Cannabis shows no liver damage risk in advanced cancer patients

Liver enzyme effects of medicinal cannabis in advanced cancer: a substudy of two randomised trials.

BMJ supportive & palliative care • • Clinical Trial • Moderately Relevant
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AI Summary

This substudy examined whether medicinal cannabis causes liver damage in patients with advanced cancer by measuring liver enzyme levels (ALT and AST) in 287 participants across two randomized clinical trials. Patients received escalating doses of CBD alone, THC/CBD combinations, or placebo, with measurements taken at baseline, day 14, and day 28. The key finding: medicinal cannabis did not cause elevation in liver enzymes at doses studied (up to 600 mg CBD/day), providing reassuring safety data for cancer patients considering cannabis treatment.

The study found no clinically meaningful differences between CBD-only and THC/CBD combination products in their effects on liver enzymes. Most importantly, no patients in either cannabis group exceeded dangerous enzyme thresholds (3× upper limit of normal, or 5× for those with liver metastases). This is significant because cancer patients often have compromised liver function, making them a vulnerable population. The first 4 weeks of treatment showed no significant adverse hepatic effects, which is crucial baseline data for long-term safety assessment.

These findings have practical implications for cancer patients exploring medicinal cannabis as a complementary treatment option. While this substudy focused specifically on short-term liver safety over 4 weeks, it provides important evidence that medicinal cannabis products don't cause acute liver enzyme elevation at clinically-used doses—a concern that had not been thoroughly evaluated in this vulnerable patient population previously. However, patients should continue regular liver function monitoring as part of their overall cancer care.

📄 Original Abstract

This substudy investigated whether medicinal cannabis causes an elevation in alanine aminotransferase (ALT) or aspartate aminotransferase (AST) in patients with advanced malignancy and determined whether different cannabis formulations (cannabidiol (CBD) alone vs tetrahydrocannabinol (THC)/CBD combination) had differing effects on enzyme levels. This analysis used data from two multicentre, randomised, placebo-controlled trials of escalating doses of CBD (MedCan1) or THC/CBD (MedCan2), including 287 patients with advanced cancer. Participants received escalating doses of CBD, THC/CBD or placebo. ALT and AST levels were measured at baseline, day 14 and day 28. Medicinal cannabis did not cause elevation of ALT or AST in patients with advanced malignancy at the doses studied (up to 600 mg CBD/day). No clinically meaningful differences in liver enzyme levels were observed between CBD-only and CBD/THC combination products. Furthermore, no patients in the cannabis groups exceeded the predefined thresholds of 3× upper limit of normal (ULN) (or 5× ULN in those with liver metastases) for ALT or AST. In patients with advanced malignancy enrolled in two clinical trials, medicinal cannabis products did not have a significant adverse impact on ALT or AST levels during the first 4 weeks of use at the doses studied.

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