ArticleArchives of toxicology2026
Pheochromocytoma in rats: a weak link in the assessment of talc carcinogenicity?
Article in Archives of toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
1 author.
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Abstract
This Letter to the Editor addresses the recent step by the International Agency for Research on Cancer (IARC) to reclassify pure talc from Group 2B "Possibly carcinogenic to humans" to Group 2A "Probably carcinogenic to humans". This change was made by IARC not based on any new data, but by reassessing previous studies, including an inhalation study on rats and mice performed in the 1980s under the auspices of the National Toxicology Program (NTP). The NTP study, however, found evidence of tumorigenicity in rats only, but not in mice. This contradicts the toxicological principle of "at least two species" for extrapolating carcinogenicity status from animals to humans. Benign and malignant pheochromocytoma, a rare condition identified in the adrenal medulla of rats in multiple NTP studies, played a special role in the IARC talc reclassification, being evaluated as the "unusual" finding requiring a precautionary approach. The Letter argues that combined benign, malignant, and complex pheochromocytoma in rats is irrelevant for the assessment of talc carcinogenicity in humans. However, with the exclusion of pheochromocytoma argumentation, the need for talc reclassification appears to be highly questionable.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.