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全反式维甲酸治疗复发性恶性胶质瘤:与肿瘤内钙化出现相关的临床和影像学稳定。

All-trans retinoic acid in relapsing malignant gliomas: clinical and radiological stabilization associated with the appearance of intratumoral calcifications.

作者信息

Defer G L, Adle-Biassette H, Ricolfi F, Martin L, Authier F J, Chomienne C, Degos L, Degos J D

机构信息

Department de Neurosciences, Hôpital Henri Mondor, Créteil, France.

出版信息

J Neurooncol. 1997 Sep;34(2):169-77. doi: 10.1023/a:1005701507111.

Abstract

PURPOSE

To evaluate the therapeutic effect of all-trans retinoic acid (ATRA) with and without cytosine arabinoside in relapsing malignant gliomas.

PATIENTS AND METHODS

9 patients (8 male, 1 female, age 53.9 +/- 11.2) with relapsing malignant gliomas (grade IV:6; grade III:3) were treated by ATRA 1 to 21 months after the end of their initial treatment. ATRA was given unceasingly during 2 to 17 months at 90 mg/d. In 6 patients it was associated to cytosine arabinoside (4 g/course, 1 to 9 courses every 4 weeks).

RESULTS

4 non-responder patients died 2.5 to 4 months after starting therapy. One patient who had been reoperated before receiving ATRA and cytosine arabinoside (5 course) had no sign of tumor recurrence after 17 months of treatment. In 4 responder patients (2 glioblastoma and 2 anaplastic astrocytoma) a clinical and radiological stabilization (time to progression) during 9 +/- 2.5 months was observed. This stabilization was associated in 3 of them with the appearance of intra tumoral calcifications visualized on repeated CT scans and confirmed in one patient by post-mortem examination. All of them had received cytosine arabinoside (1 to 9 courses) with ATRA; however small calcifications were also observed in one non-responder patient who did not receive aracytine.

CONCLUSION

These results suggest: a) a therapeutic effect of ATRA in combination with cytosine arabinoside in patients with relapsing malignant gliomas b) that intratumoral calcifications are related to the effects of ATRA on differentiation and/or on endothelial t-PA production and that these effects explain the tumor progression arrest in responder patients. The transient efficiency is probably related to the pharmacokinetics of ATRA or to changes of cellular mechanisms that modulate the cell response to the drug and is a critical issue for this therapy.

摘要

目的

评估全反式维甲酸(ATRA)联合或不联合阿糖胞苷治疗复发性恶性胶质瘤的疗效。

患者与方法

9例复发性恶性胶质瘤患者(8例男性,1例女性,年龄53.9±11.2岁),其中IV级6例,III级3例,在初始治疗结束后1至21个月接受ATRA治疗。ATRA在2至17个月内持续给予,剂量为90mg/d。6例患者联合阿糖胞苷(4g/疗程,每4周1至9个疗程)。

结果

4例无反应患者在开始治疗后2.5至4个月死亡。1例在接受ATRA和阿糖胞苷(5个疗程)治疗前接受过再次手术的患者,治疗17个月后无肿瘤复发迹象。4例有反应患者(2例胶质母细胞瘤和2例间变性星形细胞瘤)在9±2.5个月内实现了临床和影像学稳定(疾病进展时间)。其中3例患者在重复CT扫描中可见瘤内钙化,1例患者经尸检证实。他们均接受了ATRA联合阿糖胞苷(1至9个疗程)治疗;然而,1例未接受阿糖胞苷的无反应患者也观察到了小钙化灶。

结论

这些结果表明:a)ATRA联合阿糖胞苷对复发性恶性胶质瘤患者有治疗作用;b)瘤内钙化与ATRA对分化和/或内皮组织型纤溶酶原激活物(t-PA)产生的影响有关,这些影响解释了有反应患者肿瘤进展的停滞。短暂的疗效可能与ATRA的药代动力学或调节细胞对药物反应的细胞机制变化有关,这是该治疗的一个关键问题。

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