Villalona-Calero M A, Eckardt J, Burris H, Kraynak M, Fields-Jones S, Bazan C, Lancaster J, Hander T, Goldblum R, Hammond L, Bari A, Drengler R, Rothenberg M, Hadovsky G, Von Hoff D D
Institute for Drug Development, Cancer Therapy and Research Center, San Antonio, TX, USA.
Ann Oncol. 1998 Jan;9(1):71-7. doi: 10.1023/a:1008251426425.
Human corticotropin-releasing factor (hCRF) is an endogenous peptide responsible for the secretion and synthesis of corticosteroids. In animal models of peritumoral brain edema, hCRF has significant anti-edematous action. This effect, which appears to be independent of the release of adrenal steroids, appears mediated by a direct effect on endothelial cells. We conducted a feasibility and phase I study with hCRF given by continuous infusion to patients with brain metastasis.
Peritumoral brain edema documented by MRI and the use of either no steroids or stable steroid doses for more than a week were required. MRIs were repeated at completion of infusion and estimations by dual echo-image sequence (Proton density and T2-weighted images) of the amount of peritumoral edema were performed. The study was performed in two stages. In the feasibility part, patients were randomized to receive either 0.66 or 1 microgram/kg/h of hCRF or placebo over 24 hours. The second part was a dose finding study of hCRF over 72 hours at escalating doses.
Seventeen patients were enrolled; only one was receiving steroids (stable doses) at study entrance; dose-limiting toxicity (hypotension) was observed at 4 micrograms/kg/h x 72 hours in two out of four patients, while zero of five patients treated at 2 micrograms/kg/h developed dose-limiting toxicities. Flushing and hot flashes were also observed. Improvement of neurological symptoms and/or exam were seen in 10 patients. Only small changes were detected by MRI. Improvement in symptoms did not correlate with changes in cortisol levels, and changes in cortisol levels were not correlated with changes in peritumoral edema.
hCRF is well tolerated in doses up to 2 micrograms/kg/h by continuous infusion x 72 hours. Hypotension limits administration of higher doses. The observation of clinical benefit in the absence of corticosteroids suggests hCRF may be an alternative to steroids for the treatment of patients with peritumoral brain edema. Further exploration of this agent in efficacy studies is warranted.
人促肾上腺皮质激素释放因子(hCRF)是一种内源性肽,负责皮质类固醇的分泌和合成。在瘤周脑水肿的动物模型中,hCRF具有显著的抗水肿作用。这种作用似乎独立于肾上腺类固醇的释放,似乎是通过对内皮细胞的直接作用介导的。我们对脑转移患者持续输注hCRF进行了一项可行性和I期研究。
需要通过MRI记录瘤周脑水肿,且患者未使用类固醇或稳定类固醇剂量超过一周。输注结束时重复进行MRI检查,并通过双回波图像序列(质子密度和T2加权图像)估计瘤周水肿量。该研究分两个阶段进行。在可行性部分,患者被随机分配在24小时内接受0.66或1微克/千克/小时的hCRF或安慰剂。第二部分是在72小时内以递增剂量进行的hCRF剂量探索研究。
共纳入17例患者;研究开始时只有1例患者接受类固醇(稳定剂量)治疗;4例患者中有2例在4微克/千克/小时×72小时时观察到剂量限制性毒性(低血压),而5例接受2微克/千克/小时治疗的患者中无一例出现剂量限制性毒性。还观察到面部潮红和潮热。10例患者的神经症状和/或检查有改善。MRI仅检测到微小变化。症状改善与皮质醇水平变化无关,皮质醇水平变化与瘤周水肿变化也无关。
连续输注72小时,hCRF剂量高达2微克/千克/小时时耐受性良好。低血压限制了更高剂量的给药。在无皮质类固醇的情况下观察到临床获益表明,hCRF可能是治疗瘤周脑水肿患者的类固醇替代药物。有必要在疗效研究中进一步探索该药物。