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GOECP/SEOR 恶性胸膜间皮瘤放射治疗临床指南

GOECP/SEOR clinical guidelines on radiotherapy for malignant pleural mesothelioma.

作者信息

Luna Javier, Bobo Andrea, Cabrera-Rodriguez Joaquín José, Pagola María, Martín-Martín Margarita, Ruiz María Ángeles González, Montijano Miguel, Rodríguez Aurora, Pelari-Mici Lira, Corbacho Almudena, Moreno Marta, Couñago Felipe

机构信息

Department of Radiation Oncology, Institute of Oncohealth, Fundación Jiménez Díaz, Madrid 28040, Spain.

Department of Radiation Oncology, Institution of Ruber Internacional Hospital, Madrid 28034, Spain.

出版信息

World J Clin Oncol. 2021 Aug 24;12(8):581-608. doi: 10.5306/wjco.v12.i8.581.

DOI:10.5306/wjco.v12.i8.581
PMID:34513595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8394157/
Abstract

Malignant pleural mesothelioma (MPM) is a rare tumor with poor prognosis and rising incidence. Palliative care is common in MPM as radical treatment with curative intent is often not possible due to metastasis or extensive locoregional involvement. Numerous therapeutic advances have been made in recent years, including the use of less aggressive surgical techniques associated with lower morbidity and mortality (, pleurectomy/decortication), technological advancements in the field of radiotherapy (intensity-modulated radiotherapy, image-guided radiotherapy, stereotactic body radiotherapy, proton therapy), and developments in systemic therapies (chemotherapy and immunotherapy). These improvements have had as yet only a modest effect on local control and survival. Advances in the management of MPM and standardization of care are hampered by the evidence to date, limited by high heterogeneity among studies and small sample sizes. In this clinical guideline prepared by the oncological group for the study of lung cancer of the Spanish Society of Radiation Oncology, we review clinical, histologic, and therapeutic aspects of MPM, with a particular focus on all aspects relating to radiotherapy, including the current evidence base, associations with chemotherapy and surgery, treatment volumes and planning, technological advances, and reradiation.

摘要

恶性胸膜间皮瘤(MPM)是一种预后较差且发病率不断上升的罕见肿瘤。由于转移或广泛的局部区域受累,通常无法进行根治性治疗,因此姑息治疗在MPM中很常见。近年来取得了许多治疗进展,包括使用侵袭性较小、发病率和死亡率较低的手术技术(胸膜切除术/剥脱术)、放射治疗领域的技术进步(调强放射治疗、图像引导放射治疗、立体定向体部放射治疗、质子治疗)以及全身治疗(化疗和免疫治疗)的发展。这些改进迄今对局部控制和生存率的影响不大。MPM管理的进展和护理的标准化受到迄今为止证据的阻碍,这些证据受到研究之间高度异质性和小样本量的限制。在西班牙放射肿瘤学会肺癌研究肿瘤学组编写的本临床指南中,我们回顾了MPM的临床、组织学和治疗方面,特别关注与放射治疗相关的所有方面,包括当前的证据基础、与化疗和手术的联合、治疗体积和计划、技术进步以及再程放疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/71ac939be69a/WJCO-12-581-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/71ac939be69a/WJCO-12-581-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/8639175d9113/WJCO-12-581-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/1c8ec13d5ccc/WJCO-12-581-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/2bc27e8ef87f/WJCO-12-581-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8211/8394157/990d3fcdfc3b/WJCO-12-581-g004.jpg
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Int J Radiat Oncol Biol Phys. 2021 Apr 1;109(5):1368-1376. doi: 10.1016/j.ijrobp.2020.11.057. Epub 2020 Nov 28.
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Consensus Statement on Proton Therapy in Mesothelioma.
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