Dalton W S, Grogan T M, Meltzer P S, Scheper R J, Durie B G, Taylor C W, Miller T P, Salmon S E
Department of Medicine, University of Arizona, College of Medicine, Tucson.
J Clin Oncol. 1989 Apr;7(4):415-24. doi: 10.1200/JCO.1989.7.4.415.
The B-cell neoplasms, multiple myeloma and non-Hodgkin's lymphoma, frequently become drug resistant, despite initial responses to chemotherapeutic drugs. Tumor cells from eight patients with clinically drug-refractory disease were evaluated by immuno-histochemical staining for monoclonal immunoglobulin (Ig) expression, nuclear proliferation antigen, P-glycoprotein (P-gly) expression, and other cellular antigens. P-gly was detected on tumor cells from six of eight patients with drug-resistant disease. Of the six patients with P-gly-positive tumors, five patients had advanced multiple myeloma and one had a drug-refractory non-Hodgkin's lymphoma. Cellular RNA analysis confirmed the over-expression of P-gly. In an effort to overcome drug resistance, a pilot study evaluated possible verapamil enhancement of chemotherapy in these eight patients. All patients had developed progressive disease while receiving a regimen containing vincristine and doxorubicin, and seven of eight patients had previously received continuous infusion vincristine and doxorubicin plus oral dexamethasone (VAD). At the time of progressive disease, continuous infusion verapamil was added to the VAD regimen. Three of the eight patients who were refractory to vincristine and doxorubicin alone responded when verapamil was added to VAD. The three patients who responded had P-gly-positive tumors. Verapamil increased the intracellular accumulation of doxorubicin and vincristine in vitro for both a P-gly-positive myeloma cell line and tumor cells from two patients with end-stage myeloma which over-expressed P-gly. The dose-limiting side effect associated with the addition of verapamil to chemotherapy was temporary impairment of cardiac function, manifest as hypotension and cardiac arrhythmia. We conclude that P-gly expression occurs in drug-refractory B-cell neoplasms and may contribute to the development of clinical drug resistance. However, other factors, such as the proliferative activity of the tumor, may also play a role in determining response to chemotherapy. The administration of verapamil along with VAD chemotherapy may partially circumvent drug resistance in patients whose tumors over-express P-gly.
B细胞肿瘤、多发性骨髓瘤和非霍奇金淋巴瘤,尽管对化疗药物最初有反应,但经常会产生耐药性。对8例临床耐药疾病患者的肿瘤细胞进行免疫组织化学染色,评估单克隆免疫球蛋白(Ig)表达、核增殖抗原、P-糖蛋白(P-gly)表达及其他细胞抗原。在8例耐药疾病患者中,有6例的肿瘤细胞检测到P-糖蛋白。在这6例P-糖蛋白阳性肿瘤患者中,5例患有晚期多发性骨髓瘤,1例患有耐药性非霍奇金淋巴瘤。细胞RNA分析证实了P-糖蛋白的过度表达。为了克服耐药性,一项初步研究评估了维拉帕米对这8例患者化疗的可能增强作用。所有患者在接受含长春新碱和阿霉素的方案治疗时均出现疾病进展,8例患者中有7例先前接受过长春新碱和阿霉素持续输注加口服地塞米松(VAD)治疗。在疾病进展时,将维拉帕米持续输注添加到VAD方案中。8例单独对长春新碱和阿霉素耐药的患者中,有3例在维拉帕米添加到VAD方案后有反应。有反应的3例患者肿瘤细胞P-糖蛋白呈阳性。维拉帕米在体外增加了P-糖蛋白阳性骨髓瘤细胞系以及来自2例晚期骨髓瘤且P-糖蛋白过度表达患者的肿瘤细胞内阿霉素和长春新碱的蓄积。将维拉帕米添加到化疗中相关的剂量限制性副作用是心脏功能暂时受损,表现为低血压和心律失常。我们得出结论,P-糖蛋白表达出现在耐药性B细胞肿瘤中,可能导致临床耐药的发生。然而,其他因素,如肿瘤的增殖活性,在决定化疗反应中也可能起作用。维拉帕米与VAD化疗联合应用可能会部分克服肿瘤过度表达P-糖蛋白患者的耐药性。