Strikingly high false positivity of surveillance FDG‐PET/CT scanning among patients with diffuse large cell lymphoma in the rituximab era

Predictive value (PV) of surveillance fluorodeoxyglucose positron emission tomography (FDG‐PET) in patients with diffuse large B‐cell lymphoma (DLBCL) treated with chemotherapy‐rituximab (R) versus chemotherapy only, remains unclear. The aim of the current study was to compare the performance of sur...

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Published inAmerican journal of hematology Vol. 88; no. 5; pp. 400 - 405
Main Authors Avivi, Irit, Zilberlicht, Ariel, Dann, Eldad J., Leiba, Ronit, Faibish, Tal, Rowe, Jacob M., Bar‐Shalom, Rachel
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.05.2013
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Summary:Predictive value (PV) of surveillance fluorodeoxyglucose positron emission tomography (FDG‐PET) in patients with diffuse large B‐cell lymphoma (DLBCL) treated with chemotherapy‐rituximab (R) versus chemotherapy only, remains unclear. The aim of the current study was to compare the performance of surveillance PET in DLBCL patients receiving CHOP (cyclophosphamide, hydroxydaunorubicin hydrochloride, vincristine, and prednisone) alone versus CHOP‐R. Institutional database was retrospectively searched for adults with newly diagnosed DLBCL, receiving CHOP or CHOP‐R, who achieved complete remission and underwent surveillance PETs. Follow‐up (FU) PET was considered positive for recurrence in case of an uptake unrelated to physiological or known benign process. Results were confirmed by biopsy, imaging and clinical FU. One hundred nineteen patients, 35 receiving CHOP and 84 CHOP‐R, who underwent 422 FU‐PETs, were analyzed. At a median PET‐FU of 3.4 years, 31 patients relapsed (17 vs. 14, respectively; P = 0.02). PET detected all relapses, with no false‐negative studies. Specificity and positive PV (PPV) were significantly lower for patients receiving CHOP‐R vs. CHOP (84% vs. 87%, P = 0.023; 23% vs. 74%, P < 0.0001), reflecting a higher false‐positive (FP) rate in subjects receiving CHOP‐R (77% vs. 26%, P < 0.001). In the latter group, FP‐rate remained persistently high up to 3 years post‐therapy. Multivariate analysis confirmed rituximab to be the most significant predictor for FP‐PET. In conclusion, routine surveillance FDG‐PET is not recommended in DLBCL treated with rituximab; strict criteria identifying patients in whom FU‐PET is beneficial are required. Am. J. Hematol. 88:400–405, 2013. © 2013 Wiley Periodicals, Inc.
Bibliography:I.A. and A.Z. contributed equally to this work.
I.A. was the principal investigator, wrote the article and takes primary responsibility for the article. A.Z. performed research, analyzed data. E.J.D. performed research. R.L. analyzed data. T.F. performed research. J.M.R. wrote the paper. R.B.S. designed and performed research, analyzed data, wrote the article.
The authors report no potential conflicts of interest.
ObjectType-Article-1
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content type line 23
ISSN:0361-8609
1096-8652
DOI:10.1002/ajh.23423