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γ相机扫描和预处理肿瘤体积作为Y-90抗CD20放射免疫治疗后反应和进展的预测指标。

Gamma camera scans and pretreatment tumor volumes as predictors of response and progression after Y-90 anti-CD20 radioimmunotherapy.

作者信息

Gokhale Abhay S, Mayadev Jyoti, Pohlman Brad, Macklis Roger M

机构信息

Department of Radiation Oncology, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2005 Sep 1;63(1):194-201. doi: 10.1016/j.ijrobp.2005.01.017.

Abstract

PURPOSE

To evaluate two potential approaches to predicting site-specific patterns of recurrence after yttrium-90 ibritumomab tiuxetan radioimmunotherapy (RIT) for CD20+ B-cell Non-Hodgkin's lymphoma. These predictive methods may be useful in evaluating the utility of local intensification of individual nodal or extranodal sites using external beam radiotherapy.

METHODS AND MATERIALS

Records and images were evaluated for 20 patients previously treated with yttrium-90 ibritumomab RIT. Intensity of isotope uptake on the pretreatment two-dimensional antibody scans and maximal extent of tumor deposits found on computed tomography images of each anatomic site were correlated with response and subsequent patterns of recurrence or progression.

RESULTS

Our data failed to suggest a significant correlation between the site-by-site two-dimensional image intensity on the pre-RIT scan and the likelihood of response at those sites. In contrast, an analysis of pretreatment target volumes did correlate significantly with progression. A collective analysis of disease sites from all 20 patients found that 83% (10/12) sites of "bulky" (maximal diameter > or = 5 cm) disease displayed evidence of progression vs. 28% (26/93) of "nonbulky" disease sites containing gross disease but no area measuring >5 cm (p < 0.001). All patients with at least one site of bulky disease had initial disease progression occur at a bulky site, with a bulky site being the sole first site of progression in approximately 50%. In patients with only nonbulky disease sites, approximately one third progressed initially at an entirely new site of disease.

CONCLUSION

We conclude that we can use tumor bulk to establish a statistical hierarchy of likely tumor progression sites and use this pattern to direct the use of additional external beam radiotherapy to augment treatment.

摘要

目的

评估两种预测钇-90替伊莫单抗放射免疫疗法(RIT)治疗CD20+B细胞非霍奇金淋巴瘤后特定部位复发模式的潜在方法。这些预测方法可能有助于评估使用外照射放疗对单个淋巴结或结外部位进行局部强化治疗的效用。

方法和材料

对20例先前接受钇-90替伊莫单抗RIT治疗的患者的记录和图像进行评估。预处理二维抗体扫描上的同位素摄取强度以及每个解剖部位的计算机断层扫描图像上发现的肿瘤沉积最大范围与反应及随后的复发或进展模式相关。

结果

我们的数据未能表明RIT扫描前逐部位二维图像强度与这些部位的反应可能性之间存在显著相关性。相比之下,对预处理靶体积的分析确实与进展显著相关。对所有20例患者的疾病部位进行综合分析发现,83%(10/12)“大肿块”(最大直径≥5 cm)疾病部位显示有进展迹象,而“非大肿块”疾病部位(包含大体疾病但无测量>5 cm区域)的这一比例为28%(26/93)(p<0.001)。所有至少有一个大肿块疾病部位的患者,初始疾病进展均发生在大肿块部位,约50%的患者大肿块部位是唯一的首个进展部位。在仅患有非大肿块疾病部位的患者中,约三分之一最初在全新的疾病部位进展。

结论

我们得出结论,可以利用肿瘤大小建立可能的肿瘤进展部位的统计层次结构,并利用这种模式指导使用额外的外照射放疗来加强治疗。

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