Yang Sheng-Hsiang, Hsiao Liang-Tsai, Chiou Tzeon-Jye, Yang Ching-Fen, Yu Yuan-Bin, Liu Chun-Yu, Gau Jyh-Pyng, Liu Jin-Hwang, Chen Po-Min, Tzeng Cheng-Hwai
Division of Hematology and Oncology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan, ROC; National Yang-Ming University School of Medicine, Taipei, Taiwan, ROC; Department of Medicine, National Yang-Ming University Hospital, Ilan, Taiwan, ROC.
Division of Hematology and Oncology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan, ROC; National Yang-Ming University School of Medicine, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2015 Jul;78(7):400-7. doi: 10.1016/j.jcma.2015.02.005. Epub 2015 Mar 20.
Primary mediastinal large B-cell lymphoma (PMBCL) is a rare malignancy that has been reported in young individuals, especially young women. Patients with PMBCL commonly receive rituximab induction. This single-institution study was designed to analyze the clinical benefits of rituximab induction and its impact on postinduction treatments (PITs), especially radiotherapy.
The benefits of rituximab induction were evaluated by complete response (CR), early treatment failure, relapse, and overall survival (OS) rates. The impact of the induction therapy on the adoption of PIT was evaluated by the proportion of patients who had received at the last follow up any PIT modality [i.e., radiotherapy or hematopoietic stem cell transplantation (HSCT)], radiotherapy alone, HSCT alone, or both modalities.
Between 1999 and 2012, 48 PMBCL patients (29 men, 60%) were identified; they had a median age of 31 years. Twenty-eight patients received rituximab induction; of these, 23 (82%) patients also underwent fludeoxyglucose-positron emission tomography (FDG-PET) evaluation. Rituximab induction was significantly associated with higher rates of CR and OS, and lower rates of early treatment failure and relapse. Regarding PIT, patients with rituximab induction were more likely to receive radiotherapy alone [with rituximab induction (25%) vs. without rituximab induction (5%)], and patients with FDG-PET evaluation were similarly more likely to receive radiotherapy alone [with FDG-PET evaluation (28.6%) vs. without FDG-PET evaluation (0%)]. In multivariate analysis, age older than 60 years [hazard ratio (HR), 16.697; 95% confidence interval (CI), 1.106-252.022; p = 0.042] and rituximab induction (HR, 0.089; 95% CI, 0.012-0.653; p = 0.017) were significantly associated with OS.
Rituximab improved the CR and OS rates of patients with PMBCL, but these improvements may be attributable to the increased use of radiotherapy (which may have also resulted from FDG-PET evaluation).
原发性纵隔大B细胞淋巴瘤(PMBCL)是一种罕见的恶性肿瘤,多见于年轻人,尤其是年轻女性。PMBCL患者通常接受利妥昔单抗诱导治疗。本单中心研究旨在分析利妥昔单抗诱导治疗的临床益处及其对诱导治疗后治疗(PIT)的影响,尤其是放疗。
通过完全缓解(CR)率、早期治疗失败率、复发率和总生存率(OS)评估利妥昔单抗诱导治疗的益处。通过在最后随访时接受任何PIT模式[即放疗或造血干细胞移植(HSCT)]、单纯放疗、单纯HSCT或两种模式的患者比例,评估诱导治疗对PIT采用情况的影响。
1999年至2012年期间,共确定48例PMBCL患者(29例男性,占60%);他们的中位年龄为31岁。28例患者接受了利妥昔单抗诱导治疗;其中23例(82%)患者还接受了氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)评估。利妥昔单抗诱导治疗与较高的CR率和OS率显著相关,与较低的早期治疗失败率和复发率相关。关于PIT,接受利妥昔单抗诱导治疗的患者更有可能单纯接受放疗[接受利妥昔单抗诱导治疗(25%)与未接受利妥昔单抗诱导治疗(5%)],接受FDG-PET评估的患者同样更有可能单纯接受放疗[接受FDG-PET评估(28.6%)与未接受FDG-PET评估(0%)]。在多变量分析中,年龄大于60岁[风险比(HR),16.697;95%置信区间(CI),1.106 - 252.022;p = 0.042]和利妥昔单抗诱导治疗(HR,0.089;95%CI,0.012 - 0.653;p = 0.017)与OS显著相关。
利妥昔单抗提高了PMBCL患者的CR率和OS率,但这些改善可能归因于放疗使用的增加(这也可能是FDG-PET评估的结果)。