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Published in: Annals of Surgical Oncology 6/2012

01-06-2012 | Melanomas

Clinical and Pathologic Factors Associated with Distant Metastasis and Survival in Patients with Thin Primary Cutaneous Melanoma

Authors: Rajmohan Murali, MBBS, MD, FRCPA, Lauren E. Haydu, BSCHE, MIPH, Georgina V. Long, MBBS, PhD, FRACP, Michael J. Quinn, MBBS, FRACS, Robyn P. M. Saw, MBBS, FRACS, Kerwin Shannon, MBBS, FRACS, Andrew J. Spillane, MD, FRACS, Jonathan R. Stretch, MBBS, DPhil, FRACS, Richard F. Kefford, MBBS, FRACP, John F. Thompson, MBBS, MD, FRACS, FACS, Richard A. Scolyer, MBBS, MD, FRCPA, FRCPath

Published in: Annals of Surgical Oncology | Issue 6/2012

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Abstract

Background

Approximately 3–5% of patients with thin (≤1 mm) cutaneous melanomas develop distant metastases. We sought to identify clinical and pathologic factors associated with distant metastasis and survival in a large number of patients with thin melanoma treated at a single institution.

Methods

We identified patients with a single invasive melanoma ≤1 mm in thickness diagnosed between January 1983 and December 2003 who developed distant metastasis (cases), and matched patients with no recorded recurrence during follow-up (control subjects). Cases and control subjects were matched for age, sex, and year of primary melanoma diagnosis. Associations of clinical and pathologic parameters with distant metastasis-free survival and melanoma-specific survival were analyzed.

Results

A total of 178 cases and 178 control subjects were identified. Factors associated with development of distant metastasis were: increasing Breslow thickness (P < 0.001), increasing Clark level of invasion (P < 0.001), increasing mitotic rate (P = 0.001), ulceration (P = 0.025), and American Joint Committee on Cancer T subcategory (P < 0.001). Multivariable models including Breslow thickness (but not Clark level) showed that factors independently associated with poorer distant metastasis-free survival were increasing age [hazard ratio (HR) 1.01, 95% confidence interval (CI) 1.00–1.02]; increasing Breslow thickness (HR 3.21, 95% CI 1.73–5.94, and HR 3.77, 95% CI 2.11–6.74 for 0.51–0.75 mm and 0.76–1.00 mm, respectively, compared with 0.01–0.50 mm); ulceration (HR 1.87, 95% CI 1.14–3.06) and mitotic rate (HR 1.13, 95% CI 1.05–1.21). Similar associations with melanoma-specific survival were found.

