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Melanoma inhibitory activity in Brazilian patients with cutaneous melanoma* * Study conducted at the Federal University of Mato Grosso do Sul (UFMS) – Campo Grande (MS), Brazil.

Abstract

BACKGROUND:

Melanoma inhibitory activity is a protein secreted by melanoma cells and has been used as a tumor marker. Increased Melanoma inhibitory activity serum levels are related to metastatic disease or tumor recurrence. Currently there are no studies on Melanoma inhibitory activity and cutaneous melanoma involving Brazilian patients.

OBJECTIVE:

To evaluate the performance and feasibility of measuring Melanoma inhibitory activity levels in Brazilian patients with cutaneous melanoma.

METHODS:

Blood was obtained from ten patients with proved metastatic cutaneous melanoma (Group 1), 15 patients resected for cutaneous melanoma without metastasis (Group 2) and 5 healthy donors (Group 3). Melanoma inhibitory activity was measured using a commercially available ELISA kit.

RESULTS:

There was a statistically significant difference of Melanoma inhibitory activity levels between patients with and without metastasis (p=0.002), and between patients with metastasis and healthy donors (p=0.002). There was no difference between patients without metastasis and healthy donors (p=0.443).

CONCLUSION:

Melanoma inhibitory activity is a tumor marker for cutaneous melanoma and the Melanoma inhibitory activity-ELISA test can be easily performed. Patients with metastasis have increased Melanoma inhibitory activity serum levels when compared to patients without metastasis and healthy donors.

Keywords:
Follow-up studies; Melanoma; Tumor markers, biological

INTRODUCTION

Cutaneous melanoma (CM) is the fifth and seventh most frequent cancer found in men and women in the United States, respectively. It is estimated that 76,690 individuals in the United States will be diagnosed with CM, and the mortality rate associated with this tumor has been on the rise. 1cancer.org [Internet]. American Cancer Society. Cancer Facts & Figures 2013. Atlanta: American Cancer Society; 2013. [cited 2014 Apr 1]. Available from: http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-036845.pdf.
http://www.cancer.org/acs/groups/content...

Patients who have undergone the resection of CM should be followed up not only for the possible detection of its recurrence and metastasis, but also for the development of a new tumor, which occurs in 3% to 6% of all patients.2Ferrone CR, Ben Porat L, Panageas KS, Berwick M, Halpern AC, Patel A, et al. Clinicopathological features of and risk factors for multiple primary melanomas. JAMA : the journal of the American Medical Association. JAMA. 2005;294:1647-54. A complete clinical exam, including physical and imaging exams of the regional lymph nodes and systemic organs, is essential for patients with advanced disease. However, there is a lack of agreement about the selection criteria used for and the timing of the laboratorial exams and imaging studies when following patients with resected melanoma.3Trotter SC, Sroa N, Winkelmann RR, Olencki T, Bechtel M. A Global Review of Melanoma Follow-up Guidelines. J Clin Aesthet Dermatol. 2013;6:18-26. Depending on the institution or oncology group, different guidelines have been applied.4Fong ZV, Tanabe KK. Comparison of melanoma guidelines in the U.S.A., Canada, Europe, Australia and New Zealand: a critical appraisal and comprehensive review. Br J Dermatol. 2014;170:20-30. For example, the National Comprehensive Cancer Network (NCCN), the European Society for Medical Oncology (ESMO), the American Academy of Dermatology (AAD), the British Association of Dermatologists (BAD), and the Guideline for Management of Melanoma in Australia and New Zealand (GMMANZ) (1F) do not have specific recommendations regarding the use of laboratory tests for the follow up of CM patients. On the other hand, the Swiss Melanoma Guideline (SMG), as well as the German Cancer Society and German Dermatologic Society, recommend that S100 blood levels be obtained in patients with clinical stage III-IV and III melanoma, respectively.5Nccn.org [Internet]. National Comprehensive Cancer Network Guidelines. [cited 2014 Apr 1]. Available from: http://www.nccn.org/professionals/physician_gls/f_guidelines.asp.
http://www.nccn.org/professionals/physic...

Esmo.org [Internet]. European Society for Medical Oncology - ESMO guidelines. [cited 2014 Apr 1]. Available from: http://www.esmo.org/Guidelines-Practice/Clinical-Practice-Guidelines/Melanoma
http://www.esmo.org/Guidelines-Practice/...

