Ocular Melanoma Center, Retina Service, Massachusetts Eye and Ear Infirmary, Boston.
JAMA Ophthalmol. 2018 Sep 1;136(9):981-986. doi: 10.1001/jamaophthalmol.2018.2466.
Despite high rates of local tumor control in patients who are treated for uveal melanoma, most patients will eventually die of metastasis. When metastasis develops, the liver is involved in most cases, and hepatic metastases are particularly refractory to treatment. Finding effective treatments has been challenging. A comparison of survival rates in patients who were treated for metastasis over approximately 30 years may offer insights into progress that has been made in prolonging survival.
To compare survival after treatment for metastasis in a cohort of patients who were treated for uveal melanoma at the Massachusetts Eye and Ear Infirmary (MEE) during an approximately 30-year period with an earlier analysis to determine if there was meaningful improvement in survival rates after treatment for metastasis.
DESIGN, SETTING, AND PARTICIPANTS: This review included patients (n = 661) who received a diagnosis of metastasis from uveal melanoma who were identified from a cohort of 3063 patients treated at MEE between January 1982 and December 2009 and followed up through December 2011. They were compared with findings from a previous study of patients treated between 1975 and 1987.
Survival rates in patients who received treatment for metastasis were compared with those who did not receive treatment. The differences in survival rates were compared with an earlier analysis that was completed at MEE. A comparison of patients with hepatic metastases and extrahepatic metastases was also completed. Kaplan-Meier analysis was used to calculate survival rates and the log rank test was used to test for statistically significant differences between the groups.
Of 620 patients with race information available, 615 (97.3%) were white; the mean (SD) age of patients was 59.71 (13.23) years and 307 (47.3%) were women. The median time from the initial treatment of the tumor to metastasis was 3.45 years (interquartile range [IQR], 2.0-5.57). Overall, the median survival time was poor (3.9 months [IQR, 1.6-10.1]). Patients who received treatment fared better than those who did not receive treatment (median survival after metastasis diagnosis, 6.3 months [IQR, 2.96-14.41] vs 1.7 months [IQR, 0.66-3.5]). This finding was similar to that of our earlier study in which median survival was 5.2 months and 2 months for treated and untreated patients, respectively.
These findings suggest that advances in treatments that lead to clinically meaningful improvements in survival times have not been realized. Similar survival rates in patients who were treated for metastasis were observed in this recent analysis compared with our earlier study. Adjuvant therapies that are initiated at the time of melanoma diagnosis may be the most effective way to prolong survival.
尽管接受治疗的葡萄膜黑色素瘤患者局部肿瘤控制率很高,但大多数患者最终仍会死于转移。当转移发生时,肝脏通常会受到影响,而肝转移尤其难以治疗。寻找有效的治疗方法一直具有挑战性。比较大约 30 年来接受治疗的转移性疾病患者的生存率,可以深入了解在延长生存方面取得的进展。
通过比较马萨诸塞州眼耳医院(MEE)治疗的葡萄膜黑色素瘤患者在大约 30 年期间接受转移性疾病治疗的生存率,与早期分析进行比较,以确定治疗转移性疾病后的生存率是否有明显提高。
设计、地点和参与者:本综述纳入了从 1982 年 1 月至 2009 年 12 月期间在 MEE 接受治疗的 3063 名患者队列中诊断出患有葡萄膜黑色素瘤转移性疾病的 661 名患者(n=661),并随访至 2011 年 12 月。他们与之前在 1975 年至 1987 年接受治疗的患者研究结果进行了比较。
比较了接受转移性疾病治疗的患者与未接受治疗的患者的生存率。比较了生存率的差异与 MEE 完成的早期分析。还比较了肝转移和肝外转移患者。Kaplan-Meier 分析用于计算生存率,对数秩检验用于检验组间的统计学显著差异。
在有种族信息的 620 名患者中,615 名(97.3%)为白人;患者的平均(SD)年龄为 59.71(13.23)岁,307 名(47.3%)为女性。从肿瘤初始治疗到转移的中位时间为 3.45 年(四分位距[IQR],2.0-5.57)。总体而言,中位生存时间较差(3.9 个月[IQR,1.6-10.1])。接受治疗的患者比未接受治疗的患者预后更好(转移性疾病诊断后的中位生存时间,6.3 个月[IQR,2.96-14.41] vs 1.7 个月[IQR,0.66-3.5])。这一发现与我们早期的研究相似,治疗组和未治疗组的中位生存时间分别为 5.2 个月和 2 个月。
这些发现表明,在治疗方面的进展并未导致生存时间的临床意义上的改善。与我们早期的研究相比,最近的分析显示,接受转移性疾病治疗的患者的生存率相似。在黑色素瘤诊断时开始的辅助治疗可能是延长生存时间的最有效方法。