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      Smartphone applications for triaging adults with skin lesions that are suspicious for melanoma

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          Abstract

          Melanoma accounts for a small proportion of all skin cancer cases but is responsible for most skin cancer‐related deaths. Early detection and treatment can improve survival. Smartphone applications are readily accessible and potentially offer an instant risk assessment of the likelihood of malignancy so that the right people seek further medical attention from a clinician for more detailed assessment of the lesion. There is, however, a risk that melanomas will be missed and treatment delayed if the application reassures the user that their lesion is low risk. To assess the diagnostic accuracy of smartphone applications to rule out cutaneous invasive melanoma and atypical intraepidermal melanocytic variants in adults with concerns about suspicious skin lesions. We undertook a comprehensive search of the following databases from inception to August 2016: Cochrane Central Register of Controlled Trials; MEDLINE; Embase; CINAHL; CPCI; Zetoc; Science Citation Index; US National Institutes of Health Ongoing Trials Register; NIHR Clinical Research Network Portfolio Database; and the World Health Organization International Clinical Trials Registry Platform. We studied reference lists and published systematic review articles. Studies of any design evaluating smartphone applications intended for use by individuals in a community setting who have lesions that might be suspicious for melanoma or atypical intraepidermal melanocytic variants versus a reference standard of histological confirmation or clinical follow‐up and expert opinion. Two review authors independently extracted all data using a standardised data extraction and quality assessment form (based on QUADAS‐2). Due to scarcity of data and poor quality of studies, we did not perform a meta‐analysis for this review. For illustrative purposes, we plotted estimates of sensitivity and specificity on coupled forest plots for each application under consideration. This review reports on two cohorts of lesions published in two studies. Both studies were at high risk of bias from selective participant recruitment and high rates of non‐evaluable images. Concerns about applicability of findings were high due to inclusion only of lesions already selected for excision in a dermatology clinic setting, and image acquisition by clinicians rather than by smartphone app users. We report data for five mobile phone applications and 332 suspicious skin lesions with 86 melanomas across the two studies. Across the four artificial intelligence‐based applications that classified lesion images (photographs) as melanomas (one application) or as high risk or 'problematic' lesions (three applications) using a pre‐programmed algorithm, sensitivities ranged from 7% (95% CI 2% to 16%) to 73% (95% CI 52% to 88%) and specificities from 37% (95% CI 29% to 46%) to 94% (95% CI 87% to 97%). The single application using store‐and‐forward review of lesion images by a dermatologist had a sensitivity of 98% (95% CI 90% to 100%) and specificity of 30% (95% CI 22% to 40%). The number of test failures (lesion images analysed by the applications but classed as 'unevaluable' and excluded by the study authors) ranged from 3 to 31 (or 2% to 18% of lesions analysed). The store‐and‐forward application had one of the highest rates of test failure (15%). At least one melanoma was classed as unevaluable in three of the four application evaluations. Smartphone applications using artificial intelligence‐based analysis have not yet demonstrated sufficient promise in terms of accuracy, and they are associated with a high likelihood of missing melanomas. Applications based on store‐and‐forward images could have a potential role in the timely presentation of people with potentially malignant lesions by facilitating active self‐management health practices and early engagement of those with suspicious skin lesions; however, they may incur a significant increase in resource and workload. Given the paucity of evidence and low methodological quality of existing studies, it is not possible to draw any implications for practice. Nevertheless, this is a rapidly advancing field, and new and better applications with robust reporting of studies could change these conclusions substantially. How accurate are smartphone applications ('apps') for detecting melanoma in adults? What is the aim of the review? We wanted to find out how well smartphone applications can help the general public understand whether their skin lesions might be melanoma. Why is improving the diagnosis of malignant melanoma skin cancer important? Melanoma is one of the most dangerous forms of skin cancer. Not recognising a melanoma (a false negative test result) could delay seeking appropriate advice and surgery to remove it. This increases the risk of the cancer spreading to other organs in the body and possibly causing death. Diagnosing a skin lesion as a melanoma when it is not present (a false positive result) may cause anxiety and lead to unnecessary surgery and further investigations. What was studied in the review? Specialised applications ('apps') that provide advice on skin lesions or moles that might cause people concern are widely available for smartphones. Some apps allow people to photograph any skin lesion they might be worried about and then receive guidance on whether to get medical advice. Apps may automatically classify lesions as high or low risk, while others can act as store‐and‐forward devices where images are sent to an experienced professional, such as a dermatologist, who then makes a risk assessment based on the photo. Cochrane researchers found two studies, evaluating five apps that used automated analysis of images and one that used a store‐and‐forward approach, to evaluate suspicious skin lesions. What are the main results of the review? The review included two studies with 332 lesions, including 86 melanomas, analysed by at least one smartphone application. Both studies used photographs of moles or skin lesions that were about to be removed because doctors had already decided they could be melanomas. The photographs were taken by doctors instead of people taking pictures of their lesions with their own smartphones. For these reasons, we are not able to make a reliable estimate about how well the apps actually work. Four apps that produce an immediate (automated) assessment of a skin lesion or mole that has been photographed by the smartphone missed between 7 and 55 melanomas. One app that sends the photograph of a mole or skin lesion to a dermatologist for assessment missed only one melanoma. Another 6 melanomas examined by the dermatologist via the application were not classified as high risk; instead the dermatologist was not able to classify the lesion as either 'atypical' (possibly a melanoma) or 'typical' (definitely not a melanoma). How reliable are the results of the studies of this review? The small number and poor quality of included studies reduces the reliability of findings. The people included were not typical of those who would use the applications in real life. The final diagnosis of melanoma was made by histology, which is likely to have been a reliable method for deciding whether patients really had melanoma*. However, the studies excluded between 2% and 18% of images because the applications failed to produce a recommendation. Who do the results of this review apply to? Studies took place in the USA and Germany. They did not report key patient information such as age and gender. The percentage of people with a final diagnosis of melanoma was 18% and 35%, much higher than that observed in community settings. The definition of eligible patients was narrow in comparison to likely users of the applications. The photographs used were taken by doctors rather than by smartphone users, which seriously impacts the applicability of results. What are the implications of this review? Current smartphone applications using automated analysis are observed to have a high chance of missing melanomas (false negatives). Store‐and‐forward image applications could have a potential role in the timely identification of people with potentially malignant lesions by facilitating early engagement of those with suspicious skin lesions, but they have resource and workload implications. The development of applications to help identify people who might have melanoma is a fast‐moving field. The emergence of new applications, higher quality and better reported studies could change the conclusions of this review substantially. How up‐to‐date is this review? The review authors searched for and used studies published up to August 2016. *In these studies biopsy was the reference standard (means of establishing final diagnoses).

