A new induction schedule of epoetin alfa 40.000 IU in anemic patients with advanced lung cancer
- PMID: 15364140
- DOI: 10.1016/j.lungcan.2004.03.017
A new induction schedule of epoetin alfa 40.000 IU in anemic patients with advanced lung cancer
Abstract
Background: Non-small cell lung cancer (NSCLC) treatment with new drugs in combination with platinum salts induce anemia G1/2 and G3/4 WHO in about 35 and 10-20% of patients, respectively, with a chemotherapy (CT) dose intensity decrease in 20% of cases. Epoetin alfa, administered at standard dosages has been shown to significantly increase hemoglobin (Hb) levels, decrease transfusion requirements, and improve quality-of-life parameters in patients undergoing chemotherapy.
Objective: This open-label, non-randomized study was conducted to evaluate the efficacy and safety of an induction dose of epoetin alfa 40.000 IU in lung cancer patients with moderate or severe anemia who were receiving CT.
Patients and methods: Twenty-four patients (8 SCLC and 16 NSCLC) were enrolled in the study to receive single subcutaneous (s.c.) injections of epoetin alfa 40.000 IU on days 1, 4, 7, 10, and 13, followed by standard treatment (10.000 IU t.i.w.) for the further 2 weeks. Nine patients had been previously treated with epoetin alfa 10.000 IU t.i.w. Twenty-two patients were receiving first-line CT and two patients were receiving docetaxel as second-line CT.
Results: After 15 days of treatment, in 21 evaluable patients, Hb was 10.5 +/- 1.3 g/dL (mean +/- S.D.), with a mean increase from baseline of 2.0 g/dL (95%CI: 1.3-2.7). Hb increase was > or =2g/dL in 11 patients, 1-1.9 g/dL in 5 patients, and <1g/dL in 5 patients. After 30 days of treatment, Hb was 11.5 +/- 0.8 g/dL (mean +/- S.D.), with a mean increase from baseline of 2.9 g/dL (95%CI: 2.4-3.4) in 20 evaluable patients. No adverse events possibly related to epoetin alfa treatment were observed.
Conclusion: An induction therapy with epoetin alfa 40.000 IU for 2 weeks followed by standard treatment allows an Hb increase of 2.9 g/dL even in advanced lung cancer patients with a moderate/severe anemia, without RBC transfusion requirements. A randomized study of the proposed induction dose of epoetin alfa 40.000 IU is actually ongoing.
Similar articles
-
Anaemia management with epoetin alfa in lung cancer patients in The Netherlands.Lung Cancer. 2007 Oct;58(1):104-11. doi: 10.1016/j.lungcan.2007.05.007. Epub 2007 Jun 29. Lung Cancer. 2007. PMID: 17601632 Clinical Trial.
-
Epoetin alfa 60,000 U once weekly followed by 120,000 U every 3 weeks increases and maintains hemoglobin levels in anemic cancer patients undergoing chemotherapy.Oncologist. 2004;9(1):90-6. Oncologist. 2004. PMID: 14755018
-
Epoetin alpha prevents anaemia and reduces transfusion requirements in patients undergoing primarily platinum-based chemotherapy for small cell lung cancer.Br J Cancer. 1999 May;80(3-4):396-402. doi: 10.1038/sj.bjc.6690369. Br J Cancer. 1999. PMID: 10408844 Free PMC article. Clinical Trial.
-
Patients previously transfused or treated with epoetin alfa at low baseline hemoglobin are at higher risk for subsequent transfusion: an integrated analysis of the Canadian experience.Oncologist. 2006 Jan;11(1):73-82. doi: 10.1634/theoncologist.11-1-73. Oncologist. 2006. PMID: 16401716 Review.
-
Clinical experience with epoetin alfa in the management of hemoglobin levels in orthopedic surgery and cancer. Implications for use in gynecologic surgery.J Reprod Med. 2001 May;46(5 Suppl):531-8. J Reprod Med. 2001. PMID: 11396387 Review.
Cited by
-
Phase II study of two dose schedules of C.E.R.A. (Continuous Erythropoietin Receptor Activator) in anemic patients with advanced non-small cell lung cancer (NSCLC) receiving chemotherapy.Trials. 2007 Mar 6;8:8. doi: 10.1186/1745-6215-8-8. Trials. 2007. PMID: 17341293 Free PMC article.
-
Anaemia: a rare but neglected problem among Finnish patients receiving chemotherapy for solid tumours.Support Care Cancer. 2011 Jan;19(1):149-53. doi: 10.1007/s00520-009-0809-x. Epub 2010 Jan 26. Support Care Cancer. 2011. PMID: 20101415
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical