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High dose chemotherapy for breast cancer: the case for trials in adjuvant therapy.

机译:乳腺癌的大剂量化疗:辅助治疗试验的情况。

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摘要

Adjuvant polychemotherapy reduces the annual mortality for breast cancer, the effect being seen for at least the first decade after primary treatment for stage II disease. However, the overall benefit is modest with an annual reduction in the odds of death of the order of 20%-30%. For patients at standard or low risk of recurrence this appears to be an acceptable benefit given low toxicity of treatment. However, some patients have a very much worse prognosis identifiable on the basis of the number of involved axillary nodes at surgery. Patients with more than 10 lymph nodes, for example, have a predicted survival of less than 30% at 5 years and around 10% at 10 years. High dose chemotherapy has shown immediate benefits in terms of complete response rates in advanced breast cancer. Potential benefits of this treatment could be even higher in the adjuvant setting given the patient's fitness and the fact that micrometastatic disease represents the best clinical analogue of the successful laboratory experimental conditions. Now that the safety factors appear to be favourable with a treatment-related mortality of less than 5% it would appear that stage II poor risk disease is an appropriate setting to test high dose chemotherapy against the best conventional therapy in randomized trials.
机译:辅助多化学疗法可降低乳腺癌的年死亡率,这种效果至少在II期疾病的主要治疗后的第一个十年中可见。但是,总体收益是适度的,每年的死亡几率降低了20%-30%。对于处于标准或低复发风险的患者,鉴于治疗毒性低,这似乎是可以接受的获益。但是,根据手术时受累腋窝结节的数量,有些患者的预后非常差。例如,淋巴结多于10个的患者在5年时的预期生存率不到30%,在10年时的生存率约为10%。就晚期乳腺癌的完全缓解率而言,高剂量化疗已显示出直接的益处。鉴于患者的健康状况以及微转移性疾病代表成功的实验室实验条件的最佳临床类似物,这种治疗在辅助治疗中的潜在益处甚至更高。既然安全因素似乎对治疗相关的死亡率低于5%有利,那么看来II期低危疾病是在随机试验中针对最佳常规疗法进行高剂量化疗试验的合适环境。

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