Dear Editor,In the letter entitled “Management of thin melanoma,” Drs. Pusiol and Piscioli outline an algorithm for classification of melanoma into one of three types; nontumorigenic microinvasive radial growth phase (RGP) thin melanoma, tumorigenic early vertical growth phase (VGP) thin melanoma, or uncertain potentially tumorigenic thin melanoma. Further, the authors suggest that treatment decisions regarding performance of sentinel lymph node biopsy (SLNB) be based on this classification alone, with the recommendation that SLNB be performed for any VGP thin melanoma with a potential for regional nodal metastasis.The decision to perform SLNB has historically been based on the probability of finding a positive sentinel lymph node using independent prognostic variables of tumor and patient characteristics. In our study of 510 patients with 512 melanoma lesions Breslow thickness 0.75‐0.99 mm, univariate analysis showed age ≤45, Breslow depth ≥0.85 mm, mitotic rate>1/mm2, and ulceration to be significantly associated with nodal disease (either positive SLNB or nodal recurrence in the follow up period). To our knowledge, RGP and VGP have not been shown to be independent prognostic indicators of risk of nodal metastasis and, although the risk is low, it has been shown that very early thin lesions and even those interpreted as melanoma in situ can metastasize.Given that SLNB is a surgical test with associated risks, the recommendation to perform SLNB has been and should continue to be based on the probability (percentage) and not the possibility (yes/no) of regional lymph node disease. As such, we feel strongly that the decision to perform SLNB should be based upon a reasonable evaluation of the likelihood of potential benefit appropriately weighed against the surgical risk.CONFLICTS OF INTERESTNone.Sincerely,Alison B. Durham, MD1Jennifer L. Schwartz, MD1Lori Lowe, MD1,2Lili Zhao, PhD3Andrew G. Johnson, BA4Kelly L. Harms MD, PhD1Christopher K. Bichakjian, MD1Amy P. Orsini, MD1Scott A. McLean, MD, PhD5Carol R. Bradford, MD5Mark S. Cohen, MD6Timothy M. Johnson, MD1,5,6Michael S. Sabel, MD6Sandra L. Wong MD, MS71Department of Dermatology, University of Michigan Hospital, Ann Arbor, Michigan2Department of Pathology, University of Michigan Health System, Ann Arbor, Michigan3Department of Biostatistics, University of Michigan Health System, Ann Arbor, Michigan4University of Michigan Medical School, Ann Arbor, Michigan5Department of Otolaryngology, University of Michigan Health System, Ann Arbor, Michigan6Surgery University of Michigan Medical School and Comprehensive Cancer Center, Ann Arbor, Michigan7Department of Surgery, Dartmouth‐Hitchcock Medical Center and Geisel School of Medicine at Dartmouth, Lebanon, New HampshireCorrespondenceAlison B. Durham, Department of Dermatology, University of Michigan Health System, 1500 E. Medical Center Dr, UH South F7672, Ann Arbor MI 48109‐5218.Email: firstname.lastname@example.orgREFERENCESDurham AB, Schwartz JL, Lowe L, et al. The natural history of thin melanoma and the utility of sentinel lymph node biopsy. J Surg Oncol. 2017.Bax MJ, Johnson TM, Harms PW, et al. Detection of occult invasion in melanoma in situ. JAMA Dermatol. 2016;152:1201–1208.
Journal of Surgical Oncology – Wiley
Published: Jan 1, 2018
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