Aad.org [Internet]. American Academy of Dermatology clinical guidelines. [cited 2014 Apr 1]. Available from: http://www.aad.org/File%20Library/Global%20navigation/Education%20and%20quality%20care/guideline-treatment-of-cutaneous-melanoma.pdf.
http://www.aad.org/File%20Library/Global...

Bad.org.uk [Internet]. British Association of Dermatologists. [cited 2014 Apr 1]. Available from: http://www.guideline.gov/content.aspx?id=24161.
http://www.guideline.gov/content.aspx?id...

Nhmrc.org.au [Internet]. Clinical practice guidelines for the management of melanoma in Australia and New Zealand. [cited 2014 Apr 1]. Available from: https://www.nhmrc.gov.au/_files_nhmrc/publications/attachments/cp111.pdf.
https://www.nhmrc.gov.au/_files_nhmrc/pu...

10 Dummer R, Guggenheim M, Arnold AW, Braun R, von Moos R; Project Group Melanoma of the Swiss Group for Clinical Cancer Research. Updated Swiss guidelines for the treatment and follow-up of cutaneous melanoma. Swiss Med Wkly. 2011;141:w13320.
-1111 Pflugfelder A, Kochs C, Blum A, Capellaro M, Czeschik C, Dettenborn T, et al. Malignant melanoma S3-guideline "diagnosis, therapy and follow-up of melanoma". J Dtsch Dermatol Ges. 2013;11:1-116, 1-126. Nonetheless, serum markers such as lactate dehydrogenase (LDH), S100b, and melanoma inhibitory activity (MIA) have been used to monitor therapy response and to detect early recurrent and/or metastatic disease.1212 Hofmann MA, Schicke B, Fritsch A, Biesold S, Gussmann F, Küchler I, et al. Impact of lymph node metastases on serum level of melanoma inhibitory activity in stage III melanoma patients. J Dermatol. 2011;38:880-6.

When monitoring patients, financial considerations are important, especially when imaging exams are used. These examinations can add substantial costs to the management of the patient. In fact, the treatment of metastatic/advanced melanoma is one of the most costly treatments among all types of cancer.1313 Reyes C, DaCosta Byfield S, Linke R, Satram-Hoang S, Teitelbaum AH. The burden of metastatic melanoma: treatment patterns, healthcare use (utilization), and costs. Melanoma Res. 2013;23:159-66. Therefore, more effort should be made to develop successful approaches for the early diagnosis and treatment of CM, as well as for the early detection of metastasis.

MIA is an 11 kDa protein expressed and secreted by melanoma cells, but not melanocytes, as it is related to CM development and progression.1414 Schmidt J, Bosserhoff AK. Processing of MIA protein during melanoma cell migration. Int J Cancer. 2009;125:1587-94.,1515 Bosserhoff AK. Melanoma inhibitory activity (MIA): an important molecule in melanoma development and progression. Pigment Cell Res. 2005;18:411-6. Increased MIA serum levels have been considered to be a reliable tumor marker in detecting and monitoring metastatic disease and for monitoring responses to therapy.1414 Schmidt J, Bosserhoff AK. Processing of MIA protein during melanoma cell migration. Int J Cancer. 2009;125:1587-94.,1616 Bosserhoff AK, Hauschild A, Hein R, Schadendorf D, Stockfleth E, Bogenrieder T, et al. Elevated MIA serum levels are of relevance for management of metastasized malignant melanomas: results of a German multicenter study. J Invest Dermatol. 2000;114:395-6.

17 Stahlecker J, Gauger A, Bosserhoff A, Büttner R, Ring J, Hein R. MIA as a reliable tumor marker in the serum of patients with malignant melanoma. Anticancer Res. 2000;20:5041-4.
-1818 Schmidt J, Riechers A, Stoll R, Amann T, Fink F, Spruss T et al. Targeting melanoma metastasis and immunosuppression with a new mode of melanoma inhibitory activity (MIA) protein inhibition. PLoS One. 2012;7:e37941. However, this is not accepted by all authors, and at this moment, no studies have been conducted regarding the role of MIA in CM involving Brazilian patients.1919 Henry L, Fabre C, Guiraud I, Bastide S, Fabbro-Peray P, Martinez J, et al. Clinical use of p-proteasome in discriminating metastatic melanoma patients: comparative study with LDH, MIA and S100B protein. Int J Cancer. 2013;133:142-8. The kit that is used to detect MIA levels is commercially available, and it is measured via an enzyme-linked immunosorbent assay (ELISA) system; therefore, the equipment and resources necessary to perform the test are relatively simple.1717 Stahlecker J, Gauger A, Bosserhoff A, Büttner R, Ring J, Hein R. MIA as a reliable tumor marker in the serum of patients with malignant melanoma. Anticancer Res. 2000;20:5041-4.

