Literature DB >> 23114473

Recurrent desmoids determine outcome in patients with Gardner syndrome: a cohort study of three generations of an APC mutation-positive family across 30 years.

Matthias Turina1, Caroline Marianne Pavlik, Karl Heinimann, Frank Behrensmeier, Hans-Peter Simmen.   

Abstract

PURPOSE: Screening of Gardner syndrome (GS) patients is tailored towards prevention of colorectal cancer (CRC). However, many patients suffer from desmoid tumors, which are challenging to treat due to invasive growth and local recurrence. The aims of our study were to determine the effectiveness of screening in GS and analyze outcome of desmoid tumors by treatment modality.
METHODS: This was a cohort study of a family of 105 descendants with GS. All family members who agreed were screened by endoscopy, and colorectal resection was performed upon pending malignancy. Resectable desmoids were excised, whereas large tumors were treated by a combination of brachytherapy (BT) and radiotherapy (RT). Main outcome measures were the incidence of CRC and overall and disease-specific mortality (ClinicalTrial.gov ID NCT01286662).
RESULTS: Thirty-seven of 105 family members have GS. Preventive colorectal resections were performed in 16 patients (15 %), with one death due to gastric cancer. In four patients who denied screening endoscopy, invasive tumors of the colon (three patients) and stomach developed. Of 33 desmoid tumors, 10 (30 %) were located in the mesentery, 17 (52 %) in the abdominal wall, and 6 (18 %) in extra-abdominal sites. Excision of 12 desmoids was performed in eight patients. Four desmoids were treated by BT and RT and showed full or partial remission.
CONCLUSIONS: Provided adequate screening, good long-term control of colorectal tumors is achievable. However, desmoid tumors determine survival and quality of life in many patients. Our data suggest good local control using a combination of brachytherapy/radiotherapy in large desmoids unsuitable for surgical resection.

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Year:  2012        PMID: 23114473     DOI: 10.1007/s00384-012-1600-x

Source DB:  PubMed          Journal:  Int J Colorectal Dis        ISSN: 0179-1958            Impact factor:   2.571


  30 in total

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Journal:  Gastroenterology       Date:  2000-12       Impact factor: 22.682

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Authors:  Polymnia Galiatsatos; William D Foulkes
Journal:  Am J Gastroenterol       Date:  2006-02       Impact factor: 10.864

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Journal:  Dis Colon Rectum       Date:  1990-08       Impact factor: 4.585

8.  Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.

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Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

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Journal:  Gastroenterology       Date:  1994-06       Impact factor: 22.682

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Journal:  Cell       Date:  1991-08-09       Impact factor: 41.582

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  3 in total

1.  Multiple desmoid tumors in a patient with Gardner's syndrome - Report of a case.

Authors:  Lílian Vital Pinheiro; João José Fagundes; Cláudio Saddy Rodrigues Coy; Cesar Cabello; Ivan Toro; Marcelo Michellino; Paulo Henrique Fachina; Marc Ward; Raquel Franco Leal; Maria de Lourdes Setsuko Ayrizono
Journal:  Int J Surg Case Rep       Date:  2014-04-18

2.  Intestinal perforation during chemotherapeutic treatment of intra-abdominal desmoid tumor in patients with Gardner's syndrome: report of two cases.

Authors:  Wei Li; Yuhong Zhou; Qian Li; Hanxing Tong; Weiqi Lu
Journal:  World J Surg Oncol       Date:  2016-07-04       Impact factor: 2.754

3.  A Case of Spontaneous Regression of Recurrent Desmoid Tumor Originating From the Internal Obturator Muscle After Delivery.

Authors:  Takuya Sueishi; Takeshi Arizono; Kenjiro Nishida; Takahiro Hamada; Akihiko Inokuchi
Journal:  World J Oncol       Date:  2016-09-03
  3 in total

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