Alsina Melissa, Fonseca Rafael, Wilson Edward F, Belle A Nelida, Gerbino Elvira, Price-Troska Tammy, Overton Rose M, Ahmann Gregory, Bruzek Laura M, Adjei Alex A, Kaufmann Scott H, Wright John J, Sullivan Daniel, Djulbegovic Benjamin, Cantor Alan B, Greipp Philip R, Dalton William S, Sebti Saïd M
Experimental Therapeutics Program, H. Lee Moffitt Cancer Center & Research Institute and Department of Oncology, University of South Florida, Tampa, FL 33612, USA.
Blood. 2004 May 1;103(9):3271-7. doi: 10.1182/blood-2003-08-2764. Epub 2004 Jan 15.
Patients with multiple myeloma (MM) with mutated RAS are less likely to respond to chemotherapy and have a shortened survival. Therefore, targeting RAS farnesylation may be a novel approach to treatment of MM. We evaluated the activity and tolerability of the farnesyltransferase (FTase) inhibitor tipifarnib (Zarnestra) in a phase 2 trial as well as its ability to inhibit protein farnesylation and oncogenic pathways in patients with relapsed MM. Forty-three patients (median age, 62 years [range, 33-82 years]) with a median of 4 (range, 1-6) chemotherapy regimens entered the study. Tipifarnib, 300 mg orally twice daily, was administered for 3 weeks every 4 weeks. The most common toxicity was fatigue occurring in 66% of patients. Other toxicities included diarrhea, nausea, neuropathy, anemia, and thrombocytopenia. Sixty-four percent of the patients had disease stabilization. Treatment with tipifarnib suppressed FTase (but not geranylgeranyltransferase I) in bone marrow and peripheral blood mononuclear cells and also inhibited the farnesylation of HDJ-2 in unfractionated mononuclear cells and purified myeloma cells. Inhibition of farnesylation did not correlate with disease stabilization. Finally, tipifarnib decreased the levels of phosphorylated Akt and STAT3 (signal transducer and activator of transcription 3) but not Erk1/2 (extracellular signal regulated kinase 1 and 2) in bone marrow cells. We conclude that tipifarnib is tolerable, can induce disease stabilization, and can inhibit farnesylation and oncogenic/tumor survival pathways.
具有RAS基因突变的多发性骨髓瘤(MM)患者对化疗的反应较小,生存期缩短。因此,靶向RAS法尼基化可能是治疗MM的一种新方法。我们在一项2期试验中评估了法尼基转移酶(FTase)抑制剂替匹法尼(Zarnestra)的活性和耐受性,以及其对复发MM患者蛋白质法尼基化和致癌途径的抑制能力。43例患者(中位年龄62岁[范围33 - 82岁]),接受过的化疗方案中位数为4个(范围1 - 6个),进入了该研究。替匹法尼,口服300 mg,每日2次,每4周给药3周。最常见的毒性是疲劳,66%的患者出现。其他毒性包括腹泻、恶心、神经病变、贫血和血小板减少。64%的患者病情稳定。替匹法尼治疗抑制了骨髓和外周血单个核细胞中的FTase(但不抑制香叶基香叶基转移酶I),也抑制了未分级单个核细胞和纯化骨髓瘤细胞中HDJ - 2的法尼基化。法尼基化的抑制与病情稳定无关。最后,替匹法尼降低了骨髓细胞中磷酸化Akt和STAT3(信号转导和转录激活因子3)的水平,但未降低Erk1/2(细胞外信号调节激酶1和2)的水平。我们得出结论,替匹法尼耐受性良好,可诱导病情稳定,并可抑制法尼基化和致癌/肿瘤存活途径。