前列腺癌基因检测的当前做法:印度的情况。

IF 0.9 4区 医学 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Indian journal of public health Pub Date : 2024-07-01 Epub Date: 2024-09-24 DOI:10.4103/ijph.ijph_686_23
Ganesh Bakshi, Senthil Rajappa, Amit Joshi, Chirag Desai, Sanjai Addla, Hemang Baxi, Vineet Talwar, Prabrajya Narayan Mohapatra, Shivam Shingla, Utkarsha Kulkarni
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引用次数: 0

摘要

背景:尽管国际指南推荐在选择前列腺癌(PCa)靶向治疗时进行基因检测,但在印度,有关 PCa 基因检测的数据十分有限:目的:了解印度目前 PCa 基因检测的实践模式:由 9 位专家组成的小组编制并验证了一份会前在线问卷,其中包括 12 个客观问题。调查问卷于 2022 年 2 月至 2022 年 5 月在全印度的肿瘤内科医生和泌尿肿瘤科医生中分发,随后在 3 个月内收集答复。采用描述性统计方法对结果进行总结,并就目前 PCa 基因检测的实践模式得出结论:结果:共收到 103 份回复。结论:35.9%的参与者建议进行基因检测:我们发现,在全印度,HRR 基因基因检测的处方频率较低。提高基因检测的质量和可及性以及提供具有成本效益的靶向疗法将有助于为转移性 PCa 患者提供个性化治疗。
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Current Practices in Genetic Testing for Prostate Cancer: The Indian Scenario.

Background: Despite genetic testing being recommended by international guidelines for the selection of targeted therapy for prostate cancer (PCa), limited data are available on genetic testing for PCa in India.

Objectives: The objective is to understand the current genetic testing practice pattern for PCa in India.

Materials and methods: A panel of 9 experts developed and validated a premeeting online questionnaire comprising 12 objective questions. The questionnaire was circulated from February 2022 to May 2022 among medical oncologists and uro-oncologists across pan-India, followed by response collection over 3 months. Descriptive statistics were used to summarize results and concluding statements were formulated on current genetic testing practice patterns for PCa.

Results: A total of 103 responses were received. Genetic testing was advised by 35.9% of the participants in <5% of patients with PCa. Patients with a family history of PCa (88.3%) were most commonly referred for genetic testing. Nearly half (50.2%) of the participants routinely tested for homologous recombination repair (HRR) genes; 52% used blood and tissue as the most preferred specimen for performing genetic testing and 44.7% followed the testing sequence of tumor tissue followed by blood. Major barriers to genetic testing were affordability and scarcity of genetic counselors, while a major change could be brought by making it cost-effective and improving access to medication.

Conclusions: We observed a lower prescription frequency of genetic testing for the HRR gene across pan-India. Improving the quality and access to genetic testing and the availability of cost-effective-targeted therapies will aid in delivering personalized care to patients with metastatic PCa.

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来源期刊
Indian journal of public health
Indian journal of public health PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
2.40
自引率
0.00%
发文量
92
审稿时长
21 weeks
期刊介绍: Indian Journal of Public Health is a peer-reviewed international journal published Quarterly by the Indian Public Health Association. It is indexed / abstracted by the major international indexing systems like Index Medicus/MEDLINE, SCOPUS, PUBMED, etc. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles. The Indian Journal of Public Health publishes articles of authors from India and abroad with special emphasis on original research findings that are relevant for developing country perspectives including India. The journal considers publication of articles as original article, review article, special article, brief research article, CME / Education forum, commentary, letters to editor, case series reports, etc. The journal covers population based studies, impact assessment, monitoring and evaluation, systematic review, meta-analysis, clinic-social studies etc., related to any domain and discipline of public health, specially relevant to national priorities, including ethical and social issues. Articles aligned with national health issues and policy implications are prefered.
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