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      Visual inspection for diagnosing cutaneous melanoma in adults

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          Abstract

          Melanoma has one of the fastest rising incidence rates of any cancer. It accounts for a small percentage of skin cancer cases but is responsible for the majority of skin cancer deaths. History‐taking and visual inspection of a suspicious lesion by a clinician is usually the first in a series of ‘tests’ to diagnose skin cancer. Establishing the accuracy of visual inspection alone is critical to understating the potential contribution of additional tests to assist in the diagnosis of melanoma. To determine the diagnostic accuracy of visual inspection for the detection of cutaneous invasive melanoma and atypical intraepidermal melanocytic variants in adults with limited prior testing and in those referred for further evaluation of a suspicious lesion. Studies were separated according to whether the diagnosis was recorded face‐to‐face (in‐person) or based on remote (image‐based) assessment. We undertook a comprehensive search of the following databases from inception up to August 2016: CENTRAL; 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. Test accuracy studies of any design that evaluated visual inspection in adults with lesions suspicious for melanoma, compared with a reference standard of either histological confirmation or clinical follow‐up. We excluded studies reporting data for ‘clinical diagnosis’ where dermoscopy may or may not have been used. Two review authors independently extracted all data using a standardised data extraction and quality assessment form (based on QUADAS‐2). We contacted authors of included studies where information related to the target condition or diagnostic threshold were missing. We estimated summary sensitivities and specificities per algorithm and threshold using the bivariate hierarchical model. We investigated the impact of: in‐person test interpretation; use of a purposely developed algorithm to assist diagnosis; and observer expertise. We included 49 publications reporting on a total of 51 study cohorts with 34,351 lesions (including 2499 cases), providing 134 datasets for visual inspection. Across almost all study quality domains, the majority of study reports provided insufficient information to allow us to judge the risk of bias, while in three of four domains that we assessed we scored concerns regarding applicability of study findings as 'high'. Selective participant recruitment, lack of detail regarding the threshold for deciding on a positive test result, and lack of detail on observer expertise were particularly problematic. Attempts to analyse studies by degree of prior testing were hampered by a lack of relevant information and by the restricted inclusion of lesions selected for biopsy or excision. Accuracy was generally much higher for in‐person diagnosis compared to image‐based evaluations (relative diagnostic odds ratio of 8.54, 95% CI 2.89 to 25.3, P < 0.001). Meta‐analysis of in‐person evaluations that could be clearly placed on the clinical pathway showed a general trade‐off between sensitivity and specificity, with the highest sensitivity (92.4%, 95% CI 26.2% to 99.8%) and lowest specificity (79.7%, 95% CI 73.7% to 84.7%) observed in participants with limited prior testing (n = 3 datasets). Summary sensitivities were lower for those referred for specialist assessment but with much higher specificities (e.g. sensitivity 76.7%, 95% CI 61.7% to 87.1%) and specificity 95.7%, 95% CI 89.7% to 98.3%) for lesions selected for excision, n = 8 datasets) . These differences may be related to differences in the spectrum of included lesions, differences in the definition of a positive test result, or to variations in observer expertise. We did not find clear evidence that accuracy is improved by the use of any algorithm to assist diagnosis in all settings. Attempts to examine the effect of observer expertise in melanoma diagnosis were hindered due to poor reporting. Visual inspection is a fundamental component of the assessment of a suspicious skin lesion; however, the evidence suggests that melanomas will be missed if visual inspection is used on its own. The evidence to support its accuracy in the range of settings in which it is used is flawed and very poorly reported. Although published algorithms do not appear to improve accuracy, there is insufficient evidence to suggest that the ‘no algorithm’ approach should be preferred in all settings. Despite the volume of research evaluating visual inspection, further prospective evaluation of the potential added value of using established algorithms according to the prior testing or diagnostic difficulty of lesions may be warranted. What is the aim of the review? Melanoma is one of the most dangerous forms of skin cancer. The aim of this Cochrane Review was to find out how accurate checking suspicious skin lesions (lumps, bumps, wounds, scratches or grazes) with the naked eye (visual inspection) can be to diagnose melanoma (diagnostic accuracy). The Review also investigated whether diagnostic accuracy was different depending on whether the clinician was face to face with the patient (in‐person visual inspection), or looked at an image of the lesion (image‐based visual inspection). Cochrane researchers included 19 studies to answer this question. Why is it important to know the diagnostic accuracy of visual examination of skin lesions suspected to be melanomas? Not recognising a melanoma when it is present (a false‐negative test result) delays surgery to remove it (excision), risking cancer spreading to other organs in the body and possibly death. Diagnosing a skin lesion (a mole or area of skin with an unusual appearance in comparison with the surrounding skin) as a melanoma when it is not (a false‐positive result) may result in unnecessary surgery, further investigations, and patient anxiety. Visual inspection of suspicious skin lesions