期刊文献+

^18氟-脱氧葡萄糖PET在儿童恶性淋巴瘤分期、疗效评估及随诊中的意义

Role of ^18F-FDG-PET in diagnosis and treatment of lymphoma in children
原文传递
导出
摘要 目的探讨^18氟-脱氧葡萄糖(^18F—FDG)正电子发射断层显像(PET)在儿童恶性淋巴瘤分期、疗效评估及随诊中的意义。方法回顾性分析88例儿童恶性淋巴瘤初诊时、化疗中期及停药后随诊过程中^18F—FDG—PET扫描结果,并与同期的CT扫描相比较。结果67例初诊儿童淋巴瘤患者,化疗前共评估了1072个解剖部位,PET和CT均提示瘤灶阳性及阴性部位分别为11.10%和77.52%,PET阳性CT阴性的部位占6.81%,而PET阴性CT阳性的占4.57%,PET在化疗前受累部位的诊断方面优于CT扫描。对26例随诊患者,在治疗中期、停药时及停药后进行了35次PET检查,32例次患儿瘤灶为阴性,PET扫描瘤灶真阴性为28例次(真阴性率为87.50%),CT为16例次(真阴性率为57.14%),在假阳性方面,CT比较高,为16例次(假阳性率为50.00%),而PET仅为4例次(假阳性率为12.50%),临床吻合度PET大于CT。结论PET对于儿童恶性淋巴瘤的临床分期、鉴别残余病灶的性质以避免不必要的过度治疗或二次活检,以及发现肿瘤的早期复发具有一定的意义。 Objective To investigate the value of Fluorine-18 fluorodeoxyglucose positron emission tomography (^18F-FDG-PET) in staging and detecting residual disease during follow-up of non-Hodgkin's lymphoma in children. Methods The results of lSF-FDG-PET of 88 pediatric NHL before and after chemotherapy was analyzed respectively. The results were compared with CT scans simuhaneously. Results 67 cases were performed for initial staging. Of the 1072 anatomy regions were analyzed by PET and CT with concordance of 88.62 % regions (positive in 11.10 % and negative in 77.52 %). Disconcordance were found in 11.38 % regions (PET positive but CT negative in 6.81%, PET negative but CT positive in 4.57 %). PET was significantly better than CT scan in the staging of pediatric NHL. 35 scans were performed in the follow-up. The true residual disease positive rate of PET and CT were 87.50 % and 57.14 % respectively. The false positive rate of PET and CT were 12.50 % and 50.00 % respectively. Conclusion ISF-FDG-PET imaging is of great value for the staging of the pediatric patients with NHL. It's a useful technique to identify the residual disease, avoid unnecessary treatment and biopsy and can predict early relapse.
出处 《白血病.淋巴瘤》 CAS 2009年第12期746-749,共4页 Journal of Leukemia & Lymphoma
基金 北京市卫生局首都医学发展科研基金(2007-1030)
关键词 氟脱氧葡萄糖F^18 正电子发射断层显像术 淋巴瘤 儿童 治疗结果 Fluorodeoxyglucose FIS Positron-Emission tomography Lymphoma Child Treatment outcome
  • 相关文献

参考文献11

  • 1张永红 段彦龙 杨菁 等.儿童伯基特淋巴瘤疗效分析[J].中华儿科学杂志,2008,46:209-214.
  • 2Juweid ME.^18F-FDG PET as a routine test for posttherapy assessment of Hodgkin's disease and aggressive non-Hodgkin's lymphoma: where is the evidence? J Nucl Med, 2008, 49: 9-12.
  • 3Terasawa T, Lau J, Bardet S, et al. Fluorine-18-fluorodeoxyglucose positron emission tomography for interim response assessment of advanced-stage Hodgkin's lymphoma and diffuse large B-cell lymphoma: a systematic review. J Clin Oncol, 2009, 27: 1906-1914.
  • 4张蕊.儿童非霍奇金淋巴瘤的残留病监测[J].中国小儿血液与肿瘤杂志,2009,14(1):8-11. 被引量:2
  • 5Hemandez-Pampaloni M, Takalkar A, Yu JQ, et al. F-18 FDG-PET imaging and correlation with CT in staging and follow-up of pediatric lymphomas. Pediatr Radiol, 2006, 36:524-531.
  • 6Zijlstra JM, Lindauer-van der Weft G, Hoekstra OS, et al. lSF- Fluorine-fluoro-deoxyglucose positron emission tomography for post-treatment evaluation of malignant lymphoma: a systematic review. Haematologica, 2006, 91: 522-529.
  • 7Juweid ME, Stroobants S, Hoekstra OS, et al. Use of positron emission tomography for response assessment of lymphoma: consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma. J Clin Oncol, 2007, 25: 571-578.
  • 8Cheson BD, Pfistner B, Juweid ME, et al. Revised response criteria for malignant lymphoma. J Clin Oncol, 2007, 25: 579-586.
  • 9Brepoels L, Stroobants S. Is [(18)F]fluorodeoxyglucose positron emission tomography the ultimate tool for response and prognosis assessment?. Hematol Oncol Clin North Am, 2007, 21: 855-869.
  • 10Terasawa T, Nihashi T, Hotta T, et al. 18F-FDG PET for posttberapy assessment of Hodgkin's disease and aggressive Non-Hodgkin's lymphoma: a systematic review. J Nucl Med, 2008, 49: 13-21.

二级参考文献26

  • 1.临床病历讨论.肝硬化伴双下肢运动障碍[N].中国医学论坛报,2003.10.30.
  • 2Cheson BD, Pfistner B, Juweid ME, et al. Revised response criteria for malignant lymphoma. J Clin Oncol, 2007;25:579-586.
  • 3Zijlstra JM, Lindauer-van der Weft G, Hoekstra OS, et al. 18F- Fluorine-fluoro-deoxyglucose positron emission tomography for post-treatment evaluation of malignant lymphoma: a systematic review. Haematologica, 2006 ;91:522-529..
  • 4Terasawa T, Nihashi T, Hotta T, et al. 18F-FDG PET for posttherapy assessment of Hodgkin' s disease and aggressive Non-Hodgkin' s lymphoma: a systematic review. J Nucl Med, 2008 Jan;49 (1): 13-21.
  • 5Busch K, Keller T, Fuchs U etd. Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t ( 8 ; 14 ) translocations in sporadic Burkitt-lymphoma. Leukemia, 2007,21 (8) : 1739-1751.
  • 6Staber PB, Vesely P, Haq N et al. The oncoprotein NPM-ALK of anaplastic large cell lymphoma induces JUNB transcription via ERK1/2 and JunB translation via mTOR signaling. Blood, 2007, (Epub ahead of print).
  • 7Amin HM and Lai R. Pathobiology of ALK + anaplastic large-cell lymphoma. Blood, 2007, [ Epub ahead of print).
  • 8Dunleavy K, Davis RE, Landgren O et al. BCL-6 and rituximab in diffuse large B-cell lymphoma: where are we?. Blood, 2007,109 (2) :843-844.
  • 9Dunleavy K, Staudt LM and Wilson WH. The BCL-2 biomarker in the era of molecular diagnosis of diffuse large B-cell lymphoma. Leuk Lymphoma, 2007,48(6) : 1061 - 1063.
  • 10Dolken G, Detection of minimal residual disease. Adv Cancer Res, 2001 ;82 : 133-85.

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部