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间碘苄胍(mIBG)治疗47例神经母细胞瘤患者:德国神经母细胞瘤试验结果

Metaiodobenzylguanidine (mIBG) in treatment of 47 patients with neuroblastoma: results of the German Neuroblastoma Trial.

作者信息

Klingebiel T, Berthold F, Treuner J, Schwabe D, Fischer M, Feine U, Maul F D, Waters W, Wehinger H, Niethammer D

机构信息

Department of Pediatric Oncology, Eberhard-Karls University, Tübingen, Federal Republic of Germany.

出版信息

Med Pediatr Oncol. 1991;19(2):84-8. doi: 10.1002/mpo.2950190203.

DOI:10.1002/mpo.2950190203
PMID:2011100
Abstract

From 1984 to 1989, 47 children with relapsed, refractory, and/or metastasized neuroblastoma were treated with 131I-metaiodobenzylguanidine (mIBG) in several different treatment combinations. At initial diagnosis, 36 children had Evans stage IV and 11 stage III disease. In 16 of the 47 children, tumor recurred after complete remission prior to mIBG treatment, 26 of 47 progressed from residual or nonresponding tumor, and in 5 of 47 tumor progression during chemotherapy was observed. Altogether the children were treated with a total of 112 courses (range 1-6) with a mean dosage of 8.9 +/- 6.7 mCi/kg body weight/treatment course. Total dose was 283.2 +/- 203.7 mCi for stage III and 388.9 +/- 218.6 mCi for stage IV. Nine of 47 children reached a complete or a very good partial remission (CR and VGPR) from mIBG treatment alone, 13 of 47 achieved partial remission (PR). In an early analysis, 10 patients treated with mIBG in the neuroblastoma trial NB 85 of the German Society of Pediatric Oncology showed no significant difference in survival time compared with 30 conventionally treated children. However, the recent therapy series has been done with higher doses of mIBG, and during improved therapeutic scanning many more bone lesions could be detected than during earlier diagnostic scanning. We conclude that mIBG treatment has not yet fulfilled the expectations for it but still seems for certain indications to be a promising tool to treat neuroblastoma in the future. Moreover, the frontier of neuroblastoma detection is still advancing.

摘要

1984年至1989年期间,47例复发性、难治性和/或转移性神经母细胞瘤患儿接受了131I-间碘苄胍(mIBG)治疗,采用了几种不同的治疗组合。初诊时,36例患儿为Evans IV期,11例为III期。在47例患儿中,16例在mIBG治疗前完全缓解后肿瘤复发,47例中有26例从残留或无反应肿瘤进展而来,47例中有5例在化疗期间观察到肿瘤进展。这些患儿总共接受了112个疗程(范围为1 - 6个疗程)的治疗,平均剂量为8.9±6.7 mCi/kg体重/疗程。III期患儿的总剂量为283.2±203.7 mCi,IV期患儿为388.9±218.6 mCi。47例患儿中有9例仅通过mIBG治疗达到完全缓解或非常好的部分缓解(CR和VGPR),47例中有13例达到部分缓解(PR)。在早期分析中,德国儿科肿瘤学会神经母细胞瘤试验NB 85中接受mIBG治疗的10例患者与30例接受传统治疗的患儿相比,生存时间无显著差异。然而,最近的治疗系列采用了更高剂量的mIBG,并且在改进的治疗扫描过程中,与早期诊断扫描相比,能够检测到更多的骨病变。我们得出结论,mIBG治疗尚未达到人们对它的期望,但对于某些适应症而言,它似乎仍是未来治疗神经母细胞瘤的一种有前景的工具。此外,神经母细胞瘤检测的前沿仍在不断推进。

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