OnCo
ideasIdea

Confirm or refute the harm of antioxidant supplements during chemotherapy

Half of patients take antioxidant vitamins during chemotherapy. One good observational study suggests they raise recurrence by 40%. Patients deserve a definitive answer, and it can be obtained cheaply by adding supplement tracking to trials already running.

The DELCaP study nested in a breast cancer chemotherapy trial found that antioxidant supplements (vitamins A, C, E, carotenoids, coenzyme Q10) taken before and during chemotherapy were associated with a 41% higher recurrence and 40% higher mortality, with similar signals for vitamin B12, iron and omega-3. Randomised harm has been shown for beta-carotene in smokers and for antioxidants during head and neck radiotherapy. A randomised trial of antioxidants during chemotherapy is now ethically difficult; the pragmatic path is prospective supplement capture in every adjuvant trial and a pre-registered pooled analysis, plus a randomised trial of a stop-supplement counselling intervention.

Hypothesis
Prospectively recorded antioxidant supplement use during adjuvant chemotherapy is associated with worse disease-free survival across tumour types after adjustment, and a pharmacist-led counselling intervention at chemotherapy start reduces antioxidant use by half and is acceptable to patients.
Rationale
The mechanism (scavenging of the reactive oxygen species that mediate cytotoxic and radiation cell kill) is coherent, the observational signal is large, and the exposure is common, modifiable and almost never recorded. Patients currently receive contradictory advice from oncologists, pharmacies and the internet.
What would test it
Add a standardised supplement questionnaire to three ongoing adjuvant chemotherapy trials (breast, colorectal, lung) with a pre-registered pooled analysis; in parallel, a cluster-randomised trial of pharmacist supplement reconciliation and counselling at chemotherapy initiation with supplement cessation and patient satisfaction as endpoints.
Maturity
early clinical
Who has to act
research
Cost to try
Medium ($1M to $50M)
Years to first evidence
5
Bottlenecks it attacks

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