Please use this identifier to cite or link to this item:
https://hdl.handle.net/1/1240
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DC Field | Value | Language |
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dc.contributor.author | Forsyth, Cecily J | en |
dc.contributor.author | Trotman, J. | en |
dc.contributor.author | Fournier, M | en |
dc.contributor.author | Lamy, T. | en |
dc.contributor.author | Seymour, J.F. | en |
dc.contributor.author | Sonet, A. | en |
dc.contributor.author | Janikova, A. | en |
dc.contributor.author | Shpilberg, O. | en |
dc.contributor.author | Gyan, E. | en |
dc.contributor.author | Tilly, H. | en |
dc.contributor.author | Estell, J. | en |
dc.contributor.author | Decaudin, D. | en |
dc.contributor.author | Fabiani, B. | en |
dc.contributor.author | Gabarre, J. | en |
dc.contributor.author | Salles, B. | en |
dc.contributor.author | Van Den Neste, E. | en |
dc.contributor.author | Canioni, D. | en |
dc.contributor.author | Garin, E. | en |
dc.contributor.author | Fulham, M. | en |
dc.contributor.author | Vander Borght, T. | en |
dc.contributor.author | Salles, G. | en |
dc.date.accessioned | 2018-12-14T02:10:46Z | en |
dc.date.available | 2018-12-14T02:10:46Z | en |
dc.date.issued | 2011-08 | en |
dc.identifier.citation | Volume 29, Issue 23, pp. 3194 - 3200 | en |
dc.identifier.issn | 0732-183x | en |
dc.identifier.uri | https://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/1240 | en |
dc.description.abstract | PURPOSE: The utility of [(18)F]fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) in assessing response at the end of induction therapy is well documented in Hodgkin's and diffuse large B-cell lymphomas, but its role in follicular lymphoma (FL) remains undetermined. We investigated the prognostic significance of PET-CT performed after first-line therapy in patients with FL treated in the prospective Primary Rituximab and Maintenance (PRIMA) study. PATIENTS AND METHODS: Results of PET-CT scans performed after induction immunochemotherapy were recorded retrospectively. Patients went on to either observation or rituximab maintenance per protocol independent of the PET-CT result. Patient characteristics and outcomes were then evaluated. RESULTS: Of 122 PET-CT scans performed at the end of the induction immunochemotherapy, 32 (26%) were reported as positive by the local investigator. Initial demographic or disease characteristics did not differ between PET-CT-positive (PET-positive) and PET-CT-negative (PET-negative) patients. PET status correlated with conventional response criteria (P < .001). Patients remaining PET positive had a significantly (P < .001) inferior progression-free survival at 42 months of 32.9% (95% CI, 17.2% to 49.5%) compared with 70.7% (95% CI, 59.3% to 79.4%) in those who became PET negative. PET status, but not conventional response (complete response or complete response unconfirmed v partial response) according to IWC 1999, was an independent predictive factor for lymphoma progression. The risk of death was also increased in PET-positive patients (hazard ratio 7.0; P = .0011). CONCLUSION: [(18)F]FDG PET-CT status at the end of immunochemotherapy induction in patients with FL is strongly predictive of outcome and should be considered a meaningful clinical end point in future studies. | en |
dc.subject | Drug Therapy | en |
dc.title | Positron emission tomography-computed tomography (PET-CT) after induction therapy is highly predictive of patient outcome in follicular lymphoma: analysis of PET-CT in a subset of PRIMA trial participants | en |
dc.type | Journal Article | en |
dc.identifier.doi | 10.1200/jco.2011.35.0736 | en |
dc.description.pubmeduri | https://www.ncbi.nlm.nih.gov/pubmed/21747087 | en |
dc.identifier.journaltitle | Journal of clinical oncology : official journal of the American Society of Clinical Oncology | en |
dc.type.studyortrial | Randomized Controlled Clinical Trial/Controlled Clinical Trial | en |
dc.relation.orcid | https://orcid.org/0000-0002-9108-3088 | en |
dc.originaltype | Text | en |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
crisitem.author.dept | Haematology | - |
Appears in Collections: | Haematology |
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