Suppr超能文献

肢端雀斑样黑素瘤的白种人患者与分期和肢端相匹配的浅表扩散性黑素瘤患者具有相同的结局。

Caucasians with acral lentiginous melanoma have the same outcome as patients with stage- and limb-matched superficial spreading melanoma.

机构信息

Department of Dermatology, Skin Cancer Center, Ruhr-University Bochum, Gudrunstrasse 56, 44791, Bochum, Germany.

出版信息

J Cancer Res Clin Oncol. 2022 Feb;148(2):497-502. doi: 10.1007/s00432-021-03630-6. Epub 2021 Apr 15.

Abstract

PURPOSE

Acral lentiginous melanoma (ALM), a relatively rare subtype of cutaneous melanoma, has been reported to have a worse prognosis than other melanomas. We aimed to assess clinical findings in Caucasian ALM patients and compare the data with a matched cohort of superficial spreading melanoma (SSM) patients.

METHODS

We studied 63 patients with ALM and 63 randomly stage- and limb-matched patients with SSM (non-ALM). In both cohorts, guideline-adjusted diagnosis, treatment and follow-up were performed.

RESULTS

We did not observe differences in prognostic factors (e.g., tumor thickness, ulceration) between the two cohorts. Both in ALM and non-ALM patients positive sentinel lymph node was a significant independent predictor for disease relapse and melanoma-specific death. However, disease relapse and melanoma-specific death rates did not significantly differ between ALM and non-ALM patients. An overall 5-year melanoma-specific survival of 82.5% and 81% was observed in ALM and non-ALM patients, respectively.

CONCLUSIONS

Our data confirm that patients with ALM have no worse outcome than non-ALM patients when correcting for significant prognostic factors. Hence, the reportedly high rates of fatal ALM cases should not be ascribed to pathobiological differences between ALM and non-ALM but are most likely are a consequence of a delay in diagnosis and thus advanced stage of ALM.

摘要

目的

肢端雀斑样黑素瘤(ALM)是一种相对罕见的皮肤黑素瘤亚型,其预后比其他黑素瘤差。我们旨在评估高加索裔 ALM 患者的临床特征,并将数据与匹配的浅表扩散性黑素瘤(SSM)患者进行比较。

方法

我们研究了 63 例 ALM 患者和 63 例随机分期和肢位匹配的 SSM 患者(非 ALM)。在两个队列中,均进行了指南调整后的诊断、治疗和随访。

结果

我们未观察到两个队列之间的预后因素(例如肿瘤厚度、溃疡)存在差异。在 ALM 和非 ALM 患者中,阳性前哨淋巴结均是疾病复发和黑素瘤特异性死亡的显著独立预测因素。然而,ALM 和非 ALM 患者的疾病复发和黑素瘤特异性死亡率无显著差异。ALM 和非 ALM 患者的 5 年总体黑素瘤特异性生存率分别为 82.5%和 81%。

结论

我们的数据证实,在纠正显著预后因素后,ALM 患者的预后并不比非 ALM 患者差。因此,报道中 ALM 病死率较高的情况不应归因于 ALM 和非 ALM 之间的病理生物学差异,而很可能是由于诊断延迟和因此 ALM 处于晚期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c9/11800941/9ca54dd828b1/432_2021_3630_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验