The Value of Local Therapies in Advanced Adrenocortical Carcinoma

Author:

Kimpel Otilia1,Altieri Barbara1ORCID,Laganà Marta2ORCID,Vogl Thomas J.3ORCID,Adwan Hamzah3,Dusek Tina4,Basile Vittoria5,Pittaway James6,Dischinger Ulrich1,Quinkler Marcus7,Kroiss Matthias18,Puglisi Soraya5ORCID,Cosentini Deborah2,Kickuth Ralph9,Kastelan Darko4ORCID,Fassnacht Martin110ORCID

Affiliation:

1. Division of Endocrinology and Diabetes, Department of Medicine, University Hospital, University of Würzburg, 97070 Würzburg, Germany

2. Medical Oncology Unit, Department of Medical & Surgical Specialties, Radiological Sciences & Public Health, University of Brescia, ASST Spedali Civili of Brescia, 25123 Brescia, Italy

3. Universitätsklinikum Frankfurt, Institut für Diagnostische und Interventionelle Radiologie, 60596 Frankfurt, Germany

4. Department of Endocrinology, University Hospital Centre Zagreb, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia

5. Internal Medicine 1, San Luigi Gonzaga Hospital, Department of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy

6. Department of Endocrinology, St Bartholomew’s Hospital, London EC1A 7BE, UK

7. Endocrinology in Charlottenburg, 10627 Berlin, Germany

8. Department of Medicine IV, University Hospital, LMU Munich, Ziemssenstraße 1, 80336 München, Germany

9. Institute of Diagnostic and Interventional Radiology, University-Hospital of Würzburg, 97080 Würzburg, Germany

10. Comprehensive Cancer Center Mainfranken, University of Würzburg, 97070 Würzburg, Germany

Abstract

International guidelines recommend local therapies (LTs) such as local thermal ablation (LTA; radiofrequency, microwave, cryoablation), transarterial (chemo)embolisation (TA(C)E), and transarterial radioembolisation (TARE) as therapeutic options for advanced adrenocortical carcinoma (ACC). However, the evidence for these recommendations is scarce. We retrospectively analysed patients receiving LTs for advanced ACC. Time to progression of the treated lesion (tTTP) was the primary endpoint. The secondary endpoints were best objective response, overall progression-free survival, overall survival, adverse events, and the establishment of predictive factors by multivariate Cox analyses. A total of 132 tumoural lesions in 66 patients were treated with LTA (n = 84), TA(C)E (n = 40), and TARE (n = 8). Complete response was achieved in 27 lesions (20.5%; all of them achieved by LTA), partial response in 27 (20.5%), and stable disease in 38 (28.8%). For the LTA group, the median tTTP was not reached, whereas it was reached 8.3 months after TA(C)E and 8.2 months after TARE (p < 0.001). The median time interval from primary diagnosis to LT was >47 months. Fewer than four prior therapies and mitotane plasma levels of >14 mg/L positively influenced the tTTP. In summary, this is one of the largest studies on LTs in advanced ACC, and it demonstrates a very high local disease control rate. Thus, it clearly supports the guideline recommendations for LTs in these patients.

Funder

Else Kröner-Fresenius-Stiftung

European Reference networks Endo-ERN

EuRanCan

COST

Publisher

MDPI AG

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