A Prospective Study of Expectant Observation as Primary Therapy for Neuroblastoma in Young Infants A Children's Oncology Group Study

被引:127
作者
Nuchtern, Jed G. [1 ,2 ,3 ]
London, Wendy B. [4 ,7 ]
Barnewolt, Carol E. [5 ]
Naranjo, Arlene [7 ,8 ]
McGrady, Patrick W. [7 ,8 ]
Geiger, James D. [9 ]
Diller, Lisa [4 ,7 ]
Schmidt, Mary Lou [10 ]
Maris, John M. [11 ,12 ]
Cohn, Susan L. [13 ]
Shamberger, Robert C. [6 ]
机构
[1] Baylor Coll Med, Div Pediat Surg, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Dept Surg, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Dept Pediat, Houston, TX 77030 USA
[4] Dana Farber Childrens Hosp Canc Ctr, Dept Pediat, Childrens Hosp Boston, Boston, MA USA
[5] Dana Farber Childrens Hosp Canc Ctr, Dept Radiol, Childrens Hosp Boston, Boston, MA USA
[6] Dana Farber Childrens Hosp Canc Ctr, Dept Surg, Childrens Hosp Boston, Boston, MA USA
[7] Childrens Oncol Grp Stat & Data Ctr, Arcadia, CA USA
[8] Univ Florida, Dept Biostat, Gainesville, FL USA
[9] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
[10] Univ Illinois, Dept Pediat, Chicago, IL USA
[11] Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA
[12] Univ Penn, Philadelphia, PA 19104 USA
[13] Univ Chicago, Dept Pediat, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
expectant observation; infant; localized; neuroblastoma; prenatal; sonography; surgery; LOCALIZED NEUROBLASTOMA; SPONTANEOUS REGRESSION; CYSTIC NEUROBLASTOMA; SINGLE INSTITUTION; COMPLICATIONS; WAIT; AGE; ANESTHETICS; RESECTION; SURVIVAL;
D O I
10.1097/SLA.0b013e31826cbbbd
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To demonstrate that expectant observation of young infants with small adrenal masses would result in excellent event-free and overall survival. Background: Neuroblastoma is the most common malignant tumor in infants, and in young infants, 90% of neuroblastomas are located in the adrenal gland. Although surgical resection is standard therapy, multiple observations suggest that expectant observation could be a safe alternative for infants younger than 6 months who have small adrenal masses. Methods: A prospective study of infants younger than 6 months with small adrenal masses and no evidence of spreading beyond the primary tumor was performed at participating Children's Oncology Group institutions. Parents could choose observation or immediate surgical resection. Serial abdominal sonograms and urinary vanillylmandelic acid and homovanillic acid measurements were performed during a 90-week interval. Infants experiencing a 50% increase in the volume of the mass, urine catecholamine values, or an increase in the homovanillic acid to vanillylmandelic acid ratio greater than 2, were referred for surgical resection. Results: Eighty-seven eligible patients were enrolled: 83 elected observation and 4 chose immediate surgery. Sixteen observational patients ultimately had surgery; 8 had International Neuroblastoma Staging System stage 1 neuroblastoma, 2 had higher staged neuroblastoma (2B and 4S), 2 had low-grade adrenocortical neoplasm, 2 had adrenal hemorrhage, and 2 had extralobar pulmonary sequestration. The 2 patients with adrenocortical tumors were resected because of a more than 50% increase in tumor volume. The 3-year event-free survival for a neuroblastoma event was 97.7 +/- 2.2% within the entire cohort of patients (n = 87). The 3-year overall survival was 100%, with a median follow-up of 3.2 years. Eighty-one percent of patients on the observation arm were spared resection. Conclusions: Expectant observation of infants younger than 6 months with small adrenal masses led to excellent event-free survival and overall survival while avoiding surgical intervention in a large majority of the patients.
引用
收藏
页码:573 / 580
页数:8
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