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Prof. Dr. Mustafa Özdoğan · Medical Oncologist

Ho-166 Therapy Found Effective for Liver Metastases from Neuroendocrine Tumours

Ho-166 Therapy Found Effective for Liver Metastases from Neuroendocrine Tumours
In this article

The Lancet Oncology reported a single-centre Dutch phase II clinical trial by Braat and colleagues, who showed that following Lutetium-177 (Lu-117) therapy, Holmium-166 (Ho-166)-based radioembolization, for neuroendocrine tumour liver metastases was effective in these patients.

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Study Details

In the study, 31 patients enrolled at University Medical Center Utrecht between October 2014 and September 2018 received holmium Ho-166 radioembolization within 20 weeks after 4 treatments with lutetium Lu-177 dotatate. This radioembolization procedure required a 3-day hospital stay.

The primary endpoint the study aimed to measure was the objective liver tumour volume response at month 3.

Responses

  • All 30 evaluable patients completed 6 months of follow-up.
  • An objective response in liver tumour volume was observed in 13 of 30 patients (43%) at month 3 and in 14 (47%) at month 6.
  • All responses were partial; 50% of patients had stable disease at month 3 and 37% at month 6.

Side Effects

Among the 31 patients who underwent radioembolization, the most common serious (grade 3 or 4) clinical and laboratory side effects within 6 months were abdominal pain (10%), increased γ-glutamyl transpeptidase (GGT) (54%) and lymphocytopenia (23%). One patient had fatal radioembolization-induced liver damage; in addition to this patient, two other patients had serious adverse events thought to be unrelated to treatment: a gastric ulcer and perforated cholecystitis.

In conclusion, [Holmium Ho-166] radioembolization in addition to peptide receptor radionuclide therapy (Lu-177) is safe and effective in patients with liver metastases from neuroendocrine cancer. Radioembolization may be considered, including after peptide receptor radionuclide therapy, in patients with large liver tumours. A future randomized, controlled clinical trial should investigate the additional benefit of this treatment for progression-free survival.

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