» Articles » PMID: 1310270

Noncytotoxic Drug Therapy for Intra-abdominal Desmoid Tumor in Patients with Familial Adenomatous Polyposis

Overview
Specialty Gastroenterology
Date 1992 Jan 1
PMID 1310270
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

Forty of 416 patients with familial adenomatous polyposis were noted to have intra-abdominal desmoid tumors, and a subgroup of 16 were treated with noncytotoxic drug therapy. Drugs used were sulindac (14 patients), sulindac plus tamoxifen (3 patients), indomethacin (4 patients), tamoxifen (4 patients), progesterone (DEPO-PROVERA; Upjohn Co., Kalamazoo, MI) (2 patients), and testolactone (1 patient). Therapy with these drugs for continuous periods of six months or more resulted in three complete and seven partial remissions. When treated patients were compared with untreated patients (n = 12), there were significant benefits for the treated group, both in reduction of desmoid size and in improvement of symptoms, despite the inherent selection bias against this. Sulindac was the only drug used in enough patients to permit independent evaluation of its effect, with one complete and seven partial reductions of tumor size. Some patients had a delayed response to sulindac, with tumor shrinkage occurring after an initial period of tumor enlargement. When using sulindac for the treatment of desmoid tumors, this phenomenon should be considered.

Citing Articles

Desmoid-type fibromatosis of the breast: a case report and literature review.

Zhao Z, Shang Q, Yang C, Liu J, Liu S, Li X Front Oncol. 2025; 15:1482024.

PMID: 40008005 PMC: 11850368. DOI: 10.3389/fonc.2025.1482024.


Nirogacestat-the pathway to approval of the first treatment for desmoid tumors, a rare disease.

Kummar S, Bui N, Messersmith W, Whiting J, Portnoy M, Lim A Ther Adv Rare Dis. 2025; 6:26330040251317546.

PMID: 39944188 PMC: 11815814. DOI: 10.1177/26330040251317546.


Clinical Benefit of Pegylated Liposomal Doxorubicin and High Prevalence of Pre-Existing Psychiatric Conditions in Patients with Desmoid-Type Fibromatosis.

Freire A, Skubitz K Cancers (Basel). 2025; 17(2).

PMID: 39858074 PMC: 11763362. DOI: 10.3390/cancers17020293.


Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint....

Zaffaroni G, Mannucci A, Koskenvuo L, de Lacy B, Maffioli A, Bisseling T Br J Surg. 2024; 111(5).

PMID: 38722804 PMC: 11081080. DOI: 10.1093/bjs/znae070.


Management of Desmoid Disease in Familial Adenomatous Polyposis.

Sommovilla J, Shepard D, Liska D Clin Colon Rectal Surg. 2024; 37(3):185-190.

PMID: 38606047 PMC: 11006445. DOI: 10.1055/s-0043-1770731.