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[恶性脑肿瘤生物反应调节剂治疗的进展]

[Advances of BRM therapy of malignant brain tumors].

作者信息

Nagai M

机构信息

Dept. of Neurosurgery, Dokkyo University School of Medicine.

出版信息

Gan To Kagaku Ryoho. 1991 Feb;18(2):188-94.

PMID:1992912
Abstract

The cooperative study on the beta-interferon (IFN) therapy for glioblastoma and malignant astrocytoma reported the response rate as 14.0%. Continuing study resulted the response rate of 24.0% to low grade astrocytoma and 20.0% to medulloblastoma. Totally, effectiveness of 19.2% to gliomas was confirmed in 120 evaluated cases. A randomized study was conducted on combination therapy with beta-interferon and chemoradiotherapy. The response rate of 41.2% (21/51) in the group treated with IFN, ACNU and Radiation was significantly higher than the rate of 19.6% (10/51) in the group treated with ACNU and radiation only. Application of IFN to a maintenance therapy is also on going. Adoptive immunotherapy has been developed as potential therapeutic method of malignant glioma. Lymphokine activated killer cells (LAK) and Tumor infiltrating lymphocytes (TIL) are put to clinical use. Clinical application of human monoclonal antibody (MAb) CLN-IgG was conducted to recurrent malignant glioma. 131I labeled MAb was administered intratumorously and the specific incorporation was confirmed by gamma-scintigraphy. Concomitant administration of interferon enhanced the efficacy of the therapy. This radio-immunotherapy holds future promise as a new therapeutic approach to gliomas.

摘要

一项关于β-干扰素(IFN)治疗胶质母细胞瘤和恶性星形细胞瘤的合作研究报告称缓解率为14.0%。后续研究显示,低级别星形细胞瘤的缓解率为24.0%,髓母细胞瘤的缓解率为20.0%。在120例评估病例中,共证实对胶质瘤的有效率为19.2%。开展了一项关于β-干扰素与放化疗联合治疗的随机研究。接受IFN、ACNU和放疗治疗的组的缓解率为41.2%(21/51),显著高于仅接受ACNU和放疗治疗的组的19.6%(10/51)。IFN用于维持治疗的研究也在进行中。过继性免疫疗法已被开发为恶性胶质瘤的潜在治疗方法。淋巴因子激活的杀伤细胞(LAK)和肿瘤浸润淋巴细胞(TIL)已投入临床使用。对复发性恶性胶质瘤进行了人单克隆抗体(MAb)CLN-IgG的临床应用。将131I标记的单克隆抗体瘤内注射,并通过γ闪烁扫描证实其特异性摄取。同时给予干扰素可增强治疗效果。这种放射免疫疗法作为一种新的胶质瘤治疗方法具有广阔前景。

相似文献

1
[Advances of BRM therapy of malignant brain tumors].[恶性脑肿瘤生物反应调节剂治疗的进展]
Gan To Kagaku Ryoho. 1991 Feb;18(2):188-94.
2
[Efficacy of interferon-beta and interleukin-2 as cytokines for malignant brain tumor treatment].[β-干扰素和白细胞介素-2作为细胞因子用于恶性脑肿瘤治疗的疗效]
Gan To Kagaku Ryoho. 1987 Dec;14(12):3235-44.
3
[Chemical modifiers in radiotherapy].[放射治疗中的化学修饰剂]
Gan No Rinsho. 1989 Sep;35(11):1369-71.
4
[Monoclonal immunotherapy with human monoclonal antibody(CLN-IgG) in glioma patients].[人单克隆抗体(CLN-IgG)对胶质瘤患者的单克隆免疫治疗]
Nihon Rinsho. 2002 Mar;60(3):497-503.
5
[Effect of human fibroblast interferon on malignant brain tumors].[人成纤维细胞干扰素对恶性脑肿瘤的作用]
No To Shinkei. 1983 Sep;35(9):905-11.
6
Autologous natural killer cell therapy for human recurrent malignant glioma.自体自然杀伤细胞疗法治疗人类复发性恶性胶质瘤。
Anticancer Res. 2004 May-Jun;24(3b):1861-71.
7
Adoptive immunotherapy of a rat glioma using lymphokine-activated killer cells and interleukin 2.使用淋巴因子激活的杀伤细胞和白细胞介素2对大鼠神经胶质瘤进行过继性免疫治疗。
Cancer Res. 1990 Jul 15;50(14):4338-43.
8
Monoclonal antibody therapy of murine lymphoma: enhanced efficacy by concurrent administration of interleukin 2 or lymphokine-activated killer cells.小鼠淋巴瘤的单克隆抗体治疗:通过同时给予白细胞介素2或淋巴因子激活的杀伤细胞提高疗效。
Cancer Res. 1990 Sep 1;50(17):5421-5.
9
A phase I trial of a new recombinant human beta-interferon (BG9015) for the treatment of patients with recurrent gliomas.一项用于治疗复发性神经胶质瘤患者的新型重组人β干扰素(BG9015)的I期试验。
Clin Cancer Res. 1997 Mar;3(3):381-7.
10
Aspects of immunobiology and immunotherapy and uses of monoclonal antibodies and biologic immune modifiers in human gliomas.免疫生物学与免疫治疗的各个方面以及单克隆抗体和生物免疫调节剂在人类胶质瘤中的应用。
Neurol Clin. 1985 Nov;3(4):901-17.

引用本文的文献

1
Human interferon beta, nimustine hydrochloride, and radiation therapy in the treatment of newly diagnosed malignant astrocytomas.人β干扰素、盐酸尼莫司汀与放射治疗联合用于新诊断恶性星形细胞瘤的治疗
J Neurooncol. 2005 Mar;72(1):57-62. doi: 10.1007/s11060-004-2160-x.