TY - JOUR
T1 - Efficacy of subsequent treatment for unresectable locally-advanced non-small cell lung cancer after relapse of concurrent chemoradiotherapy with durvalumab consolidation therapy
T2 - A single-center retrospective study
AU - Nishibori, Yuichiro
AU - Kenmotsu, Hirotsugu
AU - Ando, Kenju
AU - Tonsho, Ayumi
AU - Matsuda, Suguru
AU - Morita, Meiko
AU - Sekikawa, Motoki
AU - Doshita, Kosei
AU - Morikawa, Noboru
AU - Miura, Keita
AU - Kodama, Hiroaki
AU - Yabe, Michitoshi
AU - Iida, Yuko
AU - Mamesaya, Nobuaki
AU - Kobayashi, Haruki
AU - Ko, Ryo
AU - Wakuda, Kazushige
AU - Ono, Akira
AU - Naito, Tateaki
AU - Murakami, Haruyasu
AU - Harada, Hideyuki
AU - Takahashi, Toshiaki
N1 - Publisher Copyright:
© 2024
PY - 2024/1
Y1 - 2024/1
N2 - Objectives: The current standard treatment for locally advanced non-small cell lung cancer (LA-NSCLC) is concurrent chemoradiation therapy (CCRT) followed by durvalumab consolidation therapy. Although the trial revealed the survival benefit of adding an immune checkpoint inhibitor (ICI) to the population, the optimal treatment strategy and efficacy of subsequent treatment after relapse remain unclear. Materials and methods: We retrospectively collected data from patients with unresectable LA-NSCLC who completed platinum-based CCRT as first-line treatment. Patients who received molecular-targeted therapy for driver gene alterations or did not receive durvalumab as consolidation therapy following the approval were excluded. We assessed differences in regimen and efficacy of subsequent treatment in patients who underwent durvalumab consolidation therapy (D group) and those who did not (CR group). Results: Among the 62 eligible patients, 32 were assigned to the D group and 30 to the CR group. Patients in the CR group were more frequently treated with an immune checkpoint inhibitor (ICI)-containing regimen than those in the D group (57 % vs. 13 %, p < 0.001). The median overall survival from initiation of subsequent treatment was shorter in the D group than in the CR group (13.0 months vs. 26.7 months, hazard ratio 2.60; 95 % confidence interval: 1.28–2.56, p = 0.008). Conclusions: Patients with unresectable LA-NSCLC who relapsed after durvalumab consolidation therapy received an ICI-containing regimen less frequently, and the efficacy of the subsequent treatment was limited.
AB - Objectives: The current standard treatment for locally advanced non-small cell lung cancer (LA-NSCLC) is concurrent chemoradiation therapy (CCRT) followed by durvalumab consolidation therapy. Although the trial revealed the survival benefit of adding an immune checkpoint inhibitor (ICI) to the population, the optimal treatment strategy and efficacy of subsequent treatment after relapse remain unclear. Materials and methods: We retrospectively collected data from patients with unresectable LA-NSCLC who completed platinum-based CCRT as first-line treatment. Patients who received molecular-targeted therapy for driver gene alterations or did not receive durvalumab as consolidation therapy following the approval were excluded. We assessed differences in regimen and efficacy of subsequent treatment in patients who underwent durvalumab consolidation therapy (D group) and those who did not (CR group). Results: Among the 62 eligible patients, 32 were assigned to the D group and 30 to the CR group. Patients in the CR group were more frequently treated with an immune checkpoint inhibitor (ICI)-containing regimen than those in the D group (57 % vs. 13 %, p < 0.001). The median overall survival from initiation of subsequent treatment was shorter in the D group than in the CR group (13.0 months vs. 26.7 months, hazard ratio 2.60; 95 % confidence interval: 1.28–2.56, p = 0.008). Conclusions: Patients with unresectable LA-NSCLC who relapsed after durvalumab consolidation therapy received an ICI-containing regimen less frequently, and the efficacy of the subsequent treatment was limited.
KW - Chemoradiation therapy
KW - Durvalumab
KW - Non-small cell lung cancer
KW - Subsequent treatment
UR - http://www.scopus.com/inward/record.url?scp=85208580154&partnerID=8YFLogxK
U2 - 10.1016/j.ctarc.2024.100849
DO - 10.1016/j.ctarc.2024.100849
M3 - Article
C2 - 39536390
AN - SCOPUS:85208580154
SN - 2213-0896
VL - 41
JO - Cancer Treatment and Research Communications
JF - Cancer Treatment and Research Communications
M1 - 100849
ER -