TY - JOUR
T1 - Development of pituitary dysfunction and destructive thyroiditis is associated with better survival in non-small cell lung cancer patients treated with programmed cell death-1 inhibitors
T2 - a prospective study with immortal time bias correction
AU - Suzuki, Koji
AU - Kobayashi, Tomoko
AU - Izuchi, Tetsushi
AU - Otake, Koki
AU - Ando, Masahiko
AU - Handa, Tomoko
AU - Miyata, Takashi
AU - Sugiyama, Mariko
AU - Onoue, Takeshi
AU - Hagiwara, Daisuke
AU - Suga, Hidetaka
AU - Banno, Ryoichi
AU - Hase, Tetsunari
AU - Inoue, Megumi
AU - Ishii, Makoto
AU - Arima, Hiroshi
AU - Iwama, Shintaro
N1 - Publisher Copyright:
Copyright © 2024 Suzuki, Kobayashi, Izuchi, Otake, Ando, Handa, Miyata, Sugiyama, Onoue, Hagiwara, Suga, Banno, Hase, Inoue, Ishii, Arima and Iwama.
PY - 2024
Y1 - 2024
N2 - Background: Immune-related adverse events (irAEs) are reported to be associated with better overall survival (OS) in non-small cell lung cancer (NSCLC) patients treated with immune checkpoint inhibitors. However, there may be a bias in that patients who develop irAEs must survive long enough to experience the irAEs, and no prospective studies adjusting for immortal time bias (ITB) have examined the relationship between OS and pituitary dysfunction or the two different types of thyroid dysfunction: destructive thyroiditis and hypothyroidism without prior thyrotoxicosis (isolated hypothyroidism). Methods: Patients with NSCLC who received nivolumab or pembrolizumab at Nagoya University Hospital between November 2, 2015 and February 1, 2023 were enrolled. Endocrine irAEs were prospectively assessed during scheduled evaluations of hormone levels. The association between irAE development and survival when considering ITB was examined by time-dependent Cox regression analysis. Results: Of the 194 patients included, 11 (5.7%), 10 (5.2%), and 5 (2.6%) developed pituitary dysfunction, destructive thyroiditis, and isolated hypothyroidism, respectively. The development of pituitary dysfunction (HR 0.36, 95% CI 0.13–0.98, p = 0.045) and destructive thyroiditis (HR 0.31, 95% CI 0.10–0.97, p = 0.044), but not isolated hypothyroidism (HR 1.15, 95% CI 0.42–3.20, p = 0.786), was significantly associated with longer OS. Conclusion: NSCLC patients developing pituitary dysfunction and destructive thyroiditis showed better OS even after adjusting for ITB, suggesting that these irAEs indicate a better prognosis.
AB - Background: Immune-related adverse events (irAEs) are reported to be associated with better overall survival (OS) in non-small cell lung cancer (NSCLC) patients treated with immune checkpoint inhibitors. However, there may be a bias in that patients who develop irAEs must survive long enough to experience the irAEs, and no prospective studies adjusting for immortal time bias (ITB) have examined the relationship between OS and pituitary dysfunction or the two different types of thyroid dysfunction: destructive thyroiditis and hypothyroidism without prior thyrotoxicosis (isolated hypothyroidism). Methods: Patients with NSCLC who received nivolumab or pembrolizumab at Nagoya University Hospital between November 2, 2015 and February 1, 2023 were enrolled. Endocrine irAEs were prospectively assessed during scheduled evaluations of hormone levels. The association between irAE development and survival when considering ITB was examined by time-dependent Cox regression analysis. Results: Of the 194 patients included, 11 (5.7%), 10 (5.2%), and 5 (2.6%) developed pituitary dysfunction, destructive thyroiditis, and isolated hypothyroidism, respectively. The development of pituitary dysfunction (HR 0.36, 95% CI 0.13–0.98, p = 0.045) and destructive thyroiditis (HR 0.31, 95% CI 0.10–0.97, p = 0.044), but not isolated hypothyroidism (HR 1.15, 95% CI 0.42–3.20, p = 0.786), was significantly associated with longer OS. Conclusion: NSCLC patients developing pituitary dysfunction and destructive thyroiditis showed better OS even after adjusting for ITB, suggesting that these irAEs indicate a better prognosis.
KW - destructive thyroiditis
KW - immune checkpoint inhibitors
KW - immune-related adverse events
KW - PD-1
KW - pituitary
UR - https://www.scopus.com/pages/publications/85210073429
UR - https://www.scopus.com/pages/publications/85210073429#tab=citedBy
U2 - 10.3389/fendo.2024.1490042
DO - 10.3389/fendo.2024.1490042
M3 - Article
AN - SCOPUS:85210073429
SN - 1664-2392
VL - 15
JO - Frontiers in Endocrinology
JF - Frontiers in Endocrinology
M1 - 1490042
ER -