Journal of Clinical Oncology, Vol 15, 2254-2261, Copyright © 1997 by American Society of Clinical Oncology
Cytotoxic therapy-induced D-xylose malabsorption and invasive infection during remission-induction therapy for acute myeloid leukemia in adults
EJ Bow, R Loewen, MS Cheang, TB Shore, M Rubinger and B Schacter
Department of Medicine, University of Manitoba and The Manitoba Cancer Treatment and Research Foundation, Winnipeg, Canada.
PURPOSE: To study the sequential changes in the intestinal absorption of an
oral pentose probe, D-xylose, in patients receiving therapy for untreated
acute myeloid leukemia (AML), and to correlate these changes to infectious
morbidity. PATIENTS AND METHODS: Serial D-xylose absorption studies were
conducted in 110 consecutive adult patients admitted to a
university-affiliated tertiary care hospital for remission-induction
therapy for untreated newly diagnosed AML. Serial serum D-xylose levels
were obtained 1 hour after a 5-g oral dose of D- xylose at baseline and
weekly for 4 weeks until marrow recovery. These results were correlated
with invasive infection using multivariate techniques. RESULTS: The mean
(+/- SEM) serum D-xylose levels were 0.88 +/- 0.03, 0.69 +/- 0.03, 0.58 +/-
0.02, 0.53 +/- 0.02, and 0.73 +/- 0.02 mmol/L at baseline and weeks 1 to 4,
respectively (P < .0001, analysis of variance [AN-OVA]). Time to
malabsorption varied with induction regimen (P = .007, log-rank test).
Bloodstream infections during week 2 correlated with malabsorption (P =
.007). Neutropenic enterocolitis correlated independently with induction
regimen (P = .009), malabsorption at week 2 (P = .02), and the development
of candidemia (P = .005). Hepatosplenic fungal infection correlated with
induction regimen (P = .03), malabsorption at week 2 (P = .02), and fever
at diagnosis (P = .003). Malabsorption was unrelated to the duration of
severe neutropenia and the administration of parenteral nutrition.
CONCLUSION: Serial D-xylose absorption studies in subjects with AML
produced a characteristic profile of cytotoxic therapy-related damage to
the functional integrity of the intestinal epithelium that was regimen
dependent, myelosuppression independent, and predictive for invasive
infectious complications. Further study to validate these observations
appears warranted.
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