首页> 外文期刊>Journal of Clinical Oncology >Interferon versus interferon plus prednisone remission maintenance therapy for multiple myeloma: a Southwest Oncology Group Study.
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Interferon versus interferon plus prednisone remission maintenance therapy for multiple myeloma: a Southwest Oncology Group Study.

机译:干扰素与干扰素加泼尼松缓解维持疗法治疗多发性骨髓瘤:西南肿瘤小组研究。

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PURPOSE: We evaluated the vincristine, doxorubicin, and dexamethasone (VAD) regimen alone or with chemosensitizers for remission induction and interferon (IFN) versus IFN plus prednisone (IFN/P) for remission maintenance in previously untreated multiple myeloma. PATIENTS AND METHODS: Two hundred thirty-three patients were registered for remission-induction therapy with VAD or VAD plus the chemosensitizers verapamil and quinine. Patients who achieved remission were randomized to maintenance therapy with IFNalpha 3 MU in the evening three times weekly or IFN plus 50 mg of prednisone (IFN/P) on the morning after IFN until relapse. RESULTS: Two hundred twenty-nine patients were eligible for induction. Fatal toxicities in nine patients who received VAD plus verapamil and quinine led to closure of this arm after 47 registrations. Subsequently, all patients received VAD induction. Despite the high early mortality rate on VAD plus sensitizers, overall survival by induction arm did not differ for median or 5-year survival with approximately 40% of patients surviving 5 years. Eighty-nine eligible patients who achieved remission were randomized to maintenance. Patients who received IFN/P had improved progression-free survival (median, 19 v9 months for IFN; P = .008). After 48 months, progression-free survival on IFN/P was at the thirtieth percentile, whereas it was below the tenth percentile on IFN alone. Median survival from start of maintenance was long on both arms (57 months for IFN/P v 46 months for IFN; P = .36). CONCLUSION: IFN/Pwas more effective than IFN alone. Improved relapse-free survival may be attributable to IFN/P or to the use of prednisone for maintenance. This latter alternative is currently being studied.
机译:目的:我们评估了长春新碱,阿霉素和地塞米松(VAD)方案,或与化学增敏剂相比,对先前未经治疗的多发性骨髓瘤的缓解诱导和干扰素(IFN)与IFN加泼尼松(IFN / P)缓解的关系进行了评估。患者与方法:233例患者接受了VAD或VAD加上化学增敏剂维拉帕米和奎宁的缓解诱导治疗。达到缓解的患者被随机分配到每周三次晚上接受IFNalpha 3 MU的维持治疗,或在IFN后的早晨于IFN加50 mg泼尼松(IFN / P)进行治疗,直至复发。结果:229例患者符合入组条件。接受VAD加上维拉帕米和奎宁的9名患者的致命毒性导致47例登记后该臂闭合。随后,所有患者均接受了VAD诱导。尽管VAD加敏化剂的早期死亡率很高,但中位或5年生存率的诱导臂总体生存率无差异,大约40%的患者生存5年。达到缓解的89位合格患者被随机分配到维持治疗。接受IFN / P的患者的无进展生存期得到了改善(中位数,IFN为19 v9个月; P = 0.008)。 48个月后,IFN / P的无进展生存期为第30个百分位数,而单独使用IFN时,无进展生存率则为第10个百分位数以下。两组从维持治疗开始的中位生存期较长(IFN / P为57个月,IFN为46个月; P = 0.36)。结论:IFN / P比单独使用IFN更有效。无复发生存期的改善可能归因于IFN / P或泼尼松的维持。目前正在研究后一种选择。

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