Choi Haesun
Department of Radiology, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Curr Oncol Rep. 2005 Jul;7(4):307-11. doi: 10.1007/s11912-005-0055-4.
Imaging technology plays a major role in treatment response assessment in solid tumors and in surveillance for recurrence or progression. Currently available response evaluation criteria, Response Evaluation Criteria in Solid Tumors (RECIST), are based on unidimensional tumor size. Recently, however, these strictly size-based criteria for evaluating responses have been criticized because they do not reflect the biologic changes of solid tumors induced by targeted therapies and thus may be misleading. This problem is evident in response evaluation in advanced gastrointestinal stromal tumor (GIST) treated with a new molecularly targeted agent, imatinib. GISTs can increase in size despite good response to imatinib, and focal progression within a responding GIST can be overlooked with current size-based imaging criteria. Modified objective criteria using a combination of tumor size and density on CT are promising in early response evaluation and in predicting long-term prognosis in patients with advanced GIST treated with imatinib. These criteria may have broad applicability as additional targeted therapies become available to treat solid tumors.
成像技术在实体瘤治疗反应评估以及复发或进展监测中发挥着重要作用。目前可用的反应评估标准,即实体瘤反应评估标准(RECIST),是基于肿瘤的一维大小。然而,最近这些严格基于大小的反应评估标准受到了批评,因为它们没有反映出靶向治疗引起的实体瘤生物学变化,因此可能会产生误导。这个问题在使用新型分子靶向药物伊马替尼治疗的晚期胃肠道间质瘤(GIST)的反应评估中很明显。尽管对伊马替尼反应良好,但GIST的大小仍可能增加,并且根据当前基于大小的成像标准,反应性GIST内的局灶性进展可能会被忽视。使用CT上肿瘤大小和密度相结合的改良客观标准在伊马替尼治疗的晚期GIST患者的早期反应评估和长期预后预测方面很有前景。随着更多靶向治疗药物可用于治疗实体瘤,这些标准可能具有广泛的适用性。