Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Oncology, Karolinska University Hospital, Stockholm, Sweden.
Int J Cancer. 2017 Dec 1;141(11):2243-2252. doi: 10.1002/ijc.30925. Epub 2017 Aug 24.
Outcome data comparing patients with multiple primary invasive cutaneous malignant melanomas (MPMs) to single primary invasive cutaneous malignant melanomas (SPMs) show conflicting results. We have analyzed differences in disease-specific survival between these patients in a nationwide population-based setting. From the Swedish Melanoma Register, 27,235 patients were identified with a first invasive cutaneous malignant melanoma (CMM) between 1990 and 2007, followed-up through 2013. Of these, 700 patients developed MPMs. Cox proportional hazard regression was used for adjusted cause-specific hazard ratios (HRs). An interval of ≤5 years between CMM diagnoses was significantly correlated to a decreased CMM-specific survival in Stage I-II MPM- vs. SPM-patients (HR 1.32; 95% CI 1.04-1.67; p = 0.02). MPM-patients with longer time interval between diagnoses experienced similar risk of CMM-death as SPM-patients. The risk of CMM-death increased by almost 50% above the expected outcome according to stage of the index CMM by the diagnosis of a second CMM (HR 1.48; 95% CI 1.19-1.85; p < 0.001). MPM vs. SPM-patients had a worse outcome (HR 1.38; 95% CI 1.05-1.83; p = 0.001). This emphasizes the importance of prevention efforts in SPM-patients to decrease the risk of subsequent CMMs and has implications for more vigilant follow-up in MPM-patients.
比较多发性原发性侵袭性皮肤恶性黑色素瘤(MPM)和单发性原发性侵袭性皮肤恶性黑色素瘤(SPM)患者的预后数据显示结果相互矛盾。我们在全国范围内基于人群的研究中分析了这些患者之间疾病特异性生存率的差异。从瑞典黑色素瘤登记处,我们确定了 1990 年至 2007 年间患有首次侵袭性皮肤恶性黑色素瘤(CMM)的 27235 例患者,并随访至 2013 年。其中,700 例患者发展为 MPM。使用 Cox 比例风险回归进行调整后的特异性风险比(HR)。CMM 诊断间隔≤5 年与 I 期-II 期 MPM-与 SPM-患者的 CMM 特异性生存率降低显著相关(HR 1.32;95%CI 1.04-1.67;p=0.02)。在诊断间隔较长的 MPM 患者中,CMM 死亡的风险与 SPM 患者相似。与指数 CMM 的分期相比,第二个 CMM 的诊断使 CMM 死亡的风险增加了近 50%(HR 1.48;95%CI 1.19-1.85;p<0.001)。MPM 与 SPM 患者的预后较差(HR 1.38;95%CI 1.05-1.83;p=0.001)。这强调了在 SPM 患者中进行预防努力以降低随后 CMM 风险的重要性,并对 MPM 患者的更密切随访产生影响。