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Self-administered ivermectin and fenbendazole in a patient with metastatic melanoma showed mixed radiographic and ctDNA responsesOne man with melanoma tries antiparasitic drugs for his cancer

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Key Takeaway
Note that there is no clinical evidence supporting the use of ivermectin or fenbendazole for melanoma treatment.

This case report describes the experience of a 74-year-old man with nodular melanoma of the right lateral neck and associated nodal and hepatic metastases who self-administered ivermectin and fenbendazole. The report focuses on the patient's clinical course and the observation of mixed responses to these interventions.

Initial results showed a reduction in metabolic activity and tumor size without new sites of involvement. Concurrently, ctDNA levels decreased from 2.04 to 0.18 MTM/mL. However, these findings were followed by a worsening of the dominant axillary nodal mass and an increase in ctDNA to 0.93 MTM/mL.

The authors emphasize that there is a lack of clinical evidence supporting the efficacy of repurposing antiparasitic drugs for cancer treatment. They suggest that spontaneous immune-mediated regression is at least as plausible as any potential effect from the patient's self-administered medications.

Clinical practice relevance is limited by the lack of evidence. The report highlights the necessity of providing safety counseling regarding the known toxicities of antiparasitic drugs and notes the absence of evidence for their use in oncology. The results are not sufficient to establish any treatment effect for ivermectin or fenbendazole.

How this fits prior evidence

This case report addresses a gap in clinical evidence regarding the use of off-label antiparasitic agents in melanoma. While other covered evidence discusses established treatments like the Encorafenib and Binimetinib combination, nivolumab-containing regimens, and mRNA vaccines, this report highlights the lack of evidence for ivermectin and fenbendazole. It does not confirm or extend the findings regarding RFS, ORR, or the role of mitophagy and PGE2 signaling in melanoma progression.

Imagine facing a serious diagnosis like melanoma and looking for any possible way to fight back. In one case, a 74-year-old man with advanced melanoma and spread to his liver and lymph nodes decided to self-administer two drugs typically used to treat parasites: ivermectin and fenbendazole.

Initially, the results looked promising. Imaging showed a decrease in the size and metabolic activity of his tumors, and his ctDNA levels (a marker for circulating tumor DNA) dropped significantly. However, this progress did not last. The cancer eventually grew larger and more active, and his ctDNA levels rose again.

It is important to note that there is currently no clinical evidence to prove these drugs work against cancer. Because the patient took them on his own, it is impossible to tell if the initial improvement was caused by the drugs or by his own immune system. Doctors warn that these medications can have toxic side effects and should not be used without medical supervision.

What this means for you:
A patient saw temporary improvement with antiparasitic drugs, but there is no evidence they work for cancer.

Common questions

Did the drugs actually work for the man's melanoma?

The results were mixed. At first, the man's tumor size and activity decreased, and his ctDNA levels dropped from 2.04 to 0.18 MTM/mL. However, this did not last. His tumors eventually grew larger and more active, and his ctDNA levels rose to 0.93 MTM/mL. Because he took the drugs himself, it is unclear if the initial drop was due to the medicine or his own immune system.

What are ivermectin and fenbendazole?

These are medications typically used to treat parasites. While they were used by this patient to treat his melanoma, there is currently no clinical evidence to support using these antiparasitic drugs as a treatment for cancer. Doctors warn that these drugs can have toxic side effects.

Is it safe to use these drugs for cancer?

There is no clinical evidence to support using ivermectin or fenbendazole for cancer treatment. Because these drugs can have toxic side effects, doctors emphasize the importance of professional medical guidance and caution against self-medicating with antiparasitic drugs for oncology purposes.

Study Details

Study typeGuideline
EvidenceLevel 5
PublishedSep 2026
View Original Abstract ↓
A 74-year-old man with nodular melanoma of the right lateral neck presented with nodal and hepatic metastases at staging. He declined guideline-directed therapy and instead pursued lifestyle modifications alongside self-administered ivermectin and fenbendazole. On serial imaging, his disease initially demonstrated reduced metabolic activity and size without new sites of involvement, paralleled by a decline in tumor-informed ctDNA (Signatera) from 2.04 to 0.18 MTM/mL. Both subsequently worsened, with ctDNA rising to 0.93 MTM/mL and the dominant axillary nodal mass increasing in size and avidity. The tumor carried a mutational burden of at least 50 mutations/Mb, placing it at the extreme upper end of the immunogenic spectrum, and spontaneous immune-mediated regression is at least as plausible an explanation as any effect of the patient’s interventions. The discussion contextualizes the growing popularity of antiparasitic repurposing in oncology, the absence of clinical evidence supporting efficacy, and the need for safety counseling given the reported toxicities of such drugs.
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