IARC group 1

IARC group 1 Carcinogens are substances, chemical mixtures, and exposure circumstances which have been classified as carcinogenic to humans by the International Agency for Research on Cancer (IARC). This category is used when there is sufficient evidence of carcinogenicity in humans. Exceptionally, an agent (chemical mixture) may be placed in this category when evidence of carcinogenicity in humans is less than sufficient, but when there is sufficient evidence of carcinogenicity in experimental animals and strong evidence in exposed humans that the agent (mixture) acts through a relevant mechanism of carcinogenicity.

This list focuses on the hazard linked to the agents. This means that while carcinogens are capable of causing cancer, it does not take their risk into account, which is the probability of causing a cancer, given the level of exposure to this carcinogen. The list is up to date as of January 2024.

Agents

Infectious conditions

Viruses

  • Human immunodeficiency virus type 1 (infection with)
  • Human T-cell lymphotropic virus type I
  • Human papillomavirus types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, and 59
  • Hepatitis B virus (chronic infection with)
  • Hepatitis C virus (chronic infection with)
  • Kaposi's sarcoma-associated herpesvirus
  • Epstein–Barr virus
  • Merkel cell polyomavirus
  • Hepatitis D virus (chronic infection with)

Bacterium

  • Helicobacter pylori (infection with)

Worms

  • Clonorchis sinensis (infection with)
  • Opisthorchis viverrini (infection with)
  • Schistosoma haematobium (infection with)

Chemical substances

  • Acetaldehyde associated with consumption of alcohol
  • Acrylonitrile
  • Aflatoxins
  • 4-Aminobiphenyl
  • Aristolochic acids, and plants containing them
  • Arsenic and inorganic arsenic compounds
  • Asbestos (all forms, including actinolite, amosite, anthophyllite, chrysotile, crocidolite, tremolite)
  • Azathioprine
  • Benzene
  • Benzidine, and dyes metabolized to
  • Benzo[a]pyrene
  • Beryllium and beryllium compounds
  • 1,3-Butadiene
  • 1,4-Butanediol dimethanesulfonate (Busulphan, Myleran)
  • Cadmium and cadmium compounds
  • Chlornapazine (N,N-Bis(2-chloroethyl)-2-naphthylamine)
  • Chlorambucil
  • Bis(chloromethyl)ether
  • Chloromethyl methyl ether
  • Chromium(VI) (Hexavalent chromium) compounds
  • Ciclosporin
  • Cyclophosphamide
  • 1,2-Dichloropropane
  • Diethylstilboestrol
  • Erionite
  • Ethanol, a chemical known as alcohol as a drug
  • Ethylene oxide
  • Etoposide alone, and in combination with cisplatin and bleomycin
  • Fluoro-edenite fibrous amphibole
  • Formaldehyde
  • Gallium arsenide
  • Lindane
  • Melphalan
  • Methoxsalen (8-Methoxypsoralen) plus ultraviolet A radiation
  • 4,4'-Methylenebis(2-chloroaniline) (MOCA)
  • MOPP and other combined chemotherapy including alkylating agents
  • Mustard gas (Sulfur mustard)
  • 2-Naphthylamine
  • Nickel compounds
  • 4-(N-Nitrosomethylamino)-1-(3-pyridyl)-1-butanone (NNK)
  • N-Nitrosonornicotine (NNN)
  • 2,3,4,7,8-Pentachlorodibenzofuran
  • 3,4,5,3’,4’-Pentachlorobiphenyl (PCB-126)
  • Pentachlorophenol
  • Perfluorooctanoic acid (PFOA), evaluated 2023
  • Polychlorinated biphenyls
  • Semustine [1-(2-Chloroethyl)-3-(4-methylcyclohexyl)-1-nitrosourea, Methyl-CCNU]
  • Silica dust, crystalline, in the form of quartz or cristobalite
  • Tamoxifen
  • 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD)
  • Thiotepa (1,1',1"-Phosphinothioylidynetrisaziridine)
  • Treosulfan
  • Trichloroethylene
  • o-Toluidine
  • Vinyl chloride
  • hydrochlorothiazide
  • voriconazole
  • tacrolimus

Radiations and physical agents thereof

Complex mixtures/agents

Exposure circumstances

See also

  • IARC group 2A
  • IARC group 2B
  • IARC group 3

Notes

  1. This evaluation applies to the group of compounds as a whole and not necessarily to all individual compounds within the group.
  2. Evaluated as a group.
  3. There is also conclusive evidence that this agent (tamoxifen) reduces the risk of contralateral breast cancer.
  4. Specific radionuclides for which there is sufficient evidence for carcinogenicity to humans are also listed individually as Group 1 agents.
  5. There is also convincing evidence in humans that these agents confer a protective effect against cancer in the endometrium and ovary.
  6. Overall evaluation upgraded to Group 1 with strong supporting evidence from other relevant data.

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