首页> 外文期刊>Journal of Clinical Oncology >Treatment of Refractory Hodgkin's Lymphoma Patients With an Iodine-131-Labeled Murine Anti-CD30 Monoclonal Antibody.
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Treatment of Refractory Hodgkin's Lymphoma Patients With an Iodine-131-Labeled Murine Anti-CD30 Monoclonal Antibody.

机译:用碘131标记的鼠抗CD30单克隆抗体治疗难治性霍奇金淋巴瘤患者。

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PURPOSE Hodgkin's lymphoma (HL) has been demonstrated to be a good target for immunotherapy since lymphocyte activation markers such as CD30 are expressed in high numbers on the malignant cells. Thus, we developed a new radioimmunoconjugate consisting of the murine anti-CD30 monoclonal antibody (MAb) Ki-4 labeled with iodine-131 ((131)I). PATIENTS AND METHODS The biodistribution of (131)I-Ki-4 was assessed via dosimetry after preinfusion of 5 mg native Ki-4 followed by 250 to 300 MBq (131)I-labeled Ki-4. Whole-body scintigraphy was performed 1 hour, 24 hours, 48 hours, 72 hours, and 6 days after the infusion. Dosimetry was calculated using the programs NucliDose ICON-IDL (version 5.0.2; Siemens, Erlanger, Germany) and MIRDOSE (version 3.1; Oak Ridge National Laboratories; Oak Ridge, TN). The therapeutic dose was given on day 8 after preinfusion of unlabeled Ki-4. Results We treated 22 patients with relapsed or refractory CD30-positive HL. Preinfusion of 5 mg native Ki-4 was sufficient to bind the soluble CD30. Imaging demonstrated localization of involved areas measuring 5 cm in diameter or more in four patients and 2.5 cm in one patient. Patients received total body doses of 0.035 Gy to 0.99 Gy. Acute toxicity was mild with grade 1 fatigue in 19 of 22 assessable patients. Seven patients experienced grade 4 degrees hematotoxicity 4 to 8 weeks after treatment. Response included one complete remission, five partial remissions, and three minor responses. CONCLUSION Treatment with (131)I-Ki-4 is effective but can be associated with severe hematotoxicity.
机译:目的霍奇金淋巴瘤(HL)已被证明是免疫治疗的良好靶标,因为淋巴细胞激活标记(例如CD30)在恶性细胞上大量表达。因此,我们开发了一种新的放射免疫偶联物,它由用碘131((131)I)标记的鼠抗CD30单克隆抗体(MAb)Ki-4组成。患者和方法(131)I-Ki-4的生物分布是在预先注入5 mg天然Ki-4,然后是250至300 MBq(131)I标记的Ki-4后,通过剂量测定法评估的。输注后1小时,24小时,48小时,72小时和6天进行全身闪烁显像。使用程序NucliDose ICON-IDL(版本5.0.2;西门子,德国埃尔兰格)和MIRDOSE(版本3.1;橡树岭国家实验室;田纳西州橡树岭)来计算剂量。在未标记Ki-4的预输注后第8天给予治疗剂量。结果我们治疗了22例复发或难治的CD30阳性HL患者。预输注5 mg天然Ki-4足以结合可溶性CD30。影像学检查显示,四名患者的直径为5厘米或以上,而一名患者的2.5厘米为直径的病变区域。患者接受的全身剂量为0.035 Gy至0.99 Gy。 22例可评估患者中有19例急性毒性为1级疲劳。 7名患者在治疗后4至8周经历了4级血液毒性。回应包括一项完全缓解,五项部分缓解和三项次要缓解。结论用(131)I-Ki-4治疗是有效的,但可能与严重的血液毒性有关。

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