Literature DB >> 27742785

Adrenocortical Cancer: A Molecularly Complex Disease Where Surgery Matters.

Eden C Payabyab1, Sanjeeve Balasubramaniam2, Maureen Edgerly3, Margarita Velarde3, Maria J Merino4, Aradhana M Venkatesan5, Harshraj Leuva6, Thomas Litman7, Susan E Bates8, Tito Fojo9.   

Abstract

The development of new therapies has lagged behind for rare cancers without defined therapeutic targets. Adrenocortical cancer is no exception. Mitotane, an older agent considered "adrenolytic," is used both to control symptoms in advanced disease and as adjuvant therapy after surgical resection. Molecular characterization of adrenocortical cancer has deepened our understanding of this genetically complex disease while identifying subgroups whose importance remains to be determined. Unfortunately, such studies have yet to demonstrate a therapeutic target for drug development, and to date, no targeted therapy has achieved meaningful outcomes. Consequently, first-line therapy for metastatic disease remains a combination regimen of etoposide, doxorubicin, and cisplatinum established in a randomized clinical trial. In addition to evaluating recent studies in adrenocortical cancer, we raise one critical clinical issue-the risk of peritoneal dissemination following laparoscopic resection of adrenocortical cancer. In a retrospective case series of 267 patients referred to the NCI for the treatment of recurrent or advanced adrenocortical cancer, we found extensive peritoneal dissemination in 25 of the 45 patients (55.6%) who had undergone laparoscopic resection, compared with only 7 of the 222 patients (3%) who had undergone an open resection (P < 0.0001). Although this has been debated in the literature, our data argue for an end to laparoscopic resection of adrenocortical cancers to avoid peritoneal dissemination, a complication of laparoscopy that is uniformly fatal. Clin Cancer Res; 22(20); 4989-5000. ©2016 AACR SEE ALL ARTICLES IN THIS CCR FOCUS SECTION, "ENDOCRINE CANCERS REVISING PARADIGMS". ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27742785     DOI: 10.1158/1078-0432.CCR-16-1570

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  5 in total

1.  Progress in Endocrine Neoplasia.

Authors:  Samuel A Wells
Journal:  Clin Cancer Res       Date:  2016-10-15       Impact factor: 12.531

2.  A Phase II Trial of Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Recurrent Adrenocortical Carcinoma.

Authors:  Marybeth S Hughes; Winifred M Lo; Tatiana Beresnev; Maria Merino; Yvonne Shutack; R Taylor Ripley; Jonathan M Hernandez; Jeremy L Davis
Journal:  J Surg Res       Date:  2018-12       Impact factor: 2.192

3.  Novel Insights into the Molecular Regulation of Ribonucleotide Reductase in Adrenocortical Carcinoma Treatment.

Authors:  Christina Bothou; Ashish Sharma; Adrian Oo; Baek Kim; Pal Perge; Peter Igaz; Cristina L Ronchi; Igor Shapiro; Constanze Hantel
Journal:  Cancers (Basel)       Date:  2021-08-20       Impact factor: 6.639

4.  Overexpression of HSD17B4 exerts tumor suppressive function in adrenocortical carcinoma and is not associated with hormone excess.

Authors:  Guanxiong Ding; Shenghua Liu; Qiang Ding; Chenchen Feng
Journal:  Oncotarget       Date:  2017-12-01

5.  Metastatic and recurrent adrenocortical cancer is not defined by its genomic landscape.

Authors:  Tito Fojo; Lyn Huff; Thomas Litman; Kate Im; Maureen Edgerly; Jaydira Del Rivero; Stefania Pittaluga; Maria Merino; Susan E Bates; Michael Dean
Journal:  BMC Med Genomics       Date:  2020-11-04       Impact factor: 3.063

  5 in total

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