Magnetic resonance imaging patterns of tumor response to chemotherapy in desmoid-type fibromatosis.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
07 2021
Historique:
revised: 06 02 2021
received: 18 10 2020
accepted: 24 04 2021
pubmed: 9 6 2021
medline: 1 1 2022
entrez: 8 6 2021
Statut: ppublish

Résumé

We aimed to investigate changes in volume and MRI T2-weighted intensity in desmoid-type fibromatosis (DF) receiving methotrexate plus vinca-alkaloids (MTX-VA) at Istituto Nazionale dei Tumori, Milan. All cases of sporadic DF treated with MTX-VA from 1999 to 2019 were reviewed. MRIs at baseline, 6 and 12 months of chemotherapy and at treatment withdrawal were retrospectively reviewed, contouring the tumor lesion and measuring diameters, volume, and mean T2-signal intensity (normalized to muscle) changes. These parameters were also evaluated according to clinical variables. Thirty-two DF patients were identified. Best RECIST response was: 25% partial response, 69% stable disease, 6% progression. A ≥65% tumor volume reduction was observed in 38%, <65% reduction in 53%, an increase in 9%. 22% had RECIST stable disease with a ≥65% tumor volume reduction. T2-signal intensity decreased by ≥50% in 47%, <50% in 41% and increased in 12%. In patients with symptomatic improvement while on therapy and in patients maintaining symptomatic improvement during follow-up, median T2-signal intensity showed a reduction along the time points (3.0, 1.9, 1.2, 1.1; 2.9, 2.0, 1.2, 1.2, respectively); in patients without symptomatic improvement and in those clinically progressing during follow-up, a reduction was not observed. High T2-signal intensity at baseline was observed in patients showing RECIST progression during follow-up. In this series, RECIST detected a lower proportion of responses as compared to volumetric and T2-signal changes. T2-signal reduction seemed to better reflect symptomatic improvement. High T2-signal intensity at baseline was related to a higher proportion of further progression.

Sections du résumé

BACKGROUND
We aimed to investigate changes in volume and MRI T2-weighted intensity in desmoid-type fibromatosis (DF) receiving methotrexate plus vinca-alkaloids (MTX-VA) at Istituto Nazionale dei Tumori, Milan.
METHODS
All cases of sporadic DF treated with MTX-VA from 1999 to 2019 were reviewed. MRIs at baseline, 6 and 12 months of chemotherapy and at treatment withdrawal were retrospectively reviewed, contouring the tumor lesion and measuring diameters, volume, and mean T2-signal intensity (normalized to muscle) changes. These parameters were also evaluated according to clinical variables.
RESULTS
Thirty-two DF patients were identified. Best RECIST response was: 25% partial response, 69% stable disease, 6% progression. A ≥65% tumor volume reduction was observed in 38%, <65% reduction in 53%, an increase in 9%. 22% had RECIST stable disease with a ≥65% tumor volume reduction. T2-signal intensity decreased by ≥50% in 47%, <50% in 41% and increased in 12%. In patients with symptomatic improvement while on therapy and in patients maintaining symptomatic improvement during follow-up, median T2-signal intensity showed a reduction along the time points (3.0, 1.9, 1.2, 1.1; 2.9, 2.0, 1.2, 1.2, respectively); in patients without symptomatic improvement and in those clinically progressing during follow-up, a reduction was not observed. High T2-signal intensity at baseline was observed in patients showing RECIST progression during follow-up.
CONCLUSIONS
In this series, RECIST detected a lower proportion of responses as compared to volumetric and T2-signal changes. T2-signal reduction seemed to better reflect symptomatic improvement. High T2-signal intensity at baseline was related to a higher proportion of further progression.

