The World Health Organization’s (WHO) cancer research arm, the International Agency for Research on Cancer (IARC), has classified three widely used medicines – hydrochlorothiazide, voriconazole, and tacrolimus – as Group 1 carcinogens, the category reserved for agents considered “carcinogenic to humans”.
The latest decision follows a review of epidemiological studies, animal experiments and mechanistic evidence, and is detailed in IARC Monographs Volume 137.
The classification, however, is not a recommendation to stop taking these medicines. IARC identifies whether an agent can cause cancer under certain circumstances (hazard identification); it does not assess the level of risk for an individual patient or weigh the benefits of treatment against potential harms.
For many patients, these medicines remain life-saving and essential when used under medical supervision.
Hydrochlorothiazide is one of the world's most commonly prescribed thiazide diuretics for treating high blood pressure and fluid retention. IARC concluded there is sufficient evidence that it causes squamous cell carcinoma of the skin and cancer of the lip, with additional but more limited evidence for some other skin cancers.
The drug is known to increase sensitivity to ultraviolet (UV) radiation, which is believed to contribute to the risk.
In India, hydrochlorothiazide is sold under brands such as
Aquazide (Sun Pharma) and Hydrazide (Cipla). It is also widely available in fixed-dose combinations with blood pressure medicines, including Telma H and Telmikind-H.
Voriconazole, on the other hand, is a broad-spectrum antifungal medicine used to treat severe fungal infections such as invasive aspergillosis, particularly in patients with weakened immune systems or organ transplants.
IARC found sufficient evidence linking the drug to squamous cell carcinoma of the skin, with evidence suggesting that its phototoxic effects may play an important role.
Popular Indian brands include VFend (Pfizer), Voritek (Cipla) and Vorizol (Natco Pharma).
Tacrolimus is an immunosuppressant used primarily to prevent organ rejection after kidney, liver or heart transplantation. It is also used to prevent graft-versus-host disease after stem-cell transplantation, while topical formulations are prescribed as second-line treatment for atopic dermatitis and vitiligo.
IARC concluded there is sufficient evidence that tacrolimus causes non-Hodgkin lymphoma and post-transplant lymphoproliferative disorder, with limited evidence for leukaemia and squamous cell skin cancer.
Popular Indian brandsfor this drug include Pangraf (Mankind Pharma), Tacrograf and Tbis (Eris Lifesciences), Takfa (Intas Pharmaceuticals), Tacrotor (Torrent Pharma), and topical formulations such as Tacroz (Glenmark) and Talimus (Ajanta Pharma).