New England Journal of Medicine· 2014Q1
Dolaşımdaki Tümör Hücrelerinde AR-V7, Prostat Kanserinde Enzalutamid ve Abiraterona Direnci Öngörüyor
AR-V7 and Resistance to Enzalutamide and Abiraterone in Prostate Cancer
- 2.705atıf
- Q1SCImago
- 2014yıl
Kısa özet
Metastatik kastrasyona dirençli prostat kanseri (mKPDK) olan erkeklerin dolaşımdaki tümör hücrelerinde (DT H) AR-V7 mRNA saptanması, enzalutamid ve abiraterona karşı dirençle ilişkilidir.
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Ana noktalar
- Enzalutamid tedavisi alan hastaların %39'unda ve abirateron tedavisi alan hastaların %19'unda AR-V7 mRNA saptandı.
- Enzalutamid alan AR-V7 pozitif hastalarda PSA yanıt oranları %0 iken, AR-V7 negatif hastalarda %53 idi (P=0.004).
- Abirateron alan AR-V7 pozitif hastalarda PSA yanıt oranları %0 iken, AR-V7 negatif hastalarda %68 idi (P=0.004).
- AR-V7 pozitifliği, her iki ilaç için de anlamlı derecede daha kısa PSA progresyonsuz sağkalımı, klinik/radyografik progresyonsuz sağkalımı ve genel sağkalım ile ilişkilendirildi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: The androgen-receptor isoform encoded by splice variant 7 lacks the ligand-binding domain, which is the target of enzalutamide and abiraterone, but remains constitutively active as a transcription factor. We hypothesized that detection of androgen-receptor splice variant 7 messenger RNA (AR-V7) in circulating tumor cells from men with advanced prostate cancer would be associated with resistance to enzalutamide and abiraterone. METHODS: We used a quantitative reverse-transcriptase-polymerase-chain-reaction assay to evaluate AR-V7 in circulating tumor cells from prospectively enrolled patients with metastatic castration-resistant prostate cancer who were initiating treatment with either enzalutamide or abiraterone. We examined associations between AR-V7 status (positive vs. negative) and prostate-specific antigen (PSA) response rates (the primary end point), freedom from PSA progression (PSA progression-free survival), clinical or radiographic progression-free survival, and overall survival. RESULTS: A total of 31 enzalutamide-treated patients and 31 abiraterone-treated patients were enrolled, of whom 39% and 19%, respectively, had detectable AR-V7 in circulating tumor cells. Among men receiving enzalutamide, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 53%, P=0.004) and shorter PSA progression-free survival (median, 1.4 months vs. 6.0 months; P<0.001), clinical or radiographic progression-free survival (median, 2.1 months vs. 6.1 months; P<0.001), and overall survival (median, 5.5 months vs. not reached; P=0.002). Similarly, among men receiving abiraterone, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 68%, P=0.004) and shorter PSA progression-free survival (median, 1.3 months vs. not reached; P<0.001), clinical or radiographic progression-free survival (median, 2.3 months vs. not reached; P<0.001), and overall survival (median, 10.6 months vs. not reached, P=0.006). The association between AR-V7 detection and therapeutic resistance was maintained after adjustment for expression of full-length androgen receptor messenger RNA. CONCLUSIONS: Detection of AR-V7 in circulating tumor cells from patients with castration-resistant prostate cancer may be associated with resistance to enzalutamide and abiraterone. These findings require large-scale prospective validation. (Funded by the Prostate Cancer Foundation and others.).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2014 · DOI ↗
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