β* asked in 社會與文化語言 · 1 decade ago

請醫學達人幫忙翻譯!!急!!贈20點

Conclusion

In a large number of clinical trials for other types of

cancer, it was concluded that immunotherapy is probably

most efficacious in early-stage cancers. As such,

immunotherapy is suitable for the adjuvant treatment of

superficial bladder cancer. Indeed, the clinical results of

immunotherapy trials are promising for their use in a

multimodality treatment strategy required for this

malignancy. Theoretically, active immunotherapy aimed

at the activation of the cellular adaptive immune system

is the most attractive form, since this treatment modality

can induce immunosurveillance through the generation

of memory effector T cells and may in this way protect

the patient from tumor recurrence and metastasis.

Ongoing and future clinical trials on active immunotherapy

for superficial bladder cancer will demonstrate

whether this theory can be supported by clinical-based

evidence. There is a great challenge in overcoming a

number of major hurdles in the clinical development of

active immunotherapy, which are, amongst others, dictated

by the heterogeneity of cancer within a patient as

well as between patients. For immunogene therapy,

efficient and targeted gene transfer as well as sustained,

stable therapeutic gene expression for a long period of

time will be essential for clinical success. For vaccination,

most vaccines are currently restricted to patients

matching a defined HLA haplotype or are based on

autologous material and therefore complex to produce.

Standard vaccines that can be applied in large patient

populations are desirable but may not be established in

the near future.

1 Answer

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  • 1 decade ago
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    結論 Conclusion

    多數其他類型癌症臨床實驗總結出,免疫療法用在初期癌症患者可能最有效.

    因此, 免疫療法適合幫助治療輕微膀胱癌患者. 確實, 免疫療法實驗的臨床結果為惡性腫瘤所用的多模態物理療法帶來希望. 理論上, 有效免疫療法是最引人注意的形式,目的在細胞適應免疫系統的活化, 因為這種治療性的物理治療能透過記憶受動器T細胞的產生誘導免疫監視, 這種方法可以防止腫瘤復發和轉移.

    對療輕微膀胱癌患者做持續和進一步的臨床有效免疫治療實驗將證明此理論是否能受到臨床實證支持. 克服許多有效免疫療法的臨床發展的障礙有著極大挑戰, 諸如單一患者及患者之間的癌症異質性. 對免疫基因治療而言, 除了有效率的和指定基因轉移還有可持續性, 長期穩定治療基因顯現對臨床試驗成敗是不可或缺的. 對預防接腫而言, 現今多數疫苗只限定給符合單型組織配對抗原患者或自體移植物質為根基的患者, 因此製造複雜. 一般疫苗能用於多數患者, 但是在近期內還尚未認可

    Source(s): Me
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