Tumor volume as a potential imaging-based risk-stratification factor in trimodality therapy for locally advanced non-small cell lung cancer

Margaret M Kozak, James D Murphy, Meike L Schipper, Jessica S Donington, Lisa Zhou, Richard I Whyte, Joseph B Shrager, Chuong D Hoang, Jose Bazan, Peter G Maxim, Edward E Graves, Maximilian Diehn, Wendy Y Hara, Andrew Quon, Quynh-Thu Le, Heather A Wakelee, Billy W Loo Jr, Margaret M Kozak, James D Murphy, Meike L Schipper, Jessica S Donington, Lisa Zhou, Richard I Whyte, Joseph B Shrager, Chuong D Hoang, Jose Bazan, Peter G Maxim, Edward E Graves, Maximilian Diehn, Wendy Y Hara, Andrew Quon, Quynh-Thu Le, Heather A Wakelee, Billy W Loo Jr

Abstract

Introduction: The role of trimodality therapy for locally advanced non-small cell lung cancer (NSCLC) continues to be defined. We hypothesized that imaging parameters on pre- and postradiation positron emission tomography (PET)-computed tomography (CT) imaging are prognostic for outcome after preoperative chemoradiotherapy (CRT)/resection/consolidation chemotherapy and could help risk-stratify patients in clinical trials.

Methods: We enrolled 13 patients on a prospective clinical trial of trimodality therapy for resectable locally advanced NSCLC. PET-CT was acquired for radiation planning and after 45 Gy. Gross tumor volume (GTV) and standardized uptake value were measured at pre- and post-CRT time points and correlated with nodal pathologic complete response, loco-regional and/or distant progression, and overall survival. In addition, we evaluated the performance of automatic deformable image registration (ADIR) software for volumetric response assessment.

Results: All patients responded with average total GTV reductions after 45 Gy of 43% (range: 27-64%). Pre- and post-CRT GTVs were highly correlated (R² = 0.9), and their respective median values divided the patients into the same two groups. ADIR measurements agreed closely with manually segmented post-CRT GTVs. Patients with GTV ≥ median (137 ml pre-CRT and 67 ml post-CRT) had 3-year progression-free survival (PFS) of 14% versus 75% for GTV less than median, a significant difference (p = 0.049). Pre- and post-CRT PET-standardized uptake value did not correlate significantly with pathologic complete response, PFS, or overall survival.

Conclusions: Preoperative CRT with carboplatin/docetaxel/45 Gy resulted in excellent response rates. In this exploratory analysis, pre- and post-CRT GTV predicted PFS in trimodality therapy, consistent with our earlier studies in a broader cohort of NSCLC. ADIR seems robust enough for volumetric response assessment in clinical trials.

Source: PubMed

3
Prenumerera