Adult growth hormone replacement therapy and neuroimaging surveillance in brain tumour survivors

被引:37
作者
Jostel, A
Mukherjee, A
Hulse, PA
Shalet, SM
机构
[1] Christie Hosp, Dept Endocrinol, Manchester M20 4BX, Lancs, England
[2] Christie Hosp, Dept Radiol, Manchester M20 4BX, Lancs, England
关键词
D O I
10.1111/j.1365-2265.2005.02282.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Systematic collections of neuroimaging data are nonexistent in brain tumour survivors treated with adult growth hormone replacement therapy (AGHRT). We present our surveillance data. Design In 1993, our unit implemented a policy of performing brain scans on every brain tumour survivor before starting AGHRT, with repeat neuroimaging at least once after 12-18 months' treatment. Reports for baseline scans and most recent scans were analysed for this retrospective study. Patients All brain tumour survivors who received AGHRT (60 patients) were included in the analysis. Measurements Evidence and extent of residual tumour, tumour progression, tumour recurrence, and secondary neoplasms (SN) on baseline scan and latest follow-up scan. Results All patients had baseline scans performed. Follow-up scans were available in 41/45 (91%) patients who received AGHRT for more than 1 year (mean duration +/- SD of GHRT was 6.7 +/- 3.6 years). Sixteen patients had residual tumours, and SNs (all meningiomas) were demonstrated in three patients on baseline scans. Appearances remained stable in 34 (83%) patients during follow-up (extending to 17.4 +/- 8.3 years after tumour diagnosis). Of the 16 residual primary tumours, an incurable ependymoma continued to grow, and one meningioma progressed slightly in size over 7.7 years. Follow-up scans also revealed continued growth of the SNs detected at baseline, and five additional meningiomas (two in patients with a previous SN, confirming an excess risk in this subgroup, P = 0.02). All SNs occurred on average 22.8 (range 17-37) years after radiotherapy. Conclusions Our data do not suggest an increased rate of recurrence or progression of childhood brain tumours during AGHRT. Nonetheless, vigilance and long-term surveillance are needed in these patients in order to detect and monitor SNs, in particular in patients with a previous history of a SN. We endorse a proactive neuroimaging policy, preferably as part of a larger, controlled trial in the future.
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收藏
页码:698 / 705
页数:8
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