by a clinician using the naked eye is usually the first of a series of ‘tests’ to diagnose melanoma. Knowing the diagnostic accuracy of visual inspection alone is important to decide whether additional tests, such as a biopsy (removing a part of the lesion for examination under a microscope) are needed to improve accuracy to an acceptable level. What did the review study? Researchers wanted to find out the diagnostic accuracy of in‐person compared with image‐based visual inspection of suspicious skin lesions. Researchers also wanted to find out whether diagnostic accuracy was improved if doctors used a 'visual inspection checklist' or depending on how experienced in visual inspection they were (level of clinical expertise). They considered the diagnostic accuracy of the first visual inspection of a lesion, for example, by a general practitioner (GP), and of lesions that had been referred for further evaluation, for example, by a dermatologist (doctor specialising in skin problems). What are the main results of the review? Only 19 studies (17 in‐person studies and 2 image‐based studies) were clear whether the test was the first visual inspection of a lesion or was a visual inspection following referral (for example, when patients are referred by a GP to skin specialists for visual inspection). First in‐person visual inspection (3 studies) The results of three studies of 1339 suspicious skin lesions suggest that in a group of 1000 lesions, of which 90 (9%) actually are melanoma: ‐ An estimated 268 will have a visual inspection result indicating melanoma is present. Of these, 185 will not be melanoma and will result in an unnecessary biopsy (false‐positive results). ‐ An estimated 732 will have a visual inspection result indicating that melanoma is not present. Of these, seven will actually have melanoma and would not be sent for biopsy (false‐negative results). Two further studies restricted to 4228 suspicious skin lesions that were all selected to be excised found similar results. In‐person visual inspection after referral, all lesions selected to be excised (8 studies) The results of eight studies of 5331 suspicious skin lesions suggest that in a group of 1000 lesions, of which 90 (9%) actually are melanoma: ‐ An estimated 108 will have a visual inspection result indicating melanoma is present, and of these, 39 will not be melanoma and will result in an unnecessary biopsy (false‐positive results). ‐ Of the 892 lesions with a visual inspection result indicating that melanoma is not present, 21 will actually be melanoma and would not be sent for biopsy (false‐negative results). Overall, the number of false‐positive results (diagnosing a skin lesion as a melanoma when it is not) was observed to be higher and the number of false‐negative results (not recognising a melanoma when it is present) lower for first visual inspections of suspicious skin lesions compared to visual inspection following referral. Visual inspection of images of suspicious skin lesions (2 studies) Accuracy was much lower for visual inspection of images of lesions compared to visual inspection in person. Value of visual inspection checklists There was no evidence that use of a visual inspection checklist or the level of clinical expertise changed diagnostic accuracy. How reliable are the results of the studies of this review? The majority of included studies diagnosed melanoma by lesion biopsy and confirmed that melanoma was not present by biopsy or by follow‐up over time to make sure the skin lesion remained negative for melanoma. In these studies, biopsy, clinical follow‐up, or specialist clinician diagnosis were the reference standards (means of establishing final diagnoses). Biopsy or follow‐up are likely to have been reliable methods for deciding whether patients really had melanoma. In a few studies, experts diagnosed the absence of melanoma (expert diagnosis), which is less likely to have been a reliable method for deciding whether patients really had melanoma. There was lots of variation in the results of the studies in this review and the studies did not always describe fully the methods they used, which made it difficult to assess their reliability. Who do the results of this review apply to? Thirteen studies were undertaken in Europe (68%), with the remainder undertaken in Asia (n = 1), Oceania (n = 4), and North America (n = 1). Mean age ranged from 30 to 73.6 years (reported in 10 studies). The percentage of individuals with melanoma ranged between 4% and 20% in first visualised lesions and between 1% and 50% in studies of referred lesions. In the majority of studies, the lesions were unlikely to be representative of the range of those seen in practice, for example, only including skin lesions of a certain size or with a specific appearance. In addition, variation in the expertise of clinicians performing visual inspection and in the definition used to decide whether or not melanoma was present across studies makes it unclear as to how visual inspection should be carried out and by whom in order to achieve the accuracy observed in studies. What are the implications of this review? Error rates from visual inspection are too high for it to be relied upon alone. Although not evaluated in this review, other technologies need to be used to ensure accurate diagnosis of skin cancer. There is considerable variation and uncertainty about the diagnostic accuracy of visual inspection alone for the diagnosis of melanoma. There is no evidence to suggest that visual inspection checklists reliably improve the diagnostic accuracy of visual inspection, so recommendations cannot be made about when they should be used. Despite the existence of numerous research studies, further, well‐reported studies assessing the diagnostic accuracy of visual inspection with and without visual inspection checklists and by clinicians with different levels of expertise are needed. How up‐to‐date is this review? The review authors searched for and used studies published up to August 2016.