MIA binds to cell surface proteins that mediate cellular attachment, and it also binds to extracellular matrix proteins such as fibronectin, laminin, and tenascin. Therefore, MIA is associated with tumor cell detachment and invasion.1818 Schmidt J, Riechers A, Stoll R, Amann T, Fink F, Spruss T et al. Targeting melanoma metastasis and immunosuppression with a new mode of melanoma inhibitory activity (MIA) protein inhibition. PLoS One. 2012;7:e37941. Following the introduction of migratory stimuli, MIA binds to the cell adhesion receptors, integrin α4 β1 and integrin α5 β1, which enable tumor cells to invade the tissues and metastasize.1818 Schmidt J, Riechers A, Stoll R, Amann T, Fink F, Spruss T et al. Targeting melanoma metastasis and immunosuppression with a new mode of melanoma inhibitory activity (MIA) protein inhibition. PLoS One. 2012;7:e37941.,2020 Bosserhoff AK, Stoll R, Sleeman JP, Bataille F, Buettner R, Holak TA. Active detachment involves inhibition of cell-matrix contacts of malignant melanoma cells by secretion of melanoma inhibitory activity. Lab Invest. 2003;83:1583-94.

The aim of this study is to evaluate the performance and feasibility of measuring MIA levels among CM patients in Brazil.

METHODS

Patients

Patients were divided into one of three groups: Group 1 was composed of 15 patients without CM metastasis; Group 2 was composed of 10 patients with CM metastasis; and Group 3 was composed of 5 healthy donors (defined as individuals who were not diagnosed with cancer). All CM patients were treated primarily by surgical excision. The clinical data of the patients and healthy donors are described in tables 1 to 3. Patients from Group 1 (n=15) had clinical stage I/II CM (Table 1). Patients from Group 2 (n=10) had clinical stage III/IV CM, and 40% of them were receiving chemotherapy treatment (Table 2). No patients underwent metastatic resection or irradiation therapy. This is not a prospective study and we do not have the patient's follow-up data. Individuals without cancer (Group 3) were also assayed to determine biologically "normal" MIA plasma levels.

TABLE 1
Clinical data and MIA serum levels of patients from Group 1 (no metastasis)
TABLE 2
Clinical data and MIA serum levels of patients from Group 2 (metastasis)
TABLE 3
Clinical data and MIA serum levels of patients from Group 3 (healthy donors)

Group 1 was composed of 8 females and 7 males with a mean age of 60.8 years, standard deviation (sd) of 13.3 years and ages ranging from 28-80 years (Table 1). Group 2 (Table 2) was composed of 2 females and 8 males with a mean age of 52.7 years (sd, ±7.7 years), with ages ranging from 39-61 years. The group of healthy donors (Table 3) was composed of 3 females and 2 males with a mean age of 40.2 years (sd, ±16.9 years), with ages ranging from 24-66 years.

Specimen handling and ELISA assays

The samples were obtained with patient's informed consent and according to a protocol approved by the Ethics Committee of the Federal University of Mato Grosso do Sul, Campo Grande, MS, Brazil (protocol No. 1038). All participants were informed about the study and signed an informed consent form

Ten milliliters of blood was obtained from each patient. Blood samples were obtained and clotted at room temperature. The serum was collected following centrifugation, and samples were frozen immediately at -20ºC until analysis. A standard ELISA method was performed using a commercially available ELISA kit (Roche® MIA-ELISA; Boehringer, Mannheim, Germany) according to the manufacturer's instructions. The cost of each kit was approximately R$3000.00 (reais, local Brazilian currency, which is approximately equivalent to USD $1,300.00); each kit can be used to conduct up to 96 tests. All samples were tested in duplicate.

