Khaddour Karam, Liu Mofei, Kim Emily Y, Bahar Furkan, Lôbo Matheus M, Giobbie-Hurder Anita, Silk Ann W, Thakuria Manisha
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Merkel Cell Carcinoma Center of Excellence, Dana-Farber Cancer Institute, Boston, MA, United States.
Front Oncol. 2024 Sep 16;14:1444590. doi: 10.3389/fonc.2024.1444590. eCollection 2024.
Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine malignancy of the skin with a predilection for metastases. This study investigates the clinical outcomes in patients presenting with Stage IV MCC according to the metastatic site(s) at presentation.
Patients who presented with one or more sites of distant metastatic MCC at initial diagnosis between 2009 and 2023 were identified. The presence or absence of one or more metastases in each organ was categorized for each patient at the time of diagnosis. Overall survival (OS) and progression-free survival (PFS) were estimated using the Kaplan-Meier method. Competing risk analysis was used to estimate the cumulative occurrence risk of MCC-specific death. Fisher's exact test was used for response rate analysis. Results were considered statically significant if < 0.05.
Thirty-four patients presented with distant metastatic MCC. There was no association between the number of metastatic sites at diagnosis and OS (= 0.58), PFS (=0.79), or response rates (=0.53). However, the presence of bone metastases was associated with significantly shorter OS (8.2 versus 25.2 months, HR: 2.4, 95% CI 1.01-5.7, = 0.04). MCC-specific death in patients with lymph node metastases was significantly lower than in patients without (HR: 0.28, 95% CI: 0.09-0.87, = 0.013). The presence of bone metastases tended to associate with an increased risk of MCC-specific death, although not statistically significant. The location of metastases was not associated with the response rate to first-line treatment. There was no significant association between site of metastases and PFS.
In this cohort of patients with metastatic MCC, the presence of bone metastases, but not the number of organs involved, was associated with significantly worse OS. The presence of lymph node metastases was associated with lower MCC-specific death. Further research is warranted in larger cohorts to investigate the impact of the location of metastases on clinical outcomes.
默克尔细胞癌(MCC)是一种罕见且侵袭性强的皮肤神经内分泌恶性肿瘤,易发生转移。本研究根据初诊时的转移部位,调查IV期MCC患者的临床结局。
确定2009年至2023年期间初诊时出现一个或多个远处转移性MCC部位的患者。在诊断时,为每位患者对每个器官中是否存在一个或多个转移灶进行分类。采用Kaplan-Meier法估计总生存期(OS)和无进展生存期(PFS)。使用竞争风险分析来估计MCC特异性死亡的累积发生风险。采用Fisher精确检验进行缓解率分析。如果P<0.05,则结果被认为具有统计学意义。
34例患者出现远处转移性MCC。诊断时转移部位的数量与OS(P=0.58)、PFS(P=0.79)或缓解率(P=0.53)之间无关联。然而,骨转移的存在与显著缩短的OS相关(8.2个月对25.2个月,HR:2.4,95%CI 1.01-5.7,P=0.04)。有淋巴结转移的患者中MCC特异性死亡显著低于无淋巴结转移的患者(HR:0.28,95%CI:0.09-0.87,P=0.013)。骨转移的存在倾向于与MCC特异性死亡风险增加相关,尽管无统计学意义。转移部位与一线治疗的缓解率无关。转移部位与PFS之间无显著关联。
在这组转移性MCC患者中,骨转移的存在而非受累器官的数量与显著更差的OS相关。淋巴结转移的存在与较低的MCC特异性死亡相关。有必要在更大的队列中进行进一步研究,以调查转移部位对临床结局的影响。