Quality Assurance in Radiotherapy (RT)-Specific Trials: Indian Scenario

IF 3 3区 医学 Q2 ONCOLOGY Clinical oncology Pub Date : 2025-02-01 Epub Date: 2024-06-01 DOI:10.1016/j.clon.2024.05.016
A. Mahata, S. Chakraborty, S. Mandal, R.B. Achari, T. Bhattacharyya, I. Mallick, M. Arunsingh, S. Chatterjee
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Abstract

Aims

There is evidence that proper radiotherapy trial quality assurance (RTTQA) translates into improved outcomes for patients. However, the practice of RTTQA is heterogeneous and implemented in a diverse manner across trials. In this paper, we review the RTTQA report for randomised trials (RCT) conducted in India and present our experience with RTTQA for various clinical trials and highlight the key achievements and challenges.

Materials and methods

Search was performed using the keywords and the variations thereof for “radiotherapy” and author affiliations from India, its states and major metropolitan cities. Pubmed search filters were used to restrict results to RCT published in the past 5 years (2019–2024). Reporting of RTTQA procedures from publications and protocols was documented along with the protocol-specified dosimetric goals. We also evaluated a few clinical trials performed in the Department of Radiation Oncology at Tata Medical Center. The different RTTQA procedures and results for four representative clinical trials have been described.

Results

A formal RTTQA process was reported by only one out of 24 randomised controlled trials and formal dosimetric goals were pre-specified by 9 of 13 trials where IMRT was used as treatment. RTTQA requirements were tailored for each clinical trial at Tata Medical Center. For the HYPORT trial, the RTTQA process focused on ensuring the matchline doses were homogenous. HYPORT B trial commissioned the use of a simultaneous integrated boost technique which emphasised conformal avoidance of dose spillage to contralateral breast and lung. HYPORT Adjuvant and PROPARA trials are multicentre clinical trials. While HYPORT Adjuvant focussed on ensuring that the dose delivery met the predefined constraints, segmentation of the target volume was important for the PROPARA trial.

Conclusion

We demonstrate different RTTQA procedures required for representative clinical trials and highlight key challenges encountered.
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RT 专项试验的质量保证:印度的情况
目的有证据表明,适当的放疗试验质量保证(RTTQA)可以改善患者的预后。然而,RTTQA的实践是异构的,并且在不同的试验中以不同的方式实现。在本文中,我们回顾了在印度进行的随机试验(RCT)的RTTQA报告,并介绍了我们在各种临床试验中使用RTTQA的经验,并强调了主要成就和挑战。材料和方法使用“放射治疗”的关键词及其变体,以及来自印度、印度各邦和主要大都市的作者所属单位进行搜索。使用Pubmed搜索过滤器将结果限制为过去5年(2019-2024年)发表的RCT。出版物和方案中的RTTQA程序报告连同方案规定的剂量学目标一起被记录下来。我们还评估了在塔塔医疗中心放射肿瘤科进行的一些临床试验。描述了四个代表性临床试验的不同RTTQA程序和结果。结果24个随机对照试验中只有1个报告了正式的RTTQA过程,13个使用IMRT治疗的试验中有9个预先规定了正式的剂量学目标。RTTQA要求是为塔塔医疗中心的每个临床试验量身定制的。对于HYPORT试验,RTTQA过程侧重于确保匹配剂量是均匀的。HYPORT B试验委托使用同时集成的增强技术,强调适形避免剂量溢出到对侧乳房和肺部。HYPORT佐剂和PROPARA试验是多中心临床试验。虽然HYPORT佐剂的重点是确保剂量递送符合预定义的限制,但对于PROPARA试验来说,靶体积的分割很重要。我们展示了代表性临床试验所需的不同RTTQA程序,并强调了遇到的关键挑战。
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来源期刊
Clinical oncology
Clinical oncology 医学-肿瘤学
CiteScore
5.20
自引率
8.80%
发文量
332
审稿时长
40 days
期刊介绍: Clinical Oncology is an International cancer journal covering all aspects of the clinical management of cancer patients, reflecting a multidisciplinary approach to therapy. Papers, editorials and reviews are published on all types of malignant disease embracing, pathology, diagnosis and treatment, including radiotherapy, chemotherapy, surgery, combined modality treatment and palliative care. Research and review papers covering epidemiology, radiobiology, radiation physics, tumour biology, and immunology are also published, together with letters to the editor, case reports and book reviews.
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