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[自体骨髓移植在儿童恶性疾病中的应用——结果与结论]

[Use of autologous bone marrow transplantation in pediatric malignant diseases--results and conclusions].

作者信息

Slavc I, Urban C, Kaulfersch W, Teubl I

出版信息

Wien Klin Wochenschr. 1987 Feb 6;99(3):74-9.

PMID:3554773
Abstract

Ultrahigh-dose myeloablative antineoplastic therapy followed by autologous bone marrow transplantation (ABMT) has become an attractive therapeutic option for patients without HLA compatible bone marrow donors. Autologous bone marrow was harvested in 9 patients. In four cases the bone marrow was also treated ex vivo with a stable derivative of 4-hydroperoxycyclophosphamide, ASTA-Z 7654, to eliminate residual tumour cells. Altogether 5 patients, namely a patient with metastatic neuroblastoma, a patient with malignant histiocytosis, a patient with recurrent sacrococcygeal malignant teratoma and two patients with acute myelogenous leukaemia in first remission are in continuous remission so far from 125 + to 821 + days (median 657 + days). These patients were transplanted at the time of minimal tumour load (first remission) and in good clinical condition 3-7 months after diagnosis, while 3 of the four patients who died were transplanted in first or repeated relapse after one to several years of chemotherapy. It is concluded that the earliest possible recognition of a refractory therapeutic situation is of utmost importance for successful ABMT. Patients with an unfavourably responding neoplasm should, therefore, be already primary candidates for ABMT.

摘要

超高剂量清髓性抗肿瘤治疗后进行自体骨髓移植(ABMT),已成为没有 HLA 相匹配骨髓供体的患者颇具吸引力的治疗选择。9 例患者采集了自体骨髓。其中 4 例的骨髓还在体外使用 4-氢过氧环磷酰胺的稳定衍生物 ASTA-Z 7654 进行处理,以清除残留肿瘤细胞。截至目前,共有 5 例患者持续缓解,时间为 125 +至 821 +天(中位数 657 +天),分别为 1 例转移性神经母细胞瘤患者、1 例恶性组织细胞增多症患者、1 例复发性骶尾部恶性畸胎瘤患者以及 2 例处于首次缓解期的急性髓性白血病患者。这些患者在肿瘤负荷最小(首次缓解期)且诊断后 3 - 7 个月临床状况良好时接受了移植,而死亡的 4 例患者中有 3 例是在化疗 1 至数年出现首次或反复复发后接受移植的。得出的结论是,对于成功的 ABMT 而言,尽早识别难治性治疗情况至关重要。因此,对治疗反应不佳的肿瘤患者应一开始就作为 ABMT 的候选对象。

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