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          To revise the staging system for cutaneous melanoma on the basis of data from an expanded American Joint Committee on Cancer (AJCC) Melanoma Staging Database. The melanoma staging recommendations were made on the basis of a multivariate analysis of 30,946 patients with stages I, II, and III melanoma and 7,972 patients with stage IV melanoma to revise and clarify TNM classifications and stage grouping criteria. Findings and new definitions include the following: (1) in patients with localized melanoma, tumor thickness, mitotic rate (histologically defined as mitoses/mm(2)), and ulceration were the most dominant prognostic factors. (2) Mitotic rate replaces level of invasion as a primary criterion for defining T1b melanomas. (3) Among the 3,307 patients with regional metastases, components that defined the N category were the number of metastatic nodes, tumor burden, and ulceration of the primary melanoma. (4) For staging purposes, all patients with microscopic nodal metastases, regardless of extent of tumor burden, are classified as stage III. Micrometastases detected by immunohistochemistry are specifically included. (5) On the basis of a multivariate analysis of patients with distant metastases, the two dominant components in defining the M category continue to be the site of distant metastases (nonvisceral v lung v all other visceral metastatic sites) and an elevated serum lactate dehydrogenase level. Using an evidence-based approach, revisions to the AJCC melanoma staging system have been made that reflect our improved understanding of this disease. These revisions will be formally incorporated into the seventh edition (2009) of the AJCC Cancer Staging Manual and implemented by early 2010.
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            A systematic revision of the literature was conducted in order to undertake a comprehensive meta-analysis of all published observational studies on melanoma. An extensive analysis of the inconsistencies and variability in the estimates was performed to provide some clues about its Epidemiology. Following a systematic literature search, relative risks (RRs) for sun exposure were extracted from 57 studies published before September 2002. Intermittent sun exposure and sunburn history were shown to play considerable roles as risk factors for melanoma, whereas a high occupational sun exposure seemed to be inversely associated to melanoma. The country of study and adjustment of the estimates adjuste for phenotype and photo-type were significantly associated with the variability of the intermittent sun exposure estimates (P = 0.024, 0.003 and 0.030, respectively). For chronic sun exposure, inclusion of controls with dermatological diseases and latitude resulted in significantly different data (P = 0.05 and 0.031, respectively). Latitude was also shown to be important (P = 0.031) for a history of sunburn; studies conducted at higher latitudes presented higher risks for a history of sunburns. Role of country, inclusion of controls with dermatological diseases and other study features seemed to suggest that "well conducted" studies supported the intermittent sun exposure hypothesis: a positive association for intermittent sun exposure and an inverse association with a high continuous pattern of sun exposure.
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              International trends in the incidence of malignant melanoma 1953-2008--are recent generations at higher or lower risk?

