Pinnix Chelsea C, Shah Jatin J, Chuang Hubert, Costelloe Colleen M, Medeiros L Jeffrey, Wogan Christine F, Reed Valerie, Smith Grace L, Milgrom Sarah, Patel Krina, Huo Jinhai, Turturro Francesco, Romaguera Jorge, Fayad Luis, Oki Yasuhiro, Fanale Michelle A, Westin Jason, Nastoupil Loretta, Hagemeister Fredrick B, Rodriguez Alma, Qazilbash Muzaffar, Shah Nina, Bashir Qaiser, Ahmed Sairah, Nieto Yago, Hosing Chitra, Rohren Eric, Dabaja Bouthaina
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2016 Mar;16(3):122-8. doi: 10.1016/j.clml.2015.12.008. Epub 2015 Dec 22.
Plasmablastic lymphoma (PBL) is an aggressive variant of diffuse large B-cell lymphoma. We sought to assess the treatment outcomes after combined-modality therapy for early-stage PBL.
We retrospectively reviewed the outcomes of 10 consecutive patients diagnosed with stage I-II PBL from February 2001 to December 2013 at a single institution. The baseline clinical characteristics, treatment modalities, overall outcomes, and treatment-related toxicity were assessed.
The median age at diagnosis was 50.5 years. All patients had extranodal disease; 2 were positive for human immunodeficiency virus. Seven patients received hyper-CVAD (cyclophosphamide, vincristine, doxorubicin, dexamethasone)-based chemotherapy, 2 received CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone), and 1 received dose-adjusted EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin). Radiotherapy (RT) was administered after a complete response to chemotherapy in 7 patients and a partial response in 1 patient. At a median follow-up period of 42 months, the estimated 2-year progression-free and overall survival rates were 90% and 100%, respectively.
PBL can be successfully treated with aggressive chemotherapy followed by RT. The treatment was well tolerated and can result in long-term survival for patients with limited-stage disease.
浆母细胞淋巴瘤(PBL)是弥漫性大B细胞淋巴瘤的一种侵袭性亚型。我们旨在评估早期PBL综合治疗后的治疗效果。
我们回顾性分析了2001年2月至2013年12月在一家机构连续诊断为I-II期PBL的10例患者的治疗结果。评估了基线临床特征、治疗方式、总体结果和治疗相关毒性。
诊断时的中位年龄为50.5岁。所有患者均有结外病变;2例人类免疫缺陷病毒检测呈阳性。7例患者接受了基于大剂量环磷酰胺、长春新碱、阿霉素、地塞米松(hyper-CVAD)的化疗,2例接受了环磷酰胺、阿霉素、长春新碱、泼尼松(CHOP)方案,1例接受了剂量调整的依托泊苷、泼尼松、长春新碱、环磷酰胺、阿霉素(EPOCH)方案。7例患者在化疗完全缓解后接受了放疗(RT),1例部分缓解后接受了放疗。中位随访期为42个月,估计2年无进展生存率和总生存率分别为90%和100%。
PBL采用积极化疗后行放疗可成功治疗。该治疗耐受性良好,可使局限性疾病患者长期生存。