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Cancer Immune Therapy Edited by G. Stuhler and P. Walden ...

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apy. Since such therapies are well tolerated <strong>by</strong> the patients, this appears to be an attractive<br />

option; however, it requires that tumor material for vaccine production is<br />

available for long periods.<br />

While the clinical responses observed in the initial trials are promising, cure is a<br />

rare exception <strong>and</strong> the question is how to improve the vaccination therapies in order<br />

to improve the response rates <strong>and</strong>, in future, offer vaccination therapy as a st<strong>and</strong>ard<br />

therapy for the treatment of various cancer. Late-stage cancers are certainly not targets<br />

for cancer immune therapy. The tumor burden is often very high, the patients<br />

often already suffer from disease-related immune suppression <strong>and</strong> the tumor cells<br />

might already be highly diversified. The selection of an immune-escape variant of<br />

the tumor is a possible adverse effect of specific immune intervention. It is conceivable<br />

to combine HCV with other treatment modalities that can help to reduce the tumor<br />

burden <strong>and</strong> to provide relief from some of the immune-suppressive activities of<br />

the tumors. It might be necessary to include in the treatment cytokines that can stabilize<br />

the tumor-specific T cell responses, <strong>and</strong> aid their long-term expansion <strong>and</strong><br />

functional integrity.<br />

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241

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