Laboratory of Stem Cell Biology, Cellular and Tissue Therapy Branch, Division of Cell and Gene Therapies,Office of Cellular, Tissues and Gene Therapies, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Leuk Lymphoma. 2011 Dec;52(12):2284-92. doi: 10.3109/10428194.2011.589547. Epub 2011 Jul 12.
This is a phase I study of 7-hydroxystaurosporine (UCN-01) and fludararbine monophosphate (FAMP) in relapsed lymphoma. UCN-01 alone was administered in cycle 1 and with FAMP in cycles 2-6. FAMP was escalated in cohorts from 1 to 5 days. UCN-01 and FAMP pharmacokinetics and apoptosis of malignant lymphocytes was evaluated. Eighteen patients were enrolled. Standard FAMP with UCN-01 was tolerated without dose-limiting toxicity (DLT) and those seen were common to either agent alone. One patient died due to Stevens-Johnson syndrome. Seven of 18 patients responded. No pharmacological effect of UCN-01 by FAMP was noted. Lymphocytosis occurred in 15 of 18 patients following UCN-01 to paradoxically increase circulating tumor cells. UCN-01 induced apoptosis in six of eight patients with chronic lymphocytic leukemia (CLL). UCN-01 does not increase FAMP toxicity. Transient lymphocytosis followed by apoptosis occurs with UCN-01. Mobilization from tissue reservoirs may play a role in the induction of cell death in malignant lymphocytes.
这是一项关于 7-羟基星形孢菌素(UCN-01)和单磷酸氟达拉滨(FAMP)在复发性淋巴瘤中的 I 期研究。UCN-01 单独在第 1 周期中给药,在第 2-6 周期中与 FAMP 联合给药。FAMP 按队列从 1 天增加到 5 天。评估了 UCN-01 和 FAMP 的药代动力学和恶性淋巴细胞凋亡。共纳入 18 例患者。标准 FAMP 联合 UCN-01 耐受良好,无剂量限制毒性(DLT),且这些毒性与单独使用任一药物时所见相似。1 例患者因 Stevens-Johnson 综合征死亡。18 例患者中有 7 例有反应。未观察到 FAMP 对 UCN-01 的药理学作用。18 例患者中有 15 例在使用 UCN-01 后出现淋巴细胞增多,这与循环肿瘤细胞增加呈矛盾。UCN-01 诱导了 8 例慢性淋巴细胞白血病(CLL)患者中的 6 例细胞凋亡。UCN-01 不会增加 FAMP 的毒性。UCN-01 会引起短暂的淋巴细胞增多,随后发生凋亡。组织储库中的动员可能在诱导恶性淋巴细胞死亡中起作用。