Clinical Pharmacology, Early Clinical Development, Pfizer Inc., 10777 Science Center Drive, San Diego, CA, 92121, USA.
Clinical Development, Early Oncology Development and Clinical Research, Pfizer Inc., San Diego, CA, USA.
Cancer Chemother Pharmacol. 2021 Jan;87(1):23-30. doi: 10.1007/s00280-020-04202-0. Epub 2020 Nov 25.
The ideal starting dose for an oncology first-in-patient (FIP) trial should be low enough to be safe but not too far removed from therapeutically relevant doses. A low starting dose combined with small dose increments could lead to a lengthy dose escalation and could expose patients unnecessarily to sub-therapeutic dosing. In the current analyses, we reviewed 59 approved small molecule oncology drugs (SMOD) with the overarching goals to assess the current approaches of FIP starting dose selection and dose escalation, and to identify potential opportunities for improving trial efficiency and minimizing number of patients receiving sub-therapeutic dose levels. Of 59 SMODs, the majority (~ 66%) were kinase inhibitors and ~ 73% were approved for solid tumor indications. Most of the trials used a 3 + 3 design for dose escalation and had a median (range) of 4 cohorts (0-11) to reach MTD from the starting dose. The maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) to starting dose ratio was highly variable with a median (range) of 8 (0.25-125). About 71% of the FIP trials had < 6 dose escalation steps to reach MTD or RP2D (with 15% ≤ 2 dose escalations), but the remaining 29% of trials had ≥ 6 dose escalation steps to reach MTD or RP2D suggesting that there is still room for increasing efficiency by reducing the number of dose escalation steps, reducing the variability in MTD to starting dose ratio, and consequently reducing significant number of patients exposed at sub-therapeutic doses in the dose escalation phase of FIP study.
肿瘤首次入组(FIP)试验的理想起始剂量应足够低以确保安全,但又不能与治疗相关剂量相差太远。起始剂量低加上剂量递增幅度小,可能导致漫长的剂量爬坡期,并使患者不必要地暴露于亚治疗剂量。在目前的分析中,我们回顾了 59 种已批准的小分子肿瘤药物(SMOD),总体目标是评估 FIP 起始剂量选择和剂量爬坡的当前方法,并确定提高试验效率和减少接受亚治疗剂量水平的患者数量的潜在机会。在 59 种 SMOD 中,大多数(约 66%)为激酶抑制剂,约 73% 为实体瘤适应症所批准。大多数试验采用 3+3 设计进行剂量爬坡,中位数(范围)为 4 个队列(0-11),从起始剂量达到最大耐受剂量(MTD)。从起始剂量到最大耐受剂量(MTD)或推荐的 2 期剂量(RP2D)的比值变化很大,中位数(范围)为 8(0.25-125)。约 71%的 FIP 试验达到 MTD 或 RP2D 所需的剂量爬坡步骤数<6(15%的试验≤2 个剂量爬坡),但其余 29%的试验达到 MTD 或 RP2D 所需的剂量爬坡步骤数≥6,这表明通过减少剂量爬坡步骤数、减少 MTD 与起始剂量比值的变异性,以及减少 FIP 研究剂量爬坡阶段暴露于亚治疗剂量的患者数量,仍有提高效率的空间。