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Impact of opioid analgesics on survival in cancer patients receiving immune checkpoint inhibitors.
Kavgaci, Gozde; Guven, Deniz Can; Kaygusuz, Yunus; Karaca, Ece; Dizdar, Omer; Kilickap, Saadettin; Aksoy, Sercan; Erman, Mustafa; Yalcin, Suayib.
Afiliación
  • Kavgaci G; Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey. drgozdekavgaci@gmail.com.
  • Guven DC; Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
  • Kaygusuz Y; Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Karaca E; Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Dizdar O; Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
  • Kilickap S; Department of Medical Oncology, Liv Hospital, Ankara, Turkey.
  • Aksoy S; Department of Medical Oncology, Istinye University Faculty of Medicine, Istanbul, Turkey.
  • Erman M; Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
  • Yalcin S; Department of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
Support Care Cancer ; 32(7): 467, 2024 Jun 27.
Article en En | MEDLINE | ID: mdl-38937345
ABSTRACT

PURPOSE:

This study aimed to assess the effects of concurrent opioid analgesic (OA) use with immune checkpoint inhibitors (ICIs) on progression-free survival (PFS) and overall survival (OS).

METHODS:

In this observational retrospective study, we included advanced cancer patients who received ICIs at Hacettepe University Hospital's Department of Medical Oncology between June 2018 and January 2023.

RESULTS:

Our study included 375 recurrent or metastatic cancer patients treated with ICIs in the first, second line, or beyond. There were no significant differences between the OA-treated and OA-untreated groups regarding median age, age group, gender, primary tumor location, ICI type, or the presence of baseline liver and lung metastases. However, the OA-treated group exhibited a significantly higher proportion of patients who had received three or more prior treatments before initiating ICIs (p = 0.015). OA-Untreatment was significantly correlated with prolonged mPFS (6.83 vs. 4.30 months, HR 0.59, 95% CI 0.44-0.79, p < 0.001) and mOS (17.05 vs. 7.68 months, HR 0.60, 95% CI 0.45-0.80, p < 0.001).

CONCLUSIONS:

Our study demonstrates an association between the concurrent use of OAs and reduced OS and PFS in patients treated with ICIs. While OA treatment serves as a surrogate marker for higher disease burden, it may also suggest a potential biological relationship between opioids and immunotherapy efficacy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inhibidores de Puntos de Control Inmunológico / Analgésicos Opioides / Neoplasias Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Support Care Cancer Asunto de la revista: NEOPLASIAS / SERVICOS DE SAUDE Año: 2024 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inhibidores de Puntos de Control Inmunológico / Analgésicos Opioides / Neoplasias Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Support Care Cancer Asunto de la revista: NEOPLASIAS / SERVICOS DE SAUDE Año: 2024 Tipo del documento: Article País de afiliación: Turquía