Department of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, Ohio, USA.
Department of Internal Medicine, The University of Cincinnati, Cincinnati, Ohio, USA.
Am J Hematol. 2023 Jan;98(1):56-65. doi: 10.1002/ajh.26755. Epub 2022 Oct 20.
Chronic lymphocytic leukemia (CLL) transformation to aggressive lymphoma, known as Richter's Transformation (RT), has a dismal prognosis. There are limited data evaluating risk of RT in patients treated with ibrutinib. We performed a retrospective analysis to determine prognostic variables associated with development of RT and overall survival (OS) at progression after treatment with ibrutinib. We identified 559 patients with CLL treated with ibrutinib from 2010-2019. After a median follow-up of 44.5 months from ibrutinib start, 179 patients progressed and were included in our analysis. After a median follow-up of 20.8 months from progression, 54 out of 179 patients developed RT. Progression on treatment (hazard ratio [HR] 4.01 [1.60-10.00], p = .003), higher LDH (HR 1.80 for 2-fold increase [1.33-2.43], p = .0001), and lymphadenopathy without lymphocytosis (HR 2.88 [1.15-7.20], p = .02) were independent prognostic variables for the development of RT at progression. Progression with lymphadenopathy without lymphocytosis continued to be an independent prognostic variable of worse OS post-progression. In a subset analysis of 50 patients who obtained a PET-CT at progression, the median SUV for patients who would develop RT was 15.2 (n = 30, range: 4.0-46.3) versus those patients who did not develop RT with a SUV of 7.7 (n = 20, range: 2.3-27.2) (p = .0030). Median OS from date of RT was 4.0 months, suggesting that prognosis for RT remains poor. A lymph node biopsy to rule out RT should be considered in patients who received ibrutinib who progress on treatment, have an elevated LDH, or progress with lymphadenopathy without lymphocytosis.
慢性淋巴细胞白血病(CLL)向侵袭性淋巴瘤的转化,即里希特转化(RT),预后较差。目前评估接受伊布替尼治疗的患者发生 RT 的风险的数据有限。我们进行了一项回顾性分析,以确定与接受伊布替尼治疗后进展时发生 RT 相关的预后变量和总生存(OS)。我们从 2010 年至 2019 年确定了 559 例接受伊布替尼治疗的 CLL 患者。从伊布替尼开始治疗的中位随访 44.5 个月后,179 例患者进展并纳入我们的分析。从进展后的中位随访 20.8 个月后,179 例患者中有 54 例发生 RT。治疗进展(风险比 [HR] 4.01 [1.60-10.00],p =.003)、较高的乳酸脱氢酶(HR 2 倍增加 [1.33-2.43],p =.0001)和无淋巴细胞增多的淋巴结病(HR 2.88 [1.15-7.20],p =.02)是进展时发生 RT 的独立预后因素。无淋巴细胞增多的淋巴结病进展仍然是进展后 OS 更差的独立预后因素。在进展时获得 PET-CT 的 50 例患者的亚组分析中,将发生 RT 的患者的 SUV 中位数为 15.2(n = 30,范围:4.0-46.3),而未发生 RT 的患者的 SUV 中位数为 7.7(n = 20,范围:2.3-27.2)(p =.0030)。从 RT 发生之日起的中位 OS 为 4.0 个月,表明 RT 的预后仍然较差。对于接受伊布替尼治疗后治疗进展、LDH 升高或无淋巴细胞增多的淋巴结病进展的患者,应考虑进行淋巴结活检以排除 RT。