Regenbogen Thomas, Chen Ling, Trinkaus Kathryn, Wang-Gillam Andrea, Tan Benjamin R, Amin Manik, Pedersen Katrina S, Park Haeseong, Suresh Rama, Lim Kian-Huat, Ratchford Emily, Brown Amberly, Lockhart A Craig
Division of Oncology, Washington University, St. Louis, MO, USA.
Division of Oncology, University of Miami, Miami, FL, USA.
J Gastrointest Oncol. 2017 Dec;8(6):985-989. doi: 10.21037/jgo.2017.08.16.
Treatment options for patients with refractory colorectal cancer are limited and typically provide a chance of only modest benefit. The goal of this study was to evaluate the benefit of inhibiting the JAK/STAT inflammatory pathway with single agent pacritinib in patients with metastatic refractory colorectal adenocarcinoma.
A single arm institutional trial was initiated and enrolled patients with metastatic colorectal cancer refractory to at least two standard lines of treatment. Pacritinib 400 mg daily was administered orally continuously in 28 day cycles.
The trial was discontinued prior to reaching the planned accrual due to an FDA hold on pacritinib and a lack of treatment benefit. Eleven patients were enrolled and seven were evaluated for response. Median baseline C-reactive protein level was 12.1 (2.1-147) mg/L. One patient had stable disease at eight weeks by RECIST criteria and six progressed. There were no grade 4 or 5 adverse events while patients were on study. The grade 2 and lower AE events experienced were consistent with prior pacritinib trials.
In seven evaluable patients there were no objective responses. The trial was discontinued prior to completing planned accrual based on a low likelihood that the progression free survival goal of 4 months would be met.
难治性结直肠癌患者的治疗选择有限,通常只能带来适度的获益机会。本研究的目的是评估单药帕西替尼抑制JAK/STAT炎症通路对转移性难治性结直肠腺癌患者的疗效。
开展一项单臂机构试验,纳入对至少两线标准治疗难治的转移性结直肠癌患者。帕西替尼每日400mg,以28天为周期持续口服给药。
由于美国食品药品监督管理局(FDA)对帕西替尼的限制以及缺乏治疗获益,该试验在达到计划入组人数之前提前终止。共入组11例患者,7例接受疗效评估。基线C反应蛋白水平中位数为12.1(2.1 - 147)mg/L。根据RECIST标准,1例患者在8周时病情稳定,6例病情进展。患者在研究期间未发生4级或5级不良事件。发生的2级及以下不良事件与既往帕西替尼试验一致。
在7例可评估患者中未观察到客观缓解。基于达到4个月无进展生存目标的可能性较低,该试验在完成计划入组前提前终止。