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Updated: Jun 21, 2026

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
Response of malignant scalp dermatofibrosarcoma to presurgical targeted growth factor inhibition
Austin K Mattox1, Ankit I Mehta, Peter M Grossi
1Preston Robert Tisch Brain Tumor Center, Duke Medical Center, Durham, North Carolina 27710, USA.
Abstract:
Dermatofibrosarcoma protuberans (DFSP) is an uncommon, locally aggressive, malignant cutaneous tumor that sparingly presents on the scalp. Dermatofibrosarcomas often result from the formation of a fusion oncogene on translocated or supernumerary ring chromosomes 17 and 22, causing the overexpression of PDGFRbeta driven by the COL1A1 promoter. Because of uncertainty surrounding appropriate treatment of aggressive scalp DFSP, the authors performed an extensive review of the available data from a MEDLINE (Ovid) search to describe the clinical presentation and treatment options for this rare tumor. Their search identified 39 different cases, including the illustrative case presented in this study. Adjuvant therapy for this malignant lesion is not universally established in the literature. In the present case, the authors successfully treated a locally invasive scalp DFSP with presurgical therapy that specifically inhibited the PDGFbeta receptor. Imatinib significantly shrank the DFSP tumor mass, reduced hypervascularity, reduced metabolic activity on PET scanning, and permitted a safe gross-total resection. Although wide excision and Mohs micrographic surgery remain the standard surgical treatments for DFSP, the authors illustrate that presurgical chemotherapeutic treatment by imatinib provides a critical adjunct to traditional therapy.
Insights
Dermatofibrosarcoma protuberans (DFSP) on the scalp is rare. Presurgical imatinib therapy targeting PDGFbeta receptor effectively shrank tumors, enabling complete resection and improving treatment for this aggressive skin cancer.
Area of Science:
- Oncology
- Dermatology
- Genetics
Background:
- Dermatofibrosarcoma protuberans (DFSP) is a rare, locally aggressive skin cancer.
- DFSP commonly arises from COL1A1-PDGFB gene fusions on ring chromosomes, leading to PDGFRbeta overexpression.
- Scalp DFSP presents unique challenges due to its rarity and potential for aggressive local invasion.
Observation:
- A comprehensive literature review identified 39 reported cases of scalp DFSP.
- The study presents a case of locally invasive scalp DFSP.
- Standard treatments like wide excision and Mohs surgery have limitations for extensive cases.
Findings:
- Presurgical treatment with imatinib, a PDGFbeta receptor inhibitor, was successfully employed.
- Imatinib significantly reduced tumor size, hypervascularity, and metabolic activity.
- This neoadjuvant therapy facilitated a safe and complete surgical resection of the DFSP.
Implications:
- Presurgical imatinib therapy offers a promising adjunct to conventional surgical treatments for aggressive scalp DFSP.
- Targeting the PDGFbeta receptor pathway represents a viable strategy for managing challenging DFSP cases.
- Further research into targeted therapies may improve outcomes for patients with rare cutaneous malignancies.
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