Evaluation of a blood miRNA/mRNA signature to follow-up Lu-PRRT therapy for G1/G2 intestinal neuroendocrine tumors

Front Endocrinol (Lausanne). 2024 Jun 14:15:1385079. doi: 10.3389/fendo.2024.1385079. eCollection 2024.

Abstract

Background: 177Lu-oxodotreotide peptide receptor therapy (LuPRRT) is an efficient treatment for midgut neuroendocrine tumors (NETs) of variable radiological response. Several clinical, biological, and imaging parameters may be used to establish a relative disease prognosis but none is able to predict early efficacy or toxicities. We investigated expression levels for mRNA and miRNA involved in radiosensitivity and tumor progression searching for correlations related to patient outcome during LuPRRT therapy.

Methods: Thirty-five patients received LuPRRT for G1/G2 midgut NETs between May 2019 and September 2021. Peripheral blood samples were collected prior to irradiation, before and 48 h after the second and the fourth LuPRRT, and at 6-month follow-up. Multiple regression analyses and Pearson correlations were performed to identify the miRNA/mRNA signature that will best predict response to LuPRRT.

Results: Focusing on four mRNAs and three miRNAs, we identified a miRNA/mRNA signature enabling the early identification of responders to LuPRRT with significant reduced miRNA/mRNA expression after the first LuPRRT administration for patients with progressive disease at 1 year (p < 0.001). The relevance of this signature was reinforced by studying its evolution up to 6 months post-LuPRRT. Moreover, nadir absolute lymphocyte count within the first 2 months after the first LuPRRT administration was significantly related to low miRNA/mRNA expression level (p < 0.05) for patients with progressive disease.

Conclusion: We present a pilot study exploring a miRNA/mRNA signature that correlates with early hematologic toxicity and therapeutic response 12 months following LuPRRT. This signature will be tested prospectively in a larger series of patients.

Keywords: PRRT therapy; hematotoxicity; intestinal neuroendocrine tumors; miRNA/mRNA signature; outcome.

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / blood
  • Biomarkers, Tumor / genetics
  • Female
  • Follow-Up Studies
  • Humans
  • Intestinal Neoplasms* / blood
  • Intestinal Neoplasms* / drug therapy
  • Intestinal Neoplasms* / genetics
  • Intestinal Neoplasms* / pathology
  • Lutetium
  • Male
  • MicroRNAs* / blood
  • MicroRNAs* / genetics
  • Middle Aged
  • Neuroendocrine Tumors* / blood
  • Neuroendocrine Tumors* / genetics
  • Neuroendocrine Tumors* / pathology
  • Neuroendocrine Tumors* / radiotherapy
  • Neuroendocrine Tumors* / therapy
  • Prognosis
  • RNA, Messenger* / blood
  • RNA, Messenger* / genetics
  • Radioisotopes
  • Radiopharmaceuticals / administration & dosage
  • Radiopharmaceuticals / therapeutic use
  • Receptors, Peptide / genetics
  • Somatostatin / analogs & derivatives
  • Somatostatin / therapeutic use

Substances

  • MicroRNAs
  • RNA, Messenger
  • Biomarkers, Tumor
  • Somatostatin
  • Lutetium-177
  • Receptors, Peptide
  • Radiopharmaceuticals
  • Lutetium
  • Radioisotopes

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the GENEBIOLuNET project, ARI grants from the Academic Hospital of Toulouse, NCT03667092.