Outcome of immunotherapy in adrenocortical carcinoma: a retrospective cohort study

Author:

Remde Hanna1ORCID,Schmidt-Pennington Laura2,Reuter Miriam1,Landwehr Laura-Sophie1ORCID,Jensen Marie2,Lahner Harald3,Kimpel Otilia1ORCID,Altieri Barbara1,Laubner Katharina4,Schreiner Jochen5,Bojunga Joerg6,Kircher Stefan7,Kunze Catarina Alisa8,Pohrt Anne9,Teleanu Maria-Veronica10,Hübschmann Daniel111213,Stenzinger Albrecht14,Glimm Hanno15161718,Fröhling Stefan1013,Fassnacht Martin119ORCID,Mai Knut2ORCID,Kroiss Matthias15

Affiliation:

1. Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg , Josef-Schneider-Straße 2, 97080 Würzburg , Germany

2. Department of Endocrinology & Metabolism, Charité—Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health , Berlin 10117 , Germany

3. Department of Endocrinology and Metabolism, University Hospital Duisburg-Essen , Hufelandstraße 55, 45147 Essen , Germany

4. Division of Endocrinology and Diabetology, Department of Medicine II, Faculty of Medicine, Medical Centre University of Freiburg, University of Freiburg , Hugstetter Straße 55, 79106 Freiburg , Germany

5. Department of Internal Medicine IV, University Hospital Munich, Ludwig-Maximilians-University München , Ziemssenstraße 5, 80336 München , Germany

6. Department of Internal Medicine 1, Division of Endocrinology, Goethe University Frankfurt, Faculty 16 Medicine , Theodor-Stern-Kai 7, 60596 Frankfurt am Main , Germany

7. Institute of Pathology, University of Würzburg , Josef-Schneider-Str. 2, 97080 Würzburg , Germany

8. Institute of Pathology, Charité—Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health , Charitéplatz 1, 10117 Berlin , Germany

9. Institute of Biometry and Clinical Epidemiology, Charité—Universitätsmedizin Berlin , Charitéplatz 1, 10117 Berlin , Germany

10. National Center for Tumor Diseases Heidelberg and German Cancer Research Center, Im Neuenheimer Feld 460 , Heidelberg 69120 , Germany

11. Computational Oncology Group, Molecular Precision Oncology Program, National Centre for Tumour Diseases (NCT), Heidelberg and German Cancer Research Centre (DKFZ) , Im Neuenheimer Feld 580, 69120 Heidelberg , Germany

12. Pattern Recognition and Digital Medicine Group, Heidelberg Institute for Stem cell Technology and Experimental Medicine (HI-STEM) gGmbH , Im Neuenheimer Feld 280, 69120 Heidelberg , Germany

13. German Cancer Consortium, Im Neuenheimer Feld 280 , Heidelberg 69120 , Germany

14. Institut für Pathologie, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 224 , Heidelberg 69120 , Germany

15. Department for Translational Medical Oncology, National Centre for Tumour Diseases (NCT/UCC) , Dresden , Germany

16. Translational Medical Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden , Dresden , Germany

17. Translational Functional Cancer Genomics, National Centre for Tumour Diseases (NCT) and German Cancer Research Center (DKFZ) , Heidelberg , Germany

18. Department for Translational Medical Oncology (DD05), National Center for Tumor Diseases Dresden (NCT/UCC), German Cancer Consortium (DKTK) , Fetscherstraße 74/PF 64, 01307 Dresden , Germany

19. Comprehensive Cancer Center Mainfranken, University of Würzburg , Würzburg, Berlin , Germany

Abstract

Abstract Objective Clinical trials with immune checkpoint inhibitors (ICI) in adrenocortical carcinoma (ACC) have yielded contradictory results. We aimed to evaluate treatment response and safety of ICI in ACC in a real-life setting. Design Retrospective cohort study of 54 patients with advanced ACC receiving ICI as compassionate use at 6 German reference centres between 2016 and 2022. Methods Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and treatment-related adverse events (TRAE) were assessed. Results In 52 patients surviving at least 4 weeks after initiation of ICI, ORR was 13.5% (6-26) and DCR was 24% (16-41). PFS was 3.0 months (95% CI, 2.3-3.7). In all patients, median OS was 10.4 months (3.8-17). 17 TRAE occurred in 15 patients, which was associated with a longer PFS of 5.5 (1.9-9.2) vs 2.5 (2.0-3.0) months (HR 0.29, 95% CI, 0.13-0.66, P = 0.001) and OS of 28.2 (9.5-46.8) vs 7.0 (4.1-10.2) months (HR 0.34, 95% CI, 0.12-0.93). Positive tissue staining for programmed cell death ligand 1 (PD-L1) was associated with a longer PFS of 3.2 (2.6-3.8) vs 2.3 (1.6-3.0, P < 0.05) months. Adjusted for concomitant mitotane use, treatment with nivolumab was associated with lower risk of progression (HR 0.36, 0.15-0.90) and death (HR 0.20, 0.06-0.72) compared to pembrolizumab. Conclusions In the real-life setting, we observe a response comparable to other second-line therapies and an acceptable safety profile in ACC patients receiving different ICI. The relevance of PD-L1 as a marker of response and the potentially more favourable outcome in nivolumab-treated patients require confirmation.

Funder

German Research Foundation

National Center for Tumor Diseases

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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