Conclusions

Clinical and pathologic predictors of distant metastasis and survival identified in this large study of patients with thin primary cutaneous melanomas will enable more accurate stratification of risk of distant metastasis and poor survival in such patients, and will assist in formulating clinical management and follow-up regimens based on the level of risk.
Literature
1.
go back to reference Reintgen C, Shivers S, Reintgen M, et al. The changing face of malignant melanoma. J Surg Oncol. 2010;101:443–6.PubMedCrossRef Reintgen C, Shivers S, Reintgen M, et al. The changing face of malignant melanoma. J Surg Oncol. 2010;101:443–6.PubMedCrossRef
2.
go back to reference McKinnon JG, Yu XQ, McCarthy WH, et al. Prognosis for patients with thin cutaneous melanoma: long-term survival data from New South Wales Central Cancer Registry and the Sydney Melanoma Unit. Cancer. 2003;98:1223–31.PubMedCrossRef McKinnon JG, Yu XQ, McCarthy WH, et al. Prognosis for patients with thin cutaneous melanoma: long-term survival data from New South Wales Central Cancer Registry and the Sydney Melanoma Unit. Cancer. 2003;98:1223–31.PubMedCrossRef
3.
go back to reference Gimotty PA, Guerry D, Ming ME, et al. Thin primary cutaneous malignant melanoma: a prognostic tree for 10-year metastasis is more accurate than American Joint Committee on Cancer staging. J Clin Oncol. 2004;22:3668–76.PubMedCrossRef Gimotty PA, Guerry D, Ming ME, et al. Thin primary cutaneous malignant melanoma: a prognostic tree for 10-year metastasis is more accurate than American Joint Committee on Cancer staging. J Clin Oncol. 2004;22:3668–76.PubMedCrossRef
4.
go back to reference Kalady MF, White RR, Johnson JL, et al. Thin melanomas: predictive lethal characteristics from a 30-year clinical experience. Ann Surg. 2003;238:528–35.PubMed Kalady MF, White RR, Johnson JL, et al. Thin melanomas: predictive lethal characteristics from a 30-year clinical experience. Ann Surg. 2003;238:528–35.PubMed
5.
go back to reference Mansson-Brahme E, Carstensen J, Erhardt K, et al. Prognostic factors in thin cutaneous malignant melanoma. Cancer. 1994;73:2324–32.PubMedCrossRef Mansson-Brahme E, Carstensen J, Erhardt K, et al. Prognostic factors in thin cutaneous malignant melanoma. Cancer. 1994;73:2324–32.PubMedCrossRef
6.
go back to reference Leiter U, Buettner PG, Eigentler TK, et al. Prognostic factors of thin cutaneous melanoma: an analysis of the central malignant melanoma registry of the German Dermatological Society. J Clin Oncol. 2004;22:3660–7.PubMedCrossRef Leiter U, Buettner PG, Eigentler TK, et al. Prognostic factors of thin cutaneous melanoma: an analysis of the central malignant melanoma registry of the German Dermatological Society. J Clin Oncol. 2004;22:3660–7.PubMedCrossRef
7.
go back to reference Slingluff CL Jr, Seigler HF. “Thin” malignant melanoma: risk factors and clinical management. Ann Plast Surg. 1992;28:89–94.PubMedCrossRef Slingluff CL Jr, Seigler HF. “Thin” malignant melanoma: risk factors and clinical management. Ann Plast Surg. 1992;28:89–94.PubMedCrossRef
8.
go back to reference Slingluff CL, Jr., Vollmer RT, Reintgen DS, et al. Lethal “thin” malignant melanoma. Identifying patients at risk. Ann Surg. 1988;208:150–61.PubMedCrossRef Slingluff CL, Jr., Vollmer RT, Reintgen DS, et al. Lethal “thin” malignant melanoma. Identifying patients at risk. Ann Surg. 1988;208:150–61.PubMedCrossRef
9.
go back to reference Guitart J, Lowe L, Piepkorn M, et al. Histological characteristics of metastasizing thin melanomas: a case-control study of 43 cases. Arch Dermatol. 2002;138:603–8.PubMedCrossRef Guitart J, Lowe L, Piepkorn M, et al. Histological characteristics of metastasizing thin melanomas: a case-control study of 43 cases. Arch Dermatol. 2002;138:603–8.PubMedCrossRef
10.
go back to reference Finley JW, Gibbs JF, Rodriguez LM, et al. Pathologic and clinical features influencing outcome of thin cutaneous melanoma: correlation with newly proposed staging system. Am Surg. 2000;66:527–31.PubMed Finley JW, Gibbs JF, Rodriguez LM, et al. Pathologic and clinical features influencing outcome of thin cutaneous melanoma: correlation with newly proposed staging system. Am Surg. 2000;66:527–31.PubMed
11.
