Literature DB >> 31361313

National Treatment Practice for Adrenocortical Carcinoma: Have They Changed and Have We Made Any Progress?

John F Tierney1, Sitaram V Chivukula1, Jennifer Poirier1, Sam G Pappas1, Erik Schadde1,2,3,4, Martin Hertl2, Electron Kebebew5, Xavier Keutgen6.   

Abstract

BACKGROUND: Adrenocortical carcinoma (ACC) is a rare malignancy with a dismal prognosis. Two landmark trials published in 2007 and 2012 showed efficacy for adjuvant mitotane in resectable ACC and etoposide/doxorubicin/cisplatin plus mitotane for unresectable ACC, respectively. In this study, we used the National Cancer Database to examine whether treatment patterns and outcomes changed after these trials.
METHODS: The National Cancer Database was used to examine treatment patterns and survival in patients diagnosed with ACC from 2006 to 2015. Treatment modalities were compared within that group and with a historical cohort (1985 to 2005). χ2 tests were performed, and Cox proportional hazards models were created.
RESULTS: From 2006 to 2015, 2752 patients were included; 38% of patients (1042) underwent surgery alone, and 31% (859) underwent surgery with adjuvant therapy. Overall 5-year survival rates for all stages after resection were 43% (median, 41 months) in the contemporary cohort and 39% (median, 32 months) in the historical cohort. After 2007, patients who underwent surgery were more likely to receive adjuvant chemotherapy (P = 0.005), and 5-year survival with adjuvant chemotherapy improved (41% vs 25%; P = 0.02). However, survival did not improve in patients with unresectable tumors after 2011 compared with 2006 to 2011 (P = 0.79). Older age, tumor size ≥10 cm, distant metastases, and positive margins were associated with lower survival after resection (hazard ratio range: 1.39 to 3.09; P < 0.03).
CONCLUSIONS: Since 2007, adjuvant therapy has been used more frequently in patients with resected ACC, and survival for these patients has improved but remains low. More effective systemic therapies for patients with ACC, especially those in advanced stages, are desperately needed.
Copyright © 2019 Endocrine Society.

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Year:  2019        PMID: 31361313     DOI: 10.1210/jc.2019-00915

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  4 in total

1.  Exquisite sensitivity of adrenocortical carcinomas to induction of ferroptosis.

Authors:  Alexia Belavgeni; Stefan R Bornstein; Anne von Mässenhausen; Wulf Tonnus; Julian Stumpf; Claudia Meyer; Evelyn Othmar; Markus Latk; Waldemar Kanczkowski; Matthias Kroiss; Constanze Hantel; Christian Hugo; Martin Fassnacht; Christian G Ziegler; Andrew V Schally; Nils P Krone; Andreas Linkermann
Journal:  Proc Natl Acad Sci U S A       Date:  2019-10-14       Impact factor: 11.205

2.  Tumor mutational burden presents limiting effects on predicting the efficacy of immune checkpoint inhibitors and prognostic assessment in adrenocortical carcinoma.

Authors:  Fangshi Xu; Yibing Guan; Peng Zhang; Li Xue; Yubo Ma; Mei Gao; Tie Chong; Bin-Cheng Ren
Journal:  BMC Endocr Disord       Date:  2022-05-14       Impact factor: 3.263

Review 3.  Management of adrenocortical carcinoma: are we making progress?

Authors:  Barbara Kiesewetter; Philipp Riss; Christian Scheuba; Peter Mazal; Elisabeth Kretschmer-Chott; Alexander Haug; Markus Raderer
Journal:  Ther Adv Med Oncol       Date:  2021-08-31       Impact factor: 5.485

4.  Role of Bclaf1 in Promoting Adrenocortical Carcinoma Proliferation: A Study Combining the Use of Bioinformatics and Molecular Events.

Authors:  Hui Zhou; Mengchen Zou; Xinyi Ding; Fei Zou
Journal:  Cancer Manag Res       Date:  2021-08-31       Impact factor: 3.989

  4 in total

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