Influence of pretreatment with everolimus or sunitinib on the subacute hematotoxicity of 177Lu-DOTATATE PRRT

Acta Oncol. 2020 Jun;59(6):644-651. doi: 10.1080/0284186X.2020.1723161. Epub 2020 Feb 8.

Abstract

Background: Peptide receptor radionuclide therapy (PRRT) is a validated treatment for somatostatin receptor overexpressing neuroendocrine tumors (NETs). The NETTER-1 trial demonstrated a pronounced positive effect on progression-free-survival compared to high dose somatostatin analogs (SSAs), with a strong tendency toward overall survival benefit. Our aim was to investigate the influence of pretreatment with everolimus and/or sunitinib on subacute hematotoxicity of PRRT. To assess the influence of prior treatment with everolimus/sunitinib might be of clinical relevance due to the link between short-term hematotoxicity and increased incidence of late hematotoxicity.Material and methods: Our single-center retrospective study enrolled all patients treated with 177Lu-DOTATATE PRRT (1-4 cycles of 7.4 GBq), between November 2013 and July 2018. Patients were assigned to two groups according to their pretreatment: no targeted agents (N = 41), or targeted agents (everolimus, sunitinib or both; N = 41). The end point was subacute hematotoxicity, defined as the nadir value between the first administration until 3 months after the last administration, using the CTCAE 4.03 classification. The impact of splenectomy was also explored.Results: Eighty percent of patients had a primary gastroenteropancreatic NET. No statistically significant differences in severe subacute hematotoxicity were seen in the pretreated group vs. the naive group for hemoglobin (grade 3/4: 12% vs. 22%), neither for leucocytes (grade 3/4: 10% vs. 7%), neutrophils (grade 3/4: 5% vs. 7%), lymphocytes (grade 3/4: 49% vs. 37%) and platelets (grade 3/4: 15% vs. 15%). Furthermore, we observed significantly lower toxicity for total white blood cells, lymphocytes and platelets in the subgroup that had splenectomy (N = 12). Limitations of this study include the potential bias in lack of use of targeted agents in patients more susceptible to toxicity, and the limited number of patients and events.Conclusions: In a patient cohort with NET pretreated with everolimus and/or sunitinib, we could not demonstrate a significant effect of prior/pretreatment with everolimus and/or sunitinib on the subacute hematotoxicity of 177Lu-DOTATATE PRRT.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Anemia / chemically induced
  • Antineoplastic Agents / therapeutic use*
  • Everolimus / therapeutic use*
  • Female
  • Hematologic Diseases / chemically induced*
  • Humans
  • Intestinal Neoplasms / blood
  • Intestinal Neoplasms / drug therapy*
  • Leukopenia / chemically induced
  • Lymphopenia / chemically induced
  • Male
  • Middle Aged
  • Neuroendocrine Tumors / blood
  • Neuroendocrine Tumors / drug therapy*
  • Octreotide / administration & dosage
  • Octreotide / adverse effects
  • Octreotide / analogs & derivatives*
  • Organometallic Compounds / administration & dosage
  • Organometallic Compounds / adverse effects*
  • Organometallic Compounds / pharmacokinetics
  • Pancreatic Neoplasms / blood
  • Pancreatic Neoplasms / drug therapy*
  • Progression-Free Survival
  • Radiopharmaceuticals / administration & dosage
  • Radiopharmaceuticals / adverse effects*
  • Receptors, Somatostatin / metabolism
  • Retrospective Studies
  • Somatostatinoma / blood
  • Somatostatinoma / drug therapy*
  • Somatostatinoma / mortality
  • Splenectomy
  • Stomach Neoplasms / blood
  • Stomach Neoplasms / drug therapy*
  • Sunitinib / therapeutic use*
  • Thrombocytopenia / chemically induced
  • Young Adult

Substances

  • Antineoplastic Agents
  • Organometallic Compounds
  • Radiopharmaceuticals
  • Receptors, Somatostatin
  • Everolimus
  • gallium Ga 68 dotatate
  • lutetium Lu 177 dotatate
  • Octreotide
  • Sunitinib

Supplementary concepts

  • Gastro-enteropancreatic neuroendocrine tumor