SAKK 16/14: Durvalumab in Addition to Neoadjuvant Chemotherapy in Patients With Stage IIIA(N2) Non–Small-Cell Lung Cancer—A Multicenter Single-Arm Phase II Trial

Author:

Rothschild Sacha I.1ORCID,Zippelius Alfred1,Eboulet Eric I.2,Savic Prince Spasenija3,Betticher Daniel4ORCID,Bettini Adrienne4,Früh Martin56,Joerger Markus5,Lardinois Didier7,Gelpke Hans8,Mauti Laetitia A.9,Britschgi Christian10,Weder Walter11,Peters Solange12ORCID,Mark Michael13,Cathomas Richard13ORCID,Ochsenbein Adrian F.6,Janthur Wolf-Dieter14,Waibel Christine15,Mach Nicolas16ORCID,Froesch Patrizia17,Buess Martin18,Bohanes Pierre19,Godar Gilles2,Rusterholz Corinne2,Gonzalez Michel20ORCID,Pless Miklos9,

Affiliation:

1. Department of Medical Oncology and Comprehensive Cancer Center, University Hospital Basel, Basel, Switzerland

2. SAKK Coordinating Center, Bern, Switzerland

3. Pathology, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland

4. Department of Oncology, HFR Fribourg—Hôpital fribourgeois, Fribourg, Switzerland

5. Department of Oncology/Hematology, Cantonal Hospital St Gallen, St Gallen, Switzerland

6. Department of Oncology, Inselspital Bern, Bern, Switzerland

7. Division of Thoracic Surgery, University Hospital Basel, Basel, Switzerland

8. Department of Thoracic and Visceral Surgery, Cantonal Hospital Winterthur, Winterthur, Switzerland

9. Department of Oncology, Cantonal Hospital Winterthur, Winterthur, Switzerland

10. Department of Medical Oncology and Hematology, Comprehensive Cancer Center Zurich, University Hospital Zurich, University of Zurich, Zurich, Switzerland

11. Department of Thoracic Surgery, University Hospital of Zurich, Zurich, Switzerland

12. Department of Oncology, University Hospital Lausanne CHUV, Lausanne, Switzerland

13. Divison of Oncology/Hematology, Cantonal Hospital Graubünden, Chur, Switzerland

14. Department of Oncology/Hematology, Cantonal Hospital Aarau, Aarau, Switzerland

15. Department of Oncology, Cantonal Hospital Baden, Baden, Switzerland

16. Department of Oncology, University Hospital Geneva, Geneva, Switzerland

17. Oncology Institute of Southern Switzerland, Bellinzona, Switzerland

18. Division of Medical Oncology, St Claraspital, Basel, Switzerland

19. Centre de Chimiothérapie Anti-Cancéreuse, Lausanne, Switzerland

20. Department of Thoracic Surgery, University Hospital Lausanne CHUV, Lausanne, Switzerland

Abstract

PURPOSE For patients with resectable stage IIIA(N2) non–small-cell lung cancer, neoadjuvant chemotherapy with cisplatin and docetaxel followed by surgery resulted in a 1-year event-free survival (EFS) rate of 48% in the SAKK 16/00 trial and is an accepted standard of care. We investigated the additional benefit of perioperative treatment with durvalumab. METHODS Neoadjuvant treatment consisted of three cycles of cisplatin 100 mg/m2 and docetaxel 85 mg/m2 once every 3 weeks followed by two doses of durvalumab 750 mg once every 2 weeks. Durvalumab was continued for 1 year after surgery. The primary end point was 1-year EFS. The hypothesis for statistical considerations was an improvement of 1-year EFS from 48% to 65%. RESULTS Sixty-eight patients were enrolled, 67 were included in the full analysis set. Radiographic response rate was 43% (95% CI, 31 to 56) after neoadjuvant chemotherapy and 58% (95% CI, 45 to 71) after sequential neoadjuvant immunotherapy. Fifty-five patients were resected, of which 34 (62%) achieved a major pathologic response (MPR; ≤ 10% viable tumor cells) and 10 (18%) among them a complete pathologic response. Postoperative nodal downstaging (ypN0-1) was observed in 37 patients (67%). Fifty-one (93%) resected patients had an R0 resection. There was no significant effect of pretreatment PD-L1 expression on MPR or nodal downstaging. The 1-year EFS rate was 73% (two-sided 90% CI, 63 to 82). Median EFS and overall survival were not reached after 28.6 months of median follow-up. Fifty-nine (88%) patients had an adverse event grade ≥ 3 including two fatal adverse events that were judged not to be treatment-related. CONCLUSION The addition of perioperative durvalumab to neoadjuvant chemotherapy in patients with stage IIIA(N2) non–small-cell lung cancer is safe and exceeds historical data of chemotherapy alone with a high MPR and an encouraging 1-year EFS rate of 73%.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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