Salmon S E, Durie B G
Arch Intern Med. 1975 Jan;135(1):131-8.
Previous studies of myeloma immunoglobulin synthesis and tumor cell number, using a marker kinetic approach, have increased knowledge about body bruden of tumor cells, kinetics of myeloma cell growth, and response to chemotherapy. On the basis of these observations, we have developed a clinical staging system that permits accurate estimation of total myeloma cell number in patients who have not had specialized immunosynthetic measurements. We have incorporated this clinical staging into a nationwide time-sharing computer network called the Myeloma Study System (MSS). With the MSS we are able to establish a file for each patient, keep track of changes in tumor cell number with treatment, and evaluate toxicity. This resource should afford an excellent test of the value of cellular kinetics for the planning and uniform evaluation of cancer chemotherapy.
以往采用标记动力学方法对骨髓瘤免疫球蛋白合成及肿瘤细胞数量进行的研究,增加了我们对肿瘤细胞体内负荷、骨髓瘤细胞生长动力学以及化疗反应的认识。基于这些观察结果,我们开发了一种临床分期系统,可对未进行专门免疫合成测量的患者的骨髓瘤细胞总数进行准确估算。我们已将此临床分期纳入一个名为骨髓瘤研究系统(MSS)的全国性分时计算机网络。借助MSS,我们能够为每位患者建立一个档案,跟踪治疗过程中肿瘤细胞数量的变化,并评估毒性。这一资源应为细胞动力学在癌症化疗规划和统一评估中的价值提供一个很好的检验。