癌症患者单次低剂量注射放射性标记小鼠单克隆抗体后的人抗小鼠抗体反应。

R O Dillman, D L Shawler, T J McCallister, S E Halpern
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引用次数: 35

摘要

我们检测了61例癌症患者在单次诊断性注射111In偶联小鼠单克隆抗体后的人抗小鼠抗体(HAMA)反应。给予含有1-5 mCi 111In的抗体1- 22mg。研究人群包括30名结直肠癌患者(四种不同的抗体),22名恶性黑色素瘤患者(四种抗体)和9名前列腺癌患者(两种抗体)。41%的患者在14天内发展为HAMA。3名患者(5%)出现IgM应答,5名患者(8%)出现IgG应答,17名患者(28%)同时出现IgM和IgG应答。只有27%的结肠癌患者发生了HAMA,而黑色素瘤患者和前列腺癌患者的这一比例分别为55%和56%。注射剂量、各项临床参数与HAMA反应无相关性。HAMA对不同单克隆抗体的反应存在差异,但群体样本太小,无法推断其重要性。大多数HAMA反应具有显著比例的独特型或同型特异性。在首次输注HAMA阴性的患者中,只有1/6的患者在随后输注相同的单克隆抗体后发生了HAMA。我们的数据表明,在单次低剂量注射用于诊断目的的放射性标记单克隆抗体后,显着百分比的癌症患者发生了HAMA。这可能对未来单克隆抗体在此类患者中的治疗应用具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human anti-mouse antibody response in cancer patients following single low-dose injections of radiolabeled murine monoclonal antibodies.

We examined the human anti-mouse antibody (HAMA) response in 61 cancer patients following a single, diagnostic injection of any one of ten 111In conjugated murine monoclonal antibodies. Between 1 and 22 mg of antibody containing 1-5 mCi 111In was administered. The populations studied included 30 patients with colorectal carcinoma (four different antibodies), 22 with malignant melanoma (four antibodies), and nine with prostate cancer (two antibodies). Forty-one percent of the patients developed HAMA within 14 days. Three patients (5%) developed an IgM response, five patients (8%) developed an IgG response, and 17 patients (28%) developed both IgM and IgG. Only 27% of the patients with colon cancer developed HAMA, compared to 55% of the melanoma patients and 56% of the prostate cancer patients. There were no correlations among injected dose, various clinical parameters, and HAMA response. There were variations in the HAMA response to different monoclonal antibodies, but population samples were too small to infer significance. Most of the HAMA responses had a significant proportion of idiotypic or isotypic specificity. Only 1/6 patients who were HAMA negative after the first infusion developed HAMA following subsequent infusions of the same monoclonal antibody. Our data demonstrate that a significant percent of cancer patients develop HAMA following a single, low-dose injection of a radiolabeled monoclonal antibody for diagnostic purposes. This may have important implications for the future therapeutic use of monoclonal antibodies in such patients.

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