Novel response to neoadjuvant anti-PD1 therapy for a patient with retrocaval melanotic schwannoma.


Journal

Melanoma research
ISSN: 1473-5636
Titre abrégé: Melanoma Res
Pays: England
ID NLM: 9109623

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 17 12 2020
medline: 2 9 2021
entrez: 16 12 2020
Statut: ppublish

Résumé

Melanotic schwannoma is a rare nerve sheath tumor composed of melanin-producing Schwann cells with the potential for metastasis. These tumors can be associated with familial tumor syndromes and can cause significant symptoms related to nerve compression and mass effect. Due to the rarity of these lesions, they can be initially misidentified as melanocytomas, pigmented dermatofibrosarcoma protuberans, neurofibromas or malignant melanomas. Surgical excision is the mainstay of treatment with limited benefit from adjuvant systemic chemotherapy or radiation. Modern treatments with immune checkpoint blockade have demonstrated significant improvements in progression-free and overall survival for a variety of cancer histologies; however, anti-PD1 therapy has yet to be evaluated in patients with melanotic schwannoma. This report demonstrates a significant improvement in symptomatology and tumor stability with neoadjuvant anti-PD1 therapy for a retrocaval melanotic schwannoma initially masquerading as malignant melanoma. This report demonstrates the potential benefit of a novel therapeutic option for patients with melanotic schwannoma.

Identifiants

pubmed: 33323721
pii: 00008390-202102000-00012
doi: 10.1097/CMR.0000000000000711
pmc: PMC7755705
mid: NIHMS1647721
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

92-97

Subventions

Organisme : NCI NIH HHS
ID : K12 CA139160
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007019
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007281
Pays : United States

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Charles C Vining (CC)

Department of Surgical Oncology.

Phillip J Hsu (PJ)

Department of Surgical Oncology.
Medical Scientist Training Program, Biological Sciences Division.

Aaron Miller (A)

Department of Pathology.

Daniel J Olson (DJ)

Department of Hematology and Oncology.

Thomas F Gajewski (TF)

Department of Hematology and Oncology.

Peter Pytel (P)

Department of Pathology.

Bruce S Bauer (BS)

Department of Plastic and Reconstructive Surgery, University of Chicago Medical Center, Chicago, Illinois, USA.

Michael J Millis (MJ)

Department of Surgical Oncology.

Kevin K Roggin (KK)

Department of Surgical Oncology.

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