Association of MRI T2 Signal Intensity With Desmoid Tumor Progression During Active Observation: A Retrospective Cohort Study.
Journal
Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354
Informations de publication
Date de publication:
04 2020
04 2020
Historique:
pubmed:
13
11
2018
medline:
5
6
2020
entrez:
13
11
2018
Statut:
ppublish
Résumé
The aim of this study was to identify predictors of desmoid progression during observation. Untreated desmoids can grow, remain stable, or regress, but reliable predictors of behavior have not been identified. Primary or recurrent desmoid patients were identified retrospectively from an institutional database. In those managed with active observation who underwent serial magnetic resonance imaging (MRIs) with T2-weighted sequences, baseline tumor size was recorded, and 2 radiologists independently estimated the percentage of tumor volume showing hyperintense T2 signal at baseline. Associations of clinical or radiographic characteristics with progression-free survival (PFS; by RECIST) were evaluated by Cox regression and Kaplan-Meier statistics. Among 160 patients with desmoids, 72 were managed with observation, and 37 of these had serial MRI available for review. Among these 37 patients, median age was 35 years and median tumor size was 4.7 cm; all tumors were extra-abdominal (41% in abdominal wall). Although PFS was not associated with size, site, or age, it was strongly associated with hyperintense T2 signal in ≥90% versus <90% of baseline tumor volume (as defined by the "test" radiologist; hazard ratio = 11.3, P = 0.003). For patients in the ≥90% group (n = 20), 1-year PFS was 55%, compared with 94% in the <90% group (n = 17). The percentage of baseline tumor volume with hyperintense T2 signal defined by a validation radiologist correlated with results of the test radiologist (ρ = 0.75). The percent tumor volume characterized by hyperintense T2 signal is associated with desmoid progression during observation and may help distinguish patients who would benefit from early intervention from those who may be reliably observed.
Sections du résumé
OBJECTIVE
The aim of this study was to identify predictors of desmoid progression during observation.
SUMMARY OF BACKGROUND DATA
Untreated desmoids can grow, remain stable, or regress, but reliable predictors of behavior have not been identified.
METHODS
Primary or recurrent desmoid patients were identified retrospectively from an institutional database. In those managed with active observation who underwent serial magnetic resonance imaging (MRIs) with T2-weighted sequences, baseline tumor size was recorded, and 2 radiologists independently estimated the percentage of tumor volume showing hyperintense T2 signal at baseline. Associations of clinical or radiographic characteristics with progression-free survival (PFS; by RECIST) were evaluated by Cox regression and Kaplan-Meier statistics.
RESULTS
Among 160 patients with desmoids, 72 were managed with observation, and 37 of these had serial MRI available for review. Among these 37 patients, median age was 35 years and median tumor size was 4.7 cm; all tumors were extra-abdominal (41% in abdominal wall). Although PFS was not associated with size, site, or age, it was strongly associated with hyperintense T2 signal in ≥90% versus <90% of baseline tumor volume (as defined by the "test" radiologist; hazard ratio = 11.3, P = 0.003). For patients in the ≥90% group (n = 20), 1-year PFS was 55%, compared with 94% in the <90% group (n = 17). The percentage of baseline tumor volume with hyperintense T2 signal defined by a validation radiologist correlated with results of the test radiologist (ρ = 0.75).
CONCLUSION
The percent tumor volume characterized by hyperintense T2 signal is associated with desmoid progression during observation and may help distinguish patients who would benefit from early intervention from those who may be reliably observed.
Identifiants
pubmed: 30418203
doi: 10.1097/SLA.0000000000003073
pmc: PMC6736761
mid: NIHMS1048932
pii: 00000658-202004000-00024
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
748-755Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA140146
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217694
Pays : United States
Références
Am J Surg. 1990 May;159(5):450-3
pubmed: 2139764
Ann Surg Oncol. 2016 Jul;23(7):2212-9
pubmed: 27020588
Hum Pathol. 1996 Sep;27(9):939-43
pubmed: 8816889
J Bone Joint Surg Am. 1984 Dec;66(9):1369-74
pubmed: 6501332
Cancer. 2010 May 1;116(9):2258-65
pubmed: 20187095
Ann Surg. 1999 Jun;229(6):866-72; discussion 872-3
pubmed: 10363901
Eur Radiol. 1997;7(7):1013-9
pubmed: 9265665
Acta Orthop Scand. 1986 Feb;57(1):1-7
pubmed: 3962627
Ann Surg. 1989 Dec;210(6):765-9
pubmed: 2531573
Clin Cancer Res. 2011 Jun 15;17(12):4082-90
pubmed: 21447727
Int Orthop. 1995;19(6):383-9
pubmed: 8567158
J Clin Oncol. 2011 Sep 10;29(26):3553-8
pubmed: 21844500
Ann Surg. 2013 Aug;258(2):347-53
pubmed: 23532110
Br J Surg. 2000 May;87(5):608-13
pubmed: 10792318
Ann Oncol. 2017 Oct 1;28(10):2399-2408
pubmed: 28961825
Cancer. 1999 Nov 15;86(10):2045-52
pubmed: 10570430
Ann Surg Oncol. 2009 Sep;16(9):2587-93
pubmed: 19568815
Eur J Cancer. 2017 Sep;83:125-131
pubmed: 28735069
Cancer Res. 2010 Oct 1;70(19):7690-8
pubmed: 20841474
Skeletal Radiol. 1987;16(1):30-6
pubmed: 3823958
Br J Surg. 1995 Apr;82(4):510-4
pubmed: 7613897