Jung Sung-Hoon, Lee Je-Jung, Kim Kihyun, Suh Cheolwon, Yoon Dok Hyun, Min Chang-Ki, Sohn Sang Kyun, Choi Chul Won, Lee Ho Sup, Kim Hyo Jung, Shin Ho-Jin, Bang Soo-Mee, Yoon Sung-Soo, Park Seong Kyu, Yhim Ho-Young, Kim Min Kyoung, Jo Jae-Cheol, Mun Yeung-Chul, Lee Jae Hoon, Kim Jin Seok
Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Oncotarget. 2017 Jun 16;8(45):79517-79526. doi: 10.18632/oncotarget.18535. eCollection 2017 Oct 3.
Primary plasma cell leukemia (pPCL) is a rare and aggressive plasma cell neoplasm, with rapidly progressing clinical course. We evaluated the treatment status and survival outcomes of 69 Korean patients with pPCL. Of them, 59 patients were treated; 15 (25.4%) were treated initially with novel agent-based regimens with upfront autologous stem cell transplantation (ASCT), 7 (11.9%) with conventional chemotherapy with upfront ASCT, 21 (35.6%) with novel agent-based regimens only, and 16 (27.1%) were treated with conventional chemotherapy alone. Overall response rates after initial therapy were significantly higher in patients treated with novel agent-based regimens compared with those treated with conventional chemotherapies (75% vs. 43.4%, 0.026). Median progression-free survival (PFS) and overall survival (OS) were 12.2 months and 16.1 months, respectively. The median PFS of the four treatment groups-conventional chemotherapy alone, novel agents alone, conventional chemotherapy with ASCT, and novel agents with ASCT-were 1.2, 9.0, 10.5, and 26.4 months, respectively ( < 0.001); the median OS of the four treatment groups were 2.9, 12.3, 14.1, and 31.1 months, respectively ( < 0.001). The median OS was also significantly better in the patients with novel agents with ASCT versus other patients. In a multivariate analysis, an increased lactate dehydrogenase level, low albumin (< 3.5 g/dL), and non-CR after front-line treatment were independently associated with poor PFS and OS. In conclusion, the use of novel agent-based therapy with ASCT and achieving a deep response to front-line treatment are important in expecting improved PFS and OS in patients with pPCL.
原发性浆细胞白血病(pPCL)是一种罕见且侵袭性的浆细胞肿瘤,临床病程进展迅速。我们评估了69例韩国pPCL患者的治疗情况和生存结果。其中,59例患者接受了治疗;15例(25.4%)最初接受了基于新型药物的方案联合早期自体干细胞移植(ASCT)治疗,7例(11.9%)接受了传统化疗联合早期ASCT治疗,21例(35.6%)仅接受基于新型药物的方案治疗,16例(27.1%)仅接受传统化疗。与接受传统化疗的患者相比,接受基于新型药物方案治疗的患者初始治疗后的总体缓解率显著更高(75%对43.4%,P = 0.026)。中位无进展生存期(PFS)和总生存期(OS)分别为12.2个月和16.1个月。四个治疗组(仅传统化疗、仅新型药物、传统化疗联合ASCT、新型药物联合ASCT)的中位PFS分别为1.2、9.0、10.5和26.4个月(P < 0.001);四个治疗组的中位OS分别为2.9、12.3、14.1和31.1个月(P < 0.00)。与其他患者相比,新型药物联合ASCT治疗的患者中位OS也显著更好。在多变量分析中,乳酸脱氢酶水平升高、白蛋白水平低(< 3.5 g/dL)以及一线治疗后未达到完全缓解与不良的PFS和OS独立相关。总之,使用基于新型药物的疗法联合ASCT并在一线治疗中获得深度缓解对于期望改善pPCL患者的PFS和OS很重要。