              The incidence of cutaneous malignant melanoma has steadily increased over the past 50 years in predominately fair-skinned populations. This increase is reported to have leveled off recently in several Northern and Western European countries, Australia, New Zealand and in North America. We studied the global patterns and time trends in incidence of melanoma by country and sex, with a focus on and age- and cohort-specific variations. We analyzed the incidence data from 39 population-based cancer registries, examining all-ages and age-truncated standardized incidence rates of melanoma, estimating the annual percentage change and incidence rate ratios from age-period-cohort models. Incidence rates of melanoma continue to rise in most European countries (primarily Southern and Eastern Europe), whereas in Australia, New Zealand, the U.S., Canada, Israel and Norway, rates have become rather stable in recent years. Indications of a stabilization or decreasing trend were observed mainly in the youngest age group (25-44 years). Rates have been rising steadily in generations born up to the end of the 1940s, followed by a stabilization or decline in rates for more recently born cohorts in Australia, New Zealand, the U.S., Canada and Norway. In addition to the birth cohort effect, there was a suggestion of a period-related influence on melanoma trends in certain populations. Although our findings provide support that primary and secondary prevention can halt and reverse the observed increasing burden of melanoma, they also indicate that those prevention measures require further endorsement in many countries. Copyright © 2012 UICC.
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                Author and article information

                Journal
                Cochrane Database of Systematic Reviews
                Wiley
                14651858
                December 04 2018
                Affiliations
                [1 ]University of Birmingham; Institute of Applied Health Research; Birmingham UK B15 2TT
                [2 ]University Hospitals Birmingham NHS Foundation Trust and University of Birmingham; NIHR Birmingham Biomedical Research Centre; Birmingham UK
                [3 ]Churchill Hospital; Department of Dermatology; Old Road Headington Oxford UK OX3 7LE
                [4 ]Addenbrooke's Hospital; Plastic Surgery; Hills Road Cambridge UK CB2 0QQ
                [5 ]University of Pittsburgh Medical Center; Internal Medicine; Department of Medicine, Office of Education UPMC Montefiore Hospital, N715 Pittsburgh USA PA, 15213
                [6 ]The University of Nottingham; c/o Cochrane Skin Group; Nottingham UK
                [7 ]Cardiff and Vale University Health Board; CEDAR Healthcare Technology Research Centre; Cardiff Medicentre, University Hospital of Wales, Heath Park Campus Cardiff Wales UK CF144UJ
                [8 ]Imperial College Healthcare NHS trust, St Mary’s Hospital; Department of Plastic and Reconstructive Surgery; London UK W2 1NY
                [9 ]University of Cambridge; Public Health & Primary Care; Strangeways Research Laboratory, Worts Causeway Cambridge UK CB1 8RN
                [10 ]University of Nottingham; Centre of Evidence Based Dermatology; Queen's Medical Centre Derby Road Nottingham UK NG7 2UH
                Article
                10.1002/14651858.CD013192
                6517294
                30521685
                8ef3ff75-dffb-46b6-ab23-cbe8e078d4aa
                © 2018
                History

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