Abdominal and intra-abdominal fibromatoses: Outcomes over time.

IF 2.3 4区 医学 Q2 PATHOLOGY
Fireneh N Beshah, Monica Sanchez-Avila, Amr Abulaban, Diego Montoya-Cerrillo, Domenika Ortiz Requena, Temitope Kehinde, Alan S Livingstone, Francis J Hornicek, Gina D'Amato, Andrew E Rosenberg, Elizabeth A Montgomery
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引用次数: 0

Abstract

Objectives: Abdominal wall and intra-abdominal fibromatoses are locally aggressive, nonmetastasizing neoplasms. Surgery has been the mainstay of local control, but new forms of therapy have been developed that may influence the clinical course and morbidity. We studied the clinical features and outcomes of patients with abdominal and intra-abdominal fibromatoses over time.

Methods: Ninety-one patients-46 with abdominal wall and 45 with intra-abdominal fibromatosis-treated in our hospital systems between 2009 and 2023 were included. The patients were allocated to 1 of 2 groups based on the year of their initial treatment: before and including 2016 vs 2017-2023. Medical records and available histologic slides were reviewed.

Results: Forty-six patients were treated between 2009 and 2016, and 45 patients were treated between 2017 and 2023. Patient ages ranged from 1 to 85 years (median, 39 years), and most patients (70%) were women (2:2 men to women). Patients self-reported as Hispanic (49%), followed by White (28%), Black (20%), and Asian (3%). A subset (21%) had familial adenomatous polyposis (FAP)/Gardner syndrome. Individuals with intra-abdominal fibromatoses (37%) were more likely to have FAP than individuals with abdominal wall fibromatosis (4%) (P < .0001). The most common initial treatment before and during vs after 2016 was surgical excision (78% and 51% respectively; P = .02), followed by active surveillance with other medical intervention (9% and 18%, respectively; P = .28) and use of tyrosine kinase inhibitors (0% and 18%, respectively; P = .014). The rate of multivisceral transplant in patients with FAP/Gardner syndrome was 47% vs 4% in patients with sporadic disease (P < .001); most transplants (92%) were performed before and during 2016. The overall tumor recurrence/persistence rate in patients who had undergone surgery was 31%. The recurrence/persistence rate in patients treated before and during 2016 was 39% (median follow-up, 24 months), which fell to 13% (median follow-up, 18 months) in individuals treated after 2016 (P = .032). The overall recurrence/persistence rate in patients with FAP/Gardner syndrome was 64% vs 21% in patients with sporadic disease (P = .002). In patients with sporadic disease, there were recurrences in 29% of patients treated before and during 2016 and in 9% of patients treated thereafter (P = .086). Intra-abdominal vs abdominal wall lesions in patients with FAP and in patients with sporadic disease were more likely to recur (26% vs 10% and 16% vs 5%), but this occurrence did not reach statistical significance (P = .15). Most recurrent tumors were treated by surgical re-excision in both groups.

Conclusions: Our data suggest that a combination of less morbid surgical approaches and the addition of nonsurgical approaches (active disease surveillance, use of tyrosine kinase inhibitors and other interventions) have resulted in substantially fewer surgical interventions over time for intra-abdominal and abdominal wall fibromatoses treated between 2009 and 2023. The overall probability of recurrences, however, in patients treated surgically remains similar.

腹部和腹腔内纤维瘤病:随时间的结果。
目的:腹壁和腹内纤维瘤是一种局部侵袭性非转移性肿瘤。手术一直是局部控制的主要方法,但新的治疗方法可能会影响临床病程和发病率。我们研究了腹部和腹腔内纤维瘤患者的临床特征和预后。方法:选取2009 - 2023年我院收治的91例腹壁纤维瘤病患者46例,腹内纤维瘤病患者45例。患者根据初始治疗年份分为两组:2016年之前及包括2016年与2017-2023年。回顾了医疗记录和现有的组织学切片。结果:2009 - 2016年治疗46例,2017 - 2023年治疗45例。患者年龄从1岁到85岁不等(中位39岁),大多数患者(70%)为女性(男女比例为2:2)。患者自述为西班牙裔(49%),其次是白人(28%)、黑人(20%)和亚洲人(3%)。一个子集(21%)患有家族性腺瘤性息肉病(FAP)/Gardner综合征。腹内纤维瘤患者(37%)比腹壁纤维瘤患者(4%)更容易发生FAP (P)。我们的数据表明,在2009年至2023年期间,发病率较低的手术方法和非手术方法(主动疾病监测、使用酪氨酸激酶抑制剂和其他干预措施)相结合,导致腹内和腹壁纤维瘤的手术干预大大减少。然而,在手术治疗的患者中,复发的总体概率仍然相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
2.90%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The American Journal of Clinical Pathology (AJCP) is the official journal of the American Society for Clinical Pathology and the Academy of Clinical Laboratory Physicians and Scientists. It is a leading international journal for publication of articles concerning novel anatomic pathology and laboratory medicine observations on human disease. AJCP emphasizes articles that focus on the application of evolving technologies for the diagnosis and characterization of diseases and conditions, as well as those that have a direct link toward improving patient care.
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