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Author Notes:

Corresponding author: Jonathan W. Friedberg, MD, MMSc, James P. Wilmot Cancer Center, University of Rochester, 601 Elmwood Ave, Box 704, Rochester, NY 14642; e-mail: jonathan_ friedberg@urmc.rochester.edu.

C.M.F., C.R.F., J.D.H., J.R.C., B.K.L., A.D.Z., and J.W.F. serve on the advisory board for this study and have full access to data for patients in this analysis. This article was written de novo by the authors, with some editorial support from the sponsor.

For author contributions and disclosures, see the full article.

Subjects:

Research Funding:

Supported by Genentech and F. Hoffmann-La Roche. Support for editorial assistance was funded by Genentech. Funded by P50CA97274 (Cerhan)

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Oncology
  • STEM-CELL TRANSPLANTATION
  • NON-HODGKINS-LYMPHOMA
  • FREE SURVIVAL
  • 1ST-LINE TREATMENT
  • END-POINT
  • RANDOMIZED-TRIAL
  • WORKING PARTY
  • UNITED-STATES
  • PHASE-III
  • R-CVP

Early Relapse of Follicular Lymphoma After Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone Defines Patients at High Risk for Death: An Analysis From the National LymphoCare Study

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Journal Title:

Journal of Clinical Oncology

Volume:

Volume 33, Number 23

Publisher:

, Pages 2516-U55

Type of Work:

Article | Final Publisher PDF

Abstract:

Purpose: Twenty percent of patients with follicular lymphoma (FL) experience progression of disease (POD) within 2 years of initial chemoimmunotherapy. We analyzed data from the National LymphoCare Study to identify whether prognostic FL factors are associated with early POD and whether patients with early POD are at high risk for death. Patients and Methods: In total, 588 patients with stage 2 to 4 FL received first-line rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). Two groups were defined: patients with early POD 2 years or less after diagnosis and those without POD within 2 years, the reference group. An independent validation set, 147 patients with FL who received first-line R-CHOP, was analyzed for reproducibility. Results: Of 588 patients, 19% (n = 110) had early POD, 71% (n = 420) were in the reference group, 8% (n = 46) were lost to follow-up, and 2% (n = 12) died without POD less than 2 years after diagnosis. Five-year overall survival was lower in the early-POD group than in the reference group (50% v 90%). This trend was maintained after we adjusted for FL International Prognostic Index (hazard ratio, 6.44; 95% CI, 4.33 to 9.58). Results were similar for the validation set (FL International Prognostic Index - adjusted hazard ratio, 19.8). Conclusion: In patients with FL who received first-line R-CHOP, POD within 2 years after diagnosis was associated with poor outcomes and should be further validated as a standard end point of chemoimmunotherapy trials of untreated FL. This high-risk FL population warrants further study in directed prospective clinical trials.

Copyright information:

© 2015 by American Society of Clinical Oncology.

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