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2.
J Surg Oncol ; 129(6): 1041-1050, 2024 May.
Article En | MEDLINE | ID: mdl-38436625

INTRODUCTION: Melanoma guidelines stem largely from data on non-Hispanic White (NHW) patients. We aimed to identify features of melanoma within non-Hispanic Black (NHB) patients to inform strategies for earlier detection and treatment. METHODS: From 2004 to 2019 Surveillance, Epidemiology, and End Results (SEER) data, we identified nonmetastatic melanoma patients with known TN category and race. Kaplan-Meier cancer-specific survival (CSS) estimates and multivariable Cox proportional hazard modeling analyses were performed. RESULTS: Of 492 597 patients, 1499 (0.3%) were NHB, who were younger (21% vs. 17% age <50) and more commonly female (54% vs. 41%) than NHW, both p < 0.0005. For NHBs, lower extremity was the most common site (52% vs. 15% for NHWs, p < 0.0001), T category was higher (55% Tis-T1 vs. 82%; 27% T3-T4 vs. 8%, p < 0.0001) and stage at presentation was higher (19% Stage III, vs. 6%, p < 0.0001). Within the NHB cohort, males were older, and more often node-positive than females. Five-year Stage III CSS was 42% for NHB males versus 71% for females, adjusting for age and clinical nodal status (hazard ratio 2.48). CONCLUSIONS: NHB melanoma patients presented with distinct tumor characteristics. NHB males with Stage III disease had inferior CSS. Focus on this high-risk patient cohort to promote earlier detection and treatment may improve outcomes.


Black or African American , Melanoma , SEER Program , Skin Neoplasms , Humans , Melanoma/pathology , Melanoma/mortality , Melanoma/therapy , Melanoma/ethnology , Male , Female , Middle Aged , Skin Neoplasms/pathology , Skin Neoplasms/mortality , Skin Neoplasms/therapy , Skin Neoplasms/ethnology , Survival Rate , Black or African American/statistics & numerical data , Aged , Adult , Prognosis , Follow-Up Studies
6.
J Drugs Dermatol ; 22(7): 712-713, 2023 07 01.
Article En | MEDLINE | ID: mdl-37410040

Syder NC, Elbuluk N. rising interest in sunscreen for skin of color: an analysis of Google trends. J Drugs Dermatol. 2023;22(7):712-713. doi:10.36849/JDD.7373.


Skin Neoplasms , Sunscreening Agents , Humans , Search Engine , Skin , Skin Neoplasms/drug therapy , Skin Neoplasms/ethnology , Skin Neoplasms/prevention & control , Skin Pigmentation
7.
J Drugs Dermatol ; 22(7): 687-689, 2023 Jul 01.
Article En | MEDLINE | ID: mdl-37410053

The various presentations of many dermatologic conditions among various skin types are slowly being elucidated throughout the recent years. These differences present as an issue as it leads to delayed diagnosis, treatment, and poorer quality of life. Herein, we present the characteristics of leukemia cutis in a skin of color patient with diagnosed chronic myelomonocytic leukemia. Adjei S, Temiz LA, Miller AC, et al. Leukemia cutis in skin of color. J Drugs Dermatol. 2023;22(7):687-689. doi:10.36849/JDD.7020.


Leukemia , Skin Neoplasms , Humans , Leukemia/diagnosis , Quality of Life , Skin , Skin Neoplasms/diagnosis , Skin Neoplasms/ethnology , Skin Neoplasms/therapy , Skin Pigmentation
9.
Melanoma Res ; 33(4): 326-331, 2023 08 01.
Article En | MEDLINE | ID: mdl-37199704

