Department of Medicine, Division of Hematology and Medical Oncology, New York Presbyterian Hospital, Weill Medical College of Cornell University, New York, New York 10021, USA.
Cancer. 2012 Nov 15;118(22):5497-506. doi: 10.1002/cncr.27592. Epub 2012 May 8.
It has been demonstrated that the humanized clivatuzumab tetraxetan (hPAM4) antibody targets pancreatic ductal carcinoma selectively. After a trial of radioimmunotherapy that determined the maximum tolerated dose of single-dose yttrium-90-labeled hPAM4 ((90) Y-hPAM4) and produced objective responses in patients with advanced pancreatic ductal carcinoma, the authors studied fractionated radioimmunotherapy combined with low-dose gemcitabine in this disease.
Thirty-eight previously untreated patients (33 patients with stage IV disease and 5 patients with stage III disease) received gemcitabine 200 mg/m(2) weekly for 4 weeks with (90) Y-hPAM4 given weekly in Weeks 2, 3, and 4 (cycle 1), and the same cycle was repeated in 13 patients (cycles 2-4). In the first part of the study, 19 patients received escalating weekly (90) Y doses of 6.5 mCi/m(2) , 9.0 mCi/m(2) , 12.0 mCi/m(2) , and 15.0 mCi/m(2) . In the second portion, 19 additional patients received weekly doses of 9.0 mCi/m(2) or 12.0 mCi/m(2) .
Grade 3/4 thrombocytopenia or neutropenia (according to version 3.0 of the National Cancer Institute's Common Terminology Criteria for Adverse Events) developed in 28 of 38 patients after cycle 1 and in all retreated patients; no grade >3 nonhematologic toxicities occurred. Fractionated dosing of cycle 1 allowed almost twice the radiation dose compared with single-dose radioimmunotherapy. The maximum tolerated dose of (90) Y-hPAM4 was 12.0 mCi/m(2) weekly for 3 weeks for cycle 1, with ≤9.0 mCi/m(2) weekly for 3 weeks for subsequent cycles, and that dose will be used in future trials. Six patients (16%) had partial responses according to computed tomography-based Response Evaluation Criteria in Solid Tumors, and 16 patients (42%) had stabilization as their best response (58% disease control). The median overall survival was 7.7 months for all 38 patients, including 11.8 months for those who received repeated cycles (46% [6 of 13 patients] ≥1 year), with improved efficacy at the higher radioimmunotherapy doses.
Fractionated radioimmunotherapy with (90) Y-hPAM4 and low-dose gemcitabine demonstrated promising therapeutic activity and manageable myelosuppression in patients with advanced pancreatic ductal carcinoma.
已证明人源化 clivatuzumab tetraxetan(hPAM4)抗体可选择性靶向胰腺导管腺癌。在一项确定单剂量钇-90 标记的 hPAM4((90)Y-hPAM4)最大耐受剂量的放射免疫治疗试验后,该研究作者研究了在这种疾病中联合低剂量吉西他滨的分次放射免疫治疗。
38 例未经治疗的患者(33 例 IV 期疾病和 5 例 III 期疾病)接受吉西他滨 200mg/m2 每周 4 周,(90)Y-hPAM4 每周在第 2、3 和 4 周(第 1 周期)给予,13 例患者重复相同的周期(第 2-4 周期)。在研究的第一部分,19 例患者接受递增剂量的每周(90)Y 6.5mCi/m2、9.0mCi/m2、12.0mCi/m2 和 15.0mCi/m2。在第二部分,另外 19 例患者接受每周 9.0mCi/m2 或 12.0mCi/m2 的剂量。
在第 1 周期后和所有复治患者中,38 例患者中有 28 例出现 3/4 级血小板减少或中性粒细胞减少(根据国立癌症研究所不良事件通用术语标准 3.0);没有发生 >3 级非血液学毒性。第 1 周期的分次剂量允许与单次放射免疫治疗相比,辐射剂量几乎增加了一倍。第 1 周期的(90)Y-hPAM4 最大耐受剂量为每周 12.0mCi/m2 持续 3 周,随后周期的剂量为每周≤9.0mCi/m2 持续 3 周,该剂量将用于未来的试验。根据实体瘤反应评估标准(RECIST),6 例患者(16%)有部分缓解,16 例患者(42%)有最佳反应(58%疾病控制)。所有 38 例患者的中位总生存期为 7.7 个月,包括接受重复周期治疗的 11.8 个月(13 例患者中有 6 例[60%]≥1 年),高放射免疫治疗剂量时疗效提高。
(90)Y-hPAM4 和低剂量吉西他滨的分次放射免疫治疗在晚期胰腺导管腺癌患者中显示出有希望的治疗活性和可管理的骨髓抑制。