Division of Surgical Oncology, Breast Surgical Oncology, UPMC Magee-Womens Hospital, University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, USA.
Breast Surgery, Private Practice, Ankara, Turkey.
Ann Surg Oncol. 2022 Oct;29(10):6327-6336. doi: 10.1245/s10434-022-12239-z. Epub 2022 Jul 25.
One fourth of early-stage breast cancer cases become metastatic during the follow-up period. Limited metastasis is a metastatic disease condition in which the number of metastatic sites and the extent of the disease both are limited, and the disease is amenable to metastatic intervention. This prospective study aimed to evaluate intervention for limited metastases in the lung, liver, or both.
The study enrolled luminal A/B and/or human epidermal growth factor receptor 2 (HER2)-neu+ patients with operable lung and/or liver metastases in the follow-up assessment after completion of primary breast cancer treatment and patients with a diagnosis of metastasis after 2014. Demographic, clinical, tumor-specific, and metastasis detection-free interval (MDFI) data were collected. Bone metastasis in addition to lung and liver metastases also was included in the analysis. The patients were divided into two groups according to the method of treatment for metastases: systemic therapy alone (ST) group or intervention (IT) group.
Until June 2020, 200 patients were enrolled in the study. The demographic data were similar between the two groups. The median follow-up time was 77 months (range 55-107 months) in the IT group (n = 119; 59.5%) and 57 months (range 39-84) in the ST-only group (n = 81; 40.5%). The median MDFI was 40 months (range 23-70 months) in the IT group, and 35 months (range 13-61 months) in the ST-only group (p = 0.47). The groups had similar surgeries for the primary tumor and axilla. Most of the patients had liver metastases (49.5%, n = 99), and 42% (n = 84) of the patients had lung metastases. Both lung and liver metastases were found in 8.5% (n = 17) of the patients. The primary tumor was estrogen receptor/progesterone receptor-positive in 75% (n = 150) of the patients, and 32% (n = 64) of the patients had HER2-neu+ tumors. Metastatic-site resection was performed for 32% (n = 64) of the patients, and 27.5% (n = 55) of the patients underwent metastatic ablative interventions. In the Kaplan-Meier survival analysis, the hazard of death (HoD) was 56% lower in the IT group than in the ST-only group (hazard ratio [HR], 0.44; 95% confidence interval [CI] 0.26-0.72; p = 0.001). The HoD was lower in the IT group than in the ST-only group for the patients younger than 55 years (HR, 0.32; 95% CI 0.17-0.62; p = 0.0007). In the multivariable Cox regression model, HoD was significantly lower for the patients who underwent intervention for metastases and had an MDFI longer than 24 months, but their liver metastases doubled the risk of death compared with lung metastases.
Metastasis-directed interventions have reduced the risk of death for patients with limited lung/liver metastases who are amenable to interventions after completion of primary cancer treatment. For a select group of patients, such as those with luminal A/B or HER2-neu+ breast cancer who are younger than 55 years with limited metastases to the lung and liver or an MDFI longer than 24 months, surgical or ablative therapy for metastases should be considered and discussed on tumor boards.
四分之一的早期乳腺癌病例在随访期间发生转移。局限性转移是一种转移性疾病,其转移部位的数量和疾病的严重程度均有限,且转移性疾病适合进行转移干预。本前瞻性研究旨在评估对肺、肝或两者均有的局限性转移进行干预的效果。
本研究纳入了在完成原发性乳腺癌治疗后随访评估时发现肺和/或肝转移的 luminal A/B 型和/或人表皮生长因子受体 2(HER2)-neu+型患者,以及在 2014 年后诊断为转移的患者。收集了人口统计学、临床、肿瘤特异性和转移无检测间隔(MDFI)数据。此外,还将骨转移纳入到肺和肝转移的分析中。根据转移治疗方法将患者分为两组:全身治疗组(ST)或干预组(IT)。
截至 2020 年 6 月,共有 200 例患者入组该研究。两组的人口统计学数据相似。干预组(n=119;59.5%)的中位随访时间为 77 个月(范围 55-107 个月),而全身治疗组(n=81;40.5%)的中位随访时间为 57 个月(范围 39-84 个月)。干预组的中位 MDFI 为 40 个月(范围 23-70 个月),全身治疗组为 35 个月(范围 13-61 个月)(p=0.47)。两组的原发性肿瘤和腋窝手术相似。大多数患者存在肝转移(49.5%,n=99),42%(n=84)的患者存在肺转移。8.5%(n=17)的患者同时存在肺和肝转移。75%(n=150)的患者原发性肿瘤为雌激素受体/孕激素受体阳性,32%(n=64)的患者存在 HER2-neu+肿瘤。32%(n=64)的患者进行了转移灶切除术,27.5%(n=55)的患者进行了转移性消融干预。在 Kaplan-Meier 生存分析中,与全身治疗组相比,干预组的死亡风险(HoD)降低了 56%(危险比 [HR],0.44;95%置信区间 [CI],0.26-0.72;p=0.001)。对于年龄小于 55 岁的患者,干预组的 HoD 比全身治疗组低 32%(HR,0.32;95% CI,0.17-0.62;p=0.0007)。在多变量 Cox 回归模型中,对于接受转移性干预且 MDFI 长于 24 个月的患者,HoD 显著降低,但与肺转移相比,肝转移会使死亡风险增加一倍。
对于完成原发性癌症治疗后适合进行转移干预的局限性肺/肝转移患者,转移定向干预降低了死亡风险。对于 luminal A/B 型或 HER2-neu+乳腺癌、年龄小于 55 岁、肺和肝局限性转移或 MDFI 长于 24 个月的特定患者,肿瘤委员会应考虑并讨论对转移灶进行手术或消融治疗。