CLL Program, Leukemia Service, Division of Hematologic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
University of Texas MD Anderson Cancer Center, Houston, TX.
Haematologica. 2019 Nov;104(11):2258-2264. doi: 10.3324/haematol.2018.207068. Epub 2019 Mar 28.
The utility of positron emission tomography-computed tomography (PET-CT) in distinguishing Richter's transformation chronic lymphocytic leukemia (CLL) progression after ibrutinib and/or idelalisib was assessed in a analysis of a phase II study of venetoclax. Patients underwent PET-CT at screening and were not enrolled/treated if Richter's transformation was confirmed pathologically. Of 167 patients screened, 57 met criteria for biopsy after PET-CT. Of 35 patients who underwent biopsy, eight had Richter's transformation, two had another malignancy, and 25 had CLL. A PET-CT maximum standardized uptake value (SUVmax) ≥10 had 71% sensitivity and 50% specificity for detecting Richter's transformation [Odds Ratio (OR): 2.5, 95%CI: 0.4-15; =0.318]. Response rate to venetoclax was similar for screening SUVmax <10 ≥10 (65% 62%) (n=127 enrolled), though median progression-free survival was longer at <10 months (24.7 15.4 months; =0.0335). Six patients developed Richter's transformation on venetoclax, of whom two had screening biopsy demonstrating CLL (others did not have a biopsy) and five had screening SUVmax <10. We have defined the test characteristics for PET-CT to distinguish progression of CLL as compared to Richter's transformation when biopsied in patients treated with B-cell receptor signaling pathway inhibitors. Overall diminished sensitivity and specificity as compared to prior reports of patients treated with chemotherapy/chemoimmunotherapy suggest it has diminished ability to discriminate these two diagnoses using a SUVmax ≥10 cutoff. This cutoff did not identify venetoclax-treated patients with an inferior response but may be predictive of inferior progression-free survival. (Registered at ).
评估了正电子发射断层扫描-计算机断层扫描(PET-CT)在伊布替尼和/或idelalisib 后区分利妥昔单抗转化慢性淋巴细胞白血病(CLL)进展的效用,这是一项 Venetoclax 二期研究的分析。患者在筛查时进行 PET-CT,如果病理证实发生利妥昔单抗转化,则不参与/治疗。在 167 例筛查患者中,57 例符合 PET-CT 后活检标准。在 35 例接受活检的患者中,8 例发生利妥昔单抗转化,2 例发生另一种恶性肿瘤,25 例发生 CLL。PET-CT 最大标准化摄取值(SUVmax)≥10 对检测利妥昔单抗转化的敏感性为 71%,特异性为 50%[优势比(OR):2.5,95%CI:0.4-15;=0.318]。Venetoclax 治疗的 SUVmax<10 和≥10 的患者的缓解率相似(65%和 62%)(n=127 例入组),但 SUVmax<10 的患者中位无进展生存期更长(24.7 个月和 15.4 个月;=0.0335)。6 例患者在 Venetoclax 治疗期间发生利妥昔单抗转化,其中 2 例在筛查活检中显示 CLL(其余患者未进行活检),5 例在筛查时 SUVmax<10。我们已经确定了在接受 B 细胞受体信号通路抑制剂治疗的患者中,用 PET-CT 区分 CLL 进展与利妥昔单抗转化的试验特征。与接受化疗/化疗免疫治疗的患者的先前报告相比,总体敏感性和特异性降低表明,使用 SUVmax≥10 作为截止值,其区分这两种诊断的能力降低。该截止值不能识别 Venetoclax 治疗反应较差的患者,但可能预示着无进展生存期较差。(注册于)。