Lee Choon-Kee, Barlogie Bart, Munshi Nikhil, Zangari Maurizio, Fassas Athanasios, Jacobson Joth, van Rhee Frits, Cottler-Fox Michele, Muwalla Firas, Tricot Guido
The Myeloma Institute for Research and Therapy, The University of Arkansas for Medical Sciences, Slot 776, 4301 West Markham, Little Rock, AR 72205, USA.
J Clin Oncol. 2003 Jul 15;21(14):2732-9. doi: 10.1200/JCO.2003.01.055.
To improve outcome in previously treated patients (at least two cycles of standard therapy) with multiple myeloma, thalidomide was combined with cytotoxic chemotherapy as induction therapy.
The regimen consisted of 4-days of oral dexamethasone, daily thalidomide, and 4 days of continuous-infusion cisplatin, doxorubicin, cyclophosphamide, and etoposide (DTPACE). Response to two cycles of DTPACE for induction was evaluated in 236 patients. Before being treated with DTPACE, 148 patients (63%) had shown progressive disease while receiving standard chemotherapy, and 55 patients (23%) had chromosome 13 abnormalities.
The partial remission rate (PR) after two cycles of DTPACE was 32%, with 16% attaining a complete remission (CR) or near-CR (nCR; defined as only immunofixation electrophoresis-positive). Patients with high lactate dehydrogenase (LDH; n = 98) showed a better response than those with normal LDH (n = 138): PR or better, 43% v 27% (P =.01); CR + nCR, 25% v 11% (P =.01). Patients with chromosome 13 abnormalities (n = 55) responded equally well as the other patients (n = 181): PR or better, 35% v 33% (P =.84); CR + nCR, 17% v 15% (P =.73). Patients who received 100% dose of DTPACE for two cycles (n = 115) achieved higher response rates than those with less than 100% dose (n = 121): PR or better, 49% v 17% (P <.0001); CR + nCR, 27% v 6% (P <.0001).
Combination therapy of oral dexamethasone and thalidomide with infusional chemotherapy is effective as induction therapy before autotransplantation, especially in patients with high-risk features.
为了改善先前接受过治疗(至少两个周期的标准治疗)的多发性骨髓瘤患者的治疗效果,将沙利度胺与细胞毒性化疗联合作为诱导治疗。
该方案包括4天的口服地塞米松、每日服用沙利度胺,以及4天持续输注顺铂、阿霉素、环磷酰胺和依托泊苷(DTPACE)。对236例患者进行了两个周期DTPACE诱导治疗的疗效评估。在接受DTPACE治疗前,148例患者(63%)在接受标准化疗时出现疾病进展,55例患者(23%)存在13号染色体异常。
两个周期DTPACE治疗后的部分缓解率(PR)为32%,16%达到完全缓解(CR)或接近完全缓解(nCR;定义为仅免疫固定电泳阳性)。乳酸脱氢酶(LDH)水平高的患者(n = 98)比LDH水平正常的患者(n = 138)反应更好:PR或更好,分别为43%对27%(P = 0.01);CR + nCR,分别为25%对11%(P = 0.01)。存在13号染色体异常的患者(n = 55)与其他患者(n = 181)反应相当:PR或更好,分别为35%对33%(P = 0.84);CR + nCR,分别为17%对15%(P = 0.73)。接受两个周期100%剂量DTPACE的患者(n = 115)比接受剂量低于100%的患者(n = 121)获得更高的缓解率:PR或更好,分别为49%对17%(P < 0.0001);CR + nCR,分别为27%对6%(P < 0.0001)。
口服地塞米松和沙利度胺与输注化疗的联合治疗作为自体移植前的诱导治疗是有效的,尤其是在具有高危特征的患者中。