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Evaluation of a blood miRNA/mRNA signature to follow-up Lu-PRRT therapy for G1/G2 intestinal neuroendocrine tumors.
Jacques, Virginie; Dierickx, Lawrence; Texier, Jean Sebastien; Brillouet, Severine; Courbon, Frederic; Guimbaud, Rosine; Vija, Lavinia; Savagner, Frederique.
Afiliação
  • Jacques V; Biochemistry Laboratory, Federative Institute of Biology, Academic Hospital, Toulouse, France.
  • Dierickx L; Inserm UMR1297, Institute of Cardiovascular and Metabolic Diseases, Toulouse, France.
  • Texier JS; Faculté de Santé, University Paul sabatier, Toulouse, France.
  • Brillouet S; Nuclear Medicine Department, Regional Center of Cancer Care Oncopole Claudius Regaud, Toulouse, France.
  • Courbon F; Nuclear Medicine Department, Regional Center of Cancer Care Oncopole Claudius Regaud, Toulouse, France.
  • Guimbaud R; Nuclear Medicine Department, Regional Center of Cancer Care Oncopole Claudius Regaud, Toulouse, France.
  • Vija L; Faculté de Santé, University Paul sabatier, Toulouse, France.
  • Savagner F; Nuclear Medicine Department, Regional Center of Cancer Care Oncopole Claudius Regaud, Toulouse, France.
Front Endocrinol (Lausanne) ; 15: 1385079, 2024.
Article em En | MEDLINE | ID: mdl-38948517
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Tumores Neuroendócrinos / MicroRNAs / Neoplasias Intestinais Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Tumores Neuroendócrinos / MicroRNAs / Neoplasias Intestinais Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article