ERYTHROPOIETIN TREATMENT UNDER POLYCHEMOTHERAPY IN PATIENTS WITH GYNECOLOGIC MALIGNANCIES - A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED MULTICENTER STUDY

Citation
C. Kurz et al., ERYTHROPOIETIN TREATMENT UNDER POLYCHEMOTHERAPY IN PATIENTS WITH GYNECOLOGIC MALIGNANCIES - A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED MULTICENTER STUDY, Gynecologic oncology, 65(3), 1997, pp. 461-466
Citations number
18
Categorie Soggetti
Oncology,"Obsetric & Gynecology
Journal title
ISSN journal
00908258
Volume
65
Issue
3
Year of publication
1997
Pages
461 - 466
Database
ISI
SICI code
0090-8258(1997)65:3<461:ETUPIP>2.0.ZU;2-8
Abstract
In order to examine the influence of erythropoietin (rHuEPO) on serum hemoglobin levels, transfusion requirements, and quality of life in pa tients with gynecologic malignancies under polychemotherapy and chroni c tumor anemia (hemoglobin <11 g/dl), we performed a prospective, rand omized, double-blinded placebo-controlled clinical trial. Between Octo ber 1992 and October 1993, 35 patients from 5 gynecologic departments were entered into this trial. Inclusion criteria were hemoglobin level <11 g/dl, ferritin level >29 ng/ml, stool negative for occult blood, and Life expectancy for more than 3 months. Patients received either 1 50 U/kg body wt rHuEPO (Erypo by Cilag-Janssen) sc three times a week for 12 weeks (n = 23) or a placebo (n = 12). If the hemoglobin levels of the 4th, 8th, or 12th week were >2 g/dl above the baseline value an d/or >12 g/dl, the patient was classified as a responder. Patients who required blood transfusions (hemoglobin <8 g/dl, erythrocytes <3 x 10 (6)/ml, or clinical symptoms of anemia) were classified as nonresponde rs. A nonvalidated quality of life questionnaire was completed by the patient at the beginning of the treatment and then every fourth week b efore receiving chemotherapy. In the rHuEPO group 56.6% of the patient s responded to the treatment (chi(2) = 10.79, P = 0.001) and only 5 pa tients (21.7%) required blood transfusions, whereas 8 of 12 patients i n the placebo group (66.6%) had to be transfused (chi(2) = 6.81, P = 0 .009). Quality of life did not differ significantly between the rHuEPO group and the placebo group of patients. Within the rHuEPO group thos e patients that responded showed a significant increase in physical ac tivity after response in comparison to the preresponsive phase (P = 0. 02, paired t test). We therefore concluded that rHuEPO significantly i ncreases serum hemoglobin levels and decreases transfusions requiremen ts while maintaining quality of life in patients with gynecological ma lignancies who are undergoing polychemotherapy. (C) 1997 Academic Pres s.