Statistical analysis

Statistical analysis was performed using the Kruskal-Wallis and post hoc Dunn tests to compare MIA levels of patients with and without metastatic disease, as well as healthy patients' samples. A significance level of 5% and a confidence interval (CI) of 95% were used. Data were collected and analyzed using Microsoft Excel® (Microsoft Corporation, Redmond, WA, USA) and SPSS 11.0 for Windows® (IBM Corporation, Armonk, NY, USA).

RESULTS

MIA serum levels in patients from Group 2 (with metastasis) were higher when compared to patients in Group 1 (without metastasis) and Group 3 (healthy donors). There was a significant difference in MIA serum levels between groups 1 and 2 (p=0.005), and between group 2 and control (p=0.007). However, there were no statistically significant differences between group 1 and control (p=1.000). MIA levels in the different groups are graphically represented on figure 1. Descriptive statistics is shown in table 4.

FIGURE 1
MIA serum levels presented as median and quartile ranges. There was no statistically signifi cant difference between the healthy donors group and the group without metastasis (p=1.000). However, differences between the group with metastasis and the other two groups were found to be statistically signifi cant (group without metastasis p=0.005; healthy donors group p=0.007)
TABLE 4
Descriptive statistics of serum levels of MIA (ng/ml) for each group

Mean MIA level in Group 3 was 5.6 ng/ml (sd, ±1.9 ng/ml) (Table 4). Therefore, it could be inferred that MIA "biologically normal values" vary between 1.8 ng/ml and 9.4 ng/ml (mean+- 2sd).

Four out of 10 patients from Group 2 had been receiving chemotherapy at the time when the blood was drawn. The MIA levels found in these patients (n=4; median MIA level = 10 ng/ml) were lower than the MIA levels found in patients who did not receive chemotherapy at the time of the blood draw (n=6; median MIA level = 30 ng/ml). Five out of the 6 patients who had not been receiving chemotherapy (83.3%) presented with MIA levels >30 ng/ml. The maximum MIA level observed in patients receiving chemotherapy was 17.6 ng/ml (Tables 2 and 4).

All patients from Groups 1 and 2 had skin color type I or II (based on Fitzpatrick's scale). Group 3 had two donors with skin color type II, two with skin color type III, and one with skin color type V. Interestingly, the MIA levels in healthy donors ranged from 4.0-6.4 ng/ml, except for the donor with skin type V, who presented with a MIA level of 8.6 ng/ml (Table 3).

DISCUSSION

To our knowledge, this is the first Brazilian study that has been conducted on MIA levels in CM patients.

Tumoral markers are mainly used in the early detection of recurrent disease and/or metastasis when following up with patients.2121 Matsushita Y, Hatta N, Wakamatsu K, Takehara K, Ito S, Takata M. Melanoma inhibitory activity (MIA) as a serum marker for early detection of post-surgical relapse in melanoma patients: comparison with 5-S-cysteinyldopa. Melanoma Res. 2002;12:319-23. In this study, we found statistically significant differences between MIA levels in patients with and without metastasis. However, there were no significant differences between MIA levels in patients with resected CM without metastasis and in healthy donors. Stahlecker et al. reported similar results.1717 Stahlecker J, Gauger A, Bosserhoff A, Büttner R, Ring J, Hein R. MIA as a reliable tumor marker in the serum of patients with malignant melanoma. Anticancer Res. 2000;20:5041-4. They found that 5.6% of patients with stage I/II disease had increased MIA levels when compared to 60% and 89.5% of patients with stage III and stage IV disease, respectively. Interestingly, patients with advanced disease and low MIA levels were the ones who had had their blood drawn following metastatic surgery, irradiation, or chemotherapy. In our study, we also found that patients with metastatic disease who had received chemotherapy showed the lowest MIA levels. Mühlbauer et al. also demonstrated that patients treated with chemotherapy had lower MIA levels. The authors attributed this finding to the reduction of systemic malignant cells in these patients.2222 Mühlbauer M, Langenbach N, Stolz W, Hein R, Landthaler M, Buettner R, et al. Detection of melanoma cells in the blood of melanoma patients by melanomainhibitory activity (MIA) reverse transcription-PCR. Clin Cancer Res. 1999;5:1099-105. Therefore, it is not a surprise that many authors have considered the MIA test to be a highly sensitive and specific test, which is clinically valuable for the follow-up and treatment monitoring of CM patients.2323 Bosserhoff AK, Kaufmann M, Kaluza B, Bartke I, Zirngibl H, Hein R, et al. Melanoma-inhibiting activity, a novel serum marker for progression of malignant melanoma. Cancer Res. 1997;57:3149-53. MIA can detect melanoma recurrence before there is clinical evidence of the disease, even in patients receiving chemotherapy.2121 Matsushita Y, Hatta N, Wakamatsu K, Takehara K, Ito S, Takata M. Melanoma inhibitory activity (MIA) as a serum marker for early detection of post-surgical relapse in melanoma patients: comparison with 5-S-cysteinyldopa. Melanoma Res. 2002;12:319-23.,2424 Faries MB, Gupta RK, Ye X, Hsueh EC, Morton DL. Melanoma-inhibiting activity assay predicts survival in patients receiving a therapeutic cancer vaccine after complete resection of American Joint Committee on Cancer Stage III Melanoma. Ann Surg Oncol. 2004;11:85-93. This is important because some studies demonstrated that the detection of disease recurrence at an early stage seems to be associated with a significantly better survival rate.2525 Garbe C1, Paul A, Kohler-Späth H, Ellwanger U, Stroebel W, Schwarz M,et al. Prospective evaluation of a follow-up schedule in cutaneous melanoma patients: recommendations for an effective follow-up strategy. J Clin Oncol. 2003;21:520-9. This means that the early detection of recurrent metastatic disease, and its subsequent surgical management, may be very important in the management of CM patients.

