Patterns of Delivery of Chemoimmunotherapy to Patients With Follicular Lymphoma in the United States: Results of the National LymphoCare Study

被引:17
作者
Martin, Peter [1 ]
Byrtek, Michelle [2 ]
Dawson, Keith [2 ]
Ziemiecki, Ryan [3 ]
Friedberg, Jonathan W. [4 ]
Cerhan, James R. [5 ]
Flowers, Christopher R. [6 ]
Link, Brian K. [7 ]
机构
[1] Weill Cornell Med Coll, Dept Med, Div Hematol Oncol, New York, NY 10065 USA
[2] Genentech Inc, San Francisco, CA 94080 USA
[3] RTI Hlth Solut, Res Triangle Pk, NC USA
[4] Univ Rochester, Dept Med, Wilmot Canc Ctr, Rochester, NY USA
[5] Mayo Clin, Dept Med, Rochester, MN USA
[6] Emory Univ, Dept Med, Atlanta, GA 30322 USA
[7] Univ Iowa, Dept Med, Iowa City, IA 52242 USA
关键词
follicular lymphoma; chemotherapy; rituximab; dose; intensity; completion; NON-HODGKINS-LYMPHOMA; CHEMOTHERAPY DOSE-INTENSITY; TRIAL; MULTICENTER; INDOLENT; IMPACT;
D O I
10.1002/cncr.28350
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDDrug choice and delivered dose of treatment potentially influence outcome in patients treated for follicular lymphoma (FL). Historically, observational studies have evaluated drug choice. The National LymphoCare Study (NLCS) is a prospective, observational study of patients with FL who were enrolled at academic and community practice sites in the United States between 2004 and 2007. In the current study, the authors report on measures of delivered dose and its impact on outcomes for the most common first-line regimens. METHODSAll evaluable patients with FL who were treated with initial rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP); rituximab plus cyclophosphamide, vincristine, and prednisone (R-CVP); or rituximab plus a fludarabine-containing regimen (R-Flu) were included. Associations between baseline factors, choice of treatment, number of cycles received, completion of therapy, and patient outcomes were assessed. RESULTSA total of 646 patients received R-CHOP, 297 received R-CVP, and 222 received R-Flu. Characteristics were similar between the 3 groups with the following exceptions. Patients receiving R-CHOP were more often found to have grade 3 FL and patients receiving R-CVP were older and had higher Follicular Lymphoma International Prognostic Index scores. The majority of patients (80%) received 5 cycles of treatment. Toxicity, but not disease progression, was commonly cited as the reason for the early discontinuation of treatment (51% vs 6%). Time to retreatment was shorter for patients receiving 4 cycles, regardless of the treatment regimen used. The number of cycles was associated with overall survival, progression-free survival, and lymphoma-related mortality for patients receiving R-CVP. CONCLUSIONSThe majority of patients with FL receiving chemoimmunotherapy in the NLCS completed 5 cycles of treatment. Strategies to improve dose delivery appear unlikely to impact outcomes, except possibly in patients receiving R-CVP. Although early treatment discontinuation appears to be associated with survival, this analysis does not implicate causality. Cancer 2013;119:4129-4136. (c) 2013 American Cancer Society. The majority of patients with follicular lymphoma complete first-line chemoimmunotherapy as intended. Strategies to improve dose delivery appear unlikely to impact outcomes.
引用
收藏
页码:4129 / 4136
页数:8
相关论文
共 15 条
[1]  
[Anonymous], BLOOD
[2]  
[Anonymous], 1997, BLOOD
[3]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[4]  
Federico M, 2012, ASCO M, V30, P8006
[5]  
Flinn IW, 2012, BLOOD, V120, P902
[6]   Follicular Lymphoma in the United States: First Report of the National LymphoCare Study [J].
Friedberg, Jonathan W. ;
Taylor, Michael D. ;
Cerhan, James R. ;
Flowers, Christopher R. ;
Dillon, Hildy ;
Farber, Charles M. ;
Rogers, Eric S. ;
Hainsworth, John D. ;
Wong, Elaine K. ;
Vose, Julie M. ;
Zelenetz, Andrew D. ;
Link, Brian K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (08) :1202-1208
[7]   Treatment of Older Patients with Mantle-Cell Lymphoma [J].
Kluin-Nelemans, H. C. ;
Hoster, E. ;
Hermine, O. ;
Walewski, J. ;
Trneny, M. ;
Geisler, C. H. ;
Stilgenbauer, S. ;
Thieblemont, C. ;
Vehling-Kaiser, U. ;
Doorduijn, J. K. ;
Coiffier, B. ;
Forstpointner, R. ;
Tilly, H. ;
Kanz, L. ;
Feugier, P. ;
Szymczyk, M. ;
Hallek, M. ;
Kremers, S. ;
Lepeu, G. ;
Sanhes, L. ;
Zijlstra, J. M. ;
Bouabdallah, R. ;
Lugtenburg, P. J. ;
Macro, M. ;
Pfreundschuh, M. ;
Prochazka, V. ;
Di Raimondo, F. ;
Ribrag, V. ;
Uppenkamp, M. ;
Andre, M. ;
Klapper, W. ;
Hiddemann, W. ;
Unterhalt, M. ;
Dreyling, M. H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (06) :520-531
[8]   Prospective, multicenter randomized GITMO/IIL trial comparing intensive (R-HDS) versus conventional (CHOP-R) chemoimmunotherapy in high-risk follicular lymphoma at diagnosis: the superior disease control of R-HDS does not translate into an overall survival advantage [J].
Ladetto, Marco ;
De Marco, Federica ;
Benedetti, Fabio ;
Vitolo, Umberto ;
Patti, Caterina ;
Rambaldi, Alessandro ;
Pulsoni, Alessandro ;
Musso, Maurizio ;
Liberati, Anna M. ;
Olivieri, Attilio ;
Gallamini, Andrea ;
Pogliani, Enrico ;
Scalabrini, Delia Rota ;
Callea, Vincenzo ;
Di Raimondo, Francesco ;
Pavone, Vincenzo ;
Tucci, Alessandra ;
Cortelazzo, Sergio ;
Levis, Alessandro ;
Boccadoro, Mario ;
Majolino, Ignazio ;
Pileri, Alessandro ;
Gianni, Alessandro M. ;
Passera, Roberto ;
Corradini, Paolo ;
Tarella, Corrado .
BLOOD, 2008, 111 (08) :4004-4013
[9]   Impact of Chemotherapy Dose Intensity on Cancer Patient Outcomes [J].
Lyman, Gary H. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2009, 7 (01) :99-108
[10]   Incidence and predictors of low chemotherapy dose-intensity in aggressive non-Hodgkin's lymphoma: A nationwide study [J].
Lyman, GH ;
Dale, DC ;
Friedberg, J ;
Crawford, J ;
Fisher, RI .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (21) :4302-4311