Interim FDG-PET Scan in Hodgkin's Lymphoma: Hopes and Caveats
- PMID: 21234093
- PMCID: PMC3017950
- DOI: 10.1155/2011/430679
Interim FDG-PET Scan in Hodgkin's Lymphoma: Hopes and Caveats
Abstract
FDG-PET has recently emerged as an important tool for the management of Hodgkins lymphoma. Although its use for initial staging and response evaluation at the end of treatment is well established, the place of interim PET for response assessment and subsequent treatment tailoring is still quite controversial. The use of interim PET after a few cycles of chemotherapy may allow treatment reduction for good responders, leading to lesser treatment toxicities as well as early treatment adaptation for bad responders with a potential higher chance for cure. Interpretation of interim PET is a rapidly moving field. Actually, visual interpretation is preferred over quantitative interpretation in this situation. The notion of minimal residual uptake emerged for faint persisting FDG uptake, but has evolved during the recent years. Guidelines using mediastinum and liver as references have been proposed at the expert meeting in Deauville 2009. Actually, several trials are ongoing both for localised and advanced disease to evaluate the FDG-PET potential for early treatment monitoring and tailoring. Until the results of these prospective randomized trials become available, treatment changes according to the interim PET results should remain inappropriate and limited to well-conducted clinical trials.
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References
-
- Fermé C, Eghbali H, Meerwaldt JH, et al. Chemotherapy plus involved-field radiation in early-stage Hodgkin’s disease. New England Journal of Medicine. 2007;357(19):1916–1927. - PubMed
-
- Favier O, Heutte N, Stamatoullas-Bastard A, et al. Survival after Hodgkin lymphoma: causes of death and excess mortality in patients treated in 8 consecutive trials. Cancer. 2009;115:1680–1691. - PubMed
-
- Straus DJ, Portlock CS, Qin J, et al. Results of a prospective randomized clinical trial of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) followed by radiation therapy (RT) versus ABVD alone for stages I, II, and IIIA nonbulky Hodgkin disease. Blood. 2004;104(12):3483–3489. - PubMed
-
- Meyer RM, Gospodarowicz MK, Connors JM, et al. Randomized comparison of ABVD chemotherapywith a strategy that includes radiation therapy inpatients with limited-stage Hodgkin’s lymphoma: National Cancer Institute of Canada Clinical Trials Group and the Eastern Cooperative Oncology group. Journal of Clinical Oncology. 2005;23:4623–4642. - PubMed
-
- Eghbali H, Brice P, Cremers GY, et al. Comparison of three radiation dose levels after EBVP regimen in favorable supradiaphragmatic clinical stages (CS) I-II Hodgkin’s Lymphoma (HL): preliminary results of the EORTC-GELA H9-F trial. Blood. 2005;106, article 814
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