In a prospective study, Bosserhoff et al. analyzed MIA expression in 350 patients without metastatic disease.2323 Bosserhoff AK, Kaufmann M, Kaluza B, Bartke I, Zirngibl H, Hein R, et al. Melanoma-inhibiting activity, a novel serum marker for progression of malignant melanoma. Cancer Res. 1997;57:3149-53. Among 32 patients who presented with high MIA levels, 16 developed detectable metastasis or recurrence following the blood draw. However, none of the patients with low MIA levels developed metastasis or recurrence. This result demonstrates the high specificity of MIA in metastasis detection. In our study, only one patient (patient number 2) showed a high MIA level (>9 ng/ml) with no clinically detectable metastasis. Unfortunately, we cannot derive a conclusion based on this information, as we are not able to presently follow-up with the patient.

The early detection and management of recurrent malignant disease is important not only for the patient, but also for health care management. Treatment costs (TCs) associated with advanced CM are much higher when compared to the TC of an early-stage disease.2626 Alexandrescu DT. Melanoma costs: a dynamic model comparing estimated overall costs of various clinical stages. Dermatol Online J. 2009;15:1. A Brazilian study assessed the TC of CM in the state of São Paulo, Brazil.2727 Souza RJ, Mattedi AP, Rezende ML, Corrêa Mde P, Duarte EM. An estimate of the cost of treating melanoma disease in the state of Sao Paulo - Brazil. An Bras Dermatol. 2009;84:237-43. It was demonstrated that the initial stages of the disease (stages 0, I, and II) consumed 4.2% of the total budget resources, while advanced stages (stages III and IV) accounted for 95.8% of the total budget costs.

Borssehoff et al. demonstrated that MIA is strongly expressed and secreted by melanoma cells and, at lower levels, by some melanocytic nevi.2828 Bosserhoff AK, Moser M, Hein R, Landthaler M, Buettner R. In situ expression patterns of melanoma-inhibiting activity (MIA) in melanomas and breast cancers. J Pathol. 1999;187:446-54. However, it is not secreted by normal melanocytes of the skin. 1515 Bosserhoff AK. Melanoma inhibitory activity (MIA): an important molecule in melanoma development and progression. Pigment Cell Res. 2005;18:411-6. In this study, one of the healthy donors had skin type V (according to Fitzpatrick's scale) and presented with higher MIA levels (8.6 ng/ml) when compared to the other healthy donors with skin types II and III (MIA levels ranged from 4.0-6.4 ng/ml). To our knowledge, differences in MIA levels according to patients' skin type have not yet been discussed in the literature. Nevertheless, the presence of CM in patients other than Caucasians is uncommon.2929 Kabigting FD1, Nelson FP, Kauffman CL , Popoveniuc G, Dasanu CA, Alexandrescu DT. Malignant melanoma in African-Americans. Dermatol Online J. 2009;15:3.

