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Midtreatment 18F-fluorodeoxyglucose positron-emission tomography in aggressive non-Hodgkin lymphoma.

AbstractBACKGROUND:
The use of (18) F-fluorodeoxyglucose positron-emission tomography (PET) scan has increased considerably in the clinical management of non-Hodgkin lymphoma patients, and its role as a prognostic factor during chemotherapy has been established recently.
METHODS:
Between May 2003 and May 2009, 91 newly diagnosed patients with primary mediastinal large B-cell lymphoma (PMLBCL) and diffuse large B-cell lymphoma (DLBCL) were treated with 12 weekly cycles of rituximab-MACOP-B (n = 12 patients with PMLBCL), 6 cycles of rituximab-CHOP21 (n = 65 patients with DLBCL, aged < 60 years and 1 patient with PMLBCL), or 8 weekly cycles of rituximab-VNCOP-B (n = 13 DLBCL patients, aged ≥ 60 years). All patients underwent a staging PET examination at baseline and a midtreatment (interim) PET examination after 6 weeks of rituximab-MACOP-B treatment, 3 cycles of rituximab-CHOP21 treatment, or 4 weeks of rituximab-VNCOP-B treatment and again at the end of the chemo-immunotherapy regimen.
RESULTS:
At midtreatment evaluation, 35 patients showed a persistently positive PET scan; only 6 (17%) of these patients achieved a continuous complete response (CCR). However, 56 patients presented with a negative interim PET, and 50 (89%) of these patients achieved and maintained a CCR. Comparison between the 2 PET groups indicated a statistically significant association between PET findings and event-free survival (P = .0001) and overall survival (P = .0001).
CONCLUSIONS:
The results of this study indicated that midtreatment PET may represent a significant step forward in helping physicians make crucial decisions on further treatment. Cancer 2011. © 2010 American Cancer Society.
AuthorsPier Luigi Zinzani, Letizia Gandolfi, Alessandro Broccoli, Lisa Argnani, Stefano Fanti, Cinzia Pellegrini, Vittorio Stefoni, Enrico Derenzini, Federica Quirini, Michele Baccarani
JournalCancer (Cancer) Vol. 117 Issue 5 Pg. 1010-8 (Mar 01 2011) ISSN: 0008-543X [Print] United States
PMID20960498 (Publication Type: Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 American Cancer Society.
Chemical References
  • Antibodies, Monoclonal, Murine-Derived
  • Fluorodeoxyglucose F18
  • Bleomycin
  • Rituximab
  • Vincristine
  • Etoposide
  • Doxorubicin
  • Cyclophosphamide
  • Mitoxantrone
  • Leucovorin
  • Prednisone
  • Methotrexate
Topics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Algorithms
  • Antibodies, Monoclonal, Murine-Derived (administration & dosage)
  • Antineoplastic Combined Chemotherapy Protocols (administration & dosage)
  • Bleomycin (administration & dosage)
  • Cyclophosphamide (administration & dosage)
  • Doxorubicin (administration & dosage)
  • Drug Administration Schedule
  • Etoposide (administration & dosage)
  • Female
  • Fluorodeoxyglucose F18
  • Humans
  • Leucovorin (administration & dosage)
  • Lymphoma, Non-Hodgkin (diagnostic imaging, drug therapy, mortality, pathology)
  • Male
  • Methotrexate (administration & dosage)
  • Middle Aged
  • Mitoxantrone (administration & dosage)
  • Monitoring, Physiologic (methods)
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • Positron-Emission Tomography (methods)
  • Prednisone (administration & dosage)
  • Retrospective Studies
  • Rituximab
  • Survival Analysis
  • Time Factors
  • Vincristine (administration & dosage)
  • Young Adult

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