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Effects of immune checkpoint inhibitor associated endocrinopathies on cancer survival.
Yang, Lisa; Murthy, Sruthi; Cortellini, Alessio; Lim, Emma A; Gonzalez, Michael; Pinato, David J; Abdel-Malek, Mariana; Mahmoud, Sarah; Martin, Niamh M.
Afiliação
  • Yang L; Department of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Murthy S; Department of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Cortellini A; Department of Surgery & Cancer, Imperial College London, London, London, United Kingdom.
  • Lim EA; Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
  • Gonzalez M; Department of Imaging, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Pinato DJ; Department of Medical Oncology, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Abdel-Malek M; Department of Surgery & Cancer, Imperial College London, London, London, United Kingdom.
  • Mahmoud S; Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
  • Martin NM; Department of Endocrinology, Imperial College Healthcare NHS Trust, London, United Kingdom.
Front Endocrinol (Lausanne) ; 15: 1369268, 2024.
Article em En | MEDLINE | ID: mdl-38681767
ABSTRACT

Objectives:

Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events (irAEs), of which endocrinopathies are common. We characterized endocrine and non-endocrine irAEs in cancer patients receiving ICIs, identified risk factors for their development and established whether endocrine and non-endocrine irAEs were differentially associated with improved cancer prognosis. Design and

methods:

Single-center, retrospective cohort study of patients with advanced or metastatic solid tumors receiving at least one ICI treatment cycle (242 men, 151 women, median age 65 years). Main outcome measures were incidence of any irAE during the study period, overall survival and time to treatment failure.

Results:

Non-endocrine irAEs occurred in 32% and endocrine irAEs in 12% of patients. Primary thyroid dysfunction was the most common endocrine irAE (9.5%) and the majority of endocrinopathies required permanent hormone replacement. Women had an increased risk of developing endocrine irAEs (p = 0.017). The biggest survival advantage occurred in patients who developed both endocrine and non-endocrine irAEs (overall survival HR 0.16, CI 0.09-0.28). Time to treatment failure was also significantly improved in patients who developed endocrine irAEs (HR 0.49, CI 0.34 - 0.71) or both (HR 0.41, CI 0.25 - 0.64) but not in those who only developed non-endocrine irAEs.

Conclusions:

Women may have increased risk of endocrine irAEs secondary to ICI treatment. This is the first study to compare the effects of endocrine irAEs with non-endocrine irAEs on survival. Development of endocrine irAEs may confer survival benefit in ICI treatment and future, prospective studies are needed to elucidate this.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças do Sistema Endócrino / Inibidores de Checkpoint Imunológico / Neoplasias Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças do Sistema Endócrino / Inibidores de Checkpoint Imunológico / Neoplasias Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article