go back to reference Australian Cancer Network Melanoma Guidelines Revision Working Party. Clinical Practice Guidelines for the management of melanoma in Australia and New Zealand. Wellington: The Cancer Council Australia and Australian Cancer Network, Sydney and New Zealand Guidelines Group; 2008. Australian Cancer Network Melanoma Guidelines Revision Working Party. Clinical Practice Guidelines for the management of melanoma in Australia and New Zealand. Wellington: The Cancer Council Australia and Australian Cancer Network, Sydney and New Zealand Guidelines Group; 2008.
12.
go back to reference Balch CM, Gershenwald JE, Soong SJ, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009;27:6199–206.PubMedCrossRef Balch CM, Gershenwald JE, Soong SJ, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009;27:6199–206.PubMedCrossRef
13.
go back to reference Murali R, Hughes MT, Fitzgerald P, et al. Interobserver variation in the histopathologic reporting of key prognostic parameters, particularly Clark level, affects pathologic staging of primary cutaneous melanoma. Ann Surg. 2009;249:641–7.PubMedCrossRef Murali R, Hughes MT, Fitzgerald P, et al. Interobserver variation in the histopathologic reporting of key prognostic parameters, particularly Clark level, affects pathologic staging of primary cutaneous melanoma. Ann Surg. 2009;249:641–7.PubMedCrossRef
14.
go back to reference Scolyer RA, Shaw HM, Thompson JF, et al. Interobserver reproducibility of histopathologic prognostic variables in primary cutaneous melanomas. Am J Surg Pathol. 2003;27:1571–6.PubMedCrossRef Scolyer RA, Shaw HM, Thompson JF, et al. Interobserver reproducibility of histopathologic prognostic variables in primary cutaneous melanomas. Am J Surg Pathol. 2003;27:1571–6.PubMedCrossRef
15.
go back to reference Balch CM, Soong SJ, Gershenwald JE, et al. Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol. 2001;19:3622–34.PubMed Balch CM, Soong SJ, Gershenwald JE, et al. Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol. 2001;19:3622–34.PubMed
16.
go back to reference Azzola MF, Shaw HM, Thompson JF, et al. Tumor mitotic rate is a more powerful prognostic indicator than ulceration in patients with primary cutaneous melanoma: an analysis of 3661 patients from a single center. Cancer. 2003;97:1488–98.PubMedCrossRef Azzola MF, Shaw HM, Thompson JF, et al. Tumor mitotic rate is a more powerful prognostic indicator than ulceration in patients with primary cutaneous melanoma: an analysis of 3661 patients from a single center. Cancer. 2003;97:1488–98.PubMedCrossRef
17.
go back to reference Francken AB, Shaw HM, Thompson JF, et al. The prognostic importance of tumor mitotic rate confirmed in 1317 patients with primary cutaneous melanoma and long follow-up. Ann Surg Oncol. 2004;11:426–33.PubMedCrossRef Francken AB, Shaw HM, Thompson JF, et al. The prognostic importance of tumor mitotic rate confirmed in 1317 patients with primary cutaneous melanoma and long follow-up. Ann Surg Oncol. 2004;11:426–33.PubMedCrossRef
18.
go back to reference Corona R, Mele A, Amini M, et al. Interobserver variability on the histopathologic diagnosis of cutaneous melanoma and other pigmented skin lesions. J Clin Oncol. 1996;14:1218–23.PubMed Corona R, Mele A, Amini M, et al. Interobserver variability on the histopathologic diagnosis of cutaneous melanoma and other pigmented skin lesions. J Clin Oncol. 1996;14:1218–23.PubMed
19.
go back to reference Lock-Andersen J, Hou-Jensen K, Hansen JP, et al. Observer variation in histological classification of cutaneous malignant melanoma. Scand J Plast Reconstr Surg Hand Surg. 1995;29:141–8.PubMedCrossRef Lock-Andersen J, Hou-Jensen K, Hansen JP, et al. Observer variation in histological classification of cutaneous malignant melanoma. Scand J Plast Reconstr Surg Hand Surg. 1995;29:141–8.PubMedCrossRef
Metadata
Title
Clinical and Pathologic Factors Associated with Distant Metastasis and Survival in Patients with Thin Primary Cutaneous Melanoma
Authors
Rajmohan Murali, MBBS, MD, FRCPA
Lauren E. Haydu, BSCHE, MIPH
Georgina V. Long, MBBS, PhD, FRACP
Michael J. Quinn, MBBS, FRACS
Robyn P. M. Saw, MBBS, FRACS
Kerwin Shannon, MBBS, FRACS
Andrew J. Spillane, MD, FRACS
Jonathan R. Stretch, MBBS, DPhil, FRACS
Richard F. Kefford, MBBS, FRACP
John F. Thompson, MBBS, MD, FRACS, FACS
Richard A. Scolyer, MBBS, MD, FRCPA, FRCPath
Publication date
01-06-2012
Publisher
Springer-Verlag
Published in
Annals of Surgical Oncology / Issue 6/2012
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-012-2265-y

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