Radiation Oncology/Sarcoma/DFSP
Appearance
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Dermatofibrosarcoma Protuberans
Epidemiology
[edit | edit source]- Cutaneous, locally aggressive, primarily low grade sarcoma
- ~10% may contain a high-grade fibrosarcoma component
- Low rate (<5%) of metastasis; higher if fibrosarcoma component
- Rare, 2-6% of soft tissue sarcomas
- Adults in 30's
- Risk factors: pregnancy, arsenic exposure, acanthosis nigricans
Clinical Presentation
[edit | edit source]- Plaque-like areas of cutaneous thickening
- Skin-colored, red-brown, or violaceous, particularly at the margins
- May arise within pre-existing scar or tattoo
- As it slowly enlarges, becomes raised ("protuberans"), firm, and nodular (fixed to dermis, but moves over deeper structures)
- At diagnosis, >75% are superficial and <5cm diameter
- Slow, indolent growth, such that the lesion may be present for years
- Distribution:
- Trunk ~50%
- Lower extremity ~20%
- Upper extremity 15%
- Head and neck 15%
Work Up
[edit | edit source]- MRI helpful to estimate extent of deep extent
- CT not routinely necessary, unless bony invasion suspected
- Metastatic workup not routinely necessary, unless suspicion from H&P
Histology
[edit | edit source]- Cell of origina is not well understood
- Histochemistry and electron microscopy suggest fibroblast lineage
- However, the cells are CD34 positive, suggesting possibly dendritic lineage
- In comparison, dermatofibromas and desmoid tumors are CD34-
- The tumors show benign-appearing spindle cells, in an irregular patterns resembling a straw mat. In early lesions there is a tumor-free zone with epidermis
- >90% have a t(17;22) translocation, resulting in a fusion of PDFG-B driven by a highly expressed collagen promoter (COL1A1)
- Results in PDFGRb activation, which is tyrosine kinase receptor
Staging
[edit | edit source]- AJCC 7th Edition (2010)
- First edition to include DFSP
- Please see the Soft Tissue Sarcoma staging page
- American Musculoskeletal Tumor Society Staging for DFSP
- Stage IA - Low or intermediate grade within the subcutaneous compartment
- Stage IB - Low or intermediate grade extending outside anatomic compartment
- Stage II - High grade histology
Natural History
[edit | edit source]- Tends to recur locally after excision alone
- Recur locally multiple times before metastasis; significant interval before development of metastases.
- Fibrosarcomatous changes predict for metastatic potential.
Treatment Overview
[edit | edit source]- Surgical resection is the primary treatment approach
- Historically, wide local excision with 3cm margins was recommended, down to and including fascia
- Mohs mapping reveals fine tentacles of tumor, and is becoming favored due to preservation of cosmesis
- Some recommend modified Mohs to include a final path margin for permanent section
- Pooled local recurrence rate with adequate margin WLE or Mohs' is <2%
- Recurrences tend to occur within 3 years of surgery
- Definitive RT not routinely; only couple reports available
- Adjuvant radiation is typically indicated if positive or close margins, further resection anatomically not possible if recurrence happens, or recurrent disease
- Given the high rate of t(17;22) leading downstream to a tyrosine kinase activation, efforts are under way to use Gleevec and other TKIs in this disease
Adjuvant Radiation Therapy
[edit | edit source]- MD Anderson
- 2013 (1972-2010) PMID 23628134 -- Dermatofibrosarcoma Protuberans: Long-term Outcomes of 53 Patients Treated With Conservative Surgery and Radiation Therapy. (Castle KO, Int J Radiat Oncol Biol Phys. 2013 Jul 1;86(3):585-90. doi: 10.1016/j.ijrobp.2013.02.024. Epub 2013 Apr 26.)
- Retrospective. 53 consecutive patients. Surgery and preoperative (13%) or postoperative (87%) RT. Median tumor size 4 cm (1-25 cm). Preop dose 50 Gy, postop dose 60-66 Gy. Gross disease 7%, positive margin 30%. Median F/U 6.5 years
- Outcome: Recurrence 4%. 5-year and 10-year OS 98%. Fibrosarcomatous change not associated with risk of LR or DM
- Toxicity: 13%; moderate/severe complications 9% at 10 years
- Conclusion: DFSP is radioresponse with excellent local control after surgery and RT. Adjuvant RT should be considered if large/recurrent tumor or where attempt at wide surgical margins would result in significant morbidity
- 1998 PMID 9531366 -- "The role of radiation therapy in the management of dermatofibrosarcoma protuberans." (Ball MT, Int J Radiat Oncol Biol Phys. 1998 Mar 1;40(4):823-7.
- Retrospective. 19 patients receiving adjuvant xrt. 60 Gy given for +microscopic margin; 65 Gy given for gross residual disease. Local control at 10 yrs was 95%
- Conclusion: adjuvant xrt should be considered for +margins or if adequate wide excision would lead to major cosmetic defect.
- 2013 (1972-2010) PMID 23628134 -- Dermatofibrosarcoma Protuberans: Long-term Outcomes of 53 Patients Treated With Conservative Surgery and Radiation Therapy. (Castle KO, Int J Radiat Oncol Biol Phys. 2013 Jul 1;86(3):585-90. doi: 10.1016/j.ijrobp.2013.02.024. Epub 2013 Apr 26.)
- Soft Tissue Tumours Working Group, The Netherlands Cancer Institute; 1997 PMID 9376187 -- Haas RL et al. "The role of radiotherapy in the local management of dermatofibrosarcoma protuberans."
- 38 consecutive pts w/ DFSP. 21 tx'd surgically, 17 tx'd w/ combined modality.
- Surgery alone had local control of 67%
- Combined modality had local control of 82% (many of these who had xrt already had multiple local recurrences.
- Harvard; 1996 PMID 8708729 -- Suit H et al. "Radiation in management of patients with dermatofibrosarcoma protuberans." J Clin Oncol. 1996 Aug;14(8):2365-9.
- 18 patients treated with postop (n=15) or definitive (n=3) xrt. Population was +/close margins or xrt alone.
- Local control at 10yrs was 88%.