Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

被引:51
作者
Rodriguez-Galindo, Carlos [1 ,2 ]
Krailo, Mark D. [3 ,4 ]
Pinto, Emilia M. [5 ]
Pashankar, Farzana [6 ]
Weldon, Christopher B. [7 ]
Huang, Li [3 ]
Caran, Eliana M. [8 ]
Hicks, John [9 ]
McCarville, M. Beth [10 ]
Malkin, David [11 ,12 ]
Wasserman, Jonathan D. [13 ]
de Oliveira Filho, Antonio G. [14 ]
LaQuaglia, Michael P. [15 ]
Ward, Deborah A. [16 ]
Zambetti, Gerard [5 ]
Mastellaro, Maria J. [17 ]
Pappo, Alberto S. [1 ]
Ribeiro, Raul C. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Global Pediat Med, 262 Danny Thomas Pl MS 721, Memphis, TN 38105 USA
[3] Childrens Oncol Grp, Stat & Data Ctr, Monrovia, CA USA
[4] Univ Southern Calif, Dept Prevent Med, Los Angeles, CA 90007 USA
[5] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
[6] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[7] Boston Childrens Hosp, Dept Surg, Boston, MA USA
[8] Inst Oncol Pediat, Dept Oncol, Sao Paulo, Brazil
[9] Texas Childrens Hosp, Dept Pathol, Houston, TX 77030 USA
[10] St Jude Childrens Res Hosp, Dept Diagnost Imaging, Memphis, TN 38105 USA
[11] Univ Toronto, Hosp Sick Children, Div Hematol Oncol, Toronto, ON, Canada
[12] Univ Toronto, Dept Pediat, Toronto, ON, Canada
[13] Hosp Sick Children, Div Endocrinol, Toronto, ON, Canada
[14] Ctr Infantil Boldrini, Dept Surg, Sao Paulo, Brazil
[15] Mem Sloan Kettering Canc Ctr, Dept Pediat Surg, 1275 York Ave, New York, NY 10021 USA
[16] St Jude Childrens Res Hosp, Dept Pharmaceut Sci, Memphis, TN 38105 USA
[17] Ctr Infantil Boldrini, Dept Oncol, Sao Paulo, Brazil
关键词
PROGNOSTIC-SIGNIFICANCE; TUMOR; MITOTANE; DOXORUBICIN; MANAGEMENT; CISPLATIN; ETOPOSIDE; SURVIVAL; REGISTRY;
D O I
10.1200/JCO.20.02871
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Adrenocortical carcinoma (ACC) is a rare aggressive pediatric malignancy with distinct biology. Its treatment follows the principles developed for adults; pediatric-specific studies are scarce. PATIENTS AND METHODS Prospective single-arm risk-stratified interventional study. Study objectives were (1) to describe the outcome of patients with stage I ACC treated with adrenalectomy alone; (2) to describe the outcome of stage II patients (completely resected > 200 cc or > 100 g) treated with adrenalectomy and retroperitoneal lymph node dissection; and (3) to describe the outcome of patients with stage III or IV treated with mitotane and chemotherapy. RESULTS Between September 2006 and May 2013, 78 patients (77 eligible, 51 females) were enrolled. The 5-year event-free survival estimates for stages I (24 patients), II (15 patients), III (24 patients), and IV (14 patients) were 86.2%, 53.3%, 81%, and 7.1%, respectively. The corresponding 5-year overall survival estimates were 95.2%, 78.8%, 94.7%, and 15.6%, respectively. On univariate analysis, age, stage, presence of virilization, Cushing syndrome, or hypertension, germline TP53 status, and presence of a somatic ATRX mutation were associated with outcome. On multivariable analysis, only stage and age were significantly associated with outcome. The probabilities of mitotane and chemotherapy feasibility events were 10.5% and 31.6%, respectively. CONCLUSION Outcome for children with stage I ACC is excellent with surgery. Outcome for patients with stage II disease is inferior despite retroperitoneal lymph node dissection. Patients with stage III ACC have an excellent outcome combining surgery and chemotherapy. Patients with stage IV ACC are older and have a poor outcome; new treatments should be explored for this high-risk group. The combination of mitotane and chemotherapy as prescribed in ARAR0332 resulted in significant toxicity; one third of patients with advanced disease could not complete the scheduled treatment.
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收藏
页码:2463 / +
页数:14
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