侵袭性纤维瘤病对他莫昔芬的反应:MRI与症状反应之间缺乏相关性。

Clinical Sarcoma Research Pub Date : 2018-05-14 eCollection Date: 2018-01-01 DOI:10.1186/s13569-018-0100-3
M Libertini, I Mitra, W T A van der Graaf, A B Miah, I Judson, R L Jones, K Thomas, E Moskovic, Z Szucs, C Benson, C Messiou
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引用次数: 29

摘要

背景:抗雌激素药物他莫昔芬是治疗侵袭性纤维瘤病常用的全身药物之一。然而,关于疗效和最佳反应评估方法的数据有限,主要由小病例系列和报告组成。方法:回顾性数据库用于识别2007年至2014年在三级转诊中心连续诊断为侵袭性纤维瘤病(AF)并使用他莫昔芬加/减非甾体抗炎药治疗的患者。记录MRI和症状变化。结果:纳入32例患者,其中男13例,女19例,中位年龄41岁。他莫昔芬治疗的中位持续时间为316天。在RECIST 1.1的9例进展性疾病患者中(28%):4例患者出现症状恶化;3例症状改善,2例症状无改变。22例病情稳定的患者中(69%):11例症状无变化;6例症状改善,5例症状加重。一名患者获得了部分缓解,症状有所改善。结论:在MRI上通过RECIST 1.1检查,没有发现症状获益和反应之间的关系。房颤的前瞻性研究应纳入关注患者症状的终点。
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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Aggressive fibromatosis response to tamoxifen: lack of correlation between MRI and symptomatic response.

Background: One of the commonly used systemic agents for the treatment of aggressive fibromatosis is the anti-oestrogen drug tamoxifen. However, data on efficacy and optimum methods of response assessment are limited, consisting mainly of small case series and reports.

Methods: A retrospective database was used to identify consecutive patients diagnosed with aggressive fibromatosis (AF) and treated with tamoxifen plus/minus non-steroidal anti-inflammatory drugs at our tertiary referral centre between 2007 and 2014. MRI and symptom changes were recorded.

Results: Thirty-two patients (13 male 19 female, median age 41 years) were included. Median duration of treatment with tamoxifen was 316 days. Of 9 patients with progressive disease by RECIST 1.1 (28%): 4 patients experienced worsening symptoms; 3 patients had improved symptoms and 2 had no change in symptoms. Of 22 patients with stable disease (69%): 11 had no change in symptoms; 6 had improved symptoms and 5 patients had worsening symptoms. One patient achieved a partial response with improved symptoms.

Conclusions: No relationship was identified between symptomatic benefit and response by RECIST 1.1 on MRI. Prospective studies in AF should incorporate endpoints focusing on patient symptoms.

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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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