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Comparison of clinicopathological features and treatment outcomes for cutaneous melanomas of the head and neck and melanomas arising at other sites: Implications for systemic therapy. 头颈部皮肤黑色素瘤与其他部位黑色素瘤的临床病理特征和治疗效果比较:对全身治疗的影响。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.06.107
Andrew T Li, Jessie X Xu, Tyler R Blah, Serigne N Lo, Robyn Pm Saw, Alexander Hr Varey, Alexander Van Akkooi, Matteo S Carlino, Ines Pires da Silva, Alexander M Menzies, Kerwin F Shannon, Georgina V Long, Richard A Scolyer, John F Thompson, Sydney Ch'ng

Background: Melanoma is increasingly recognized as a heterogeneous disease, with conflicting evidence regarding whether cutaneous head and neck melanoma (CHNM) represents a distinct entity.

Objective: Comparison of clinicopathological features and treatment outcomes of CHNM and cutaneous melanomas of other sites (CMOS).

Methods: Patients with CHNM and CMOS diagnosed between 2000 and 2018 were included. Locoregional control, distant metastasis-free survival, melanoma-specific survival (MSS), and overall survival (OS) were described using the Kaplan-Meier method. Cox regression analyses were performed to examine associations between prognostic factors and outcomes. Additional analyses of survival from time of stage IV disease diagnosis were undertaken, stratified by receipt of BRAF-targeted therapy and immune checkpoint inhibitor immunotherapy.

Results: Of 3007 CHNM and 10,637 CMOS patients, CHNM had more adverse pathological features (median age 65.9 vs 58.5, P < .001; median Breslow thickness 1.7 mm vs 1.2 mm, P < .001; and ulceration 21.2% vs 18.2%, P < .001). CHNM had worse locoregional control (hazard ratio (HR) 1.17, P < .001) and distant metastasis-free survival (HR 1.25, P < .001) but there were no significant differences in MSS or OS. Among stage IV patients who received immune checkpoint inhibitor, CHNM had better MSS (HR 0.56, P = .001) and OS (HR 0.57, P < .001) on multivariable analyses.

Limitations: Retrospective study, offset by prospective data collection.

Conclusion: CHNM is associated with a distinct clinicopathological and prognostic profile.

背景:黑色素瘤越来越被认为是一种异质性疾病:黑色素瘤越来越被认为是一种异质性疾病,关于皮肤头颈部黑色素瘤(CHNM)是否代表一个独特的实体,存在相互矛盾的证据:比较头颈部皮肤黑色素瘤和其他部位皮肤黑色素瘤(CMOS)的临床病理特征和治疗效果:纳入2000-2018年间确诊的CHNM和CMOS患者。采用 Kaplan-Meier 法描述了局部控制率(LRC)、无远处转移生存率(DMFS)、黑色素瘤特异性生存率(MSS)和总生存率(OS)。研究人员还进行了 Cox 回归分析,以检验预后因素与结果之间的关联。此外,还根据接受 BRAF 靶向疗法和免疫检查点抑制剂(ICI)免疫疗法的情况,对 IV 期疾病诊断后的存活率进行了分析:结果:在3007名CHNM和10637名CMOS患者中,CHNM患者的不良病理特征更明显(中位年龄65.9岁对58.5岁,p局限性:局限性:回顾性研究,由前瞻性数据收集抵消:结论:CHNM 与独特的临床病理和预后特征相关。
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引用次数: 0
Technology pearl: Utilizing dermatoscope adapter to obtain high-resolution histopathologic photographs with modern multilens smartphone cameras. 技术明珠:利用皮肤镜适配器,用现代多镜头智能手机相机获取高分辨率组织病理学照片。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.08.053
Elizabeth P Long, Brooke A Burgess, Joshua L Owen
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引用次数: 0
A phase 2 open-label study of cemiplimab in patients with advanced cutaneous squamous cell carcinoma (EMPOWER-CSCC-1): Final long-term analysis of Groups 1, 2, and 3, and primary analysis of fixed-dose treatment Group 6. 针对晚期皮肤鳞状细胞癌患者的塞米普利单抗 2 期开放标签研究(EMPOWER-CSCC-1):第1、2和3组的最终长期分析以及固定剂量治疗第6组的主要分析。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.06.108
Brett G M Hughes, Alexander Guminski, Samantha Bowyer, Michael R Migden, Chrysalyne D Schmults, Nikhil I Khushalani, Anne Lynn S Chang, Jean-Jacques Grob, Karl D Lewis, George Ansstas, Fiona Day, Rahul Ladwa, Brian N Stein, Eva Muñoz Couselo, Friedegund Meier, Axel Hauschild, Dirk Schadendorf, Nicole Basset-Seguin, Badri Modi, Sophie Dalac-Rat, Lara A Dunn, Lukas Flatz, Laurent Mortier, Sarah Guégan, Lucie M Heinzerling, Janice M Mehnert, Sabiha Trabelsi, Ainara Soria-Rivas, Alexander J Stratigos, Claas Ulrich, Deborah J Wong, Marie Beylot-Barry, Paolo Bossi, Cristina Bugés Sánchez, Sunandana Chandra, Caroline Robert, Jeffery S Russell, Ann W Silk, Jocelyn Booth, Suk-Young Yoo, Frank Seebach, Israel Lowy, Matthew G Fury, Danny Rischin

Background: In the phase 2 EMPOWER-CSCC-1 study (NCT02760498), cemiplimab demonstrated antitumor activity against metastatic (mCSCC) and locally advanced cutaneous squamous cell carcinoma (laCSCC).

