Medical Department II, University Hospital Würzburg, Würzburg, Germany.
Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
J Nucl Med. 2023 Dec 1;64(12):1889-1894. doi: 10.2967/jnumed.123.266074.
Because of gastral and extranodal manifestations, guideline-compatible diagnostic work-up of marginal zone lymphoma is challenging. We aimed to determine the diagnostic performance of C-X-C motif chemokine receptor 4 (CXCR4)-directed PET/CT compared with routine diagnostics, along with PET/CT-based retrospective changes in therapeutic management. The predictive potential of the PET signal was also investigated, and the number of patients eligible for CXCR4-directed radioligand therapy in a theranostic setting was determined. For this study, 100 marginal zone lymphoma patients underwent CXCR4-directed PET/CT. We compared staging results and treatment decisions from molecular imaging with respective results from guideline-compatible work-up (CT, esophagogastroduodenoscopy, and bone marrow-derived biopsy). Prognostic performance of the in vivo CXCR4 PET signal for progression-free survival (PFS) was evaluated (using log-rank test and Kaplan-Meier curves). Relative to CT, CXCR4-directed imaging led to Ann Arbor (AA) staging changes for 27 of 100 patients (27.0%). Among those, clinically relevant upstaging from AA I or AA II to AA III or AA IV was observed for 23 patients (85.2%), along with respective changes in therapeutic management (escalation, 6/23 [26.1%]; deescalation, 17/23 [73.9%]). CXCR4 PET/CT yielded diagnostic accuracy of 94.0% relative to esophagogastroduodenoscopy and 76.8% relative to bone marrow-derived biopsy. An increased CXCR4 PET signal was linked to shorter PFS (707 d vs. median PFS not reached; hazard ratio, 3.18; 95% CI, 1.37-7.35; = 0.01). CXCR4-directed radioligand therapy would have been feasible for 18 of 100 patients (18.0%). Relative to CT, CXCR4-directed PET/CT led to AA changes for 27 of 100 patients. Chemokine receptor PET/CT may improve current diagnostic algorithms and influence management relative to CT alone, potentially obviating some biopsies.
由于胃和结外表现,边缘区淋巴瘤的指南一致的诊断工作具有挑战性。我们旨在确定 C-X-C 基序趋化因子受体 4 (CXCR4) 导向的 PET/CT 与常规诊断相比的诊断性能,以及基于 PET/CT 的治疗管理的回顾性变化。还研究了 PET 信号的预测潜力,并确定了在治疗性设置中适合接受 CXCR4 导向放射性配体治疗的患者数量。 在这项研究中,100 例边缘区淋巴瘤患者接受了 CXCR4 导向的 PET/CT。我们将分子成像的分期结果和治疗决策与指南一致的工作(CT、食管胃十二指肠镜和骨髓衍生活检)的结果进行了比较。评估了体内 CXCR4 PET 信号对无进展生存期 (PFS) 的预后性能(使用对数秩检验和 Kaplan-Meier 曲线)。 与 CT 相比,CXCR4 导向的成像导致 100 例患者中的 27 例(27.0%)出现 Ann Arbor (AA) 分期改变。在这些患者中,23 例(85.2%)从 AA I 或 AA II 临床相关升级为 AA III 或 AA IV,同时治疗管理也发生了相应变化(升级,23/23 [6.1%];降级,17/23 [73.9%])。与食管胃十二指肠镜相比,CXCR4 PET/CT 的诊断准确性为 94.0%,与骨髓衍生活检相比为 76.8%。增加的 CXCR4 PET 信号与较短的 PFS 相关(707 d 与未达到的中位 PFS;风险比,3.18;95%CI,1.37-7.35; = 0.01)。100 例患者中有 18 例(18.0%)适合接受 CXCR4 导向的放射性配体治疗。 与 CT 相比,CXCR4 导向的 PET/CT 导致 100 例患者中的 27 例发生 AA 改变。趋化因子受体 PET/CT 可改善当前的诊断算法,并相对于单独 CT 影响治疗,可能避免一些活检。