Driessen Christoph, Kraus Marianne, Joerger Markus, Rosing Hilde, Bader Jürgen, Hitz Felicitas, Berset Catherine, Xyrafas Alexandros, Hawle Hanne, Berthod Gregoire, Overkleeft Hermann S, Sessa Christiana, Huitema Alwin, Pabst Thomas, von Moos Roger, Hess Dagmar, Mey Ulrich J M
Department of Oncology/Hematology, Kantonsspital St. Gallen, Switzerland
Department of Oncology/Hematology, Kantonsspital St. Gallen, Switzerland.
Haematologica. 2016 Mar;101(3):346-55. doi: 10.3324/haematol.2015.135780. Epub 2015 Dec 11.
Downregulation of the unfolded protein response mediates proteasome inhibitor resistance in multiple myeloma. The Human Immunodeficieny Virus protease inhibitor nelfinavir activates the unfolded protein response in vitro. We determined dose-limiting toxicity and recommended dose for phase II of nelfinavir in combination with the proteasome inhibitor bortezomib. Twelve patients with advanced hematologic malignancies were treated with nelfinavir (2500-5000 mg/day p.o., days 1-14, 3+3 dose escalation) and bortezomib (1.3 mg/m(2), days 1, 4, 8, 11; 21-day cycles). A run in phase with nelfinavir monotherapy allowed pharmakokinetic/pharmakodynamic assessment of nelfinavir in the presence or absence of concomittant bortezomib. End points included dose-limiting toxicity, activation of the unfolded protein response, proteasome activity, toxicity and response to trial treatment. Nelfinavir 2×2500 mg was the recommended phase II dose identified. Nelfinavir alone significantly up-regulated expression of proteins related to the unfolded protein response in peripheral blood mononuclear cells and inhibited proteasome activity. Of 10 evaluable patients in the dose escalation cohort, 3 achieved a partial response, 4 stable disease for 2 cycles or more, while 3 had progressive disease as best response. In an exploratory extension cohort with 6 relapsed, bortezomib-refractory, lenalidomide-resistant myeloma patients treated at the recommended phase II dose, 3 reached a partial response, 2 a minor response, and one progressive disease. The combination of nelfinavir with bortezomib is safe and shows promising activity in advanced, bortezomib-refractory multiple myeloma. Induction of the unfolded protein response by nelfinavir may overcome the biological features of proteasome inhibitor resistance. (clinicaltrials.gov identifier: 01164709).
未折叠蛋白反应的下调介导了多发性骨髓瘤对蛋白酶体抑制剂的耐药性。人类免疫缺陷病毒蛋白酶抑制剂奈非那韦在体外可激活未折叠蛋白反应。我们确定了奈非那韦与蛋白酶体抑制剂硼替佐米联合使用时的剂量限制毒性和II期推荐剂量。12例晚期血液系统恶性肿瘤患者接受奈非那韦(口服2500 - 5000 mg/天,第1 - 14天,3 + 3剂量递增)和硼替佐米(1.3 mg/m²,第1、4、8、11天;21天为一个周期)治疗。奈非那韦单药治疗的导入期允许在有或无硼替佐米伴随的情况下对奈非那韦进行药代动力学/药效学评估。终点包括剂量限制毒性、未折叠蛋白反应的激活、蛋白酶体活性、毒性以及对试验治疗的反应。确定奈非那韦2×(2500 mg)为推荐的II期剂量。单独使用奈非那韦可显著上调外周血单个核细胞中与未折叠蛋白反应相关的蛋白质表达,并抑制蛋白酶体活性。在剂量递增队列的10例可评估患者中,3例获得部分缓解,4例疾病稳定2个周期或更长时间,而3例最佳反应为疾病进展。在一个探索性扩展队列中,6例复发的、对硼替佐米耐药且对来那度胺耐药的骨髓瘤患者接受推荐的II期剂量治疗,3例达到部分缓解,2例轻微缓解,1例疾病进展。奈非那韦与硼替佐米联合使用安全,在晚期、对硼替佐米耐药的多发性骨髓瘤中显示出有前景的活性。奈非那韦诱导未折叠蛋白反应可能克服蛋白酶体抑制剂耐药的生物学特性。(临床试验.gov标识符:01164709)