6 ]
Martin, Linda W. [7 ]
Gay, Carl M. [8 ]
Petersen, Cordula [9 ]
Gale, Davina [10 ]
Emeribe, Ugochinyere A. [11 ]
Georgoulia, Nefeli [11 ]
Perez, Ignacio E. Diaz [11 ]
Spicer, Jonathan D. [12 ]
机构
[1] German Ctr Lung Res, Airway Res Ctr North, Lung Clin Grosshansdorf, Grosshansdorf, Germany
[2] Inst Catala Oncol ICO Hosp, Med Oncol Dept, Barcelona, Spain
[3] Inst Curie, Inst Thorax Curie Montsouris, Paris, France
[4] UVSQ, Paris Saclay, Versailles, France
[5] Univ Milan, Dept Oncol & Hemato Oncol, Milan, Italy
[6] Fdn IRCCS Ist Nazl Tumori, Radiotherapy, Milan, Italy
[7] Univ Virginia, Dept Surg, Div Thorac Surg, Charlottesville, VA USA
[8] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[9] Univ Med Ctr Hamburg Eppendorf, Dept Radiotherapy & Radiat Oncol, Hamburg, Germany
[10] AstraZeneca, Cambridge, England
[11] AstraZeneca, Gaithersburg, MD USA
[12] McGill Univ, Hlth Ctr, Dept Surg, Montreal, PQ, Canada
关键词
Anti-PD-L1; Immunotherapy; Durvalumab; NSCLC; MDT; CELL LUNG-CANCER; PEMBROLIZUMAB; OUTCOMES; PLACEBO;
D O I
10.1016/j.clc.2024.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: In the AEGEAN trial, neoadjuvant durvalumab plus platinum-based chemotherapy (D+CT) followed by adjuvant durvalumab, versus neoadjuvant chemotherapy alone, significantly improved pathological complete response (pCR) rate and event-free survival (EFS) in patients with resectable NSCLC. In the PACIFIC trial, consolidation durvalumab significantly improved progression-free (PFS) and overall survival (OS) for patients with unresectable stage III NSCLC after chemoradiotherapy. Strong pathological and clinical outcomes with chemoimmunotherapy have generated interest in its use to enable patients with borderline-resectable NSCLC to undergo surgery. Additionally, for patients initially deemed resectable but who later become unresectable/inoperable during neoadjuvant treatment, consolidation immunotherapy after chemoradiotherapy should be explored. Patients and methods: MDT-BRIDGE (NCT05925530) is a multicenter, phase II, non-randomized study in similar to 140 patients with EGFR/ALK wild-type, stage IIB-IIIB (N2) NSCLC. Following baseline multidisciplinary team (MDT) assessment to determine resectable/borderline-resectable status, all patients receive 2 cycles of neoadjuvant D+CT every 3 weeks, followed by MDT reassessment of resectability. Patients deemed resectable receive 1-2 additional cycles of D+CT followed by surgery (Cohort 1). Patients deemed unresectable receive standard-of-care chemoradiotherapy (Cohort 2). Cohort 1 patients who become ineligible for surgery can enter Cohort 2. Following surgery or chemoradiotherapy, patients receive adjuvant or consolidation durvalumab for 1 year. The primary endpoint is resection rate in all patients. Additional endpoints include resecDNA dynamics pre- and post-surgery (including correlation with clinical outcomes), and safety. Conclusion: Enrollment began in February 2024; primary completion is anticipated in April 2026.
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页数:10
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