Journal article
Outcomes following watchful waiting for stage II-IV follicular lymphoma patients in the modern era
British journal of haematology, Vol.172(5), pp.724-734
03/2016
DOI: 10.1111/bjh.13895
PMID: 26729445
Abstract
To examine the effectiveness of an initial management strategy of watchful waiting for follicular lymphoma (FL) in clinical practice, we compared outcomes for patients diagnosed 2004-2007 in the United States initially managed with watchful waiting with outcomes following initial rituximab monotherapy and chemoimmunotherapy. In total, 1754 stage II-IV patients in the National LymphoCare Study underwent watchful waiting (n = 386), rituximab monotherapy (n = 296) or rituximab plus chemotherapy (n = 1072) as initial management strategy. Female patients and those who received treatment in the Northeast or in an academic setting more commonly underwent watchful waiting versus initial chemoimmunotherapy; whereas patients with grade 3 histology, anaemia, elevated lactate dehydrogenase, extranodal involvement, B symptoms or performance status ≥1 more commonly received chemoimmunotherapy. Although time to new treatment and progression-free survival following first- and second-line therapy were improved with chemoimmunotherapy, and time to chemotherapy was improved with rituximab monotherapy, there were no differences in overall survival between watchful waiting and chemoimmunotherapy or rituximab monotherapy. With 8-year overall survival estimates of 74%, initial management with watchful waiting in the context of sequential therapy remains a viable option for FL patients in the modern era. This trial was registered at www.clinicaltrials.gov (NCT00097565).
Details
- Title: Subtitle
- Outcomes following watchful waiting for stage II-IV follicular lymphoma patients in the modern era
- Creators
- Loretta J Nastoupil - The University of Texas MD Anderson Cancer Center, Houston, TX, USABrian K Link - Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USARajni Sinha - University Oncology & Hematology Associates, Chattanooga, TN, USAJames R Cerhan - Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USAMichelle Byrtek - Genentech/Roche, South San Francisco, CA, USARyan Ziemiecki - Biostatistics, RTI Health Solutions, Research Triangle Park, NC, USAXiaolei Zhou - Biostatistics, RTI Health Solutions, Research Triangle Park, NC, USAMichael Taylor - GenentechJonathan W Friedberg - James P. Wilmot Cancer Center, University of Rochester, Rochester, NY, USAKeith Dawson - Genentech/Roche, South San Francisco, CA, USAChristopher R Flowers - Winship Cancer Institute, Emory University, Atlanta, GA, USA
- Resource Type
- Journal article
- Publication Details
- British journal of haematology, Vol.172(5), pp.724-734
- DOI
- 10.1111/bjh.13895
- PMID
- 26729445
- NLM abbreviation
- Br J Haematol
- ISSN
- 0007-1048
- eISSN
- 1365-2141
- Grant note
- name: Genentech Inc./F. Hoffmann-La Roche Ltd
- Language
- English
- Date published
- 03/2016
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Epidemiology; Internal Medicine
- Record Identifier
- 9984094564002771
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