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Journal ArticleDOI

Surgery versus radiation therapy for patients with aggressive fibromatosis or desmoid tumors: A comparative review of 22 articles.

TLDR
Desmoid tumors (aggressive fibromatoses) are benign neoplasms with high rates of recurrence after surgery, and Radiotherapy is sometimes reported to prevent recurrences, but not in all studies.
Abstract
BACKGROUND Desmoid tumors (aggressive fibromatoses) are benign neoplasms with high rates of recurrence after surgery. Radiotherapy is sometimes reported to prevent recurrences, but not in all studies. In order to evaluate the effect of radiation, comparative analysis was performed. METHODS The authors conducted a MEDLINE search and collected all articles in the English language on the treatment of “desmoid tumor” or “aggressive fibromatosis” from the years 1983–1998. They categorized treatment into three groups: surgery alone (S), surgery with radiotherapy (S + RT), or radiotherapy alone (RT). The S and S + RT groups were each subdivided according to whether margins were free (−), positive (+), or unknown. Each subgroup was divided into cases with primary, recurrent, or unknown tumor. RESULTS The local control rates after treatment for cases in the S group with (−) margins, (+) margins, and overall were 72%, 41%, and 61%, respectively. For the S + RT group the local control results were 94%, 75%, and 75%, respectively, significantly different when compared with the results for the S group. For the RT group, the local control was 78%, significantly superior to that of the S group (61%). Cases with primary and recurrent tumors had significantly superior local control rates with S + RT or RT versus S. Radiotherapy complications noted were fibrosis, paresthesias, edema, and fracture. CONCLUSIONS RT or S + RT results in significantly better local control than S. Even after dividing the groups into cases with free and positive margins and cases with primary and recurrent tumors, the best local control is achieved with RT or S + RT. Cancer 2000;88:1517–23. © 2000 American Cancer Society.

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Journal ArticleDOI

Quality of Surgery and Outcome in Extra-Abdominal Aggressive Fibromatosis: A Series of Patients Surgically Treated at a Single Institution

TL;DR: Presence of microscopic disease does not necessarily affect long-term disease-free survival in patients with primary presentation of extra-abdominal desmoid tumors, and function-sparing surgery may be a reasonable choice when feasible without leaving macroscopic residual disease.
Journal ArticleDOI

Desmoid-Type Fibromatosis: A Front-Line Conservative Approach to Select Patients for Surgical Treatment

TL;DR: A conservative policy could be a safe approach to primary and recurrent DF, which could avoid unnecessary morbidity from surgery and/or radiation therapy, and a multidisciplinary, stepwise approach should be prospectively tested in DF.
Journal ArticleDOI

The pharmacological treatment of aggressive fibromatosis: a systematic review

TL;DR: The evidence in the literature supports the opinion that both non-cytotoxic and cytotoxic chemotherapies are effective against AF, however, the lack of sufficient patient numbers and randomized trials compromises the validity of the reported results and mandates further investigation.
References
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Journal ArticleDOI

The desmoid syndrome. New aspects in the cause, pathogenesis and treatment of the desmoid tumor.

TL;DR: The direct relationship of the growth rate to the level of endogenous estrogen in the female patients and the demonstration of significant amounts of estradiol but not progesterone receptors in the tumor cytosol further suggest that the Growth rate of desmoid tumor is regulated by steroid sex hormones.
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The Desmoid Tumor: Not a Benign Disease

TL;DR: It is confirmed that desmoid tumors are malignant soft-tissue neoplasms that warrant aggressive therapy and have independent predictive value for recurrence.
Journal ArticleDOI

Extra-abdominal desmoid tumors.

TL;DR: Recommendations are made for wide local excision when anatomically feasible or marginal excision and postoperative radiation therapy when function of the extremity would be severely compromised if excision with wide margins were done.
Journal ArticleDOI

Individualizing management of aggressive fibromatoses.

TL;DR: It is fundamental that treatment recommendations should be made based on the risk:benefit analysis for the individual patient, dependent on tumor characteristics and location, as well as patient characteristics and preferences.
Journal ArticleDOI

Radiation therapy in the treatment of aggressive fibromatoses (desmoid tumors).

TL;DR: Radiation therapy is recommended in those situations where wide‐field resection without significant morbidity is not possible for gross local disease and if minimally positive margins exist after resection in a patient who may be followed carefully, frequent follow‐up and prompt treatment at recurrence may be an effective alternative to immediate radiation therapy.
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