Temsirolimus and rituximab in patients with relapsed or refractory mantle cell lymphoma: a phase 2 study

被引:126
作者
Ansell, Stephen M. [1 ]
Tang, Hui [2 ]
Kurtin, Paul J. [3 ]
Koenig, Patricia A. [5 ]
Inwards, David J. [1 ]
Shah, Keith [5 ]
Ziesmer, Steven C. [1 ]
Feldman, Andrew L. [3 ]
Rao, Radha [5 ]
Gupta, Mamta [1 ]
Erlichman, Charles [4 ]
Witzig, Thomas E. [1 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[3] Mayo Clin, Div Hematopathol, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
[5] N Cent Canc Treatment Grp, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
ANTI-CD20; MONOCLONAL-ANTIBODY; NON-HODGKINS-LYMPHOMA; SINGLE-AGENT TEMSIROLIMUS; B-CELLS; CANCER; PATHWAY; IMMUNOCHEMOTHERAPY; MULTICENTER; SENSITIVITY; INHIBITION;
D O I
10.1016/S1470-2045(11)70062-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Temsirolimus is a mammalian target of rapamycin (mTOR) inhibitor with single-agent antitumour activity in patients with mantle cell lymphoma. We therefore tested its efficacy and toxicity in combination with rituximab (an antiCD20 antibody) in patients with relapsed or refractory mantle cell lymphoma. Methods In a phase 2 study, patients (aged 18 years) at 35 centres in the USA were given temsirolimus 25 mg/week, and rituximab 375mg/m(2) per week for 4 weeks during the first cycle and thereafter a single dose of rituximab every other 28-day cyde. Both drugs were administered intravenously. Responding patients after six cycles could continue treatment for a total of 12 cycles, and were then observed without additional maintenance treatment. The primary, endpoint was the proportion of patients with either rituximab-sensitive or rituximab-refractory disease who had at least a partial response. The analyses were done on all patients who were treated. The study was registered with ClinicalTrials.gov, number NCT00109967. Findings 71 patients with mantle cell lymphoma were enrolled and 69 were assessable and were included in the final analysis. The overall response rate (ORR) was 59% (41 of 69 patients)-13 (19%) patients had complete responses and 28 (41%) had partial responses. The ORR was 63% (30 of 48; 95% CI 47-76) for rituximab-sensitive patients, and 52% (11 of 21; 30-74) for rituximab-refractory patients. The most common treatment-related grade 3 or 4 adverse events in rituximab-sensitive and rituximab-refractory patients were thrombocytopenia (eight [17%] and eight [38%], respectively), neutropenia (ten [21%] and five [24%], respectively), fatigue (eight [17%] and two [10%], respectively), leucopenia (six [13%] and three [14%], respectively), pneumonia (five [10%] and two [10%], respectively), lymphopenia (five [10%] and two [10%], respectively), pneumonitis (four [8%] and none, respectively), oedema (four [8%] and none, respectively), dyspnoea (three [6%] and two [10%], respectively), and hypertriglyceridaemia (three [6%] and two [10%], respectively). Interpretation mTOR inhibitors in combination with rituximab could have a role in the treatment of patients with relapsed and refractory mantle cell lymphoma.
引用
收藏
页码:361 / 368
页数:8
相关论文
共 30 条
[1]  
[Anonymous], 1997, BLOOD
[2]   Low-dose, single-agent temsirolimus for relapsed mantle cell lymphoma - A phase 2 trial in the North Central Cancer Treatment Group [J].
Ansell, Stephen M. ;
Inwards, David J. ;
Rowland, Kendrith M., Jr. ;
Flynn, Patrick J. ;
Morton, Roscoe F. ;
Moore, Dennis F., Jr. ;
Kaufmann, Scott H. ;
Ghobrial, Irene ;
Kurtin, Paul J. ;
Maurer, Matthew ;
Allmer, Christine ;
Witzig, Thomas E. .
CANCER, 2008, 113 (03) :508-514
[3]   Mantle cell lymphoma: A clinicopathologic study of 80 cases [J].
Argatoff, LH ;
Connors, JM ;
Klasa, RJ ;
Horsman, DE ;
Gascoyne, RD .
BLOOD, 1997, 89 (06) :2067-2078
[4]   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
[5]  
Coiffier B, 1998, BLOOD, V92, P1927
[6]   Patterns and Outcome of Relapse After Autologous Stem Cell Transplantation for Mantle Cell Lymphoma [J].
Dietrich, Sascha ;
Tielesch, Blanca ;
Rieger, Michael ;
Nickelsen, Maike ;
Pott, Christiane ;
Witzens-Harig, Mathias ;
Kneba, Michael ;
Schmitz, Norbert ;
Ho, Antony D. ;
Dreger, Peter .
CANCER, 2011, 117 (09) :1901-1910
[7]  
Dudkin L, 2001, CLIN CANCER RES, V7, P1758
[8]   Phase II trial of temsirolimus in patients with relapsed or refractory multiple myeloma [J].
Farag, Sherif S. ;
Zhang, Shuhong ;
Jansak, Buffy S. ;
Wang, Xiaojing ;
Kraut, Eric ;
Chan, Kenneth ;
Dancey, Janet E. ;
Grever, Michael R. .
LEUKEMIA RESEARCH, 2009, 33 (11) :1475-1480
[9]   European phase II study of rituximab (chimeric anti-CD20 monoclonal antibody) for patients with newly diagnosed mantle-cell lymphoma and previously treated mantle-cell lymphoma, immunocytoma, and small B-cell lymphocytic lymphoma [J].
Foran, JM ;
Rohatiner, AZS ;
Cunningham, D ;
Popescu, RA ;
Solal-Celigny, P ;
Ghielmini, M ;
Coiffier, B ;
Johnson, PWM ;
Gisselbrecht, C ;
Reyes, F ;
Radford, JA ;
Bessell, EM ;
Souleau, B ;
Benzohra, A ;
Lister, TA .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :317-324
[10]   Mantle cell lymphoma - does primary intensive immunochemotherapy improve overall survival for younger patients? [J].
Geisler, Christian ;
Kolstad, Arne ;
Laurell, Anna ;
Raty, Riikka .
LEUKEMIA & LYMPHOMA, 2009, 50 (08) :1249-1256