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. 2011 Jan 4;104(1):37-42.
doi: 10.1038/sj.bjc.6605997. Epub 2010 Nov 9.

Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients

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Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients

M H Nieuwenhuis et al. Br J Cancer. .

Abstract

Background: The optimal treatment of desmoid tumours is controversial. We evaluated desmoid management in Dutch familial adenomatous polyposis (FAP) patients.

Methods: Seventy-eight FAP patients with desmoids were identified from the Dutch Polyposis Registry. Data on desmoid morphology, management, and outcome were analysed retrospectively. Progression-free survival (PFS) rates and final outcome were compared for surgical vs non-surgical treatment, for intra-abdominal and extra-abdominal desmoids separately. Also, pharmacological treatment was evaluated for all desmoids.

Results: Median follow-up was 8 years. For intra-abdominal desmoids (n=62), PFS rates at 10 years of follow-up were comparable after surgical and non-surgical treatment (33% and 49%, respectively, P=0.163). None of these desmoids could be removed entirely. Eventually, one fifth died from desmoid disease. Most extra-abdominal and abdominal wall desmoids were treated surgically with a PFS rate of 63% and no deaths from desmoid disease. Comparison between NSAID and anti-estrogen treatment showed comparable outcomes. Four of the 10 patients who received chemotherapy had stabilisation of tumour growth, all after doxorubicin combination therapy.

Conclusion: For intra-abdominal desmoids, a conservative approach and surgery showed comparable outcomes. For extra-abdominal and abdominal wall desmoids, surgery seemed appropriate. Different pharmacological therapies showed comparable outcomes. If chemotherapy was given for progressively growing intra-abdominal desmoids, most favourable outcomes occurred after combinations including doxorubicin.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Progression-free interval after primary surgical (black line) and non-surgical (grey line) treatment for mesenterial desmoid tumours in FAP patients (log-rank test, P=0.163).
Figure 2
Figure 2
Progression-free interval after primary treatment for extra-abdominal and abdominal wall desmoid tumours in FAP patients.
Figure 3
Figure 3
Progression-free interval after NSAIDs (n=12, black line), and hormonal therapy or combination therapy (n=11, grey line), irrespective of previous surgery (log-rank test, P=0.111).

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References

    1. Arvanitis ML, Jagelman DG, Fazio VW, Lavery IC, McGannon E (1990) Mortality in patients with familial adenomatous polyposis. Dis Colon Rectum 33: 639–642 - PubMed
    1. Ballo MT, Zagars GK, Pollack A, Pisters PW, Pollack RA (1999) Desmoid tumor: prognostic factors and outcome after surgery, radiation therapy, or combined surgery and radiation therapy. J Clin Onc 17: 158–167 - PubMed
    1. Bertagnolli MM, Morgan JA, Fletcher CDM, Raut CP, Dileo P, Gill RR, Demetri GD, George S (2008) Multimodality treatment of mesenteric desmoid tumours. Eur J Cancer 44: 2404–2410 - PubMed
    1. Bertario L, Russo A, Sala P, Eboli M, Giarola M, Varesco L, Pierotti MA, Radice P, Hereditary Colorectal Tumours Registry (2001) Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis. Int J Cancer 95: 102–107 - PubMed
    1. Bonvalot S, Eldweny H, Haddad V, Rimareix F, Missenard G, Oberlin O, Vanel D, Terrier P, Blay JY, Le Cesne A, Le Pechoux C (2008) Extra-abdominal primary fibromatosis: aggressive management could be avoided in a subgroup of patients. EJSO 34: 462–468 - PubMed

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