What is changing in the natural history of chronic lymphocytic leukemia?

Citation
S. Molica et D. Levato, What is changing in the natural history of chronic lymphocytic leukemia?, HAEMATOLOG, 86(1), 2001, pp. 8-12
Citations number
22
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
HAEMATOLOGICA
ISSN journal
03906078 → ACNP
Volume
86
Issue
1
Year of publication
2001
Pages
8 - 12
Database
ISI
SICI code
0390-6078(200101)86:1<8:WICITN>2.0.ZU;2-#
Abstract
Background and Objectives. In the last few years there has been a trend tow ards an improvement in overall survival of patients with chronic lymphocyti c leukemia (CLL). Studies based on tumor registries of the general populati on or including patients referred to hematologic institutions have analyzed reasons for these changes, However, results need to be validated on indepe ndent series. Design and Methods. We retrospectively evaluated 518 CLL patients diagnosed at our institution between January 1970 and December 1998. In this cohort of patients we looked at characteristics affecting natural history such as age and sex distribution, stage at diagnosis, survival probability and impa ct of the disease status an the actuarial survival, Trends in these variabl es were analyzed after splitting the whole series into three groups accordi ng to the period in which the diagnosis was made, Group I consisted of 75 p atients diagnosed between 1970 and 1979, group II consisted of 149 patients diagnosed in the period 1980-1989, group III was composed of 293 patients diagnosed between 1991 and 1998. Results. Age and sex distribution did not reflect different periods of diag nosis. The proportion of patients in whom diagnosis was established in law clinical stage (stage A) was higher in the group III (72%) than in groups I or II (26.3% and 50.3%, respectively) (p < 0.0001). Differences in the sta ge distribution affected life-expectancy which was longer for patients diag nosed in the nineties (median survival, 93 months) than in those diagnosed in the eighties (median survival, 54 months) or in the seventies (median su rvival, 38 months) (p < 0.0001), Finally, survival analyses by stage showed an improvement of life-expectancy when dealing with patients of high risk category (p = 0.005). Interpretation and Conclusions. CLL patients diagnosed in the last decade e njoy the best clinical outcome, mostly as a result of a greater proportion of patients in the low-risk clinical stage and a relatively longer survival of the high risk group. It is not clear whether these changes represent tr ue modifications of the natural history of CU. At the beginning of the thir d millennium CLL continues to be a fatal disease with a significant impact on life-expectancy. (C) 2001, Ferrata Storti Foundation.