1994
DOI: 10.1182/blood.v84.9.3242.bloodjournal8493242
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Second cancer risk after interferon therapy? [letter; comment]

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Cited by 8 publications
(14 citation statements)
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“…On the other hand, Kampmeier et al (17) found a significant increase of secondary malignancies in HCL patients treated with IFNa and explained this rather surprising finding by a disease related increased risk for secondary malignancies, irrespective of the treatment (1,18). However, several other studies could not confirm an increase of secondary malignancies in IFNa treated HCL patients (19)(20)(21)(22)(23). Moreover, IFNa treatment for hepatitis, renal cancer, chronic myeloid leukemia, and multiple myeloma is not associated with an increased incidence of secondary cancers (24)(25)(26)(27)(28).…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, Kampmeier et al (17) found a significant increase of secondary malignancies in HCL patients treated with IFNa and explained this rather surprising finding by a disease related increased risk for secondary malignancies, irrespective of the treatment (1,18). However, several other studies could not confirm an increase of secondary malignancies in IFNa treated HCL patients (19)(20)(21)(22)(23). Moreover, IFNa treatment for hepatitis, renal cancer, chronic myeloid leukemia, and multiple myeloma is not associated with an increased incidence of secondary cancers (24)(25)(26)(27)(28).…”
Section: Discussionmentioning
confidence: 99%
“…Among 69 patients treated with IFN-α2b followed for a median of 91 months, 13 (19%) developed a second malignancy, half of which were of hematologic origin. However, this association has not been uniformly observed (81). Given the fact that the purine analogs are immunosuppressive, it will be important to determine whether patients treated with either 2´-DCF or 2-CdA are at risk for second malignancies.…”
Section: Risk Of Second Malignanciesmentioning
confidence: 99%
“…The occurrence of preceding, concurrent and subsequent secondary malignancies, both haematological and nonhaematological, has been reported and was found to be statistically significant in some series (Bernstein, Newton & Ross, 1990;Kampmeier et al, 1994;Au et al,1998;Chadha et al, 2005;Hisada et al, 2007) but not in others (Troussard, Henry-Amar & Flandrin, 1994;Kurzrock et al, 1997;Cheson et al, 1999;Flinn et al, 2000;Federico et al, 2002). Some reports have found an association with the type of therapy received whereas others (Au et al, 1998) have found a relation to the original tumour burden.…”
Section: Discussionmentioning
confidence: 98%