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Updated: Jul 16, 2026

High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents (HPHC)
Published on: May 10, 2016
Identifying carcinogenic hazards among pharmaceutical agents: An update from the IARC Monographs programme
Elisa Pasqual1, Andrew Kunzmann1, Julia Rezende da Silva1
1International Agency for Research on Cancer, World Health Organization, Lyon, France.
Background:
We aim to review the evaluation of pharmaceuticals classified as human carcinogens by the International Agency for Research on Cancer (IARC) Monographs programme (1971-2024) and the recommended evaluation priorities (2024-2029) for pharmaceuticals. This work aims to stimulate epidemiological research that can contribute to human cancer and mechanistic evidence for cancer hazard identification.
Methods:
Data on cancer in humans or experimental animals, and mechanistic evidence, for pharmaceuticals evaluated as IARC Group 1, 2 A, and 2B (carcinogenic, probably carcinogenic, and possibly carcinogenic to humans, respectively) between 1971 and 2026 were extracted from published IARC monographs. Pharmaceuticals given high priority for evaluation by the IARC Monographs Advisory Group for the period 2025-2029 were summarised, highlighting available data in human cancer or mechanistic studies.
Results:
77 pharmaceuticals have been evaluated as Group 1 (n = 24), 2 A (n = 13), or 2B (n = 40). 22 pharmaceuticals were recommended with high priority for evaluation, including 8 antineoplastic, 4 hormonal, and 2 immunosuppressant agents. The IARC Advisory Group gave high priority for evaluation to several commonly used pharmaceuticals, including several treatments in cancer patients (anthracyclines, cisplatin, textured implants), highlighting evidence of increased haematological and solid malignancies; GLP-1 agonists; paracetamol; progestogen-only contraceptives; and clomiphene citrate. Evidence from studies conducted in humans with cancer or mechanistic endpoints largely contributed to this prioritisation.
Discussion:
Pharmacoepidemiology data with cancer or mechanistic endpoints can largely contribute to cancer hazard identification of pharmaceuticals within the IARC Monographs programme. These data can inform policy decision-making for patients and workers protection.
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