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B 细胞受体通路抑制剂治疗后慢性淋巴细胞白血病患者正电子发射断层扫描-计算机断层扫描的应用。

Utility of positron emission tomography-computed tomography in patients with chronic lymphocytic leukemia following B-cell receptor pathway inhibitor therapy.

机构信息

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.

出版信息

Haematologica. 2019 Nov;104(11):2258-2264. doi: 10.3324/haematol.2018.207068. Epub 2019 Mar 28.

Abstract

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 ).

摘要

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)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d1/6821597/671f46667983/1042258.fig1.jpg

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