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单克隆抗体-蓖麻毒蛋白A链免疫偶联物Xomazyme-791治疗转移性结肠癌患者的I期研究。

Phase I study of monoclonal antibody-ricin A chain immunoconjugate Xomazyme-791 in patients with metastatic colon cancer.

作者信息

LoRusso P M, Lomen P L, Redman B G, Poplin E, Bander J J, Valdivieso M

机构信息

Department of Internal Medicine, Wayne State University School of Medicine, Harper Hospital, Detroit, Michigan 48201, USA.

出版信息

Am J Clin Oncol. 1995 Aug;18(4):307-12. doi: 10.1097/00000421-199508000-00008.

DOI:10.1097/00000421-199508000-00008
PMID:7625372
Abstract

The immunoconjugate XMMCO-791/RTA consists of ricin A chain bound to a murine monoclonal antibody MoAb 791T. This monoclonal antibody (MoAb) binds to a glycoprotein of 72 kD, which is expressed on human colorectal carcinoma, ovarian carcinoma, and osteogenic sarcoma. XMMCO-791/RTA was tested in a Phase I trial with proposed dose escalation steps of 0.02, 0.04, 0.15, and 0.2 mg/kg per day. Twelve patients with metastatic colorectal carcinoma were treated at 0.02, 0.03, and 0.04 mg/kg per day dose levels administered over 1 hour on days 1-5. Study-related toxicities were hypotension (6 patients); greater than 10% weight gain (6 patients); peripheral edema (9 patients); fever (4 patients); confusion (3 patients); diarrhea (3 patients); proteinuria, as identified by dipstick (3 patients), greater than 0.6 mg/dl decrease in serum albumin (11 patients); greater than 25% decrease in oncotic pressure (10 patients), and a decrease in ionized calcium (8 patients). Six patients received a second course of treatment. HAMA levels developed in 9 patients and titers increased with number of courses administered. Decreased overall toxicity, in comparison to the first course, was noted, but one patient had an allergic-type response (hypotension, crushing chest pain, diaphoresis) after the test dose of the second course (HAMA level > 10,000 IgG). Life-threatening toxicity in the form of fluid shift, resulting in noncardiac pulmonary edema and third-spacing occurred after course 1 in 1 of 3 patients at the 0.04 mg/kg per day level. No further dose escalation was attempted and no antitumor activity was seen.

摘要

免疫偶联物XMMCO - 791/RTA由与鼠单克隆抗体MoAb 791T结合的蓖麻毒素A链组成。这种单克隆抗体(MoAb)与一种72kD的糖蛋白结合,该糖蛋白在人结肠直肠癌、卵巢癌和成骨肉瘤中表达。XMMCO - 791/RTA在一项I期试验中进行了测试,提议的剂量递增步骤为每天0.02、0.04、0.15和0.2mg/kg。12例转移性结肠直肠癌患者在第1 - 5天以每天0.02、0.03和0.04mg/kg的剂量水平给药1小时。与研究相关的毒性包括低血压(6例患者);体重增加超过10%(6例患者);外周水肿(9例患者);发热(4例患者);意识模糊(3例患者);腹泻(3例患者);试纸检测发现蛋白尿(3例患者);血清白蛋白下降超过0.6mg/dl(11例患者);胶体渗透压下降超过25%(10例患者),以及离子钙下降(8例患者)。6例患者接受了第二个疗程的治疗。9例患者出现人抗鼠抗体(HAMA)水平升高,且滴度随给药疗程数增加而升高。与第一个疗程相比,总体毒性有所降低,但有1例患者在第二个疗程的试验剂量后出现过敏型反应(低血压、压榨性胸痛、多汗)(HAMA水平>10,000 IgG)。在每天0.04mg/kg剂量水平的3例患者中,有1例在第1个疗程后出现了以液体转移为形式的危及生命的毒性,导致非心源性肺水肿和第三间隙积液。未尝试进一步提高剂量,且未观察到抗肿瘤活性。

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