Identifiants

pubmed: 34102009
doi: 10.1002/cam4.3973
pmc: PMC8267164
doi:

Substances chimiques

Vinca Alkaloids 0
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4356-4365

Informations de copyright

© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

Références

Pathology. 2014 Feb;46(2):95-104
pubmed: 24378391
Ann Surg. 2020 Apr;271(4):748-755
pubmed: 30418203
J Clin Oncol. 1999 Mar;17(3):1086
pubmed: 10071306
Tech Coloproctol. 2010 Jun;14(2):141-6
pubmed: 20352275
Ann Oncol. 2012 Jan;23(1):182-186
pubmed: 21444357
Am J Clin Oncol. 1999 Apr;22(2):193-5
pubmed: 10199460
J Clin Oncol. 2007 Feb 10;25(5):501-6
pubmed: 17290057
Cancer Med. 2019 Sep;8(11):5047-5057
pubmed: 31301110
J Med Imaging Radiat Oncol. 2019 Dec;63(6):751-757
pubmed: 31448875
Ann Surg Oncol. 2009 Sep;16(9):2587-93
pubmed: 19568815
Radiographics. 2016 May-Jun;36(3):767-82
pubmed: 27163593
Radiology. 2009 May;251(2):447-56
pubmed: 19261927
Eur J Cancer. 2015 Dec;51(18):2800-7
pubmed: 26602014
Cancer J. 2017 Mar/Apr;23(2):86-91
pubmed: 28410293
Br J Radiol. 2016;89(1058):20150308
pubmed: 26577289
Eur J Cancer. 2009 Jan;45(2):228-47
pubmed: 19097774
Ann Surg Oncol. 2016 Jul;23(7):2212-9
pubmed: 27020588
Ann Surg Oncol. 2013 Dec;20(13):4096-102
pubmed: 24052312
Cancer. 2001 Sep 1;92(5):1259-64
pubmed: 11571741
Eur J Cancer. 2015 Jan;51(2):186-92
pubmed: 25500145
PLoS One. 2012;7(11):e48372
pubmed: 23133631
Eur J Cancer. 2017 May;76:60-67
pubmed: 28282612
Eur J Cancer. 2015 Jan;51(2):127-36
pubmed: 25434922
N Engl J Med. 2018 Dec 20;379(25):2417-2428
pubmed: 30575484
Eur J Cancer. 2020 Mar;127:96-107
pubmed: 32004793
Clin Cancer Res. 2011 Jun 15;17(12):4082-90
pubmed: 21447727
Clin Sarcoma Res. 2018 May 14;8:13
pubmed: 29785261
Clin Cancer Res. 2010 Oct 1;16(19):4884-91
pubmed: 20724445
Lancet Oncol. 2019 Sep;20(9):1263-1272
pubmed: 31331699
AJR Am J Roentgenol. 1987 Jun;148(6):1247-50
pubmed: 3034013
Eur J Radiol. 2017 Jul;92:103-110
pubmed: 28624006

Auteurs

Edoardo Zanchetta (E)

Postgraduation School in Radiodiagnostics, Università degli Studi di Milano, Milan, Italy.
Unit of Radiology, ASST Santi Paolo e Carlo, Milan, Italy.
Diagnostic and Interventional Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Chiara Maura Ciniselli (CM)

Unit of Bioinformatics and Biostatistics, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Annalisa Bardelli (A)

Unit of Bioinformatics and Biostatistics, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Chiara Colombo (C)

Sarcoma Service, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Silvia Stacchiotti (S)

Sarcoma Service, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Giacomo Giulio Baldi (GG)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Salvatore Provenzano (S)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Rossella Bertulli (R)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Federica Bini (F)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandra Casale (A)

Diagnostic and Interventional Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Francesca Gabriella Greco (FG)

Diagnostic and Interventional Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Andrea Ferrari (A)

Oncological Pediatrics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Paolo Verderio (P)

Unit of Bioinformatics and Biostatistics, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Marco Fiore (M)

Sarcoma Service, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandro Gronchi (A)

Unit of Bioinformatics and Biostatistics, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Paolo Giovanni Casali (PG)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Oncological Pediatrics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Department of Oncology and Haemato-Oncology, Università degli Studi, Milano, Italy.

Carlo Morosi (C)

Diagnostic and Interventional Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Elena Palassini (E)

Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

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