Division of Surgical Oncology, Department of Surgery, Dr Sardjito Hospital/Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Jl Kesehatan No. 1, Yogyakarta, 55281, Indonesia.
Department of Radiology, Dr Sardjito Hospital/Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, 55281, Indonesia.
World J Surg Oncol. 2020 May 30;18(1):117. doi: 10.1186/s12957-020-01893-w.
More than one third of breast cancer patients including those that are diagnosed in early stages will develop distant metastasis. Patterns of distant metastasis and the associated risks according to the molecular subtypes are not completely revealed particularly in populations of patients with delayed diagnosis and advanced stages.
Breast cancer patients (n = 1304) admitted to our institute (2014-2017) were evaluated to identify the metastatic patterns and the associated risks. Metastatic breast cancers at diagnosis were found in 245 patients (18.7%), and 1059 patients were then grouped into non-metastatic and metastatic groups after a median follow-up of 3.8 years.
Infiltration of the tumor to the skin and chest wall prevailed as the most powerful predictor for distant metastasis (OR 2.115, 95% CI 1.544-2.898) particularly in the luminal A-like subtype (OR 2.685, 95% CI 1.649-4.371). Nodal involvement was also significantly associated with the risk of distant metastasis (OR 1.855, 95% CI 1.319-2.611), and the risk was higher in the Luminal A-like subtype (OR 2.572, 95% CI 1.547-4.278). Luminal A-like subtype had a significant higher risk of bone metastasis (OR 1.601, 95% CI 1.106-2.358). In respect to treatment, a combination of anthracyclines and taxanes-based chemotherapy was significantly associated with lower distant organ spread in comparison with anthracycline-based chemotherapy (OR 0.510, 95% CI 0.355-0.766) and the effect was stronger in Luminal A-like subtype (OR 0.417, 95% CI 0.226-0.769). Classification into Luminal and non-Luminal subtypes revealed significant higher risks of bone metastasis in the Luminal subtype (OR 1.793, 95% CI 1.209-2.660) and pulmonary metastasis in non-Luminal breast cancer (OR 1.445, 95% CI 1.003-2.083).
In addition to guiding the treatment plan, a comprehensive analysis of clinicopathological variables including the molecular subtypes could assist in the determination of distant metastasis risks of breast cancer patients. Our study offers new perspectives concerning the risks of distant metastasis in breast cancer subtypes in order to plan intensive surveillance or escalation of treatment particularly in a setting where patients are predominantly diagnosed in late stages.
包括早期诊断的乳腺癌患者在内,超过三分之一的患者会发生远处转移。特别是在诊断延迟和晚期患者人群中,远处转移的模式和相关风险,根据分子亚型,尚未完全揭示。
评估了我院(2014-2017 年)收治的 1304 例乳腺癌患者,以确定转移模式和相关风险。在诊断时发现转移性乳腺癌的患者有 245 例(18.7%),在中位随访 3.8 年后,1059 例患者被分为非转移性和转移性组。
肿瘤浸润皮肤和胸壁是远处转移的最强预测因子(OR 2.115,95%CI 1.544-2.898),尤其是在 Luminal A 样亚型中(OR 2.685,95%CI 1.649-4.371)。淋巴结受累也与远处转移风险显著相关(OR 1.855,95%CI 1.319-2.611),在 Luminal A 样亚型中风险更高(OR 2.572,95%CI 1.547-4.278)。Luminal A 样亚型发生骨转移的风险显著增加(OR 1.601,95%CI 1.106-2.358)。在治疗方面,与蒽环类药物为基础的化疗相比,蒽环类药物联合紫杉烷类药物化疗显著降低了远处器官转移的风险(OR 0.510,95%CI 0.355-0.766),在 Luminal A 样亚型中效果更强(OR 0.417,95%CI 0.226-0.769)。Luminal 和非 Luminal 亚型分类显示,Luminal 亚型骨转移风险显著增加(OR 1.793,95%CI 1.209-2.660),非 Luminal 乳腺癌肺转移风险增加(OR 1.445,95%CI 1.003-2.083)。
除了指导治疗方案外,综合分析包括分子亚型在内的临床病理变量有助于确定乳腺癌患者的远处转移风险。我们的研究为乳腺癌亚型远处转移风险提供了新的视角,以便在患者主要在晚期诊断的情况下,计划进行密集监测或治疗升级。