首页> 外文期刊>Cancer: A Journal of the American Cancer Society >High rates of tumor growth and disease progression detected on serial pretreatment fluorodeoxyglucose-positron emission tomography/computed tomography scans in radical radiotherapy candidates with nonsmall cell lung cancer.
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High rates of tumor growth and disease progression detected on serial pretreatment fluorodeoxyglucose-positron emission tomography/computed tomography scans in radical radiotherapy candidates with nonsmall cell lung cancer.

机译:在非小细胞肺癌的放疗候选者中进行系列预处理氟脱氧葡萄糖-正电子发射断层显像/计算机断层显像扫描可检测到较高的肿瘤生长和疾病进展。

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BACKGROUND: The authors studied growth and progression of untreated nonsmall cell lung cancer (NSCLC) by comparing diagnostic and radiotherapy (RT) planning fluorodeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT) scans before proposed radical chemo-RT. METHODS: Patients enrolled on a prospective clinical trial were eligible for this analysis if they underwent 2 pretreatment whole body FDG-PET/CT scans, >7 days apart. Scan 1 was performed for diagnosis/disease staging and scan 2 for RT planning. Interscan comparisons included disease stage, metabolic characteristics, tumor doubling times, and change in treatment intent. RESULTS: Eighty-two patients underwent planning PET/CT scans between October 2004 and February 2007. Of these, 28 patients (61% stage III, 18% stage II) had undergone prior staging PET/CT scans. The median interscan period was 24 days (range, 8-176 days). Interscan disease progression (TNM stage) was detected in 11 (39%) patients. The probability of upstaging within 24 days was calculated to be 32% (95% confidence interval [CI], 18%-49%). Treatment intent changed from curative to palliative in 8 (29%) cases, in 7 because of PET. For 17 patients who underwent serial PET/CT scans under standardized conditions, there was a mean relative interscan increase of 19% in tumor maximum standardized uptake value (SUV) (P=.022), 16% in average SUV (P=.004), and 116% in percentage injected dose (P=.002). Estimated doubling time of FDG avid tumor was 66 days (95% CI, 51-95 days). CONCLUSIONS: Rapid tumor progression was detected in patients with untreated, predominantly stage III, NSCLC on serial FDG-PET/CT imaging, highlighting the need for prompt diagnosis, staging, and initiation of therapy in patients who are candidates for potentially curative therapy.
机译:背景:作者通过比较计划进行的根治性化学放疗前的诊断和放疗(RT)计划的氟脱氧葡萄糖(FDG)-正电子发射断层扫描(PET)/计算机断层扫描(CT)扫描,研究了未经治疗的非小细胞肺癌(NSCLC)的生长和进展。 。方法:如果参加一项前瞻性临床试验的患者接受了两次治疗前的全身FDG-PET / CT扫描(相隔> 7天),则有资格进行此分析。扫描1用于诊断/疾病分期,扫描2用于RT计划。扫描间比较包括疾病阶段,代谢特征,肿瘤倍增时间和治疗意图的改变。结果:2004年10月至2007年2月,有82例患者进行了计划的PET / CT扫描。其中,有28例患者(III期为61%,II期为18%)已经接受过分期PET / CT扫描。中间扫描期间为24天(范围8-176天)。在11名(39%)患者中检测到Interscan疾病进展(TNM分期)。 24天之内升级的可能性为32%(95%置信区间[CI],18%-49%)。 8例(29%)患者因PET的治疗意图从治愈变为姑息。对于在标准条件下进行连续PET / CT扫描的17例患者,平均最大相对摄取值(SUV)平均相对扫描间增加19%(P = .022),平均SUV平均16%(P = .004) )和116%的注射剂量(P = .002)。 FDG狂热肿瘤的估计倍增时间为66天(95%CI,51-95天)。结论:在连续FDG-PET / CT成像中,未经治疗的,主要为III期,NSCLC的患者被检测出肿瘤的快速进展,这突出表明有可能进行潜在治疗的患者需要迅速诊断,分期和开始治疗。

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