Objectives: To report final analysis of weight-based cemiplimab in mCSCC and laCSCC (Groups 1 and 2), fixed-dose cemiplimab in mCSCC (Group 3), and primary analysis of fixed-dose cemiplimab in mCSCC/laCSCC (Group 6).

Methods: Patients received cemiplimab (3 mg/kg intravenously [IV] every 2 weeks [Groups 1 and 2]) or cemiplimab (350 mg IV [Groups 3 and 6]) every 3 weeks. The primary endpoint was objective response rate (ORR). Duration of response (DOR) and progression-free survival (PFS) are presented per protocol, according to post-hoc sensitivity analyses that only include the period of protocol-mandated imaging assessments.

Results: At 42.5 months, ORR for Groups 1-3 (n=193) was 47.2%, estimated 12-month DOR was 88.3%, and median PFS was 26.0 months. At 8.7 months, ORR for Group 6 (n=165 patients) was 44.8%; median DOR and median PFS were not reached. Serious treatment-emergent adverse event rates (grade ≥3) were Groups 1-3: 31.1% and Group 6: 34.5%.

Limitations: Non-randomized study, non-survival primary endpoint.

Conclusion: EMPOWER-CSCC-1 provides the largest prospective data on long-term efficacy and safety for anti-programmed cell death-1 therapy in advanced CSCC.

研究背景在2期EMPOWER-CSCC-1研究(NCT02760498)中,cemiplimab对转移性皮肤鳞状细胞癌(mCSCC)和局部晚期皮肤鳞状细胞癌(laCSCC)具有抗肿瘤活性:报告基于体重的塞米单抗在mCSCC和laCSCC(第1组和第2组)、固定剂量的塞米单抗在mCSCC(第3组)中的最终分析结果,以及固定剂量的塞米单抗在mCSCC/laCSCC(第6组)中的主要分析结果:患者接受每2周一次的cemiplimab(3毫克/千克静脉注射[IV][第1组和第2组])或每3周一次的cemiplimab(350毫克静脉注射[第3组和第6组])治疗。主要终点是客观反应率(ORR)。反应持续时间(DOR)和无进展生存期(PFS)根据仅包括方案规定的成像评估期的事后敏感性分析按方案列出:42.5个月时,1-3组(n=193)的ORR为47.2%,估计12个月的DOR为88.3%,中位PFS为26.0个月。8.7个月时,第6组(165名患者)的ORR为44.8%;未达到中位DOR和中位PFS。严重治疗突发不良事件(≥3级)发生率为:第1-3组:31.1%,第6组:34.5%:局限性:非随机研究,主要终点为非存活:EMPOWER-CSCC-1为晚期CSCC抗程序性细胞死亡-1疗法的长期疗效和安全性提供了最大规模的前瞻性数据。
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引用次数: 0
Response to Caplan et al, "Clinico-mycological and therapeutic updates on cutaneous dermatophytic infections in the era of Trichophyton indotineae; Focus on Griseofulvin". 对 Caplan 等人的回应,"在 indotineae 毛癣菌时代,皮肤皮癣菌感染的临床霉菌学和治疗最新进展;聚焦 Griseofulvin"。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.08.054
Ananta Khurana, Savitha Sharath, Kabir Sardana, Anuradha Chowdhary
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引用次数: 0
Diagnostic value of direct immunofluorescence testing in the evaluation of alopecia: A single-institution retrospective cohort study of 346 studies. 直接免疫荧光检测在脱发评估中的诊断价值:一项由 346 项研究组成的单一机构回顾性队列研究。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.08.055
Michelle D Colbert, Giang H Nguyen, Carilyn N Wieland, Michael J Camilleri, Heather Hardway, Julia S Lehman
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引用次数: 0
Frailty and functional dependency in a multicenter cohort of older adults with psoriasis: Prevalence and extent of and implications for psoriasis management. 患有银屑病的老年人多中心队列中的虚弱和功能依赖:银屑病的发病率、程度及其对银屑病管理的影响。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-06 DOI: 10.1016/j.jaad.2024.07.1527
Elke L M Ter Haar, Juul M P A van den Reek, Mahshid Sadat Chenarani Moghadam, Yvonne Schoon, Marloes M Kleinpenning, Elke M G J de Jong, Satish F K Lubeek
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引用次数: 0
This Month in JAAD International: November 2024: Pressure ulcers and qualitative research. 本月 JAAD 国际:2024 年 11 月:压疮与定性研究。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-05 DOI: 10.1016/j.jaad.2024.09.001
Jonathan Kantor
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引用次数: 0
The ethical and responsible use of sick call. 有道德和负责任地使用病假。
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-02 DOI: 10.1016/j.jaad.2024.08.049
Albert E Zhou, Christian Gronbeck, Brett Sloan, Jane M Grant-Kels
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引用次数: 0
54695 Access to specialist care and perceived care quality among melanoma and non-melanoma skin cancer patients: A Medical Expenditure Panel Survey Analysis 54695 黑色素瘤和非黑色素瘤皮肤癌患者获得专科护理的机会和感知的护理质量:医疗支出小组调查分析
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.jaad.2024.07.064
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引用次数: 0
52898 Among scalp non-responder patients with eyebrow/eyelash regrowth in the first year, continued treatment with baricitinib resulted in meaningful scalp responses for patients with severe alopecia areata 52898 在第一年眉毛/睫毛再生的头皮非应答患者中,继续使用巴利昔尼治疗可使重度斑秃患者的头皮出现有意义的应答
IF 12.8 1区 医学 Q1 DERMATOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.jaad.2024.07.071
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引用次数: 0
期刊
Journal of the American Academy of Dermatology
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