Department of Hematology, Oncology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.
Department of Hematology and Transplantology, Medical University of Gdańsk, Gdańsk, Poland.
Hematol Oncol. 2019 Oct;37(4):383-391. doi: 10.1002/hon.2624. Epub 2019 Jun 14.
Richter transformation (RT) of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) to Hodgkin lymphoma (HL) is a rare and unexpected event in the course of the disease and data on this phenomenon is still limited. To better understand the clinical and histological characteristics and the outcomes of HL variant of RT (HvRS) the Polish Lymphoma Research Group performed a nationwide survey which identified 22 patients with histologically proven HvRS diagnosed between 2002 and 2016. There were 16 (73%) males. The median age at CLL/SLL and HvRS diagnosis was 59 (39-77) and 64 (40-77) years, respectively. The median interval between CLL/SLL and HvRS diagnosis was 38 months (range: 0-187). All patients had an advanced stage HL, and majority, 17 (77%), presented with B symptoms. The predominant subtypes of HL were nodular sclerosis (12; 55%) and mixed cellularity (9; 41%). Eighteen patients received non-palliative treatment, including 13 who received driamycin, bleomycin, vinblastine, and dacarbazine (ABVD) regimen first line. Objective response was: 50%, with 33% complete remissions (61% and 46% for ABVD, respectively). Median overall survival reached 13.3 months (95% CI, 3.7-NA). The only adverse prognostic factor for survival was a higher number (≤1 versus ≥2) of prior lines of treatment given for CLL/SLL with HR 3.57 (95% CI, 1.16-10.92). We conclude, HvRS harbors a poor prognosis, especially in patients heavily pretreated for CLL/SLL. Response to standard first-line anti-HL chemotherapy is unsatisfactory, and new agents should be tested to improve the outcome.
Richter 转化(RT)慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)至霍奇金淋巴瘤(HL)是疾病过程中的罕见和意外事件,关于这种现象的数据仍然有限。为了更好地了解 HL 变体的 RT(HvRS)的临床和组织学特征和结果,波兰淋巴瘤研究组进行了一项全国性调查,该调查确定了 2002 年至 2016 年间诊断出的 22 例经组织学证实的 HvRS 患者。男性 16 例(73%)。CLL/SLL 和 HvRS 诊断时的中位年龄分别为 59(39-77)和 64(40-77)岁。CLL/SLL 和 HvRS 诊断之间的中位间隔为 38 个月(范围:0-187)。所有患者均为晚期 HL,多数患者 17 例(77%)出现 B 症状。HL 的主要亚型为结节性硬化症(12 例;55%)和混合细胞性(9 例;41%)。18 例患者接受了非姑息性治疗,包括 13 例患者接受了阿霉素、博来霉素、长春新碱和达卡巴嗪(ABVD)一线治疗。客观缓解率为 50%,完全缓解率为 33%(ABVD 分别为 61%和 46%)。中位总生存期达到 13.3 个月(95%CI,3.7-N/A)。生存的唯一不良预后因素是为 CLL/SLL 接受的治疗线数较多(≤1 与≥2),风险比为 3.57(95%CI,1.16-10.92)。我们得出结论,HvRS 预后不良,尤其是在为 CLL/SLL 接受过多线治疗的患者中。对标准一线抗 HL 化疗的反应不理想,应测试新的药物以改善预后。