Westmead Breast Cancer Institute, University of Sydney, Westmead Hospital, Westmead, NSW 2145, Australia.
Eur J Cancer. 2010 Jul;46(11):1990-6. doi: 10.1016/j.ejca.2010.03.003. Epub 2010 Apr 10.
The objective of this study is to determine whether the aggregate tumour size of every focus in multifocal breast cancer more accurately predicts 10-year survival than current staging systems which use the largest or dominant tumour size.
This study examined the original histological reports of 848 consecutive patients with invasive breast cancer treated in New South Wales (NSW), Australia between 1 April 1995 and 30 September 1995. Multifocal tumours were assessed using two estimates of pathologic tumour size: largest tumour focus diameter and the aggregate diameter of every tumour focus. The 10-year survival of patients with multifocal tumours measured in both ways was compared to that with unifocal tumours.
At a median follow-up of 10.4 years, 27 of 94 patients (28.7%) with multifocal breast cancer have died of breast cancer compared to 141 of 754 (18.7%) with unifocal breast cancer (P=.022). Ten-year survival was not affected by size for tumours measuring 20mm or less, whether or not dominant tumour size (87.9%) or aggregate tumour size (87.0%) was used for multifocal tumours, compared to unifocal tumours (88.1%). For tumours larger than 20mm, 10-year survival was 72.1% for unifocal tumours compared to 54.7% (P=.008) for multifocal tumours using dominant tumour size, but this was 69.5% and not significant when multifocal tumours were classified using aggregate tumour size (P=.49). Multivariate analysis also confirmed the above-mentioned results after adjustment for important prognostic factors.
Aggregate size of every focus should be considered along with other prognostic factors for metastasis when treatment is planned. The current convention of using the largest (dominant) lesion as a measure of stage and associated breast cancer survival needs further validation.
本研究旨在确定多灶性乳腺癌中每个病灶的肿瘤总大小是否比目前使用最大或主要肿瘤大小的分期系统更能准确预测 10 年生存率。
本研究检查了 1995 年 4 月 1 日至 1995 年 9 月 30 日期间在澳大利亚新南威尔士州(NSW)治疗的 848 例浸润性乳腺癌连续患者的原始组织学报告。使用两种病理肿瘤大小估计值评估多灶性肿瘤:最大肿瘤焦点直径和每个肿瘤焦点的总直径。以这两种方式测量的多灶性肿瘤患者的 10 年生存率与单灶性肿瘤进行了比较。
在中位随访 10.4 年时,94 例多灶性乳腺癌患者中有 27 例(28.7%)死于乳腺癌,而 754 例单灶性乳腺癌患者中有 141 例(18.7%)死于乳腺癌(P=.022)。无论是否使用主要肿瘤大小(87.9%)或多灶性肿瘤的总肿瘤大小(87.0%),对于直径为 20mm 或更小的肿瘤,10 年生存率不受大小影响,与单灶性肿瘤(88.1%)相比。对于直径大于 20mm 的肿瘤,单灶性肿瘤的 10 年生存率为 72.1%,而使用主要肿瘤大小的多灶性肿瘤为 54.7%(P=.008),但当使用多灶性肿瘤总肿瘤大小进行分类时,这一数字为 69.5%,差异无统计学意义(P=.49)。多变量分析在调整了重要预后因素后也证实了上述结果。
在制定治疗计划时,应考虑每个病灶的总大小以及其他转移的预后因素。目前使用最大(主要)病变作为分期和相关乳腺癌生存率衡量标准的惯例需要进一步验证。