Treatment patterns and prognosis in inoperable stage III NSCLC after concurrent chemoradiotherapy with or without immune checkpoint inhibition: Historical overview

e20578 Background: To investigate the impact of treatment patterns in inoperable stage III NSCLC following concurrent chemoradiotherapy with or without immune checkpoint inhibition (cCRT±ICI). Methods: Patients were stratified by treatment year and divided into three subgroups: A (2011–2014), B (201...

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Published inJournal of clinical oncology Vol. 40; no. 16_suppl; p. e20578
Main Authors Flörsch, Benedikt, Taugner, Julian, Käsmann, Lukas, Kenndoff, Saskia, Guggenberger, Julian, Tufman, Amanda, Reinmuth, Niels, Duell, Thomas, Belka, Claus, Eze, Chukwuka, Manapov, Farkhad
Format Journal Article
LanguageEnglish
Published 01.06.2022
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Summary:e20578 Background: To investigate the impact of treatment patterns in inoperable stage III NSCLC following concurrent chemoradiotherapy with or without immune checkpoint inhibition (cCRT±ICI). Methods: Patients were stratified by treatment year and divided into three subgroups: A (2011–2014), B (2015–2017) and C (2018–2020). Patient- and treatment-related characteristics regarding to PFS and OS were analyzed. Survival parameters were calculated from the last day of thoracic radiotherapy (TRT). Results: 136 consecutive enrolled patients were included. Median follow-up (FU) was 35.7 months; median age was 66.9 years. All patients completed TRT to a total dose ≥60.0 Gy; Median radiotherapy planning target volume (PTV) was 700 cc (range: 172.5–2293.2). Thirty-six (26%) patients received ICI. Median PFS in subgroups A, B and C was 8.0, 8.2 and 26.3 months (p = 0.007). Median OS was 19.9 months, 23.4 months and not reached in subgroups A, B and C (p < 0.05). In subgroup C, median PFS was 14.2 vs. 26.3 months in patients treated with and without ICI. On multivariate analysis for the entire cohort, PTV > 700cc was a negative prognosticator of PFS (HR: 1.522; p = 0.042) and OS (HR: 2.671; p = 0.001); ICI was a predictor of improved PFS (HR: 0.571; p = 0.071) and longer OS (HR: 0.401; p = 0.062). In the Non-ICI cohort, multivariate analyses revealed PTV > 700cc (HR: 1.630; p = 0.047) and SUVmax > 13.75 (HR: 1.859; p = 0.012) were predictors of reduced PFS; PTV > 700cc (HR: 1.958; p = 0.017), SUVmax > 13.75 (HR: 2.405; p = 0.002) and total lung V20 > 30 (HR: 3.357; p < 0.05) were predictors of longer OS. Conclusions: Regardless of ICI, patients receiving multimodal therapy after 2018 demonstrated improved survival compared to patients treated earlier. Both PTV > 700cc and ICI were predictive for PFS and OS in the entire cohort.
ISSN:0732-183X
1527-7755
DOI:10.1200/JCO.2022.40.16_suppl.e20578