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首页> 外文期刊>Cancer biology & therapy >A phase II trial of perifosine, an oral alkylphospholipid, in recurrent or metastatic head and neck cancer.
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A phase II trial of perifosine, an oral alkylphospholipid, in recurrent or metastatic head and neck cancer.

机译:Perfosine(口服烷基磷脂)在复发或转移性头颈癌中的II期试验。

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BACKGROUND: Novel, effective therapies are warranted in the management of recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN). Perifosine is an oral alkylphospholipid that inhibits AKT phosphorylation and has shown preclinical antitumor activity in head and neck cancer cell lines and xenografts. PATIENTS AND METHODS: We conducted a phase II trial of perifosine in patients with incurable, recurrent or metastatic SCCHN. Previous therapy for recurrent or metastatic disease was limited to no more than one prior chemotherapy and one prior targeted/biologic agent regimen. Patients had to have measurable disease, Eastern Cooperative Oncology Group performance status 0-2, and adequate laboratory parameters. Perifosine was given as a loading dose of 150 mg every 6 hours x 6 doses orally in the first two days, with antiemetic prophylaxis, followed by 100 mg/day orally without interruption. Administration via gastrostomy tube was allowed. Tumor response was assessed every two cycles (eight weeks). Biomarkers in pathways potentially affected by perifosine, including AKT, P-AKT, P38, p53 and p21 were measured on tumor tissue by immunohistochemistry by manual and automated methods. RESULTS: Nineteen patients were enrolled. No objective responses were observed. One patient had stable disease as best response and 18 patients progressed at first evaluation. The median overall survival time was 5.5 months and the median progression-free survival time was 1.7 months. The most frequent toxicities were gastrointestinal (constipation, nausea, vomiting) and fatigue. One patient developed grade 4 anorexia. Although the sample size was small, a significant correlation was detected between high expression of P38 and AKT in baseline tumor tissue and better survival. CONCLUSIONS: Perifosine in the doses and schedule used lacks single-agent activity in SCCHN. Our data do not justify further investigation of perifosine as a single agent in SCCHN.
机译:背景:在头颈部复发或转移性鳞状细胞癌(SCCHN)的治疗中,需要新颖,有效的治疗方法。 Perifosine是一种口服烷基磷脂,可抑制AKT磷酸化,并已在头颈癌细胞系和异种移植物中显示出临床前抗肿瘤活性。患者与方法:我们对患有顽固性,复发性或转移性SCCHN的患者进行了periposine的II期试验。先前针对复发性或转移性疾病的疗法仅限于不超过一种先前的化疗和一种先前的靶向/生物制剂方案。患者必须具有可测量的疾病,东部合作肿瘤小组的工作状态为0-2,并且实验室参数适当。前两天给予Perifosine的剂量为每6小时150毫克x 6剂口服,并采取止吐预防措施,然后每天口服100 mg,不得中断。允许通过胃造口管给药。每两个周期(八周)评估一次肿瘤反应。通过手动和自动方法,通过免疫组织化学法在肿瘤组织上测量了可能受过磷辛酸影响的途径中的生物标志物,包括AKT,P-AKT,P38,p53和p21。结果:19例患者入选。没有观察到客观反应。一名患者病情稳定,最佳反应,初次评估时有18名患者进展。中位总生存时间为5.5个月,中位无进展生存时间为1.7个月。最常见的毒性是胃肠道(便秘,恶心,呕吐)和疲劳。一名患者发展为4级厌食症。尽管样本量很小,但是在基线肿瘤组织中P38和AKT的高表达与更好的存活率之间存在显着的相关性。结论:所用剂量和时间表中的Perifosine在SCCHN中缺乏单药活性。我们的数据不足以证明进一步研究perfofosine作为SCCHN中的单一药物的可能性。

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