首页> 外文期刊>European Journal of Nuclear Medicine and Molecular Imaging >Utility of FMISO PET in advanced head and neck cancer treated with chemoradiation incorporating a hypoxia-targeting chemotherapy agent.
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Utility of FMISO PET in advanced head and neck cancer treated with chemoradiation incorporating a hypoxia-targeting chemotherapy agent.

机译:FMISO PET在掺有低氧靶向化疗剂的化学放射治疗的晚期头颈癌中的效用。

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PURPOSE: The purpose of the study was to evaluate [(18)F]fluoromisonidazole (FMISO) PET in advanced head and neck cancer during hypoxia-targeting therapy. METHODS: Fifteen of 16 patients in a phase I trial of chemoradiation plus tirapazamine (specific cytotoxin for hypoxic cells) in advanced (T3/4 and/or N2/3) head and neck cancer underwent serial [(18)F]fluorodeoxyglucose (FDG) and FMISO PET. We have previously reported excellent early clinical outcome of these patients and now review FMISO PET results in the context of longer follow-up of this patient cohort. RESULTS: Based on blinded qualitative scoring by two readers, FMISO PET was positive in 13/15 patients at baseline: 12/15 of primary sites and 8/13 neck nodes were scored as positive. All sites of corresponding FDG and FMISO abnormality at baseline showed marked qualitative reduction of uptake within 4 weeks of commencing therapy, consistent with effective hypoxia-targeted therapy. With a median follow-up of 6.9 years, there have been only four locoregional failures, while three other patients have died of metachronous lung cancer. The 5-year overall survival was 50% (95% CI 27-73%), the 5-year failure-free survival was 44% (95% CI 22-68%) and the 5-year freedom from locoregional failure was 68% (95% CI 38-88%). CONCLUSION: The high prevalence of hypoxia demonstrated on FMISO PET imaging is consistent with the advanced disease stage of these patients and would be expected to predict an adverse prognosis. Evidence of the early resolution of FMISO abnormality during treatment, associated with excellent locoregional control in this patient cohort, supports further investigation of hypoxia-targeting agents in advanced head and neck cancer.
机译:目的:本研究的目的是评估在低氧靶向治疗期间晚期头颈癌中的[(18)F]氟代咪唑(FMISO)PET。方法:在放化疗加替拉帕明(低氧细胞特异性细胞毒素)的I期临床试验的16例患者中,有15例在晚期(T3 / 4和/或N2 / 3)头颈癌患者中接受了连续的[(18F)]氟脱氧葡萄糖(FDG)治疗)和FMISO PET。我们先前已经报道了这些患者的出色的早期临床结果,现在在对该患者队列进行更长时间随访的情况下回顾了FMISO PET结果。结果:根据两名读者的盲定性评分,在基线时FMISO PET在13/15患者中为阳性:原发部位的12/15和8/13颈部结点为阳性。在开始治疗的4周内,所有与之对应的FDG和FMISO异常的部位均显示出明显的定性摄取,与有效的低氧靶向治疗相一致。中位随访时间为6.9年,仅发生了4个局部区域衰竭,而其他3例患者则因异时性肺癌死亡。 5年总生存率为50%(95%CI 27-73%),5年无衰竭生存率为44%(95%CI 22-68%),5年无局部衰竭的自由度为68 %(95%CI 38-88%)。结论:FMISO PET成像显示低氧流行率高,与这些患者的疾病晚期相符,有望预示不良预后。在该患者队列中,治疗期间FMISO异常的早期解决与出色的局部区域控制相关的证据支持进一步研究低氧靶向药物在晚期头颈癌中的作用。

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