Small and Isolated Immunohistochemistry-positive Cells in Melanoma Sentinel Lymph Nodes Are Associated With Disease-specific and Recurrence-free Survival Comparable to that of Sentinel Lymph Nodes Negative for Melanoma.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
06 2019
Historique:
entrez: 16 5 2019
pubmed: 16 5 2019
medline: 19 2 2020
Statut: ppublish

Résumé

Although immunohistochemistry (IHC) has improved our ability to detect melanoma metastases in sentinel lymph nodes (SLN), the American Joint Committee on Cancer (AJCC) does not provide a lower threshold for determining if a SLN is positive for metastasis. Existing literature suggests that even a small aggregate or an enlarged, abnormal cell detectable by IHC can be associated with an adverse outcome. In our experience, however, some SLNs contain small solitary cells the size of neighboring lymphocytes demonstrable only by IHC. We sought to determine their clinical significance. A total of 821 patients underwent a SLN biopsy at our institution over a 12-year period. In all, 639 (77.8%) were SLN-negative, 125 (15.2%) were SLN-positive, and 57 (6.9%) had rare IHC-positive cells of undetermined clinical significance with no disease progression over a mean 59-month follow-up. Kaplan-Meier method with pair-wise comparisons revealed no significant difference in disease-specific survival and recurrence-free survival between SLN-negative and rare IHC-positive groups. There were significant differences in survival and recurrence between patients in the rare IHC-positive group and those with melanoma metastases, including those with solitary melanoma cells and those with tumor burdens ≤0.2 mm. While the lower diagnostic threshold for metastatic melanoma on IHC-stained sections needs to be studied further, our data suggest that rare IHC-positive cells lacking cytomorphologic features of overt malignancy are equivocal for melanoma and could impart a similar prognosis as patients with no evidence of SLN involvement.

Identifiants

pubmed: 31091203
doi: 10.1097/PAS.0000000000001229
pii: 00000478-201906000-00004
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

755-765

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001086
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Robert E LeBlanc (RE)

Departments of Pathology and Laboratory Medicine.

Dorothea T Barton (DT)

Surgery and Dermatology.

Zhongze Li (Z)

Biostatistics Shared Resource, Norris Cotton Cancer Center.

Christina V Angeles (CV)

Departments of Surgery.

Marc S Ernstoff (MS)

Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY.

Eryn Bagley (E)

Medicine, Hematology and Oncology Program, Dartmouth Hitchcock Medical Center, Geisel School of Medicine at Dartmouth, Lebanon, NH.

Daniel Wimmer (D)

Inform Diagnostics, Irving, TX.

Sandra L Wong (SL)

Departments of Surgery.

Richard J Barth (RJ)

Departments of Surgery.

Keisuke Shirai (K)

Medicine, Hematology and Oncology Program, Dartmouth Hitchcock Medical Center, Geisel School of Medicine at Dartmouth, Lebanon, NH.

Shaofeng Yan (S)

Departments of Pathology and Laboratory Medicine.

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