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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Stereotactic body radiotherapy (SBRT) can delay polymetastatic conversion in patients affected by liver oligometastases
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Stereotactic body radiotherapy (SBRT) can delay polymetastatic conversion in patients affected by liver oligometastases

机译:立体定向体放射疗法(SBRT)可以延迟受肝脏脱极酶影响的患者的多塑类转化

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Purpose SBRT demonstrated to increase survival in oligometastatic patients. Nevertheless, little is known regarding the natural history of oligometastatic disease (OMD) and how SBRT may impact the transition to the polymetastatic disease (PMD). Methods 97 liver metastases in 61 oligometastatic patients were treated with SBRT. Twenty patients (33%) had synchronous oligometastases, 41 (67%) presented with metachronous oligometastases. Median number of treated metastases was 2 (range 1-5). Results Median follow-up was 24 months. Median tPMC was 11 months (range 4-17 months). Median overall survival (OS) was 23 months (range 16-29 months). Cancer-specific survival predictive factors were having further OMD after SBRT (21 months versus 15 months; p = 0.00), and local control of treated metastases (27 months versus 18 months; p = 0.031). Median PFS was 7 months (range 4-12 months). Patients with 1 metastasis had longer median PFS as compared to those with 2-3 and 4-5 metastases (14.7 months versus 5.3 months versus 6.5 months; p = 0.041). At the last follow-up, 50/61 patients (82%) progressed, 16 of which (26.6%) again as oligometastatic and 34 (56%) as polymetastatic. Conclusion In the setting of oligometastatic disease, SBRT is able to delay the transition to the PMD. A proportion of patients relapse as oligometastatic and can be eventually evaluated for a further SBRT course. Interestingly, those patients retain a survival benefit as compared to those who had PMD. Further studies are needed to explore the role of SBRT in OMD and to identify treatment strategies able to maintain the oligometastatic state.
机译:目的证明SBRT可提高少转移患者的生存率。然而,关于少转移性疾病(OMD)的自然史以及SBRT如何影响向多转移性疾病(PMD)的转变,我们知之甚少。方法对61例少转移性肝癌患者的97例肝转移瘤进行SBRT治疗。20名患者(33%)出现同步性少转移,41名患者(67%)出现异时性少转移。治疗转移瘤的中位数为2(范围1-5)。结果平均随访24个月。tPMC中位数为11个月(范围4-17个月)。中位总生存期(OS)为23个月(范围16-29个月)。肿瘤特异性生存预测因素包括SBRT后的进一步OMD(21个月对15个月;p=0.00)和治疗转移的局部控制(27个月对18个月;p=0.031)。中位PFS为7个月(范围4-12个月)。与2-3和4-5转移患者相比,1转移患者的中位PFS更长(14.7个月对5.3个月对6.5个月;p=0.041)。在最后一次随访中,50/61患者(82%)进展,其中16例(26.6%)再次为少转移,34例(56%)为多转移。结论在少转移性疾病的情况下,SBRT可以延迟向PMD的转移。一部分患者复发为少转移,最终可接受进一步SBRT治疗。有趣的是,与患有PMD的患者相比,这些患者的生存率有所提高。需要进一步的研究来探索SBRT在OMD中的作用,并确定能够维持低转移状态的治疗策略。

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