Department of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan.
Department of Hematology Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Jpn J Clin Oncol. 2021 Jan 1;51(1):70-77. doi: 10.1093/jjco/hyaa169.
A phase 1 dose-escalation study of polatuzumab vedotin (pola) was conducted to assess safety, pharmacokinetics and preliminary antitumor activity of pola in Japanese patients with relapsed/refractory B-cell non-Hodgkin lymphoma.
Patients received pola (1.0 or 1.8 mg/kg) intravenously every 21 days until disease progression or intolerance. Intra-patient dose escalation was prohibited. Tolerability was determined by the standard 3 + 3 rule. Blood sampling was performed to characterize pharmacokinetics. Antitumor activity was evaluated through computed tomography and bone marrow sampling.
Four patients received pola 1.0 mg/kg; three received 1.8 mg/kg. Patients had follicular lymphoma (n = 4) or diffuse large B-cell lymphoma (n = 3), median age of 62 years, received a median of 3 prior therapies; six were female. Pola was well tolerated in both cohorts, with no dose-limiting toxicities observed. The most common adverse event was peripheral sensory neuropathy (n = 4). Grade 3 adverse events were cholecystitis and neutrophil count decreased (one each; both 1.0 mg/kg), and syncope and cataract (one each; both 1.8 mg/kg). The plasma half-life of antibody-conjugate monomethyl auristatin E was 4.43-7.98 days, and systemic exposure of unconjugated monomethyl auristatin E was limited in both cohorts. Four patients achieved objective responses (three complete, one partial) without disease progression during the study.
This phase 1 dose-escalation study demonstrated that pola has an acceptable safety profile and offers encouraging antitumor activity to Japanese patients with relapsed/refractory B-cell non-Hodgkin lymphoma. Pola 1.8 mg/kg, the recommended phase 2 dose, was tolerable in Japanese patients.
一项 polatuzumab vedotin(pola)的 1 期剂量递增研究旨在评估 pola 在日本复发/难治性 B 细胞非霍奇金淋巴瘤患者中的安全性、药代动力学和初步抗肿瘤活性。
患者每 21 天静脉注射 pola(1.0 或 1.8mg/kg),直至疾病进展或不耐受。禁止患者内剂量递增。耐受性由标准的 3+3 规则确定。通过计算机断层扫描和骨髓取样评估抗肿瘤活性。进行血样采集以描述药代动力学。
4 名患者接受 pola 1.0mg/kg;3 名患者接受 1.8mg/kg。患者患有滤泡性淋巴瘤(n=4)或弥漫性大 B 细胞淋巴瘤(n=3),中位年龄 62 岁,接受了中位数为 3 次的既往治疗;6 名女性。在两个队列中,pola 均具有良好的耐受性,未观察到剂量限制毒性。最常见的不良事件是周围感觉神经病(n=4)。3 级不良事件为胆囊炎和中性粒细胞计数减少(各 1 例;均为 1.0mg/kg),以及晕厥和白内障(各 1 例;均为 1.8mg/kg)。单甲基奥瑞他汀 E 抗体偶联物的血浆半衰期为 4.43-7.98 天,两个队列中未缀合的单甲基奥瑞他汀 E 的全身暴露均有限。4 名患者在研究期间未发生疾病进展,获得了客观缓解(3 例完全缓解,1 例部分缓解)。
这项 1 期剂量递增研究表明,pola 具有可接受的安全性,并为日本复发/难治性 B 细胞非霍奇金淋巴瘤患者提供了令人鼓舞的抗肿瘤活性。pola 1.8mg/kg,即推荐的 2 期剂量,在日本患者中耐受良好。