Multivariate analysis of febrile neutropenia occurrence in patients with non-Hodgkin lymphoma: data from the INC-EU Prospective Observational European Neutropenia Study

被引:74
作者
Pettengell, Ruth [1 ]
Bosly, Andre [2 ]
Szucs, Thomas D. [3 ]
Jackisch, Christian [4 ]
Leonard, Robert [5 ]
Paridaens, Robert [6 ]
Constenla, Manuel [7 ]
Schwenkglenks, Matthias [3 ]
机构
[1] St Georges Univ London, London SW17 0RE, England
[2] Clin Univ UCL, Serv Hematol, Godinne, Belgium
[3] Univ Basel, Univ Basel Hosp, ECPM Execut Off, European Ctr Pharmaceut Med, Basel, Switzerland
[4] Klinikum Offenbach, Dept Obstet & Gynaecol, Offenbach, Germany
[5] Charing Cross Hosp, Canc Serv & Clin Haematol, London, England
[6] Univ Hosp Gasthuisberg, Dept Med Oncol, B-3000 Louvain, Belgium
[7] Complexo Hosp Pontevedra, Serv Oncol, Pontevedra, Spain
关键词
Non-Hodgkin lymphoma; neutropenia; chemotherapy; risk factors; RELATIVE DOSE INTENSITY; B-CELL LYMPHOMA; CHEMOTHERAPY-INDUCED NEUTROPENIA; COLONY-STIMULATING FACTORS; CHOP CHEMOTHERAPY; ELDERLY-PATIENTS; CANCER-PATIENTS; BREAST-CANCER; PROGNOSTIC-SIGNIFICANCE; PREDICTIVE MODEL;
D O I
10.1111/j.1365-2141.2008.07514.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myelosuppression, particularly febrile neutropenia (FN), are serious dose-limiting toxicities that occur frequently during the first cycle of chemotherapy. Identifying patients most at risk of developing FN might help physicians to target prophylactic treatment with colony-stimulating factor (CSF), in order to decrease the incidence, or duration, of myelosuppression and facilitate delivery of chemotherapy as planned. We present a risk model for FN occurrence in the first cycle of chemotherapy, based on a subgroup of 240 patients with non-Hodgkin lymphoma (NHL) enroled in our European prospective observational study. Eligible patients had an International Prognostic Index of 0-3, and were scheduled to receive a new myelosuppressive chemotherapy regimen with at least four cycles. Clinically relevant factors significantly associated with cycle 1 FN were older age, increasing planned cyclophosphamide dose, a history of previous chemotherapy, a history of recent infection, and low baseline albumin (< 35 g/l). Prophylactic CSF use and higher weight were associated with a significant protective effect. The model had high sensitivity (81%) and specificity (80%). Our model, together with treatment guidelines, may rationalise the clinical decision of whether to support patients with CSF primary prophylaxis based on their risk factor profile. Further validation is required.
引用
收藏
页码:677 / 685
页数:9
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