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免疫毒素N901阻断型蓖麻毒素在小细胞肺癌患者中的应用。

Use of the immunotoxin N901-blocked ricin in patients with small-cell lung cancer.

作者信息

Epstein C, Lynch T, Shefner J, Wen P, Maxted D, Braman V, Ariniello P, Coral F, Ritz J

机构信息

ImmunoGen, Inc., Boston, MA.

出版信息

Int J Cancer Suppl. 1994;8:57-9. doi: 10.1002/ijc.2910570712.

Abstract

In patients with small-cell lung cancer (SCLC), relapse with resistant disease often causes death. N901-blocked ricin (N901-bR), a murine monoclonal antibody (MAb)-blocked ricin immunotoxin, is a potential therapeutic for SCLC. N901-bR targets CD56, present on SCLC and cells of neuro-ectodermal origin. N901-bR kills up to 5 logs of CD56-positive cells at a concentration of 0.25 nM, while CD56-negative cells require 1000-fold more drug to achieve similar cell kill. We treated 21 patients with relapsed or refractory SCLC with a single 7-day course of N901-bR as a continuous infusion. We determined the MTD and toxicity profile, demonstrated drug binding to tumor cells in biopsies of lung, liver and bone marrow, and determined the time to development of human anti-mouse and anti-ricin antibodies. One patient had a documented PR and 6 patients demonstrated stable disease. Toxicity included transient elevation of liver enzymes, mild thrombocytopenia, hypoalbuminemia, fever, malaise, and evidence of capillary leak syndrome. Toxicities were controllable and reversible. No apparent drug-related central- or peripheral-nervous-system toxicity was noted by serial neurologic examinations, EMGs, and nerve conduction studies. Trials of N901-bR are planned in SCLC patients achieving CR and PR following chemoradiotherapy, and in relapsed/refractory patients. Anti-B4-bR will be added as an immunosuppressant in order to permit delivery of multiple courses of N901-bR. Additional trials will investigate synergy with conventional chemotherapeutics and the use of N901-bR as a sensitizing agent for chemotherapy-resistant tumors.

摘要

在小细胞肺癌(SCLC)患者中,耐药性疾病复发常导致死亡。N901封闭型蓖麻毒素(N901-bR)是一种鼠单克隆抗体(MAb)封闭型蓖麻毒素免疫毒素,是SCLC的一种潜在治疗药物。N901-bR靶向CD56,其存在于SCLC和神经外胚层来源的细胞上。N901-bR在浓度为0.25 nM时可杀死多达5个对数的CD56阳性细胞,而CD56阴性细胞需要多1000倍的药物才能达到类似的细胞杀伤效果。我们对21例复发或难治性SCLC患者进行了为期7天的单次N901-bR连续输注治疗。我们确定了最大耐受剂量(MTD)和毒性特征,证明药物在肺、肝和骨髓活检中与肿瘤细胞结合,并确定了人抗鼠和抗蓖麻毒素抗体产生的时间。1例患者有记录的部分缓解(PR),6例患者病情稳定。毒性包括肝酶短暂升高、轻度血小板减少、低白蛋白血症、发热、不适以及毛细血管渗漏综合征的证据。毒性是可控且可逆的。通过系列神经学检查、肌电图(EMG)和神经传导研究未发现明显的与药物相关的中枢或外周神经系统毒性。计划对放化疗后达到完全缓解(CR)和PR的SCLC患者以及复发/难治性患者进行N901-bR试验。将添加抗B4-bR作为免疫抑制剂,以便能够给予多疗程的N901-bR。其他试验将研究与传统化疗药物的协同作用以及N901-bR作为化疗耐药肿瘤致敏剂的用途。

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