Other available tumoral markers for CM include S100 and LDH. Most studies on these markers have demonstrated that MIA has better sensitivity and prognostic potential than S100.3030 Loppin M, Quillien V, Adamski H, Ollivier I, Garlantézec R, Chevrant-Breton J.Protein S100 beta and Melanoma Inhibitory Activity (MIA): a prospective study of their clinical value for the early detection of metastasis in malignant melanoma. Ann Dermatol Venereol. 2007;134:535-40.,3131 Schmitz C1, Brenner W, Henze E, Christophers E, Hauschild A. Comparative study on the clinical use of protein S-100B and MIA (melanoma inhibitory activity) in melanoma patients. Anticancer Res. 2000;20:5059-63. Moreover, most of these studies have measured S100 using immunoradiometric and immunoluminescent assays or polymerase chain reaction (PCR).3232 Tas F, Yasasever V, Duranyildiz D, Camlica H, Ustuner Z, Aydiner A, et al. Clinical value of protein S100 and melanoma-inhibitory activity (MIA) in malignant melanoma. Am J Clin Oncol. 2004;27:225-8.

33 Faries MB, Gupta RK, Ye X, Lee C, Yee R, Leopoldo Z, et al. A Comparison of 3 tumor markers (MIA, TA90IC, S100B) in stage III melanoma patients. Cancer Invest. 2007;25:285-93.
-3434 Garbe C, Leiter U, Ellwanger U, Blaheta HJ, Meier F, Rassner G, et al. Diagnostic value and prognostic significance of protein S-100beta, melanoma-inhibitory activity, and tyrosinase/MART-1 reverse transcription-polymerase chain reaction in the follow-up of high-risk melanoma patients. Cancer. 2003;97:1737-45. We know that the ELISA test is routinely used in most clinical laboratories throughout Brazil, as its application is very broad and ranges from oncology to mycology.3535 Figueiró-Filho EA Senefonte FR, Lopes AH, de Morais OO, Souza Júnior VG, Maia TL, et al. Frequency of HIV-1, rubella, syphilis, toxoplasmosis, cytomegalovirus, simple herpes virus, hepatitis B, hepatitis C, Chagas disease and HTLV I/II infection in pregnant women of State of Mato Grosso do Sul. Rev Soc Bras Med Trop. 2007;40:181-7.,3636 Oliveira AL, Paniago AM, Sanches MA, Dorval ME, Oshiro ET, Leal CR, et al. Asymptomatic infection in family contacts of patients with human visceral leishmaniasis in Tres Lagoas, Mato Grosso do Sul State, Brazil. Cad Saude Publica. 2008;24:2827-33. However, PCR and the other aforementioned assays are more specialized and may not be present in all laboratories, while ELISA is.

Cost is a very important issue when introducing a new marker or exam, especially in developing countries where resources are limited. One of the objectives of this study was to evaluate the feasibility of performing MIA-ELISA in Brazil. The cost of each MIA-ELISA kit is approximately R$3000.00 (reais, local Brazilian currency, which is approximately equivalent to USD $1300.00). Each kit permits up to 96 tests to be performed at the same time. Therefore, the cost of each test is approximately R$30.00, plus the costs associated with the use of disposable materials such as syringes, needles and tubes. The kit is commercially sold by Roche® and was easily purchased by our team. The kit can be easily stored at 5ºC to 10ºC for up to 18 months, and the serum to be analyzed can be stored at -20ºC for up to 1 month, according to the manufacturer's instructions. These features enable small laboratories to perform the test, as these laboratories would have fewer patients and samples to test. Compared to the prostate-specific antigen (PSA) exam that is currently used for the screening and monitoring of patients with prostate cancer, we can regard the MIA test as feasible for use among Brazilian CM patients.3737 Toledano A, Chiche R, Lamallem H, Kanoui A, Beley S, Thibault F,et al. Elevation of PSA after prostate radiotherapy: rebound or biochemical recurrence? Prog Urol. 2008;18:557-61.

CONCLUSION

In conclusion, patients with clinically proven metastasis presented with MIA serum levels that were significantly higher when compared to those obtained among patients without metastasis and healthy donors. There were no significant differences between patients without metastasis and healthy donors in terms of MIA serum levels. Overall, this test is easy to perform and cost- effective.

