HemaSphere (Feb 2023)

Interim Positron Emission Tomography During Frontline Chemoimmunotherapy for Follicular Lymphoma

  • Reid W. Merryman,
  • Laure Michaud,
  • Robert Redd,
  • Patrizia Mondello,
  • Hyesun Park,
  • Gabriela Spilberg,
  • Matthew Robertson,
  • Eleanor Taranto,
  • Gulrayz Ahmed,
  • Matthew Chase,
  • Erin Jeter,
  • Inhye E. Ahn,
  • Jennifer R. Brown,
  • Jennifer Crombie,
  • Matthew S. Davids,
  • David C. Fisher,
  • Eric Jacobsen,
  • Caron A. Jacobson,
  • Austin I. Kim,
  • Ann S. LaCasce,
  • Samuel Y. Ng,
  • Oreofe O. Odejide,
  • Erin M. Parry,
  • Gilles Salles,
  • Andrew D. Zelenetz,
  • Philippe Armand,
  • Heiko Schöder,
  • Heather Jacene

DOI
https://doi.org/10.1097/HS9.0000000000000826
Journal volume & issue
Vol. 7, no. 2
p. e826

Abstract

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While most patients with follicular lymphoma (FL) have excellent outcomes with frontline chemoimmunotherapy (CIT), a subset of patients will experience early progression, which is associated with poor subsequent outcomes. Novel biomarkers are needed to identify high-risk patients earlier. We hypothesized that interim positron emission tomography (PET) would predict progression-free survival (PFS) in this population. We retrospectively identified 128 patients with grade 1–3A FL who had an interim PET after 2–4 cycles of frontline CIT at 2 academic centers. PET scans were analyzed using Deauville score (DS) and change in maximum standardized uptake value (ΔSUVmax). Interim PET DS was a significant predictor of PFS (P < 0.003). Patients with a DS of 3 had outcomes similar to those of patients with a DS of 4, so were categorized as PET-positive for additional analyses. Interim PET remained a strong predictor of PFS (DS 3-5, hazard ratio [HR] 2.4, P = 0.006) in a multivariable analysis and was also an early predictor of both a positive end-of-treatment PET (P < 0.001) and progression of disease within 24 months (POD24) (P = 0.006). An optimal ΔSUVmax cutoff of 75% was selected using the bootstrap method. ΔSUVmax <75% was also a significant predictor of PFS on univariable and multivariable analyses (HR 2.8, P < 0.003). In a separate cohort of 50 patients with high-grade FL, interim PET interpreted using either DS (P < 0.001) or ΔSUVmax75% (P = 0.034) was also a significant predictor of inferior PFS. In conclusion, interim PET is an independent predictor of PFS and may be useful as a tool for response-adapted treatment strategies in FL.