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HIGH-DOSE IFN-ALPHA-2B VS CISPLATIN, VINBLASTINE, DTIC + IL-2 & IFN IN MELANOMA

HIGH-DOSE IFN-ALPHA-2B VS CISPLATIN, VINBLASTINE, DTIC + IL-2 & IFN IN MELANOMA
高剂量 IFN-ALPHA-2B 与顺铂、长春碱、DTIC IL-2
批准号:
7607496
负责人:
MARK R ALBERTINI
金额:
$0.17万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-12-01 至 2007-09-16

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中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. [from ClinicalTrials.gov website (edited)] Interferon alfa may interfere with the growth of cancer cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Interleukin-2 may stimulate a person's white blood cells to kill melanoma cells. It is not yet known whether interferon alfa given alone over 1 year is more effective than interferon alfa given with combination chemotherapy and interleukin-2 for 3 months for melanoma. This is a randomized Phase III trial to compare the effectiveness of interferon alfa with or without combination chemotherapy consisting of cisplatin, vinblastine, and dacarbazine, plus interleukin-2, in preventing recurrences in patients with resected high-risk melanoma.
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Administration of intratumoral immunocytokine to activate immune rejection of spontaneous canine melanoma
Administration of intratumoral immunocytokine to activate immune rejection of spontaneous canine melanoma
Administration of intratumoral immunocytokine to activate immune rejection of spontaneous canine melanoma
Administration of intratumoral immunocytokine to activate immune rejection of spontaneous canine melanoma
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