首页> 外文期刊>International journal of gynecological cancer: official journal of the International Gynecological Cancer Society >A pilot phase 2 study of oregovomab murine monoclonal antibody to CA125 as an immunotherapeutic agent for recurrent ovarian cancer.
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A pilot phase 2 study of oregovomab murine monoclonal antibody to CA125 as an immunotherapeutic agent for recurrent ovarian cancer.

机译:一项针对CA125的oregovomab鼠单克隆抗体作为复发性卵巢癌的免疫治疗剂的2期试验性研究。

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This prospective, open-label, pilot phase 2 study examined the clinical and immunologic effects of oregovomab (OvaRex) in heavily pretreated patients with recurrent ovarian cancer (OC). Thirteen women were administered intravenous oregovomab (2 mg) at weeks 0, 2, 4, 8, and 12, followed by quarterly doses for up to 2 years or disease progression. Concomitant chemotherapy was not permitted. Eligibility criteria included recurrence after one or more platinum-based chemotherapy regimens, CA125 >35 U/mL, evaluable or measurable disease. Tumor burden was evaluated by physical or radiologic methods pretreatment, weeks 12, 24, and every 24 weeks thereafter. Immune responses, including antibodies and T cells to oregovomab and CA125, were demonstrated in over half the patients. Stabilization of disease and survival >2 years was observed in 3 of 13 patients and coincided with robust immune responses. Shrinkage of marker lesions was not observed; however, four patients showed decreases in CA125 levels. Treatment was well tolerated without serious adverse events or discontinuations due to therapy. This pilot study supports immunologic activity and safety of oregovomab in recurrent OC. Further study of this agent in the consolidation and adjuvant setting is ongoing to establish its clinical utility.
机译:这项前瞻性,开放标签的2期试验性研究检查了奥戈单抗(OvaRex)在经过大量预处理的复发性卵巢癌(OC)患者中的临床和免疫学作用。在第0、2、4、8和12周时,对13名妇女进行了静脉奥雷珠单抗(2毫克)给药,随后每2个月进行一次剂量给药,直至2年或疾病进展。不允许同时进行化学疗法。入选标准包括一种或多种铂类化疗方案后复发,CA125> 35 U / mL,可评估或可测量的疾病。通过物理或放射学方法预处理,第12、24周以及此后每24周评估肿瘤负担。在超过一半的患者中显示出了针对oregovomab和CA125的免疫反应,包括抗体和T细胞。在13名患者中的3名患者中观察到疾病稳定和生存期超过2年,并且与强大的免疫反应相吻合。没有观察到标志物病变的缩小;但是,有4名患者的CA125水平下降。治疗耐受良好,没有严重的不良事件或因治疗而中断治疗。这项前瞻性研究支持复发性OC中oregovomab的免疫活性和安全性。该药物在巩固和佐剂环境中的进一步研究正在进行中,以建立其临床效用。

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