American Society of Hematology/American Society of Clinical Oncology clinical practice guideline update on the use of epoetin and darbepoetin in adult patients with cancer

被引:108
作者
Rizzo, J. Douglas [1 ]
Brouwers, Melissa [2 ]
Hurley, Patricia [3 ]
Seidenfeld, Jerome [3 ]
Arcasoy, Murat O. [4 ]
Spivak, Jerry L. [5 ]
Bennett, Charles L. [6 ]
Bohlius, Julia [7 ]
Evanchuk, Darren [8 ]
Goode, Matthew J.
Jakubowski, Ann A. [9 ]
Regan, David H. [10 ]
Somerfield, Mark R. [3 ]
机构
[1] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[2] McMaster Univ, Hamilton, ON, Canada
[3] Amer Soc Clin Oncol, Alexandria, VA USA
[4] Duke Univ, Sch Med, Durham, NC USA
[5] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[6] S Carolina Coll Pharm, Columbia, SC USA
[7] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[8] Commonwealth Hematol Oncol PC, Stoneham, MA USA
[9] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[10] NW Canc Specialists, Vancouver, WA USA
关键词
ERYTHROPOIESIS-STIMULATING AGENTS; CHEMOTHERAPY-INDUCED ANEMIA; QUALITY-OF-LIFE; RECOMBINANT-HUMAN-ERYTHROPOIETIN; PLACEBO-CONTROLLED TRIAL; CELL LUNG-CANCER; EVERY; WEEKS; DOUBLE-BLIND; MYELODYSPLASTIC SYNDROMES; RECEIVING CHEMOTHERAPY;
D O I
10.1182/blood-2010-08-300541
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To update American Society of Hematology/American Society of Clinical Oncology recommendations for use of erythropoiesis-stimulating agents (ESAs) in patients with cancer. Methods: An Update Committee reviewed data published between January 2007 and January 2010. MEDLINE and the Cochrane Library were searched. Results: The literature search yielded one new individual patient data analysis and four literature-based meta-analyses, two systematic reviews, and 13 publications reporting new results from randomized controlled trials not included in prior or new reviews. Recommendations: For patients undergoing myelosuppressive chemotherapy who have a hemoglobin (Hb) level less than 10 g/dL, the Update Committee recommends that clinicians discuss potential harms (eg, thromboembolism, shorter survival) and benefits (eg, decreased transfusions) of ESAs and compare these with potential harms (eg, serious infections, immune-mediated adverse reactions) and benefits (eg, rapid Hb improvement) of RBC transfusions. Individual preferences for assumed risk should contribute to shared decisions on managing chemotherapy-induced anemia. The Committee cautions against ESA use under other circumstances. If used, ESAs should be administered at the lowest dose possible and should increase Hb to the lowest concentration possible to avoid transfusions. Available evidence does not identify Hb levels >= 10 g/dL either as thresholds for initiating treatment or as targets for ESA therapy. Starting doses and dose modifications after response or nonresponse should follow US Food and Drug Administration-approved labeling. ESAs should be discontinued after 6 to 8 weeks in nonresponders. ESAs should be avoided in patients with cancer not receiving concurrent chemotherapy, except for those with lower risk myelodysplastic syndromes. Caution should be exercised when using ESAs with chemotherapeutic agents in diseases associated with increased risk of thromboembolic complications. Table 1 lists detailed recommendations. (Blood.2010;116(20):4045-4059)
引用
收藏
页码:4045 / 4059
页数:15
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