Desmoid Tumors in the Active Surveillance Era: Evaluation of Treatment Options and Pain Relief in a Single-Center Retrospective Analysis

Author:

Rastrelli Marco12,Chiusole Benedetta3ORCID,Cavallin Francesco4ORCID,Del Fiore Paolo1ORCID,Angelini Andrea5ORCID,Cerchiaro Maria Chiara5,Ruggieri Pietro5ORCID,Sbaraglia Marta67,Mocellin Simone12,Brunello Antonella3ORCID

Affiliation:

1. Soft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV—IRCCS, 35128 Padua, Italy

2. Department of Surgery, Oncology and Gastroenterology (DISCOG), University of Padua, 35128 Padua, Italy

3. Oncology 1, Department of Oncology, Veneto Institute of Oncology IOV—IRCCS, 35128 Padua, Italy

4. Independent Statistician, 36020 Solagna, Italy

5. Department of Orthopedics and Orthopedic Oncology, University of Padova, 35128 Padua, Italy

6. Department of Medicine (DIMED), University of Padua School of Medicine, 35128 Padua, Italy

7. Department of Pathology, Azienda Ospedale Università Padova, 35128 Padua, Italy

Abstract

In patients with desmoid tumors (DTs), active surveillance has been increasingly preferred over surgery, while treatment (including pharmacological therapy, radiotherapy, and/or surgery) is performed in cases with confirmed disease progression. This study aimed to evaluate event-free survival and pain management according to different treatment strategies. We evaluated event-free survival, including recurrence after initial surgical treatment or changes in the therapeutic management after initial non-surgical treatment and pain management according to different treatment strategies. All patients referred for DT in 2001–2021 at our institutions were stratified into four groups: those treated surgically prior to 2012 (SGPre12) or after 2012 (SGPost12), those treated pharmacologically (MG), and those under active surveillance (ASG). An event was defined as recurrence after initial surgical treatment or a change in therapeutic management. Overall, 123 patients were included in the study: 28 in SGPre12, 41 in SGPost12, 38 in MG, and 16 in ASG. Pharmacological treatment resolved painful symptoms in 16/27 (60%) patients (p = 0.0001). The median follow-up duration was 40 months (IQR 23–74). Event-free survival at 1, 3, and 5 years was: 85%, 70%, and 62% in SGPre12; 76%, 58%, and 49% in SGPost12; 49%, 31%, and 31% in MG; and 45%, 45%, and 45% in ASG. Our findings support the role of active surveillance as initial management, as demonstrated by the fact that about half the patients did not experience any progression, while surgery can be reserved as a first-line approach for selected patients. In terms of pain relief, medical therapy led to symptom resolution in more than half the cases.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

Reference21 articles.

1. Fletcher, C.D.M., Krishnan, K., and Mertens, U.F. (2002). Pathology and Genetics of Tumours of Soft Tissue and Bone, IARC Press.

2. WHO Classification of Tumours Editorial Board (2020). WHO Classification of Tumours of Soft Tissue and Bone, IARC Press. [5th ed.].

3. Desmoid Tumor Working Group (2020). The management of desmoid tumours: A joint global consensus-based guideline approach for adult and paediatric patients. Eur. J. Cancer, 127, 96–107.

4. A prognostic nomogram for prediction of recurrence in desmoid fibromatosis;Crago;Ann. Surg.,2013

5. Surgical versus non-surgical approach in primary desmoid-type fibromatosis patients: A nationwide prospective cohort from the French Sarcoma Group;Penel;Eur. J. Cancer,2017

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