Terasawa Teruhiko, Lau Joseph, Bardet Stéphane, Couturier Olivier, Hotta Tomomitsu, Hutchings Martin, Nihashi Takashi, Nagai Hirokazu
Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA 02111, USA.
J Clin Oncol. 2009 Apr 10;27(11):1906-14. doi: 10.1200/JCO.2008.16.0861. Epub 2009 Mar 9.
To systematically review the prognostic accuracy of fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) for interim response assessment of patients with untreated advanced-stage Hodgkin's lymphoma (HL) or diffuse large B-cell lymphoma (DLBCL).
MEDLINE, EMBASE, SCOPUS, and Biologic Abstracts were searched for relevant studies. Two assessors independently reviewed studies for inclusion and extracted data. Relevant unpublished data were requested from the investigators if unavailable from publications. A meta-analysis of the prognostic accuracy was performed.
Thirteen studies involving 360 advanced-stage HL patients and 311 DLBCL patients met our inclusion criteria. Advanced-stage HL studies included few unfavorable-risk patients. DLBCL studies were heterogeneous. FDG-PET had an overall sensitivity of 0.81 (95% CI, 0.72 to 0.89) and a specificity of 0.97 (95% CI, 0.94 to 0.99) for advanced-stage HL, and a sensitivity of 0.78 (95% CI, 0.64 to 0.87) and a specificity of 0.87 (95% CI, 0.75 to 0.93) for DLBCL. Meta-regression and subgroup analyses did not identify factors that affect prognostic accuracy.
For low- to intermediate-risk advanced-stage HL, FDG-PET performed after a few cycles of standard chemotherapy seems to be a reliable prognostic test to identify poor responders, warranting prospective studies to assess PET-based treatment strategies. For DLBCL, no reliable conclusions can be drawn due to heterogeneity. Interim PET remains an unproven test for routine clinical practice. Its use should be reserved for research settings where treatment regimens and imaging conditions are standardized.
系统评价氟-18-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)用于未经治疗的晚期霍奇金淋巴瘤(HL)或弥漫性大B细胞淋巴瘤(DLBCL)患者中期反应评估的预后准确性。
检索MEDLINE、EMBASE、SCOPUS和生物学文摘数据库中的相关研究。两名评估者独立审查研究以确定是否纳入并提取数据。若出版物中没有相关未发表数据,则向研究者索取。对预后准确性进行荟萃分析。
13项研究纳入了360例晚期HL患者和311例DLBCL患者,符合我们的纳入标准。晚期HL研究中低风险患者较少。DLBCL研究具有异质性。FDG-PET对晚期HL的总体敏感性为0.81(95%CI,0.72至0.89),特异性为0.97(95%CI,0.94至0.99);对DLBCL的敏感性为0.78(95%CI,0.64至0.87),特异性为0.87(95%CI,0.75至0.93)。荟萃回归和亚组分析未发现影响预后准确性的因素。
对于低至中度风险的晚期HL,在几个周期的标准化化疗后进行FDG-PET似乎是一种可靠的预后检测方法,可识别反应较差的患者,需要进行前瞻性研究以评估基于PET的治疗策略。对于DLBCL,由于异质性无法得出可靠结论。中期PET在常规临床实践中仍是未经证实的检测方法。其应用应仅限于治疗方案和成像条件标准化的研究环境。