Cutaneous malignant melanomas of the head and neck (HNM) are proposed to have notable histological and clinical differences from those at other sites (other melanoma); however, HNMs among Asians have remained poorly understood. This study aimed to investigate the clinicopathological features and prognostic factors of HNM in Asians. Asian melanoma patients who underwent surgical treatment from January 2003 to December 2020 were retrospectively reviewed. The clinicopathological features and risk factors for local recurrence, lymph node metastasis, and distant metastasis were analyzed. Among 230 patients, 28 (12.2%) were diagnosed with HNM, and 202 (87.8%) with other melanoma. The histologic subtype significantly differed as the nodular type was predominant in HNM whereas the acral lentiginous type was predominant in other melanoma ( P  < 0.001). HNM was significantly associated with higher local recurrence ( P  = 0.045), lymph node metastasis ( P  = 0.048), distant metastasis ( P  = 0.023), and lower 5-year disease-free survival ( P  = 0.022) than other melanoma. Ulceration was the risk factor for lymph node metastasis based on multivariable analysis ( P  = 0.013). A high proportion of HNM present as the nodular subtype in Asians, leading to poor outcomes and low survival. Therefore, more cautious surveillance, evaluation, and aggressive treatment are required.


Asian , Head and Neck Neoplasms , Melanoma , Skin Neoplasms , Humans , Asian/statistics & numerical data , Head and Neck Neoplasms/ethnology , Head and Neck Neoplasms/mortality , Head and Neck Neoplasms/pathology , Head and Neck Neoplasms/surgery , Lymphatic Metastasis , Melanoma/ethnology , Melanoma/mortality , Melanoma/pathology , Melanoma/surgery , Neoplasm Staging , Prognosis , Retrospective Studies , Skin Neoplasms/ethnology , Skin Neoplasms/mortality , Skin Neoplasms/pathology , Skin Neoplasms/surgery , Skin Ulcer/ethnology , Skin Ulcer/etiology , Melanoma, Cutaneous Malignant
10.
J Am Acad Dermatol ; 89(3): 529-536, 2023 09.
Article En | MEDLINE | ID: mdl-37224968

BACKGROUND: Asian American and Pacific Islander (AAPI) melanoma patients have higher mortality than non-Hispanic White (NHW) patients. Treatment delays may contribute, but whether AAPI patients have longer time from diagnosis to definitive surgery (TTDS) is unknown. OBJECTIVES: Investigate TTDS differences between AAPI and NHW melanoma patients. METHODS: Retrospective review of AAPI and NHW melanoma patients in the National Cancer Database (NCD) (2004-2020). The association of race with TTDS was evaluated by multivariable logistic regression, controlling for sociodemographic characteristics. RESULTS: Of 354,943 AAPI and NHW melanoma patients identified, 1155 (0.33%) were AAPI. AAPI patients had longer TTDS for stage I, II, and III melanoma (P < .05 for all). Adjusting for sociodemographic factors, AAPI patients had 1.5 times the odds of a TTDS between 61 and 90 days and twice the odds of a TTDS >90 days. Racial differences in TTDS persisted in Medicare and private insurance types. Uninsured AAPI patients had the longest TTDS (mean, 53.26 days), while those with private insurance had the shortest TTDS (mean, 34.92 days; P < .001 for both). LIMITATION: AAPI patients comprised 0.33% of the sample. CONCLUSIONS: AAPI melanoma patients have increased odds of treatment delays. Associated socioeconomic differences should inform efforts to reduce disparities in treatment and survival.


Asian , Health Services Accessibility , Melanoma , Pacific Island People , Skin Neoplasms , Time-to-Treatment , Aged , Humans , Asian/statistics & numerical data , Cross-Sectional Studies , Medicare/statistics & numerical data , Melanoma/epidemiology , Melanoma/ethnology , Melanoma/therapy , United States/epidemiology , Skin Neoplasms/epidemiology , Skin Neoplasms/ethnology , Skin Neoplasms/therapy , Health Services Accessibility/statistics & numerical data
14.
J Cancer Res Clin Oncol ; 148(2): 497-502, 2022 Feb.
Article En | MEDLINE | ID: mdl-33856527

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.


