Journal Information
Vol. 95. Issue 1.
Pages 106-108 (1 January 2020)
Visits
5468
Vol. 95. Issue 1.
Pages 106-108 (1 January 2020)
Research Letter
Open Access
Imaging tests in cutaneous malignant melanoma staging: a retrospective cohort
Visits
5468
Luiza Boava Souzaa, Gabriel Peresb, Juliano Vilaverde Schmittb,
Corresponding author
julivs@gmail.com

Corresponding author.
a Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu, SP, Brazil
b Department of Dermatology and Radiotherapy, Hospital das Clínicas, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu, SP, Brazil
This item has received

Under a Creative Commons license
Article information
Full Text
Bibliography
Download PDF
Statistics
Figures (1)
Tables (2)
Table 1. Features of patients included in the study (n=93).
Table 2. Patients comparison according to the performance of chest X-rays.
Show moreShow less
Full Text
Dear Editor,

There is no consensus regarding the staging process of melanoma, with a diversity of protocols across the world and between different institutions in the same country.1

Considering the continuous increase in the incidence of melanoma and the financial demands of health systems, it is required that the management of these patients promotes good clinical results and cost–benefit ratio.2,3

The present study evaluated the frequency of imaging tests in the staging of cutaneous melanoma patients, the rates of true and false positivity, the impact of the examination on the prognosis of the patient, and the associated demographic and clinical characteristics.

This was a retrospective cohort study analyzing medical records of cases of cutaneous melanoma treated and followed at the institution between 1999 and 2016, excluding tumors in situ.

Medical records in which the anatomopathological examination did not allow adequate staging of the initial tumor were excluded. Staging exams were those performed within three months of the initial diagnosis.

The results of chest radiographs (CR) and axial computed tomography (CT) of the head, neck, chest, abdomen, and pelvis were evaluated according to the radiological reports. Positivity was true when histological evidence of the neoplasm was obtained, or when the patient's evolution showed clinically evident recurrence.

Continuous variables were analyzed by Student's t-test and the Mann–Whitney test, depending on the normality of the distributions as assessed by the Shapiro–Wilk test. Categorical variables were compared using the chi-squared test.

The impact of radiological examination on survival from the initial diagnosis was assessed by Cox regression. Two-tailed values of p<0.05 were considered significant.

We identified 93 cases included in the study, of which 57 had initial imaging tests. Table 1 shows the baseline characteristics of the patients and the imaging tests.

Table 1.

Features of patients included in the study (n=93).

Baseline features  n (%) 
Sex
Female  44 (47.3) 
Male  49 (52.7) 
Age at diagnosis (years)  62 (49–75)a 
Follow-up time (months)  55 (22–88)a 
Death in the follow-up  30 (32.3) 
Death by melanoma  16 (17.2) 
Clinical type
Superficial spreading  44 (47.3) 
Nodular  15 (16.1) 
Acral lentiginous  16 (17.2) 
Lentigo maligna  18 (19.4) 
Location
Head and neck  26 (28) 
Trunk  31 (33.3) 
Members  36 (38.7) 
Presence of ulceration  27 (29) 
Breslow thickness (mm)  1.3 (0.6–4)a 
Imaging tests for staging
Altered exams/exams performed  13/57 (22.8) 
False positives findings/exams performed  9/57 (15.8) 
True positive findings on chest X-rays  0/51 (0) 
False positive findings on chest X-rays  3/51 (5.9) 
True positive findings on CTs  3/11 (27.3) 
Preclinical  2/11 (18.2) 
False positive findings on CTs  6/11 (54.5) 
a

Median (p25–p75).

CT, computed tomography.

We had a balanced sample between the sexes, with lesions treated between the sixth and eighth decade of life, followed-up for a median period of 4.6 years, and initial tumors of intermediate thickness, with 32% fatality during follow-up.

There were frequent incidental findings on initial imaging exams, with no truly positive findings at baseline CR. However, the imaging tests were performed selectively, with a greater regularity for the CRs.

Regarding the initial staging exams, only four of 57 patients presented findings indicating systemic metastasis of melanoma (through CT). All lesions were ulcerated, with a median Breslow thickness of 9.8 (1.5–15)mm, one quarter of which had clinical regional lymph node involvement, one quarter had bone invasion by the primary tumor, and one quarter had microsatellitosis.

Patients who did or did not perform initial CR did not differ in demographic and tumor staging characteristics (Table 2). In addition, general and specific mortality adjusted for age, sex, Breslow thickness, and ulceration were not different between these groups (p=0.63 and p=0.81 – Cox regression).

Table 2.

Patients comparison according to the performance of chest X-rays.

