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Elevated cerebrospinal fluid fibronectin concentration at diagnosis indicates poor prognosis in children with acute lymphoblastic leukemia
Author(s) -
Rautonen Jukka,
Koskiniemi Marjaleena,
Siimes Martti A.,
Salonen EevaMarjatta,
Vaheri Antti
Publication year - 1989
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910430108
Subject(s) - cerebrospinal fluid , medicine , subclinical infection , gastroenterology , confidence interval , lymphoblastic leukemia , leukemia , infiltration (hvac) , relative risk , pathophysiology , physics , thermodynamics
We investigated whether the concentration of fibronectin (FN) in the cerebrospinal fluid (CSF) could be used for identifying patients with subclinical blast‐cell infiltration in the central nervous system (CNS) and an increased risk of CNS relapse later in the course of their leukemia. Our series comprised 36 children with newly diagnosed acute lymphoblastic leukemia (ALL). The mean follow‐up time was 54 months (range 5 to 96 months). The median concentration of CSF‐FN at diagnosis was 2.24 mg/l (range 0.78 to 7.04 mg/l). The 3‐year continuous complete remission rate for the 16 patients with CSF‐FN concentrations <2mg/l was 93% as compared with 37% for the 19 patients with CSF‐FN >2mg/l (p = 0.001). When multivariate analysis was performed, the CSF‐FN concentration retained its prognostic significance. When all relapses were considered as failures, the relative risks of relapse for patients with CSF‐FN <2mg/l and >2mg/l were I and 15.8 (95% confidence limits 1.8‐135.6, p<0.02), respectively. If only CNS relapses (isolated and combined) were considered as failures, relative risks for the above‐mentioned groups were I and 11.6 (1.4‐99.5, p<0.05), respectively. We conclude that determination of the CSF‐FN concentration may provide a new means of evaluating the CSF in children with ALL and may prove to be a sensitive indicator of leukemic CNS infiltration.