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          Most cited references242

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          Final version of 2009 AJCC melanoma staging and classification.

          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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            Dermoscopy of pigmented skin lesions: results of a consensus meeting via the Internet.

            There is a need for better standardization of the dermoscopic terminology in assessing pigmented skin lesions. The virtual Consensus Net Meeting on Dermoscopy was organized to investigate reproducibility and validity of the various features and diagnostic algorithms. Dermoscopic images of 108 lesions were evaluated via the Internet by 40 experienced dermoscopists using a 2-step diagnostic procedure. The first-step algorithm distinguished melanocytic versus nonmelanocytic lesions. The second step in the diagnostic procedure used 4 algorithms (pattern analysis, ABCD rule, Menzies method, and 7-point checklist) to distinguish melanoma versus benign melanocytic lesions. kappa Values, log odds ratios, sensitivity, specificity, and positive likelihood ratios were estimated for all diagnostic algorithms and dermoscopic features. Interobserver agreement was fair to good for all diagnostic methods, but it was poor for the majority of dermoscopic criteria. Intraobserver agreement was good to excellent for all algorithms and features considered. Pattern analysis allowed the best diagnostic performance (positive likelihood ratio: 5.1), whereas alternative algorithms revealed comparable sensitivity but less specificity. Interobserver agreement on management decisions made by dermoscopy was fairly good (mean kappa value: 0.53). The virtual Consensus Net Meeting on Dermoscopy represents a valid tool for better standardization of the dermoscopic terminology and, moreover, opens up a new territory for diagnosing and managing pigmented skin lesions.
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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 ]School of Medicine; Division of Epidemiology and Public Health; University of Nottingham Nottingham UK NG7 2UH
                [4 ]Churchill Hospital; Department of Dermatology; Old Road Headington Oxford UK OX3 7LE
                [5 ]St George's Hospital; Department of Plastic Surgery; London UK
                [6 ]Oxford University Hospitals NHS Foundation Trust; Department of Plastic and Reconstructive Surgery; Oxford UK
                [7 ]NHS Lothian/University of Edinburgh; Department of Plastic Surgery; 25/6 India Street Edinburgh UK EH3 6HE
                [8 ]University Hospital of Wales; Welsh Institute of Dermatology; Heath Park Cardiff UK CF14 4XW
                [9 ]Norfolk and Norwich University Hospital NHS Trust; Department of Plastic and Reconstructive Surgery; Colney Lane Norwich UK NR4 7UY
                [10 ]The University of Nottingham; c/o Cochrane Skin Group; Nottingham UK
                [11 ]University of Cambridge; Public Health & Primary Care; Strangeways Research Laboratory, Worts Causeway Cambridge UK CB1 8RN
                [12 ]University of Nottingham; Centre of Evidence Based Dermatology; Queen's Medical Centre Derby Road Nottingham UK NG7 2UH
                Article
                10.1002/14651858.CD013194
                6492463
                30521684
                6ce85f59-8905-4bff-9e8e-59dffd410d6b
                © 2018
                History

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