Talha Ayaz1, Vignesh Ramachandran2*, Asad Loya3
1Department of Radiology, University of Texas Medical Branch, Galveston, Texas, USA
2Department of Dermatology, New York University, New York, NY, USA
3Department of Ophthalmology, Baylor College of Medicine, Houston, Texas, USA
*Correspondence author: Vignesh Ramachandran, Department of Dermatology, New York University, New York, NY, USA; Email: [email protected]
Published Date: 15-04-2023
Copyright© 2023 by Ramachandran V, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Editorial
Melanoma can be deadly if not detected and treated early. The association of race with survival in cutaneous malignancies has been researched previously and it has been noted that Hispanic patients have worse melanoma-specific survival compared to non-Hispanic white patients [1]. While research has shown that Hispanic race can be a factor in melanoma survival rates, the specific impact of Hispanic subpopulations on melanoma outcomes is not well understood. In recent years, the Hispanic population in the United States has grown rapidly and is expected to continue to do so in the coming decades. These populations represent diverse individuals from various countries of origins, ethnic backgrounds, and differing cultures. In fact, the Hispanic nomenclature includes diverse worldwide subpopulations and clinical investigations often focus on the ethnic group, resulting in an incomplete characterization of skin malignancies and survival among distinct Latino groups. It is important to understand the unique melanoma survival patterns among different Hispanic subpopulations as these populations are heterogenous.
Herein, we investigated melanoma survival among Hispanic subpopulations using the National Cancer Institute’s Surveillance, Epidemiology and End Results (SEER) database in comparison to non-Hispanic whites in conjunction with the North American Association of Central Cancer Registries National Hispanic Identification Algorithm.
The SEER-18 registry pools cancer incidence and survival data from 34.6% of the U.S. population 389,920 melanoma cases were extracted (1973-2015) [2]. After applying inclusion criteria (age 18 and above, first malignancy, primary site codes C44.0-44.9 [all skin sites], known cause of death/complete follow-up), the North American Association of Central Cancer Registries National Hispanic Identification Algorithm was used to identify patient ethnicity (defined as Hispanic or non-Hispanic) and specific subpopulation of origin. The North American Association of Central Cancer Registries National Hispanic Identification Algorithm aims to augment existing research databases to provide information on Hispanic subpopulations in an effort to make health services research more inclusive and specific as it pertains to data on Hispanic populations. Hispanics with an unspecified background or identified by surname match only were excluded from the present study. Overall, a total of 246,241 cases were analyzed (mean age 57.35 years ±16.17, mean follow-up 93.03 months). Survival outcomes were assessed via multivariate Cox regression models compared to non-Hispanic whites as reference using IBM SPSS Statistics (Armonk, NY). The adjusted covariates utilized in the study included:
The results, all-cause and cause-specific mortality, are depicted in Table 1.
NHIA Derived Origin | Overall Survival | Cause-Specific Survival | ||||
HR (95% CI) | p – value | HR (95% CI) | p – value | |||
Non-Hispanic | ref | ref | ref | ref | ||
Mexican | 1.611 (1.478, 1.756) | < .001 | 1.805 (1.629, 2.000) | < .001 | ||
Cuban | .970 (.711, 1.323) | 0.847 | .831 (.523, 1.321) | 0.433 | ||
Dominican | 1.499 (.749, 2.998) | 0.253 | 1.250 (.403, 3.877) | 0.699 | ||
Puerto Rican | 1.826 (1.437, 2.320) | 0.481 | 2.178 (1.609, 2.949) | < .001 | ||
South/Central American (excluding Brazil) | 1.146 (.979, 1.342) | 0.090 | 1.273 (1.051, 1.541) | 0.013 | ||
Other Spanish Origin including Europe | 1.509 (1.259, 1.810) | < .001 | 1.845 (1.435, 2.373) | < .001 |
Table 1: Adjusted cox regression analysis based off Hispanic origin.
The U.S. has a burgeoning minority population projected to supplant the Caucasian majority by 2045. Of this minority population, Hispanics comprise the largest minority group. Historically, Hispanics from all countries of origin have been grouped together. This categorization fails to recognize heterogeneity within the Hispanic population. This is not just true of everyday life, but is a marked shortcoming in our medical literature in which these individuals are grouped together for statistical analyses. In study, we aim to address this shortcoming for melanoma outcomes in patients of Hispanic origin by delving into a subpopulation analysis of this heterogenous ethnic group. It was noted that all-cause and cause-specific mortality were significantly worse for all Hispanic subpopulations compared to non-Hispanic whites except for Cubans and Dominicans.
