Area under the curve of methotrexate and creatinine clearance are outcome-determining factors in primary CNS lymphomas

被引:104
作者
Ferreri, AJM
Guerra, E
Regazzi, M
Pasini, F
Arnbrosetti, A
Pivnik, A
Gubkin, A
Calderoni, A
Spina, M
Brandes, A
Ferrarese, F
Rognone, A
Govi, S
Dell'Oro, S
Locatelli, M
Villa, E
Reni, M
机构
[1] San Raffaele H Sci Inst, Dept Radiochemotherapy, I-20132 Milan, Italy
[2] San Raffaele H Sci Inst, Lab Stand Chim Clin, Milan, Italy
[3] Univ Pavia, IRCCS Policlin San Matteo, Dept Pharmacol, I-27100 Pavia, Italy
[4] Osped Civile, Div Clin Oncol Med, I-37126 Verona, Italy
[5] Policlin GB Rossi, Div Ematol, Verona, Italy
[6] Russian Acad Med Sci, Hematol Ctr, Hematol & Intens Care Dept, Moscow, Russia
[7] Inselspital Bern, Inst Med Onkol, Bern, Switzerland
[8] Ist Nazl Tumori, Ctr Riferimento Oncol, Div Oncol Med A, Aviano, Italy
[9] Azienda Osped Univ, Dept Med Oncol, Padua, Italy
[10] Osped Reg Treviso, Div Radioterapia, Treviso, Italy
关键词
primary central nervous system lymphoma; methotrexate; plasmatic clearance; dose intensity; area under the curve; chemotherapy;
D O I
10.1038/sj.bjc.6601472
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although high-dose methotrexate (HD-MTX) is the most effective drug against primary CNS lymphomas (PCNSL), outcome-determining variables related to its administration schedule have not been defined. The impact on toxicity and outcome of the area under the curve (AUC(MTX)), dose intensity (Dl(MTX)) and infusion rate (IRMTX) of MTX and plasmatic creatinine clearance (CLcrea) was investigated in a retrospective series of 45 PCNSL patients treated with three different HD-MTX-based combinations. Anticonvulsants were administered in 31 pts (69%). Age > 60 years, anticonvulsant therapy, slow lR(MTX) (less than or equal to 800 mg m(-2) h(-1)), and reduced DIMTX (less than or equal to1000 mg m(-2) wk(-1)) were significantly correlated with low AUC(MTX) values. Seven patients (16%) experienced severe toxicity, which was independently associated with slow CLcrea. A total of 18 (40%) patients achieved complete remission after chemotherapy, which was independently associated with slow CLcrea. In all, 22 patients were alive at a median follow-up of 31 months, with a 3-year OS of 40 +/- 9%; slow CLcrea and AUC(MTX) > 1100 mumol h l(-1) were independently associated with a better survival. Slow CLcrea and high AUC(MTX) are favourable outcome-determining factors in PCNSL, while slow CLcrea is significantly related to higher toxicity. AUC(MTX) significantly correlates with age, anticonvulsant therapy, IRMTX, and DIMTX. These findings, which seem to support the choice of an MTX dose greater than or equal to 3 g m(-2) in a 4-6-h infusion, every 3-4 weeks, deserve to be assessed prospectively in future trials. MTX dose adjustments in patients with fast CLcrea should be investigated.
引用
收藏
页码:353 / 358
页数:6
相关论文
共 26 条
[1]   Predictive factors of histologic response to primary chemotherapy in osteosarcoma of the extremity: Study of 272 patients preoperatively treated with high-dose methotrexate, doxorubicin, and cisplatin [J].
Bacci, G ;
Ferrari, S ;
Delepine, N ;
Bertoni, F ;
Picci, P ;
Mercuri, M ;
Bacchini, P ;
del Prever, AB ;
Tienghi, A ;
Comandone, A ;
Campanacci, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :658-663
[2]   Treatment of primary CNS lymphoma with methotrexate and deferred radiotherapy: A report of NABTT 96-07 [J].
Batchelor, T ;
Carson, K ;
O'Neill, A ;
Grossman, SA ;
Alavi, J ;
New, P ;
Hochberg, F ;
Priet, R .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (06) :1044-1049
[3]   Combination chemotherapy with high-dose methotrexate and cytarabine with or without brain irradiation for primary central nervous system lymphomas [J].
Calderoni, A ;
Aebi, S .
JOURNAL OF NEURO-ONCOLOGY, 2002, 59 (03) :227-230
[4]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[5]   COMBINED MODALITY THERAPY FOR PRIMARY CNS LYMPHOMA [J].
DEANGELIS, LM ;
YAHALOM, J ;
THALER, HT ;
KHER, U .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (04) :635-643
[6]   Combination chemotherapy and radiotherapy for primary central nervous system lymphoma: Radiation Therapy Oncology Group study 93-10 [J].
DeAngelis, LM ;
Seiferheld, W ;
Schold, SC ;
Fisher, B ;
Schultz, CJ .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (24) :4643-4648
[7]  
DELEPINE N, 1995, ANTICANCER RES, V15, P489
[8]   METHOTREXATE CEREBROSPINAL-FLUID AND SERUM CONCENTRATIONS AFTER INTERMEDIATE-DOSE METHOTREXATE INFUSION [J].
EVANS, WE ;
HUTSON, PR ;
STEWART, CF ;
CAIRNES, DA ;
BOWMAN, WP ;
RIVERA, G ;
CROM, WR .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1983, 33 (03) :301-307
[9]   CLINICAL PHARMACODYNAMICS OF HIGH-DOSE METHOTREXATE IN ACUTE LYMPHOCYTIC-LEUKEMIA - IDENTIFICATION OF A RELATION BETWEEN CONCENTRATION AND EFFECT [J].
EVANS, WE ;
CROM, WR ;
ABROMOWITCH, M ;
DODGE, R ;
LOOK, AT ;
BOWMAN, WP ;
GEORGE, SL ;
PUI, CH .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (08) :471-477
[10]   Therapeutic management of primary central nervous system lymphoma: Lessons from prospective trials [J].
Ferreri, AJM ;
Reni, M ;
Villa, E .
ANNALS OF ONCOLOGY, 2000, 11 (08) :927-937