Single agent rituximab in patients with follicular or mantle cell lymphoma:: clinical and biological factors that are predictive of response and event-free survival as well as the effect of rituximab on the immune system:: a study of the Swiss Group for Clinical Cancer Research (SAKK)

被引:135
作者
Ghielmini, A
Rufibach, K
Salles, G
Leoncini-Franscini, L
Léger-Falandry, C
Cogliatti, S
Fey, M
Martinelli, G
Stahel, R
Lohri, A
Ketterer, N
Wernli, A
Cerny, T
Schmitz, SFH
机构
[1] SAKK, Swiss Grp Clin Canc Res, Bern, Switzerland
[2] Ist Europeo Oncol, Milan, Italy
[3] Ctr Hosp Lyon Sud, Lyon, France
关键词
rituximab; predictive factors; toxicity; Fc-gamma receptor; follicular lymphoma; mantle cell lymphoma;
D O I
10.1093/annonc/mdi320
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Predictive factors of rituximab efficacy and its effect on the immune system are still not defined. Patients and methods: Three hundred and six patients with follicular or mantle cell lymphoma received four weekly doses of rituximab (induction) and no further treatment (arm A) or four more doses at 2-month intervals (arm 13). Results: Response rate to induction was 44%. Independent predictive factors for response were disease bulk < 5 cm, follicular histology, normal hemoglobin and low lymphocyte count. Factors associated with event-free survival (EFS) were having responded to induction, having received not more than one line of therapy, Ann Arbor stage I-III, high lymphocyte count, disease bulk < 5 cm, Fc-gamma receptor genotype VV and receiving prolonged treatment. B cells were suppressed by treatment but recovered after a median of 12 months in arm A and 18 months in arm B. The median IgM level after 1 year was normal in arm A but was decreased to 73% of baseline in arm B. We observed 24 serious adverse events, equally distributed between arms. Ten patients receiving induction only and six patients receiving prolonged treatment developed a second tumor. Conclusions: We defined the characteristics predicting response and EFS to rituximab. Prolonged treatment results in longer EFS at the cost of a longer reduction in B cell and IgM levels, but without additional clinical toxicity.
引用
收藏
页码:1675 / 1682
页数:8
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