There are multiple explanations for such disparities with many more to be uncovered through further research. There is evidence that Hispanic subpopulations vary in genetic ancestry (familial melanoma and polygenic or epigenetic mechanisms may influence the penetrance of melanoma, especially in those with genetic mutation associations), migration history, acculturation (which is defined as assimilation to a different culture, typically the dominant one), environmental exposures (such as carcinogens, pollution), and behavioral and lifestyle practices [3,4]. Fitzpatrick skin type classifications have been shown to vary for subpopulations, with a variable presence of higher risk skin types in Mexican and Puerto Rican groups, which is similar to what our findings have reflected in terms of worse survival outcomes in these populations [5]. These biopsychosocial mechanisms may not only contribute to melanoma risk, but also clinical outcomes. For instance, sunbathing is an acceptable practice in some subpopulations of Hispanic culture (e.g., European), possibly stemming from a false perception of skin cancer risk. Not only do severe sunburns increase melanoma risk, but there is growing evidence of ultraviolet signature mutations associated with melanoma risk, which is a divergence from the commonly-held belief that melanoma is not associated with ultraviolet light exposure [6]. As such, these cultural practices may eventually manifest in late-stage presentation and subsequent poor survival.
Limitations include self-reported race, data entry errors, inability to account for lifestyle and modifiable risk factors, and a retrospective design. Furthermore, SEER only allows for retrospective analyses to be conducted. Nevertheless, this is the first study to assess survival disparities by Hispanic subpopulation, laying a foundation for future investigation to build upon our framework and findings.
In conclusion, the study of Hispanic subpopulations is crucial for improving our understanding of skin cancers and conditions, particularly in the context of melanoma survival outcomes as well as other skin cancers. The Hispanic population is diverse and heterogeneous, with unique genetic, environmental, and cultural factors that can impact cancer risk, prevention, and treatment. By focusing on specific subgroups within this population, we can identify patterns and variations that may not be evident in larger racial or ethnic categories. This approach can help us to develop more targeted prevention and treatment strategies that are tailored to the needs of individual patients, improving their chances of survival and quality of life. Moreover, this approach can help to address health disparities and inequities that may exist within the Hispanic population. This is particularly important given the projected growth of the Hispanic population in the United States and the potential for disparities to worsen if they are not addressed.
Moving forward, it may be prudent to implement standardized demographic subgroups for Hispanics in clinic and in research studies via intake questionnaires. Increased physician awareness of disparities amongst Hispanic communities and individualizing care to address biopsychosocial parameters influencing skin cancer care is advisable.
Keywords: Hispanic; Subpopulation; Melanoma; Survival; Disparities; Latino; Outcomes; Cancer
Conflict of Interest
The authors have no conflict of interest to declare.
References
- Ward-Peterson M, Acuna JM, Alkhalifah MK, Nasiri AM, Al-Akeel ES, Alkhaldi TM, et al. Association between race/ethnicity and survival of melanoma patients in the United States over 3 decades: a secondary analysis of SEER data. Medicine. 2016;95(17).
- Surveillance, Epidemiology, and End Results (SEER) Program (http://www.seer.cancer.gov) SEER*Stat Database: Incidence – SEER 18 Regs Custom Data (with additional treatment fields), Nov 2017 Sub (1973-2015 varying) – Linked To County Attributes – Total U.S., 1969-2016 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, released April 2018, based on the November 2017 submission.
- Read J, Wadt KA, Hayward NK. Melanoma genetics. J Med Genet. 2016;53(1):1-14.
- Martinez Tyson D, Medina-Ramirez P, Flores AM, Siegel R, Aguado Loi C. Unpacking Hispanic ethnicity-cancer mortality differentials among Hispanic subgroups in the United States, 2004-2014. Front Public Health. 2018;31;6:219.
- Robinson JK, Penedo FJ, Hay JL, Jablonski NG. Recognizing Latinos’ range of skin pigment and phototypes to enhance skin cancer prevention. Pigment Cell. Melanoma Res. 2017;30(5):488-92.
- Brash DE. UV signature mutations. Photochem Photobiol. 2015;91(1):15-26.
Article Type
Editorial
Publication History
Received Date: 23-03-2023
Accepted Date: 08-04-2023
Published Date: 15-04-2023
Copyright© 2023 by Ramachandran V, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation: Ramachandran V, et al. Differences in Melanoma Survival in Hispanic Subpopulations. J Dermatol Res. 2023;4(1):1-3.
NHIA Derived Origin | Overall Survival | Cause-Specific Survival | ||||
HR (95% CI) | p – value | HR (95% CI) | p – value | |||
Non-Hispanic | ref | ref | ref | ref | ||
Mexican | 1.611 (1.478, 1.756) | < .001 | 1.805 (1.629, 2.000) | < .001 | ||
Cuban | .970 (.711, 1.323) | 0.847 | .831 (.523, 1.321) | 0.433 | ||
Dominican | 1.499 (.749, 2.998) | 0.253 | 1.250 (.403, 3.877) | 0.699 | ||
Puerto Rican | 1.826 (1.437, 2.320) | 0.481 | 2.178 (1.609, 2.949) | < .001 | ||
South/Central American (excluding Brazil) | 1.146 (.979, 1.342) | 0.090 | 1.273 (1.051, 1.541) | 0.013 | ||
Other Spanish Origin including Europe | 1.509 (1.259, 1.810) | < .001 | 1.845 (1.435, 2.373) | < .001 |
Table 1: Adjusted cox regression analysis based off Hispanic origin.