Use of epoetin in patients with cancer: evidence-based clinical practice guidelines of the American Society of Clinical Oncology and the American Society of Hematology

被引:149
作者
Rizzo, JD
Lichtin, AE
Woolf, SH
Seidenfeld, J
Bennett, CL
Cella, D
Djulbegovic, B
Goode, MJ
Jakubowski, AA
Lee, SJ
Miller, CB
Rarick, MU
Regan, DH
Browman, GP
Gordon, MS
机构
[1] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[2] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[3] Virginia Commonwealth Univ, Richmond, VA USA
[4] Blue Cross & Blue Shield Assoc Technol Evaluat Ct, Chicago, IL USA
[5] VA Chicago Hlth Care Syst, Chicago, IL USA
[6] Evanston Northwestern Healthcare, Evanston, IL USA
[7] Univ S Florida, Res Inst, H Lee Moffitt Canc Ctr, Tampa, FL USA
[8] Univ S Florida, Res Inst, Res Inst, Tampa, FL USA
[9] Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[11] St Agnes Hosp, Baltimore, MD USA
[12] NW Kaiser Permanente, Portland, OR USA
[13] NW Canc Specialists, Portland, OR USA
[14] Hamilton Reg Canc Ctr, Hamilton, ON L8V 1C3, Canada
[15] Univ Arizona, Hlth Sci Ctr, Phoenix, AZ USA
关键词
D O I
10.1182/blood-2002-06-1767
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anemia resulting from cancer or its treatment is an important clinical problem increasingly treated with the recombinant hematopoietic growth factor erythropoietin. To address uncertainties regarding indications and efficacy, the American Society of Clinical Oncology and the American Society of Hematology developed an evidence-based clinical practice guideline for the use of epoetin in patients with cancer. The guideline panel found good evidence to recommend use of epoetin as a treatment option for patients with chemotherapy-associated anemia with a hemoglobin (Hgb) concentration below 10 g/dL. Use of epoetin for patients with less severe anemia (Hgb level below 12 g/dL but never below 10 g/dL) should be determined by clinical circumstances. Good evidence from clinical trials supports the use of subcutaneous epoetin thrice weekly (150 U/kg) for a minimum of 4 weeks. Less strong evidence supports an alternative weekly (40 000 U/wk) dosing regimen, based on common clinical practice. With either administration schedule, dose escalation should be considered for those not responding to the initial dose. In the absence of response, continuing epoetin beyond 6-8 weeks does not appear to be beneficial. Epoetin should betitrated once the hemoglobin concentration reaches 12 g/dL. Evidence from one randomized controlled trial supports use of epoetin for patients with anemia associated with low-risk myelodysplasia not receiving chemotherapy; however, there are no published high quality studies to support its use for anemia in other hematologic malignancies in the absence of chemotherapy. Therefore, for anemic patients with hematologic malignancies it is recommended that physicians initiate conventional therapy and observe hematologic response before considering use of epoetin. (C) 2002 by The American Society of Hematology and The American Society of Clinical Oncology.
引用
收藏
页码:2303 / 2320
页数:18
相关论文
共 69 条
[1]  
Abels, 1996, Oncologist, V1, P140
[2]   ERYTHROPOIETIN FOR ANEMIA IN CANCER-PATIENTS [J].
ABELS, R .
EUROPEAN JOURNAL OF CANCER, 1993, 29A :S2-S8
[3]  
*AHCPR, 2000, AHCPR REQ TOP NOM EV
[4]  
*AHCPR, 1998, AHCPR ANN NEW EV REP
[5]   SUBCUTANEOUS VERSUS INTRAVENOUS ADMINISTRATION OF ERYTHROPOIETIN IMPROVES ITS EFFICIENCY FOR THE TREATMENT OF ANEMIA IN HEMODIALYSIS-PATIENTS [J].
ALBITAR, S ;
MEULDERS, Q ;
HAMMOUD, H ;
SOUTIF, C ;
BOUVIER, J ;
POLLINI, J .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1995, 10 :40-43
[6]  
[Anonymous], 1996, J Clin Oncol, V14, P671
[7]  
[Anonymous], 2002, P AM SOC CLIN ONCOLO
[8]   The effects of normal as compared with low hematocrit values in patients with cardiac disease who are receiving hemodialysis and epoetin [J].
Besarab, A ;
Bolton, WK ;
Browne, JK ;
Egrie, JC ;
Nissenson, AR ;
Okamoto, DM ;
Schwab, SJ ;
Goodkin, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (09) :584-590
[9]   Pure red-cell aplasia and antierythropoietin antibodies in patients treated with recombinant erythropoietin. [J].
Casadevall, N ;
Nataf, J ;
Viron, B ;
Kolta, A ;
Kiladjian, J ;
Martin-Dupont, P ;
Michaud, P ;
Papo, T ;
Ugo, V ;
Teyssandier, I ;
Varet, B ;
Mayeux, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (07) :469-475
[10]   RECOMBINANT-HUMAN-ERYTHROPOIETIN TREATMENT IN CISPLATIN-ASSOCIATED ANEMIA - A RANDOMIZED, DOUBLE-BLIND TRIAL WITH PLACEBO [J].
CASCINU, S ;
FEDELI, A ;
DELFERRO, E ;
FEDELI, SL ;
CATALANO, G .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (05) :1058-1062