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Poster session 03

877P - Characteristics of malignant cutaneous adnexal tumors in a single-institution study

Date

10 Sep 2022

Session

Poster session 03

Topics

Clinical Research;  Pathology/Molecular Biology;  Surgical Oncology

Tumour Site

Basal Cell and Squamous Cell Cancers of the Skin

Presenters

Erica Koch

Citation

Annals of Oncology (2022) 33 (suppl_7): S356-S409. 10.1016/annonc/annonc1059

Authors

E.C. Koch1, M. Vilbert1, T. Pimentel Muniz1, D. Ghazarian2, I. Hirsch1, M.F. Silva Almeida Ribeiro1, L. Mantle1, D. Hogg1, S. Saibil1, A. Spreafico1, M.O. Butler1

Author affiliations

  • 1 Division Of Medical Oncology And Hematology, Princess Margaret Cancer Centre, M5S 1Z5 - Toronto/CA
  • 2 Laboratory Medicine & Pathobiology, Princess Margaret Cancer Centre, M5G 2C1 - Toronto/CA

Resources

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Abstract 877P

Background

Malignant cutaneous adnexal tumors (MCATs) comprise a heterogeneous group of rare neoplasms. Little is known about their natural history, with limited information regarding prognostic factors and long-term outcomes described.

Methods

In this single-center retrospective cohort study, we included patients diagnosed with MCATs between 2014 and 2021. Clinicopathologic variables and outcome measures were analyzed. X2, Fisher’s exact and Mann-Whitney U tests were used to compare groups and Cox proportional hazards models were fitted. The log-rank test was used to assess recurrence free survival (RFS) and overall survival (OS).

Results

We identified 114 patients with MCATs. Characteristics are displayed in table. The most frequent histological subtypes were porocarcinoma in 41 (36%), sebaceous carcinoma in 28 (25%) and eccrine carcinoma in 17 (15%) patients. Porocarcinoma was significantly associated with organ-transplant and hematological cancer (p=0.03), and other skin cancers (p < 0.01). Disease recurred following surgical resection in 24 patients (21%) and median RFS was 68 months (95% CI 45.7-90.3). Head and neck tumors (p=0.05), larger size (p=0.04) and higher stage (p<0.01) were associated with increased risk of recurrence. Among 49 patients with stage I, 34 underwent completion of surgical resection after excisional biopsy, and it was associated with a longer OS (HR: 0.26 95% CI 0.08-0.78 p=0.01). Only 13 (11%) patients had stage IV disease at diagnosis, and the most common site of metastasis was the lung. Median OS for stage IV was 37 months (95%CI 20.6-53.3) (median follow-up 17 months). Median follow-up was 24 months for patients with localized disease and median OS was not reached (95% CI NE). Table: 877P

MCATs - n (%)
Age (years) – median (range) 73 (27-95)
Sex male 75 (66)
Histology groups Sweat gland Sebaceous Follicular 83 (73) 28 (25) 3 (2)
Primary site Head and neck Trunk Extremities 73 (64) 15 (13.2) 26 (22.8)
Comorbidities Organ transplant Hematological cancer Other skin cancer 25 (22) 8 (7) 54 (47)

Conclusions

Patients with MCATs have a good prognosis when detected early and are adequately resected. Careful dermatological surveillance in immunosuppressed patients is warranted.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

E.C. Koch: Financial Interests, Personal, Invited Speaker: Novartis, MSD; Financial Interests, Personal, Advisory Board: Novartis, MSD; Financial Interests, Institutional, Other, Funding: Alamos Gold Inc.; Financial Interests, Institutional, Research Grant: Novartis. M. Vilbert: Financial Interests, Institutional, Funding: Alamos Gold Inc. T. Pimentel Muniz: Financial Interests, Institutional, Research Grant: Novartis; Financial Interests, Institutional, Funding: Alamos Gold Inc. S. Saibil: Financial Interests, Personal, Advisory Board: Novartis. A. Spreafico: Financial Interests, Personal, Advisory Board: Merck, Bristol Myers Squibb, Oncorus, Janssen, Medison & Immunocore; Financial Interests, Institutional, Research Grant: Novartis, Bristol Myers Squibb, Symphogen AstraZeneca/MedImmune, Merck, Bayer, Surface Oncology, Northern Biologics, Janssen Oncology/Johnson & Johnson, Roche, Regeneron, Alkermes, Array Biopharma/Pfizer, GSK, Oncorus, Treadwell, Amgen. M.O. Butler: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, EMD Serono, GlaxoSmithKline, Immunocore, Merck, Novartis, Pfizer, Sanofi; Financial Interests, Institutional, Research Grant: Merck; Financial Interests, Personal, Other, Safety Review Board: Adaptimmune, GlaxoSmithKline. All other authors have declared no conflicts of interest.

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