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Current Practices in Genetic Testing for Prostate Cancer: The Indian Scenario
被引:0
作者:
Bakshi, Ganesh
[1
]
Rajappa, Senthil
[2
]
Joshi, Amit
[3
]
Desai, Chirag
[4
]
Addla, Sanjai
[5
]
Baxi, Hemang
[6
]
Talwar, Vineet
[7
]
Mohapatra, Prabrajya Narayan
[8
]
Shingla, Shivam
[9
]
Kulkarni, Utkarsha
[10
]
机构:
[1] PD Hinduja Hosp & Med Res Ctr, Mumbai, Maharashtra, India
[2] Basavatarakam Indo Amer Canc Hosp & Res Inst, Hyderabad, Telangana, India
[3] Tata Mem Hosp, Mumbai, Maharashtra, India
[4] Hemato Oncol Clin, Ahmadabad, Gujarat, India
[5] Apollo Hosp, Apollo Hlth St,Jubilee Hills, Hyderabad 500096, Telangana, India
[6] HCG Canc Ctr, Ahmadabad, Gujarat, India
[7] Rajeev Gandhi Canc Inst & Res Ctr, Delhi, India
[8] Apollo Canc Ctr, Kolkata, West Bengal, India
[9] Nanavati Max Super Special Hosp, Mumbai, Maharashtra, India
[10] AstraZeneca Pharma India Ltd, Oncol, Bengaluru, Karnataka, India
关键词:
Genetic testing;
germline testing;
prostate cancer;
somatic tumor testing;
HOMOLOGOUS RECOMBINATION;
TUMOR-TISSUE;
RISK;
MUTATIONS;
MEN;
D O I:
10.4103/ijph.ijph_686_23
中图分类号:
R1 [预防医学、卫生学];
学科分类号:
1004 ;
120402 ;
摘要:
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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页码:396 / 400
页数:5
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