Abstract

Desmoid tumor is a rare disease, which is histologically characterized by local invasion, monoclonality, and fibroblast proliferation; and clinically characterized by a variable and often unpredictable course. The treatment of desmoid tumor is mainly surgical resection, but the recurrence rate is high. In recent years, a variety of treatment methods, including endocrine therapy, surgery, radiotherapy, chemotherapy, non-steroidal anti-inflammatory drugs, targeted drugs, interferon and more, have been used and achieved certain curative effects. In addition, in view of the inertia characteristics of desmoid tumor, observation is also a first-line scheme recommended by multiple guidelines. In the past, the research progress of targeted therapy for desmoid tumor is relatively slow and the curative effect is limited. Thus, targeted therapy is usually used as a remedial treatment after the failure of other conventional treatment methods. However, in recent years, with the rapid progress in the basic research of targeted therapy, some new targeted drugs are increasingly used for the clinical treatment of desmoid tumor and have achieved good results. Herein, we described a patient with aggressive fibromatosis in the abdominal cavity. Following a combined treatment using anlotinib and celecoxib, the patient achieved a partial response with mild toxicity. Simultaneously, the patient’s pain symptoms completely disappeared. This case indicates that the combination of anlotinib and NSAIDs could be an effective treatment for desmoid tumor.

Highlights

  • Desmoid tumors (DTs), known as aggressive fibromatosis, are local tumors of mesenchymal origin that can cause significant morbidity due to their infiltrating nature [1, 2]

  • The patient’s tumor was significantly reduced and the progression-free survival (PFS) exceeded 18 months. This is the first case of successful treatment of DT using the combination of anlotinib and non-steroidal anti-inflammatory drugs (NSAIDs), which has not been previously reported

  • The World Health Organization (WHO) defines invasive fibromatosis as clonal fibroblastic proliferative tumor formed in deep soft tissue, which is characterized by invasive growth, local recurrence and no distant metastasis [17, 18]

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Summary

BACKGROUND

Desmoid tumors (DTs), known as aggressive fibromatosis, are local tumors of mesenchymal origin that can cause significant morbidity due to their infiltrating nature [1, 2]. There is no clinical study on using anlotinib for the treatment of DTs. We have recently encountered a rare case of isolated aggressive fibromatosis located in the abdominal cavity. The patient’s tumor was significantly reduced and the progression-free survival (PFS) exceeded 18 months This is the first case of successful treatment of DT using the combination of anlotinib and non-steroidal anti-inflammatory drugs (NSAIDs), which has not been previously reported. A color Doppler ultrasound examination at the local hospital (2020-04-12) showed that there was an inhomogeneous echo mass about 9.5cm*7.7cm*6.8cm in the right front of the abdominal aorta in the upper mid-abdomen. The patient is expected to obtain long-term survival with the continuation of treatment using anlotinib in combination with celecoxib

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