  • Financial Support: FUNDECT
  • How to cite this article: Odashiro M, Hans-Filho G, Pereira PR, Motta-Castro ARC, Stief AC, Pontes ERJC, Odashiro AN. Melanoma inhibitory activity in Brazilian patients with cutaneous melanoma. An Bras Dermatol. 2015;90(3):327-32.
  • *
    Study conducted at the Federal University of Mato Grosso do Sul (UFMS) – Campo Grande (MS), Brazil.

ACKNOWLEDGEMENTS

We acknowledge FUNDECT (Fundação do Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado do Mato Grosso do Sul) for providing the funds to purchase the MIA-ELISA kit.

Reference

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  • 2
    Ferrone CR, Ben Porat L, Panageas KS, Berwick M, Halpern AC, Patel A, et al. Clinicopathological features of and risk factors for multiple primary melanomas. JAMA : the journal of the American Medical Association. JAMA. 2005;294:1647-54.
  • 3
    Trotter SC, Sroa N, Winkelmann RR, Olencki T, Bechtel M. A Global Review of Melanoma Follow-up Guidelines. J Clin Aesthet Dermatol. 2013;6:18-26.
  • 4
    Fong ZV, Tanabe KK. Comparison of melanoma guidelines in the U.S.A., Canada, Europe, Australia and New Zealand: a critical appraisal and comprehensive review. Br J Dermatol. 2014;170:20-30.
  • 5
    Nccn.org [Internet]. National Comprehensive Cancer Network Guidelines. [cited 2014 Apr 1]. Available from: http://www.nccn.org/professionals/physician_gls/f_guidelines.asp.
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  • 6
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  • 9
    Nhmrc.org.au [Internet]. Clinical practice guidelines for the management of melanoma in Australia and New Zealand. [cited 2014 Apr 1]. Available from: https://www.nhmrc.gov.au/_files_nhmrc/publications/attachments/cp111.pdf.
    » https://www.nhmrc.gov.au/_files_nhmrc/publications/attachments/cp111.pdf
  • 10
    Dummer R, Guggenheim M, Arnold AW, Braun R, von Moos R; Project Group Melanoma of the Swiss Group for Clinical Cancer Research. Updated Swiss guidelines for the treatment and follow-up of cutaneous melanoma. Swiss Med Wkly. 2011;141:w13320.
  • 11
    Pflugfelder A, Kochs C, Blum A, Capellaro M, Czeschik C, Dettenborn T, et al. Malignant melanoma S3-guideline "diagnosis, therapy and follow-up of melanoma". J Dtsch Dermatol Ges. 2013;11:1-116, 1-126.
  • 12
    Hofmann MA, Schicke B, Fritsch A, Biesold S, Gussmann F, Küchler I, et al. Impact of lymph node metastases on serum level of melanoma inhibitory activity in stage III melanoma patients. J Dermatol. 2011;38:880-6.
  • 13
    Reyes C, DaCosta Byfield S, Linke R, Satram-Hoang S, Teitelbaum AH. The burden of metastatic melanoma: treatment patterns, healthcare use (utilization), and costs. Melanoma Res. 2013;23:159-66.
  • 14
    Schmidt J, Bosserhoff AK. Processing of MIA protein during melanoma cell migration. Int J Cancer. 2009;125:1587-94.
  • 15
    Bosserhoff AK. Melanoma inhibitory activity (MIA): an important molecule in melanoma development and progression. Pigment Cell Res. 2005;18:411-6.
  • 16
    Bosserhoff AK, Hauschild A, Hein R, Schadendorf D, Stockfleth E, Bogenrieder T, et al. Elevated MIA serum levels are of relevance for management of metastasized malignant melanomas: results of a German multicenter study. J Invest Dermatol. 2000;114:395-6.
  • 17
    Stahlecker J, Gauger A, Bosserhoff A, Büttner R, Ring J, Hein R. MIA as a reliable tumor marker in the serum of patients with malignant melanoma. Anticancer Res. 2000;20:5041-4.
  • 18
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Publication Dates

  • Publication in this collection
    June 2015

History

  • Received
    05 Nov 2013
  • Accepted
    31 July 2014
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