Melanoma/diagnosis , Melanoma/ethnology , Skin Neoplasms/diagnosis , Skin Neoplasms/ethnology , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Cohort Studies , Extremities/pathology , Female , Follow-Up Studies , Germany/epidemiology , Humans , Male , Melanoma/mortality , Melanoma/pathology , Middle Aged , Neoplasm Staging , Prognosis , Skin Neoplasms/mortality , Skin Neoplasms/pathology , Survival Analysis , White People/statistics & numerical data , Young Adult
16.
Med Clin North Am ; 105(4): 643-661, 2021 Jul.
Article En | MEDLINE | ID: mdl-34059243

Melanoma accounts for approximately 1% of all skin cancers but contributes to almost all skin cancer deaths. The developing picture suggests that melanoma phenotypes are driven by epigenetic mechanisms that reflect a complex interplay between genotype and environment. Furthermore, the growing consensus is that current classification standards, notwithstanding pertinent clinical history and appropriate biopsy, fall short of capturing the vast complexity of the disease. This article summarizes the current understanding of the clinical picture of melanoma, with a focus on the tremendous breakthroughs in molecular classification and therapeutics.


Melanoma/diagnosis , Melanoma/genetics , Neoplasm Staging/methods , Skin Neoplasms/genetics , Skin Neoplasms/pathology , Aged , Biopsy , Drug Therapy/methods , Epigenesis, Genetic/genetics , Female , GTP Phosphohydrolases/antagonists & inhibitors , Genotype , Humans , Immunotherapy/methods , Incidence , Male , Melanoma/epidemiology , Melanoma/therapy , Membrane Proteins/antagonists & inhibitors , Mohs Surgery/methods , Molecular Targeted Therapy/methods , Mutation/genetics , Proto-Oncogene Proteins B-raf/antagonists & inhibitors , Skin Neoplasms/ethnology , Skin Neoplasms/mortality , United States/epidemiology , Young Adult
17.
Dermatol Online J ; 27(3)2021 Mar 15.
Article En | MEDLINE | ID: mdl-33865287

Hori nevus, also known as acquired bilateral nevus of Ota-like macules, is a form of dermal melanocytosis found most commonly in women of East Asian heritage. It presents as discrete brown macules on the bilateral cheeks which later coalesce into confluent grey-brown macules and small patches. Herein, we report a classic case of Hori nevus and discuss the histologic findings and differential diagnosis. We also review the proposed pathophysiology, genetic considerations, and treatment options.


Cheek/pathology , Facial Neoplasms/pathology , Nevus, Pigmented/pathology , Skin Neoplasms/pathology , Adult , Asian People , Diagnosis, Differential , Facial Neoplasms/ethnology , Facial Neoplasms/radiotherapy , Female , Humans , Lasers, Solid-State/therapeutic use , Nevus, Pigmented/ethnology , Nevus, Pigmented/radiotherapy , Skin Neoplasms/ethnology , Skin Neoplasms/radiotherapy
18.
JNCI Cancer Spectr ; 5(2)2021 04.
Article En | MEDLINE | ID: mdl-33733052

Background: European studies reported an increased risk of nonmelanoma skin cancer associated with hydrochlorothiazide (HCTZ)-containing products. We examined the risks of basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) associated with HCTZ compared with angiotensin-converting enzyme inhibitors (ACEIs) in a US population. Methods: We conducted a retrospective cohort study in the US Food and Drug Administration's Sentinel System. From the date of HCTZ or ACEI dispensing, patients were followed until a SCC or BCC diagnosis requiring excision or topical chemotherapy treatment on or within 30 days after the diagnosis date or a censoring event. Using Cox proportional hazards regression models, we estimated the hazard ratios (HRs), overall and separately by age, sex, and race. We also examined site- and age-adjusted incidence rate ratios (IRRs) by cumulative HCTZ dose within the matched cohort. Results: Among 5.2 million propensity-score matched HCTZ and ACEI users, the incidence rate (per 1000 person-years) of BCC was 2.78 and 2.82, respectively, and 1.66 and 1.60 for SCC. Overall, there was no difference in risk between HCTZ and ACEIs for BCC (HR = 0.99, 95% confidence interval [CI] = 0.97 to 1.00), but there was an increased risk for SCC (HR = 1.04, 95% CI = 1.02 to 1.06). HCTZ use was associated with higher risks of BCC (HR = 1.09, 95% CI = 1.07 to 1.11) and SCC (HR = 1.15, 95% CI = 1.12 to 1.17) among Caucasians. Cumulative HCTZ dose of 50 000 mg or more was associated with an increased risk of SCC in the overall population (IRR = 1.19, 95% CI = 1.05 to 1.35) and among Caucasians (IRR = 1.27, 95% CI = 1.10 to 1.47). Conclusions: Among Caucasians, we identified small increased risks of BCC and SCC with HCTZ compared with ACEI. Appropriate risk mitigation strategies should be taken while using HCTZ.


