Growth hormone replacement therapy in children with medulloblastoma: Use and effect on tumor control

被引:81
作者
Packer, RJ
Boyett, JM
Janss, AJ
Stavrou, T
Kun, L
Wisoff, J
Russo, C
Geyer, R
Phillips, P
Kieran, M
Greenberg, M
Goldman, S
Hyder, D
Heideman, R
Jones-Wallace, D
August, GP
Smith, SH
Moshang, T
机构
[1] George Washington Univ, Childrens Natl Med Ctr, Dept Neurol, Washington, DC 20010 USA
[2] George Washington Univ, Childrens Natl Med Ctr, Dept Pediat, Washington, DC 20010 USA
[3] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Neurooncol, Memphis, TN 38105 USA
[5] Childrens Hosp Philadelphia, Dept Oncol, Philadelphia, PA 19104 USA
[6] Childrens Hosp Philadelphia, Dept Neurol, Philadelphia, PA 19104 USA
[7] Childrens Hosp Philadelphia, Dept Endocrinol, Philadelphia, PA 19104 USA
[8] NYU, Dept Neurosurg, New York, NY 10016 USA
[9] SUNY Coll Buffalo, Childrens Hosp Buffalo, Buffalo, NY 14222 USA
[10] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[11] Univ Calif San Francisco, Dept Neurosurg, San Francisco, CA 94143 USA
[12] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
[13] Childrens Mem Hosp, Chicago, IL 60614 USA
[14] Childrens Hosp & Reg Med Ctr, Dept Pediat, Seattle, WA USA
[15] Dana Farber Canc Inst, Boston, MA 02115 USA
[16] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
D O I
10.1200/JCO.2001.19.2.480
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Progress has been made in the treatment of medulloblastoma, the most common childhood malignant brain tumor: However, many long-term survivors will have posttherapy growth hormone insufficiency with resultant linear growth retardation. Growth hormone replacement therapy (GHRT) may significantly improve growth, but there is often reluctance to initiate GHRT because of concerns of an increased likelihood of tumor relapse. Patients and Methods: This study retrospectively reviewed the use of GHRT for survivors of medulloblastoma in 11 neuro-oncology centers in North America who received initial treatment for disease between 1980 and 1993 to determine its impact on disease control. A Landmark analysis was used to evaluate the relative risk of relapse in surviving patients. Results: Five hundred forty-five consecutive patients less than 15 years of age at diagnosis were identified. Six-year progression-free survival (mean +/- SD) was 40% +/- 5% in children less than 3 years of age at diagnosis compared with 59% +/- 3% for older patients. Older patients with total or near-total resections (P =.003) and localized disease at diagnosis (P <.0001) had the highest likelihood of survival. One hundred seventy patients (33% +/- 3% of the cohort) received GHRT. GHRT use varied widely among institutions, ranging from 5% to 73%. GHRT was begun a mean of 3.9 years after diagnosis, later in children younger than 3 years at diagnosis (5.4 years). By Landmark analyses, for those surviving 2, 3, and 5 years after diagnosis, there was no evidence that GHRT increased the rate of disease relapse. Conclusion: This large retrospective review demonstrates that GHRT is underutilized in survivors of medulloblastoma and is used relatively late in the course of the illness. GHRT is not associated with an increased likelihood of disease relapse. J Clin Oncol 19:480-487. (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:480 / 487
页数:8
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