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伊布替尼用于初治慢性淋巴细胞白血病/小淋巴细胞淋巴瘤日本患者的I期研究。

Phase I study of ibrutinib in Japanese patients with treatment-naïve chronic lymphocytic leukemia/small lymphocytic lymphoma.

作者信息

Shibayama Hirohiko, Teshima Takanori, Choi Ilseung, Hatake Kiyohiko, Sekiguchi Naohiro, Yoshinari Nozomi

出版信息

J Clin Exp Hematop. 2019;59(4):179-186. doi: 10.3960/jslrt.19023.

Abstract

This phase I study evaluated the safety and efficacy of single-agent ibrutinib in Japanese patients with treatment-naïve chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (aged 20-69 years and ineligible for chemotherapy using fludarabine or cyclophosphamide, or aged ≥70 years). Eight patients received oral ibrutinib 420 mg once daily until progressive disease or unacceptable toxicity. The primary endpoint was safety; secondary endpoints included the overall response rate (ORR). At the time of final analysis (August 22, 2018), eight patients (all with CLL; median age, 68.5 years) had received ibrutinib for a median of 32.2 months (range, 10.4-35.9); all patients had discontinued study treatment, with 50.0% of patients switching to marketing-approved ibrutinib as subsequent anticancer therapy. All patients had ≥1 adverse event (AE); the most common AEs included a decreased platelet count, upper respiratory tract infection, increased lymphocyte count, diarrhea, nasopharyngitis, peripheral edema and rash. Four patients (50.0%) had a total of eight grade ≥3 AEs, most commonly lung infection and decreased neutrophil count. Eight serious AEs were reported in four patients (50.0%); these included a case of muscle hemorrhage (grade 3), decreased neutrophil count (grade 4) that led to dose reduction and one case of fatal cardiac arrest. The ORR was 87.5% (7/8 patients [exact 95% confidence interval 47.3-99.7]). One patient had a complete response, six had a partial response and one had a partial response with lymphocytosis. Ibrutinib had an acceptable safety profile and high ORR in Japanese patients with treatment-naïve CLL.

摘要

本I期研究评估了单药伊布替尼在未经治疗的日本慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤患者(年龄20 - 69岁,不符合使用氟达拉滨或环磷酰胺进行化疗的条件,或年龄≥70岁)中的安全性和疗效。8例患者接受口服伊布替尼420 mg,每日1次,直至疾病进展或出现不可接受的毒性。主要终点为安全性;次要终点包括总缓解率(ORR)。在最终分析时(2018年8月22日),8例患者(均为CLL;中位年龄68.5岁)接受伊布替尼治疗的中位时间为32.2个月(范围10.4 - 35.9个月);所有患者均停止了研究治疗,50.0%的患者转为使用已上市批准的伊布替尼作为后续抗癌治疗。所有患者均发生≥1次不良事件(AE);最常见的AE包括血小板计数减少、上呼吸道感染、淋巴细胞计数增加、腹泻、鼻咽炎、外周水肿和皮疹。4例患者(50.0%)共发生8次≥3级AE,最常见的是肺部感染和中性粒细胞计数减少。4例患者(50.0%)报告了8次严重AE;其中包括1例肌肉出血(3级)、导致剂量减少的中性粒细胞计数减少(4级)和1例致命性心脏骤停。ORR为87.5%(8例患者中的7例[确切95%置信区间47.3 - 99.7])。1例患者完全缓解,6例部分缓解,1例部分缓解伴淋巴细胞增多。伊布替尼在未经治疗的日本CLL患者中具有可接受的安全性和高ORR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0733/6954169/3ecd9e6dd722/jslrt-59-179-g001.jpg

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