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抗CD16/CD30双特异性抗体作为难治性霍奇金淋巴瘤的潜在治疗方法。

Anti-CD16/CD30 bispecific antibodies as possible treatment for refractory Hodgkin's disease.

作者信息

Hartmann F, Renner C, Jung W, Pfreundschuh M

机构信息

Medizinische Klinik I, Universitätskliniken des Saarlandes, Homburg, Germany.

出版信息

Leuk Lymphoma. 1998 Oct;31(3-4):385-92. doi: 10.3109/10428199809059232.

Abstract

Fifteen patients with refractory Hodgkin's disease were treated in a phase I/II dose escalation trial with the NK-cell activating bispecific monoclonal antibody HRS-3/A9 which is directed against the Fcgamma-receptor III (CD16 antigen) and the Hodgkin's associated CD30 antigen, respectively. HRS-3/A9 was given four times every 3-4 days starting with 1 mg/m2. The treatment was well tolerated and the maximum tolerated dose was not reached at 64 mg/m2, the highest dose given due to limited amounts of HRS-3/A9 available. Mild to moderate side effects occured in six patients and consisted of fever, pain in involved lymph nodes, and a maculopapulous rash. Median counts of NK-cells and of all lymphocyte subsets were considerably decreased in the patients before therapy and showed no consistent changes under therapy. Eight patients developed human anti-mouse immunoglobulin antibodies, and five patients showed an allergic reaction after attempted retreatment. One complete and one partial remission (lasting 6 and 3 months, respectively), three minor responses (lasting 1 to 15 months), two disease stabilizations (for 2 and 17 months, respectively), and one mixed response were achieved. There was no clearcut dose-side effect or dose-response correlation. Our results encourage further clinical trials with this novel immunotherapeutic approach and emphasize the necessity to reduce the immunogenicity of the murine bispecific antibodies.

摘要

15例难治性霍奇金病患者参与了一项I/II期剂量递增试验,使用的是NK细胞激活双特异性单克隆抗体HRS-3/A9,该抗体分别靶向Fcγ受体III(CD16抗原)和霍奇金病相关的CD30抗原。HRS-3/A9每3 - 4天给药4次,起始剂量为1mg/m²。治疗耐受性良好,由于可用的HRS-3/A9数量有限,最高给药剂量为64mg/m²时未达到最大耐受剂量。6例患者出现轻度至中度副作用,包括发热、受累淋巴结疼痛和斑丘疹。治疗前患者的NK细胞及所有淋巴细胞亚群的中位数计数显著降低,治疗期间未出现一致的变化。8例患者产生了人抗鼠免疫球蛋白抗体,5例患者在尝试再次治疗后出现过敏反应。获得了1例完全缓解和1例部分缓解(分别持续6个月和3个月)、3例轻微反应(持续1至15个月)、2例病情稳定(分别持续2个月和17个月)以及1例混合反应。未发现明确的剂量 - 副作用或剂量 - 反应相关性。我们的结果鼓励对这种新型免疫治疗方法进行进一步的临床试验,并强调降低鼠源性双特异性抗体免疫原性的必要性。

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