|
| |||||||||||||||||||||||||||||||||||
A total of 651 children with ALL who were treated at the Children's Welfare Teaching Hospital in Baghdad and who had complete medical records were included in this analysis. There were 408 patients with standard-risk disease, with a median age of 4.9 years (range, 1.1 to 9.8) and a median white-cell count at presentation of 9050 per cubic millimeter (range, 400 to 47,000). The remaining 243 patients were at high risk and had a median age of 8 years (range, 1.3 to 15.0) and a median white-cell count at presentation of 78,600 per cubic millimeter (range, 800 to 600,000). All children were treated according to the UKALL X and XI protocols (between 1990 and 1997) and the Medical Research Council ALL 97 protocol (between 1998 and 2002).3,4 Medication shortage was defined as no treatment or incomplete treatment owing to unavailability of chemotherapeutic agents. The absence of chemotherapy administration or decreased or delayed administration due to toxic effects or myelosuppression was not considered to be a medication shortage.
The shortage of chemotherapeutic agents was evident from the increase in the proportion of the 651 patients who received less than 50% of the prescribed chemotherapy: 20.1% between 1990 and 1994 to 54.3% between 2000 and 2002. With a median follow-up period of 8.4 years (range, 3.5 to 16.9), the overall survival rate for patients who received all prescribed chemotherapy was significantly greater than that for patients who missed any chemotherapy (P<0.001). This difference was also significant within the standard-risk group (P=0.004) and within the high-risk group (P=0.02) (Figure 1). In a multivariate analysis of the data (including age, white-cell count at presentation, hemoglobin level, presence or absence of organomegaly, and year of treatment), as compared with receipt of all chemotherapy, missed chemotherapy was associated with a significantly worse outcome within the standard-risk group (relative risk, 2.90, 95% confidence interval [CI], 1.41 to 6.22; P=0.005) and within the high-risk group (relative risk, 2.55; 95% CI, 1.29 to 5.18; P=0.008). Relapse was the most common cause of treatment failure, occurring in 217 of the 651 patients (33.3%). There was a significant inverse relationship between the amount of prescribed chemotherapy that was administered and the risk of relapse (relative risk, 0.96, 95% CI, 0.93 to 0.99; P=0.01) (i.e., the more prescribed chemotherapy received, the lower the risk of relapse).
|
Haydar Frangoul, M.D.
Vanderbilt University School of Medicine
Nashville, TN 37232-6310
haydar.frangoul{at}vanderbilt.edu
Mazin F. Al-Jadiry, M.D.
Baghdad Medical College
Baghdad, Iraq
Yu Shyr, Ph.D.
Fei Ye, Ph.D.
Bashar Shakhtour, M.S.
Vanderbilt University School of Medicine
Nashville, TN 37232-6310
Salma A. Al-Hadad, M.D.
Baghdad Medical College
Baghdad, Iraq
References
| |||||||||||||||||||||||||||||||||||
HOME | SUBSCRIBE | SEARCH | CURRENT ISSUE | PAST ISSUES | COLLECTIONS | PRIVACY | HELP | beta.nejm.org Comments and questions? Please contact us. The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved. |