Welt Sydney, Ritter Gerd, Williams Clarence, Cohen Leonard S, Jungbluth Achim, Richards Elizabeth A, Old Lloyd J, Kemeny Nancy E
Department of Medicine at Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Clin Cancer Res. 2003 Apr;9(4):1347-53.
In previous studies, humanized A33 (huA33) demonstrated modest antitumor activity in chemotherapy-resistant colorectal cancer patients. In addition, unexpected major tumor responses were observed in patients treated with a specific chemotherapy regimen [carmustine, vincristine, fluorouracil, and streptozocin (BOF-Strep)] administered after huA33 protocols. We designed the present Phase I, open label, cohort, dose-escalation study of huA33 and a fixed dose of BOF-Strep to (a) determine the maximum tolerated dose of huA33 immunotherapy administered with chemotherapy, (b) determine whether chemotherapy modifies huA33 immunogenicity, and (c) develop preliminary information regarding antitumor activity.
Stage IV fluorouracil/leucovorin and irinotecan-refractory colorectal cancer patients (n = 16) received escalating weekly doses of huA33 (5-40 mg/m(2)) with BOF-Strep chemotherapy.
Four patients requiring radiotherapy or surgery were removed early. Of 12 evaluable patients, grade 3 and 4 neutropenia (n = 2) and grade 3 thrombocytopenia (n = 1) were observed. Seven of 12 (58.3%) patients developed anti-huA33 activity. Three patients had radiographic partial responses for 7.5, 5.5, and 14 months with greater than 85% decline in serum carcinoembryonic antigen levels. One mixed response (4.5 months with a serum carcinoembryonic antigen decline of 38%) was also observed.
huA33 can be safely combined with BOF-Strep chemotherapy. The present report provides compelling evidence supporting our previous observations of major antitumor activity with the combination of huA33 and BOF-Strep chemotherapy. huA33 is still immunogenic when administered with chemotherapy. Future studies to evaluate the immunogenicity of new huA33 antibodies and identify which drugs in the BOF-Strep regimen are critical for enhanced antitumor efficacy are planned.
在先前的研究中,人源化A33(huA33)在化疗耐药的结直肠癌患者中显示出适度的抗肿瘤活性。此外,在按照huA33方案给药后接受特定化疗方案[卡莫司汀、长春新碱、氟尿嘧啶和链脲佐菌素(BOF-Strep)]治疗的患者中观察到了意外的显著肿瘤反应。我们设计了本项关于huA33和固定剂量BOF-Strep的I期开放标签队列剂量递增研究,以(a)确定与化疗联合使用时huA33免疫疗法的最大耐受剂量,(b)确定化疗是否会改变huA33的免疫原性,以及(c)获取有关抗肿瘤活性的初步信息。
IV期氟尿嘧啶/亚叶酸钙和伊立替康难治性结直肠癌患者(n = 16)接受每周递增剂量的huA33(5 - 40 mg/m²)联合BOF-Strep化疗。
4名需要放疗或手术的患者提前退出。在12名可评估的患者中,观察到3级和4级中性粒细胞减少(n = 2)以及3级血小板减少(n = 1)。12名患者中有7名(58.3%)产生了抗huA33活性。3名患者出现影像学部分缓解,持续时间分别为7.5、5.5和14个月,血清癌胚抗原水平下降超过85%。还观察到1例混合反应(4.5个月,血清癌胚抗原下降38%)。
huA33可安全地与BOF-Strep化疗联合使用。本报告提供了有力证据,支持我们先前关于huA33与BOF-Strep化疗联合具有显著抗肿瘤活性的观察结果。huA33与化疗联合使用时仍具有免疫原性。计划开展未来研究,以评估新型huA33抗体的免疫原性,并确定BOF-Strep方案中的哪些药物对增强抗肿瘤疗效至关重要。