1999
DOI: 10.1016/s0016-5085(99)70294-5
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The relationship between infliximab treatment and lymphoma in Crohn's disease

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Cited by 194 publications
(106 citation statements)
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“…A recent and extensive meta-analysis has also recently confirmed the increased colorectal and small bowel cancer risk in Crohn's disease [12] . Moreover, other malignancies have been reported in Crohn's disease, including myeloid and lymphoid malignancies [13] , possibly related, in part, to wider use of immunosuppressants or biological agents (e.g., infliximab) [14,15] . …”
Section: Crohn's Disease and Cancer Riskmentioning
confidence: 99%
“…A recent and extensive meta-analysis has also recently confirmed the increased colorectal and small bowel cancer risk in Crohn's disease [12] . Moreover, other malignancies have been reported in Crohn's disease, including myeloid and lymphoid malignancies [13] , possibly related, in part, to wider use of immunosuppressants or biological agents (e.g., infliximab) [14,15] . …”
Section: Crohn's Disease and Cancer Riskmentioning
confidence: 99%
“…The same problem, i.e., an inability to distinguish therapy-related effects from effects of the disease, is encountered in case-control studies whose results have indicated increased lymphoma risks after treatment with nonsteroidal antiinflammatory drugs (NSAIDs) and aspirin (18,19) and with corticosteroids (20,21). Reports based on case series and comparisons with age-matched healthy population controls have also linked tumor necrosis factor (TNF) blockade treatment to increased lymphoma risk (8,(22)(23)(24). Importantly, though, none of the above studies has been able to pinpoint the specific effects of disease activity on lymphoma risk, let alone distinguish them from the effects of treatment.…”
mentioning
confidence: 99%
“…In light of the recent introduction of potent therapy with tumor necrosis factor ␣ (TNF␣) inhibitors in RA and other inflammatory conditions (a treatment with which development of malignant lymphomas remains a concern [21,22]), it has become increasingly important to determine how the 2 disease groups interact. Thus, we need not only to obtain a better assessment of the "expected" risk of malignant lymphoma in patients with RA (before the introduction of TNF␣ inhibitor therapy), but also to try to separate potential risk factors (genetic or environmental) common to RA and malignant lymphomas from lymphomagenic factors related to the rheumatic disease itself or its treatment.…”
mentioning
confidence: 99%