Grogan T M, Spier C M, Salmon S E, Matzner M, Rybski J, Weinstein R S, Scheper R J, Dalton W S
Department of Pathology, University of Arizona, College of Medicine, Tucson 85724.
Blood. 1993 Jan 15;81(2):490-5.
Multidrug-resistant (MDR) myeloma patients failing chemotherapy may express P-glycoprotein (PGP), which serves as an efflux pump protecting the neoplastic cells. Unknown is whether PGP expression might relate to prior cytotoxic drug exposure. To address this question, we studied 106 consecutive bone marrow samples from 104 myeloma patients with samples studied either before or after therapy and at the time of relapse. We performed an established immunocytochemical assay of PGP using an MDR-1-specific monoclonal antibody and correlated PGP status with prior chemotherapy dosage. Myeloma patients with no prior therapy had a low incidence of PGP expression (6%, 3/47), whereas those receiving chemotherapy had a significantly higher incidence (43%, 21/49) (P < .0001). A substantially higher incidence of PGP expression (50%, 83%, respectively) occurred when the total vincristine dose exceeded 20 mg and when doxorubicin exceeded 340 mg. In the 11 patients who received both high vincristine and doxorubicin dosages (> 20 mg, > 340 mg total dose) there was 100% incidence of PGP expression in the tumor cells. These data provided the basis for a predictive mathematical model from which dose-related PGP expression normograms were generated. Time with myeloma for PGP-negative patients (mean 33 months) had overlapping confidence limits with PGP-positive patients (mean 42 months), suggesting that disease duration was not a significant variable. PGP expression did not correlate with other clinical factors or immunophenotypic factors. Our findings indicate a strong correlation between PGP expression in myeloma and past chemotherapy in myeloma, in particular, related to prior exposure to the natural product agents vincristine and doxorubicin. Additionally, the proportion of PGP-positive plasma cells was significantly higher in the doxorubicin-treated patients than the nondoxorubicin-treated patients (87.7% v 65.17%; P = .013). Combined high vincristine and doxorubicin total dosage appear highly predictive of PGP expression.
化疗失败的多药耐药(MDR)骨髓瘤患者可能表达P-糖蛋白(PGP),它作为一种外排泵保护肿瘤细胞。PGP表达是否与先前接触细胞毒性药物有关尚不清楚。为解决这个问题,我们研究了104例骨髓瘤患者的106份连续骨髓样本,样本在治疗前或治疗后以及复发时进行研究。我们使用MDR-1特异性单克隆抗体对PGP进行了既定的免疫细胞化学检测,并将PGP状态与先前的化疗剂量相关联。未接受过先前治疗的骨髓瘤患者PGP表达发生率较低(6%,3/47),而接受化疗的患者发生率显著更高(43%,21/49)(P<0.0001)。当长春新碱总剂量超过20mg以及阿霉素超过340mg时,PGP表达发生率显著更高(分别为50%,83%)。在11例接受高剂量长春新碱和阿霉素(>20mg,总剂量>340mg)的患者中,肿瘤细胞中PGP表达发生率为100%。这些数据为一个预测数学模型提供了基础,据此生成了剂量相关的PGP表达正态图。PGP阴性患者的骨髓瘤病程(平均33个月)与PGP阳性患者(平均42个月)的置信区间重叠,表明疾病持续时间不是一个显著变量。PGP表达与其他临床因素或免疫表型因素无关。我们的研究结果表明,骨髓瘤中PGP表达与骨髓瘤过去的化疗之间存在很强的相关性,特别是与先前接触天然产物药物长春新碱和阿霉素有关。此外,阿霉素治疗患者中PGP阳性浆细胞的比例显著高于未接受阿霉素治疗的患者(87.7%对65.17%;P=0.013)。长春新碱和阿霉素的联合高总剂量似乎高度预测PGP表达。