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在老年乳腺癌患者中实现辅助化疗的最佳剂量强度:英国机构的一项 10 年回顾性研究。

Achieving optimal dose intensity with adjuvant chemotherapy in elderly breast cancer patients: a 10-year retrospective study in a UK institution.

机构信息

Queens University/Belfast City Hospital, Lisburn Road, Belfast BT9 7BL.

出版信息

Breast J. 2012 Jan-Feb;18(1):16-22. doi: 10.1111/j.1524-4741.2011.01177.x. Epub 2011 Oct 17.

DOI:10.1111/j.1524-4741.2011.01177.x
PMID:21999862
Abstract

The study was to determine if breast cancer patients aged 65 and above could be given adjuvant chemotherapy safely while achieving an acceptable relative dose intensity of at least 85%. We identified all patients aged 65 and over who received adjuvant chemotherapy over the 10 year period, November 1999 to October 2009, and determined the proportion that achieved a relative dose intensity of at least 85% as well as the tolerability of their treatment. A total of 101 patients were identified, with a median age of 69 years (range 65-78).Of these, 25.7% of patients had at least one major comorbidity, 84.2% had a tumor size of 5 cm or less, 73.3% were node positive and 58.4% were hormone receptor positive. The chemotherapy regimens used were AC (Doxorubicin and Cyclophosphamide), FEC (Fluorouracil, Epirubicin, and Cyclophosphamide), CMF (Cyclophosphamide, Methotrexate, and Fluorouracil) and ECMF (Epirubicin followed by CMF). Seventy-nine patients (78.2%) achieved the relative dose intensity of at least 85%. With respect to toxicity, 11.9% of patients developed febrile neutropenia and 23.8% of patients required hospital admission during the treatment period, but there were no treatment-related deaths in the group. A significant proportion of patients aged 65 and above achieved the intended dose intensity of at least 85% over this 10-year period, with manageable toxicity levels. This supports the use of these regimens as adjuvant chemotherapy for breast cancer in this age group.

摘要

这项研究旨在确定 65 岁及以上的乳腺癌患者是否可以安全地接受辅助化疗,同时实现至少 85%的可接受相对剂量强度。我们确定了在 1999 年 11 月至 2009 年 10 月的 10 年期间接受辅助化疗的所有 65 岁及以上的患者,并确定了达到至少 85%相对剂量强度的患者比例以及其治疗的耐受性。共确定了 101 例患者,中位年龄为 69 岁(范围 65-78 岁)。其中,25.7%的患者至少有一种主要合并症,84.2%的患者肿瘤大小为 5cm 或更小,73.3%的患者淋巴结阳性,58.4%的患者激素受体阳性。使用的化疗方案为 AC(多柔比星和环磷酰胺)、FEC(氟尿嘧啶、表柔比星和环磷酰胺)、CMF(环磷酰胺、甲氨蝶呤和氟尿嘧啶)和 ECMF(表柔比星后用 CMF)。79 例(78.2%)达到了至少 85%的相对剂量强度。关于毒性,11.9%的患者发生发热性中性粒细胞减少症,23.8%的患者在治疗期间需要住院治疗,但该组无治疗相关死亡。在这 10 年期间,相当一部分 65 岁及以上的患者达到了至少 85%的预期剂量强度,毒性水平可控制。这支持在该年龄组中使用这些方案作为辅助化疗治疗乳腺癌。

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