Antihypertensive Agents/adverse effects , Carcinoma, Basal Cell/chemically induced , Carcinoma, Squamous Cell/chemically induced , Hydrochlorothiazide/adverse effects , Photosensitizing Agents/adverse effects , Skin Neoplasms/chemically induced , Adult , Age Factors , Aged , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Angiotensin-Converting Enzyme Inhibitors/adverse effects , Antihypertensive Agents/administration & dosage , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/ethnology , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/ethnology , Dose-Response Relationship, Drug , Female , Humans , Hydrochlorothiazide/administration & dosage , Incidence , Male , Middle Aged , Photosensitizing Agents/administration & dosage , Propensity Score , Proportional Hazards Models , Racial Groups/statistics & numerical data , Retrospective Studies , Risk Factors , Sex Factors , Skin Neoplasms/epidemiology , Skin Neoplasms/ethnology , Ultraviolet Rays , United States/epidemiology , United States/ethnology , White People
20.
Eur J Cancer ; 145: 210-220, 2021 03.
Article En | MEDLINE | ID: mdl-33503528

BACKGROUND: As most clinical trials evaluating BRAF and MEK inhibitor combination therapy (B + Minh) have been conducted in Western countries, little is known about the effect of B + Minh among East Asian populations. MATERIAL AND METHODS: Data from patients with advanced melanoma treated using B + Minh (either dabrafenib + trametinib or encorafenib + binimetinib) were retrospectively collected from 16 institutes in Japan. Response rates, adverse events, patterns of failure and survival were analysed. RESULTS: We analysed 112 of 144 collected patient records and, of these, 14 had acral/mucosal melanoma. The response rate for the entire cohort was 75.0%. There were no statistical differences in response rates between acral/mucosal and cutaneous melanomas (64.3% versus 76.5%), whereas previous treatment using immune checkpoint inhibitors (ICIs) did not affect response (72.7% versus 73.9%) to B + Minh, response to ICI after B + Minh was only 20%. Patients who achieved complete response had the best overall survival rates at 24 months (94.7%). Elevated serum lactate dehydrogenase levels and 3 or more metastatic sites were independently associated with survival. The most common relapse site was the brain (17.9%). More than half of the patients (58.8%) experienced grade III/IV pyrexia. CONCLUSION: B + Minh was effective among Japanese patients with melanoma, including those with acral/mucosal melanoma. Factors associated with survival were similar to previous Western studies. B + Minh response was not affected by the previous use of ICI; however, vigilance against brain metastasis during B + Minh therapy is required as the brain was our most commonly encountered relapse site.


Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Melanoma/drug therapy , Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors , Protein Kinase Inhibitors/therapeutic use , Proto-Oncogene Proteins B-raf/antagonists & inhibitors , Skin Neoplasms/drug therapy , Adult , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Asian People , Female , Humans , Japan/epidemiology , Male , Melanoma/enzymology , Melanoma/ethnology , Melanoma/mortality , Middle Aged , Mitogen-Activated Protein Kinase Kinases/metabolism , Progression-Free Survival , Protein Kinase Inhibitors/adverse effects , Proto-Oncogene Proteins B-raf/metabolism , Retrospective Studies , Skin Neoplasms/enzymology , Skin Neoplasms/ethnology , Skin Neoplasms/mortality , Time Factors , Young Adult
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