Partial response after intensive chemotherapy for adrenal cortical carcinoma in a child

✍ Scribed by Aricò, Maurizio ;Bossi, Grazia ;Livieri, Chiara ;Raiteri, Emanuela ;Severi, Francesca

• Publisher: John Wiley and Sons
• Year: 1992
• Tongue: English
• Weight: 267 KB
• Volume: 20
• Category: Article
• ISSN: 0098-1532
• DOI: 10.1002/mpo.2950200314

✦ Synopsis

Abstract

Adrenocortical carcinoma (ACC) in childhood is a rare tumor with high fatality rate. Available reports provide event free survival rates ranging between 10 to 50%. Optimal treatment has not yet been established; surgery plays a major role, and the value of adjuvant chemotherapy needs to be evaluated further, especially in children who develop recurrent disease and those with metastases at diagnosis. Optimal therapy of ACC has not been established. Surgery has been curative after complete tumor resection. Children with inoperable, recurrent and metastatic ACC have been treated with O, P'DDD, with response rates ranging from 10 to 60% in different series [7,11–20]. Radiotherapy [21] and other anti‐cancer drugs have been used [4–22] but their efficacy has not been established. Combination chemotherapy containing oncovin, cisPlatinum, epipodophyllotoxin and cyclophosphamide (OPEC) produced regression of metastatic ACC in a 5‐year‐old male [23].

We report one girl with relapsed disseminated ACC who showed good, even if temporary, control of the disease, with disappearance of lung, liver and spleen metastases, and marked reduction of the adrenal mass, following combined chemotherapy according to the “eight‐drugs‐in‐one‐day” protocol. © 1992 Wiley‐Liss, Inc.