Raghavendra Akshara Singareeka, Kettner Nicole M, Kwiatkowski Danielle, Damodaran Senthil, Wang Yan, Ramirez David, Gombos Dan S, Hunt Kelly K, Shen Yu, Keyomarsi Khandan, Tripathy Debu
Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Experimental Radiation, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
NPJ Breast Cancer. 2025 Jan 26;11(1):7. doi: 10.1038/s41523-025-00722-1.
Endocrine therapy with CDK4/6 inhibitors is standard for estrogen receptor-positive, HER2-negative metastatic breast cancer (ER+/HER2- MBC), yet clinical resistance develops. Previously, we demonstrated that low doses of palbociclib activate autophagy, reversing initial G1 cell cycle arrest, while high concentrations induce off-target senescence. The autophagy inhibitor hydroxychloroquine (HCQ) induced on-target senescence at lower palbociclib doses. We conducted a phase I trial (NCT03774472 registered in ClinicalTrials.gov on 8/20/2018) of HCQ (400, 600, 800 mg/day) with palbociclib (75 mg/day continuous) and letrozole, using a 3 + 3 design. Primary objectives included safety, tolerability, and determining the recommended phase 2 dose (RP2D) of HCQ. Secondary objectives included tumor response and biomarker analysis. Fourteen ER+/HER2- MBC patients were evaluable [400 mg (n = 4), 600 mg (n = 4), 800 mg (n = 6)]. Grade 3 adverse events (AEs) included hematological (3 at 800 mg), skin rash (2 at 600 mg), and anorexia (1 at 400 mg), with no serious AEs. The best responses were partial (2), stable (11), and progression (1). Tumor reductions ranged from 11% to 30%, with one 55% increase. The two partial responders sustained tumor size reductions of 30% to 55% over an extended treatment period, lasting nearly 300 days. Biomarker analysis in responders demonstrated significant decreases in Ki67, Rb, and nuclear cyclin E levels and increases in autophagy markers p62 and LAMP1, suggesting a correlation between these biomarkers and treatment response. This phase I study demonstrated that HCQ is safe and well-tolerated and the RP2D was established at 800 mg/day with continuous low-dose palbociclib (75 mg/day) and letrozole (2.5 mg/day). These findings suggest that adding HCQ could potentially enhance the efficacy of low-dose palbociclib and standard letrozole therapy, pending verification in larger randomized studies.
对于雌激素受体阳性、人表皮生长因子受体2阴性的转移性乳腺癌(ER+/HER2- MBC),使用细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂进行内分泌治疗是标准疗法,但临床耐药仍会出现。此前,我们证明低剂量的哌柏西利可激活自噬,逆转最初的G1期细胞周期停滞,而高浓度则会诱导脱靶衰老。自噬抑制剂羟氯喹(HCQ)在较低的哌柏西利剂量下可诱导靶向衰老。我们采用3+3设计,对HCQ(400、600、800毫克/天)联合哌柏西利(75毫克/天持续给药)及来曲唑进行了一项I期试验(于2018年8月20日在ClinicalTrials.gov注册,编号NCT03774472)。主要目标包括安全性、耐受性以及确定HCQ的推荐2期剂量(RP2D)。次要目标包括肿瘤反应和生物标志物分析。14例ER+/HER2- MBC患者可进行评估[400毫克组(n = 4),600毫克组(n = 4),800毫克组(n = 6)]。3级不良事件(AE)包括血液学不良事件(800毫克组3例)、皮疹(600毫克组2例)和厌食(400毫克组1例),无严重不良事件。最佳反应为部分缓解(2例)、病情稳定(11例)和疾病进展(1例)。肿瘤缩小幅度为11%至30%,有1例增大了55%。两名部分缓解者在延长的治疗期内肿瘤大小持续缩小30%至55%,持续近300天。对缓解者的生物标志物分析显示,Ki67、视网膜母细胞瘤(Rb)和细胞核周期蛋白E水平显著降低,自噬标志物p62和溶酶体相关膜蛋白1(LAMP1)增加,表明这些生物标志物与治疗反应之间存在相关性。这项I期研究表明,HCQ安全且耐受性良好,RP2D确定为800毫克/天,联合持续低剂量的哌柏西利(75毫克/天)及来曲唑(2.5毫克/天)。这些发现表明,添加HCQ可能会增强低剂量哌柏西利和标准来曲唑治疗的疗效,有待在更大规模的随机研究中进行验证。