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Updated Survival Follow-Up for Phase Ib Trial of the Histone Deacetylase Inhibitor Abexinostat With Pazopanib in Patients With Solid Tumor Malignancies

帕唑帕尼 组蛋白脱乙酰基酶 组蛋白脱乙酰酶抑制剂 医学 内科学 肿瘤科 癌症研究 药理学 生物 癌症 组蛋白 遗传学 舒尼替尼 基因
作者
Erica S. Tsang,Rahul Aggarwal,Emily K. Bergsland,Susan Calabrese,Alexandrine Rozie,Sibapriya Chaudhuri,Mallika Sachdev Dhawan,Nela Pawłowska,Jennifer A. Grabowsky,Scott Thomas,Pamela N. Münster
出处
期刊:JCO precision oncology [American Society of Clinical Oncology]
卷期号:8 (8): e2400328-e2400328 被引量:3
标识
DOI:10.1200/po.24.00328
摘要

PURPOSE Histone deacetylase (HDAC) inhibition downregulates hypoxia-inducible factor-1α and modulates multiple metabolomic pathways relevant in cancer. Here we report a potential novel biomarker to predict exceptional responders (>3 years) in patients receiving HDAC and vascular endothelial growth factor (VEGF) inhibition. PATIENTS AND METHODS Patients with solid tumor malignancies were enrolled in this phase Ib trial of abexinostat (4/7 ×21 days) and pazopanib (28/28 days), with a dose expansion in renal cell carcinoma (RCC). Plasma was analyzed for metabolomics and peripheral blood mononuclear cells (PBMCs) for VEGF and HDAC2 expression levels. RESULTS Fifty-one patients were enrolled: n = 36 patients in dose escalation and n = 15 in dose expansion. After the initial report in 2017, six patients had remained on study: four with RCC and one each with medullary thyroid and thymic neuroendocrine carcinoma. One patient with RCC remains on treatment for >11 years after progression on five systemic therapies. Overall, the median duration of therapy measured 5.6 (1-133) months. The median duration of therapy in exceptional responders measured 44.1 (39.8-133+) months. The median overall survival in patients with high PBMC HDAC2 expression versus low HDAC2 was 32.3 versus 9.2 months ( P = .004) for all patients and 43.3 versus 25.1 months for patients with RCC ( P = .09). Exceptional responders had lower kynurenine levels both pre- and post-treatment ( P = .002, P < .001, respectively). HDAC2 and kynurenine expression levels were inversely correlated ( P = .02). CONCLUSION Abexinostat added to pazopanib shows extended tolerability and long-term responses and survival. PBMC HDAC2 levels, the abexinostat target, are relevant predictors of response. In addition, metabolomic assessment points to kynurenine as a predictor for exceptional response to combined VEGF plus HDAC inhibition.
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