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Experiences of metastatic prostate cancer patients with a mainstream genetic testing pathway.

코호트 1/5 보강
International journal of cancer 📖 저널 OA 49.7% 2022: 0/3 OA 2023: 1/3 OA 2024: 6/16 OA 2025: 32/61 OA 2026: 131/241 OA 2022~2026 2026 Vol.158(4) p. 984-993
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
767 patients who received germline genetic testing, 5% to 8% experienced clinically significant anxiety or depression at some point in time.
I · Intervention 중재 / 시술
germline genetic testing, 5% to 8% experienced clinically significant anxiety or depression at some point in time
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Anxiety, depression, distress, decisional conflict regarding genetic testing, decision regret and knowledge of genetics were assessed.

Vlaming M, Bleiker EMA, Schijven G, Kiemeney LALM, van Melick HHE, Hunting JCB

📝 환자 설명용 한 줄

Patients with metastatic prostate cancer (mPCa) are eligible for germline genetic testing.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 연구 설계 cohort study

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↓ .bib ↓ .ris
APA Vlaming M, Bleiker EMA, et al. (2026). Experiences of metastatic prostate cancer patients with a mainstream genetic testing pathway.. International journal of cancer, 158(4), 984-993. https://doi.org/10.1002/ijc.70194
MLA Vlaming M, et al.. "Experiences of metastatic prostate cancer patients with a mainstream genetic testing pathway.." International journal of cancer, vol. 158, no. 4, 2026, pp. 984-993.
PMID 41078342 ↗
DOI 10.1002/ijc.70194

Abstract

Patients with metastatic prostate cancer (mPCa) are eligible for germline genetic testing. This study assessed the experiences of mPCa patients undergoing genetic testing after being counselled by non-genetic healthcare professionals (ngHCPs: urologists, oncologists, nurses). We assessed the psychosocial impact, decision-making difficulties and knowledge of genetics. In a prospective cohort study across 15 hospitals in the Netherlands, genetic testing was discussed and requested by ngHCPs. Patients completed questionnaires shortly after receiving pre-test genetic counselling and 4 weeks and 6 months after receiving their genetic test results. Anxiety, depression, distress, decisional conflict regarding genetic testing, decision regret and knowledge of genetics were assessed. Of 767 patients who received germline genetic testing, 5% to 8% experienced clinically significant anxiety or depression at some point in time. Although up to 49% of participants had significantly elevated distress scores as assessed with the Distress Thermometer, more than 90% stated that the testing process did not affect their feelings of distress. Patients with high educational levels had more favourable outcomes than patients with low educational levels on distress and decisional conflict (odds ratios 0.36 [0.23-0.57] and 0.44 [0.21-0.93], respectively). Furthermore, only 50% of the knowledge questions about genetics were answered correctly. To conclude, germline genetic testing within a mainstreaming pathway does not lead to increased levels of general anxiety or depression in most mPCa patients. However, the poorer outcomes on several psychosocial measures for patients with low educational levels are a point of concern.

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