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Differential role of residual metabolic tumor volume in inoperable stage III NSCLC after chemoradiotherapy ± immune checkpoint inhibition
by
Eze Chukwuka
, Tufman Amanda
, Unterrainer Marcus
, Li, Minglun
, Manapov Farkhad
, Mittlmeier, Lena M
, Belka Claus
, Reinmuth Niels
, Käsmann Lukas
, Taugner Julian
, Ricke Jens
, Bartenstein, Peter
, Kunz, Wolfgang G
in
Chemoradiotherapy
/ Chemotherapy
/ Clinical outcomes
/ Fluorine isotopes
/ Immune checkpoint inhibitors
/ Immunotherapy
/ Lung cancer
/ Metabolism
/ Monoclonal antibodies
/ Non-small cell lung carcinoma
/ Patients
/ Positron emission tomography
/ Radiation therapy
/ Small cell lung carcinoma
/ Subgroups
/ Survival
/ Targeted cancer therapy
/ Tumors
2022
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Differential role of residual metabolic tumor volume in inoperable stage III NSCLC after chemoradiotherapy ± immune checkpoint inhibition
by
Eze Chukwuka
, Tufman Amanda
, Unterrainer Marcus
, Li, Minglun
, Manapov Farkhad
, Mittlmeier, Lena M
, Belka Claus
, Reinmuth Niels
, Käsmann Lukas
, Taugner Julian
, Ricke Jens
, Bartenstein, Peter
, Kunz, Wolfgang G
in
Chemoradiotherapy
/ Chemotherapy
/ Clinical outcomes
/ Fluorine isotopes
/ Immune checkpoint inhibitors
/ Immunotherapy
/ Lung cancer
/ Metabolism
/ Monoclonal antibodies
/ Non-small cell lung carcinoma
/ Patients
/ Positron emission tomography
/ Radiation therapy
/ Small cell lung carcinoma
/ Subgroups
/ Survival
/ Targeted cancer therapy
/ Tumors
2022
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Differential role of residual metabolic tumor volume in inoperable stage III NSCLC after chemoradiotherapy ± immune checkpoint inhibition
by
Eze Chukwuka
, Tufman Amanda
, Unterrainer Marcus
, Li, Minglun
, Manapov Farkhad
, Mittlmeier, Lena M
, Belka Claus
, Reinmuth Niels
, Käsmann Lukas
, Taugner Julian
, Ricke Jens
, Bartenstein, Peter
, Kunz, Wolfgang G
in
Chemoradiotherapy
/ Chemotherapy
/ Clinical outcomes
/ Fluorine isotopes
/ Immune checkpoint inhibitors
/ Immunotherapy
/ Lung cancer
/ Metabolism
/ Monoclonal antibodies
/ Non-small cell lung carcinoma
/ Patients
/ Positron emission tomography
/ Radiation therapy
/ Small cell lung carcinoma
/ Subgroups
/ Survival
/ Targeted cancer therapy
/ Tumors
2022
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Differential role of residual metabolic tumor volume in inoperable stage III NSCLC after chemoradiotherapy ± immune checkpoint inhibition
Journal Article
Differential role of residual metabolic tumor volume in inoperable stage III NSCLC after chemoradiotherapy ± immune checkpoint inhibition
2022
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Overview
BackgroundThe PET-derived metabolic tumor volume (MTV) is an independent prognosticator in non-small cell lung cancer (NSCLC) patients. We analyzed the prognostic value of residual MTV (rMTV) after completion of chemoradiotherapy (CRT) in inoperable stage III NSCLC patients with and without immune checkpoint inhibition (ICI).MethodsFifty-six inoperable stage III NSCLC patients (16 female, median 65.0 years) underwent 18F-FDG PET/CT after completion of standard CRT. rMTV was delineated on 18F-FDG PET/CT using a standard threshold (liver SUVmean + 2 × standard deviation). 21/56 patients underwent additional ICI (CRT-IO, 21/56 patients) thereafter. Patients were divided in volumetric subgroups using median split dichotomization (MTV ≤ 4.3 ml vs. > 4.3 ml). rMTV, clinical features, and ICI-application were correlated with clinical outcome parameters (progression-free survival (PFS), local PFS (LPFS), and overall survival (OS).ResultsOverall, median follow-up was 52.0 months. Smaller rMTV was associated with longer median PFS (29.3 vs. 10.5 months, p = 0.015), LPFS (49.9 vs. 13.5 months, p = 0.001), and OS (63.0 vs. 23.0 months, p = 0.003). CRT-IO patients compared to CRT patients showed significantly longer median PFS (29.3 vs. 11.2 months, p = 0.034), LPFS (median not reached vs. 14.0 months, p = 0.016), and OS (median not reached vs. 25.2 months, p = 0.007). In the CRT subgroup, smaller rMTV was associated with longer median PFS (33.5 vs. 8.6 months, p = 0.001), LPFS (49.9 vs. 10.1 months, p = 0.001), and OS (63.0 vs. 16.3 months, p = 0.004). In the CRT-IO subgroup, neither PFS, LPFS, nor OS were associated with MTV (p > 0.05 each). The findings were confirmed in subsequent multivariate analyses.ConclusionIn stage III NSCLC, smaller rMTV is highly associated with superior clinical outcome, especially in patients undergoing CRT without ICI. Patients with CRT-IO show significantly improved outcome compared to CRT patients. Of note, clinical outcome in CRT-IO patients is independent of residual MTV. Hence, even patients with large rMTV might profit from ICI despite extensive tumor load.
Publisher
Springer Nature B.V
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