首页> 美国卫生研究院文献>BMJ Open >Phase I/II study protocol to assess safety and efficacy of adoptive cell therapy with anti-PD-1 plus low-dose pegylated-interferon-alpha in patients with metastatic melanoma refractory to standard of care treatments: the ACTME trial
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Phase I/II study protocol to assess safety and efficacy of adoptive cell therapy with anti-PD-1 plus low-dose pegylated-interferon-alpha in patients with metastatic melanoma refractory to standard of care treatments: the ACTME trial

机译:阶段I / II研究方案以评估抗PD-1加上低剂量聚乙二醇化干扰素-Nα的安全性和功效转移性黑色素瘤难以解决护理治疗方法:ACTME试验

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摘要

Treatment with anti-PD-1 immunotherapy does not lead to long-lasting clinical responses in approximately 60% of patients with metastatic melanoma. These refractory patients, however, can still respond to treatment with tumour infiltrating lymphocytes (TIL) and interferon-alpha (IFNa). A combination of TIL, pegylated-interferon-alpha (PEG-IFNa) and anti-PD-1 is expected to provide a safe, feasible and effective therapy for patients with metastatic melanoma, who are refractory to standard of care treatment options.
机译:用抗PD-1免疫疗法治疗不会导致大约60%的转移性黑素瘤患者的长期临床反应。然而,这些耐火患者仍可致致响应肿瘤渗透淋巴细胞(TIL)和干扰素-α(IFNA)的治疗。预期TIL,PEG化 - 干扰素-α(PEG-IFNA)和抗PD-1的组合,为转移性黑素瘤的患者提供安全,可行和有效的治疗,他们是护理选项的标准令人难以忍受的。

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