Non-cancer mortality among people diagnosed with lymphohaematopoietic neoplasm in Australia.

OBJECTIVES: There is some evidence that people diagnosed with cancer have increased risks of dying from other diseases. This may particularly be so for cancers such as the lymphohaematopoietic neoplasms (LHN) which are now managed more as chronic diseases than acute events. METHODS: The non-cancer mortality of people diagnosed with LHN in Australia between 1982 and 2006 was compared to the mortality of the age- and sex-matched Australian population. RESULTS: Australians diagnosed with LHN had about an 80% higher risk (SMR = 1.82; 95% CI = 1.79-1.85) of dying from a non-cancer cause of death than the general population, with this increased risk particularly evident in the first 3-12 months after diagnosis. While the relative risk varied by LHN subtypes, all had an inflated relative risk. Despite younger patients having a lower absolute mortality risk, their relative mortality risk was particularly high; this decreased as age increased. The causes of death with the highest relative risks were infections and diseases of blood and blood-forming organs. CONCLUSIONS: The consistently increased risks of non-cancer causes of death compared to the general population for patients diagnosed with LHN highlight the importance that general practitioners and haematologists should bear in mind the patient's other medical conditions as well as the LHN diagnosis.

Maternal consumption of coffee and tea during pregnancy and risk of childhood ALL: results from an Australian case-control study.

OBJECTIVES: To investigate whether maternal coffee and/or tea consumption during the last 6 months of pregnancy was associated with risk of childhood ALL. METHODS: Data on coffee and tea drinking during pregnancy from 337 case mothers and 697 control mothers were analyzed using unconditional multivariable logistic regression. A meta-analysis of our findings with those of previous studies was also conducted. RESULTS: There was little evidence of an overall association between maternal coffee consumption and risk of ALL: OR 0.89 (95% CI 0.61, 1.30), although there was some suggestion that higher levels of intake might increase the risk in children of non-smoking mothers: OR for 2+ cups/day = 1.44 (95% CI 0.85, 2.42); this was supported by our meta-analysis. Risk was also elevated among cases with chromosomal translocations. The overall OR for maternal tea consumption was 0.82 (95% CI 0.56, 1.18), although the OR for T-cell ALL was 0.21 (95% CI 0.08, 0.51). Among ALL cases with translocations, the ORs for tea consumption tended to be elevated: OR = 1.70 (95% CI 0.79-3.68) for 2+ cups/day. CONCLUSIONS: The observed increased risk associated with coffee and tea consumption may be confined to ALL with translocations. These associations should be explored further in large international consortia.

Maternal folate and other vitamin supplementation during pregnancy and risk of acute lymphoblastic leukemia in the offspring.

The Australian Study of Causes of Acute Lymphoblastic Leukemia in Children (Aus-ALL) was designed to test the hypothesis, raised by a previous Western Australian study, that maternal folic acid supplementation during pregnancy might reduce the risk of childhood acute lymphoblastic leukemia (ALL). Aus-ALL was a national, population-based, multicenter case-control study that prospectively recruited 416 cases and 1,361 controls between 2003 and 2007. Detailed information was collected about maternal use of folic acid and other vitamin supplements before and during the index pregnancy. Data were analyzed using logistic regression, adjusting for matching factors and potential confounders. A meta-analysis with the results of previous studies of folic acid supplementation was also conducted. We found weak evidence of a protective effect of maternal folate supplementation before pregnancy against risk of childhood ALL, but no evidence for a protective effect of its use during pregnancy. A meta-analysis including this and 2 other studies, but not the study that raised the hypothesis, also found little evidence that folate supplementation during pregnancy protects against ALL: the summary odds ratios (ORs) for folate supplementation were 1.06 [95% confidence interval (CI): 0.77-1.48] with reference to no folate supplementation and 1.02 (95% CI: 0.86-1.20) with reference to no vitamin supplementation. For vitamin supplementation in general, the summary OR from a meta-analysis of 5 studies-including Aus-ALL-was 0.83 (95% CI: 0.73-0.94). Vitamin supplementation in pregnancy may protect against childhood ALL, but this effect is unlikely to be large or, if real, specifically due to folate.