Channar Aneeta, Naqvi Syed Arsalan Ahmed, Khan Muhammad Ali, Bibi Arifa, Saxena Akshat, Tripathi Nikita, Iftikhar Ahmad, Raina Ammad, Khakwani Kaneez Zahra Rubab, Riaz Irbaz Bin, Husnain Muhammad
Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
The University of Arizona, Tucson, Arizona, USA.
Cancer Rep (Hoboken). 2025 Apr;8(4):e70171. doi: 10.1002/cnr2.70171.
The treatment landscape for multiple myeloma continues to evolve. Recently, the addition of anti-CD38 monoclonal antibodies (mAbs) to the triplet regimen, comprising a proteasome inhibitor, an immunomodulatory agent, and a steroid, for transplant-eligible newly diagnosed multiple myeloma (TENDMM) has shown promising results.
To evaluate the overall efficacy and safety of quadruplet therapy with an anti-CD38 mAb compared to a triplet regimen.
A systematic search of Medline, Scopus, and EMBASE databases from inception to July 2024 identified relevant randomized controlled trials (RCTs). Efficacy and safety outcomes were derived using random-effects meta-analysis. Summarized outcomes include hazard ratios (HR) for progression-free survival (PFS) and overall survival (OS), odds ratios (OR) for response rates, measurable residual disease (MRD) negativity rate, and grade 3 or higher adverse events (G ≥ 3 AEs).
Five RCTs involving 2963 patients were included. A statistically significant PFS was observed for quadruplet therapy when compared to the triplet regimen (HR 0.44; 95% Confidence Interval [CI] 0.35-0.56). PFS benefit was consistent for the standard risk (SR) group (HR 0.38; 95% CI 0.27-0.52) and high risk (HiR) group (HR 0.62; 95% CI 0.41-0.92). No statistically significant benefit was observed for OS (HR 0.55; 95% CI 0.28-1.08). A statistically significant benefit was observed for the overall response rate (OR 1.77; 95% CI 1.02-3.06) and MRD negativity rate (OR 2.67; 95% CI 1.79-3.99). No significant differences were observed for G ≥ 3 AE (OR 1.21; 95% CI 0.92-1.58), lymphopenia (OR 1.09; 95% CI 0.62-1.89), and anemia (OR 1.06; 95% CI 0.83-1.37). However, a significantly increased risk was observed for all-grade thrombocytopenia (OR 1.64; 95% CI 1.37-1.97), neutropenia (OR 2.24; 95% CI 1.67-3.02) and infections (OR 1.88; 95% CI 1.07-3.31).
Quadruplet therapy demonstrated a favorable efficacy and safety profile, with consistent benefit across subgroups. The findings support its potential as the new standard of care for TENDMM.
多发性骨髓瘤的治疗格局持续演变。最近,对于适合移植的新诊断多发性骨髓瘤(TENDMM),在由蛋白酶体抑制剂、免疫调节剂和类固醇组成的三联方案中加入抗CD38单克隆抗体(mAb)已显示出有前景的结果。
评估与三联方案相比,抗CD38 mAb四联疗法的总体疗效和安全性。
对Medline、Scopus和EMBASE数据库从创建至2024年7月进行系统检索,以确定相关的随机对照试验(RCT)。使用随机效应荟萃分析得出疗效和安全性结果。汇总结果包括无进展生存期(PFS)和总生存期(OS)的风险比(HR)、缓解率的优势比(OR)、可测量残留病(MRD)阴性率以及3级或更高等级不良事件(G≥3 AE)。
纳入了5项涉及2963例患者的RCT。与三联方案相比,四联疗法观察到具有统计学意义的PFS(HR 0.44;95%置信区间[CI] 0.35 - 0.56)。标准风险(SR)组(HR 0.38;95% CI 0.27 - 0.52)和高风险(HiR)组(HR 0.62;95% CI 0.41 - 0.92)的PFS获益一致。OS未观察到具有统计学意义的获益(HR 0.55;95% CI 0.28 - 1.08)。总体缓解率(OR 1.77;95% CI 1.02 - 3.06)和MRD阴性率(OR 2.67;95% CI 1.79 - 3.99)观察到具有统计学意义的获益。G≥3 AE(OR 1.21;95% CI 0.92 - 1.58)、淋巴细胞减少(OR 1.09;95% CI 0.62 - 1.89)和贫血(OR 1.06;95% CI 0.83 - 1.37)未观察到显著差异。然而,所有等级血小板减少(OR 1.64;95% CI 1.37 - 1.97)、中性粒细胞减少(OR 2.24;95% CI 1.67 - 3.02)和感染(OR 1.88;95% CI 1.07 - 3.31)的风险显著增加。
四联疗法显示出良好的疗效和安全性概况,各亚组均有一致的获益。这些发现支持其作为TENDMM新护理标准的潜力。