Variable  Performed (n=51)  Unperformed (n=42)  p 
Sex      0.72 
Female  25 (49%)  19 (45.2%)   
Male  26 (51%)  23 (54.8%)   
Age at diagnosisa  57.4 (17.9)  63.4 (15.6)  0.09 
Breslow thickness (mm)b  1.4 (0.6–4)  1 (0.5–3.5)  0.46 
Ulceration present  14 (27.5%)  13 (31%)  0.71 
a

Mean (standard deviation).

b

Median (p25–p75).

Of the patients with negative baseline tests, 24.5% (13/53) evolved to metastatic disease identified at follow-up imaging tests, reaching 61.5% (8/13) after clinical manifestation of relapse. Five of the 13 cases of recurrence (38.5%) presented metastatic disease in the follow-up CRs.

Of the five patients who had findings of asymptomatic metastasis on imaging examinations, three had previously progressed to stage III. The median follow-up time for pre-clinical identification of distant metastatic disease at imaging examinations was 24 (9–29) months.

Fig. 1 shows the patients’ overall survival curves from the initial diagnosis, according to the performance and alterations of the follow-up imaging tests, adjusted for age, sex, Breslow thickness, and ulceration, where more aggressive behavior of tumors with clinically identified metastatic disease is observed (p<0.01 – Cox regression).

Figure 1.

Global survival according to the performance and changes of the imaging exams during follow-up. *Including chest X-rays and axial tomography. The exams were performed selectively.

(0.07MB).

The results of the present study suggest that imaging tests to stage asymptomatic patients are not very productive and should be considered only for locally advanced cases with thick and ulcerated tumors. The studies by Gjørup et al., in 2016, and Ferrándiz et al., also in 2016, together identified only three positive cases between CR and CT in the staging of 913 asymptomatic patients up to stage IIC.4,5

At follow-up, the frequency of positive findings in asymptomatic patients increased, but was often preceded by regional spread of the tumor. In any case, clinically manifest distant metastasis indicated a disease of aggressive behavior.

Despite the limitations inherent in retrospective studies, the results disfavored CR in the staging of asymptomatic patients, except for locally very advanced cases. During the follow-up, the positivity increases, but the tumors are usually preceded by locoregional recurrence and distant metastatic disease symptoms, within the three first years of follow-up.

Financial support

None declared.

Author's contribution

Luiza Boava Souza: Approval of the final version of the manuscript; conception and planning of the study; elaboration and writing of the manuscript; obtaining, analyzing and interpreting the data; critical review of the literature; critical review of the manuscript.

Gabriel Peres: Approval of the final version of the manuscript; elaboration and writing of the manuscript; critical review of the manuscript.

Juliano Vilaverde Schmitt: Statistical analysis; approval of the final version of the manuscript; conception and planning of the study; elaboration and writing of the manuscript; obtaining, analyzing and interpreting the data; effective participation in research orientation; critical review of the literature; critical review of the manuscript.

Conflicts of interest

None declared.

References
[1]
S.C. Trotter, N. Sroa, R.R. Winkelmann, T. Olencki, M. Bechtel.
A global review of melanoma follow-up guidelines.
J Clin Aesthet Dermatol, 6 (2013), pp. 18-26
[2]
N. Naser.
Cutaneous melanoma: a 30-year-long epidemiological study conducted in a city in southern Brazil, from 1980–2009.
An Bras Dermatol, 86 (2011), pp. 932-941
[3]
B. Hollingsworth.
Cost, production, efficiency, or effectiveness: where should we focus?.
Lancet Glob Health, 1 (2013), pp. e249-e250
[4]
C.A. Gjørup, H.W. Hendel, R.K. Pilegaard, C.B. Willert, L.R. Hölmich.
Routine X-ray of the chest is not justified in staging of cutaneous melanoma patients.
Dan Med J, (2016), pp. 63
[5]
L. Ferrándiz, M. Silla-Prósper, A. García-de-la-Oliva, F.M. Mendonça, T. Ojeda-Vila, D. Moreno-Ramírez.
Yield of computed tomography at baseline staging of melanoma.
Actas Dermosifiliogr, 107 (2016), pp. 55-61

How to cite this article: Souza LB, Peres G, Schmitt JV. Imaging tests in cutaneous malignant melanoma staging: a retrospective cohort. An Bras Dermatol. 2019;95:106–8.

Study conducted at the Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu, SP, Brazil.

Copyright © 2020. Sociedade Brasileira de Dermatologia
Download PDF
Idiomas
Anais Brasileiros de Dermatologia
Article options
Tools
en pt
Cookies policy Política de cookies
To improve our services and products, we use "cookies" (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here. Utilizamos cookies próprios e de terceiros para melhorar nossos serviços e mostrar publicidade relacionada às suas preferências, analisando seus hábitos de navegação. Se continuar a navegar, consideramos que aceita o seu uso. Você pode alterar a configuração ou obter mais informações aqui.