Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, USA.
Dignity Health Cancer Institute, Phoenix, AZ, USA.
Blood Cancer J. 2023 Mar 6;13(1):32. doi: 10.1038/s41408-023-00794-x.
Minimal residual disease (MRD) assays allow response assessment in patients with multiple myeloma (MM), and negativity is associated with improved survival outcomes. The role of highly sensitive next generation sequencing (NGS) MRD in combination with functional imaging remains to be validated. We performed a retrospective analysis on MM patients who underwent frontline autologous stem cell transplant (ASCT). Patients were evaluated at day 100 post-ASCT with NGS-MRD and positron emission tomography (PET-CT). Patients with ≥ 2 MRD measurements were included in a secondary analysis for sequential measurements. 186 patients were included. At day 100, 45 (24.2%) patients achieved MRD negativity at a sensitivity threshold of 10. MRD negativity was the most predictive factor for longer time to next treatment (TTNT). Negativity rates did not differ according to MM subtype, R-ISS Stage nor cytogenetic risk. PET-CT and MRD had poor agreement, with high rates of PET-CT negativity in MRD-positive patients. Patients with sustained MRD negativity had longer TTNT, regardless of baseline risk characteristics. Our results show that the ability to measure deeper and sustainable responses distinguishes patients with better outcomes. Achieving MRD negativity was the strongest prognostic marker and could help guide therapy-related decisions and serve as a response marker for clinical trials.
微小残留病灶 (MRD) 检测可用于评估多发性骨髓瘤 (MM) 患者的治疗反应,阴性结果与改善的生存结局相关。高灵敏度下一代测序 (NGS) MRD 与功能成像的联合应用的作用仍有待验证。我们对接受一线自体造血干细胞移植 (ASCT) 的 MM 患者进行了回顾性分析。患者在 ASCT 后第 100 天接受 NGS-MRD 和正电子发射断层扫描 (PET-CT) 评估。≥ 2 次 MRD 测量的患者纳入二次分析以进行连续测量。共纳入 186 例患者。在第 100 天,45 例 (24.2%) 患者在 10-10 灵敏度阈值下达到 MRD 阴性。MRD 阴性是预测下一次治疗时间 (TTNT) 更长的最主要因素。阴性率与 MM 亚型、R-ISS 分期或细胞遗传学风险无关。PET-CT 和 MRD 的一致性较差,MRD 阳性患者的 PET-CT 阴性率较高。持续 MRD 阴性的患者 TTNT 更长,无论基线风险特征如何。我们的研究结果表明,能够测量更深层次和可持续的反应可区分预后更好的患者。达到 MRD 阴性是最强的预后标志物,有助于指导治疗相关决策,并作为临床试验的反应标志物。