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Interim Positron Emission Tomography During Frontline Chemoimmunotherapy for Follicular Lymphoma.
Merryman, Reid W; Michaud, Laure; Redd, Robert; Mondello, Patrizia; Park, Hyesun; Spilberg, Gabriela; Robertson, Matthew; Taranto, Eleanor; Ahmed, Gulrayz; Chase, Matthew; Jeter, Erin; Ahn, Inhye E; Brown, Jennifer R; Crombie, Jennifer; Davids, Matthew S; Fisher, David C; Jacobsen, Eric; Jacobson, Caron A; Kim, Austin I; LaCasce, Ann S; Ng, Samuel Y; Odejide, Oreofe O; Parry, Erin M; Salles, Gilles; Zelenetz, Andrew D; Armand, Philippe; Schöder, Heiko; Jacene, Heather.
Affiliation
  • Merryman RW; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Michaud L; Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Redd R; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Mondello P; Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY and Weill Cornell Medicine, New York, NY, USA.
  • Park H; Department of Imaging, Dana-Farber Cancer Institute/Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA.
  • Spilberg G; Department of Imaging, Dana-Farber Cancer Institute/Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA.
  • Robertson M; Department of Imaging, Dana-Farber Cancer Institute/Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA.
  • Taranto E; Division of Hematology and Oncology, Hospital of the University of Pennsylvania.
  • Ahmed G; Medical College of Wisconsin, Milwaukee, WI, USA.
  • Chase M; Divisions of Hematology and Medical Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Jeter E; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Ahn IE; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Brown JR; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Crombie J; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Davids MS; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Fisher DC; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Jacobsen E; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Jacobson CA; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Kim AI; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • LaCasce AS; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Ng SY; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Odejide OO; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Parry EM; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Salles G; Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY and Weill Cornell Medicine, New York, NY, USA.
  • Zelenetz AD; Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY and Weill Cornell Medicine, New York, NY, USA.
  • Armand P; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Schöder H; Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Jacene H; Department of Imaging, Dana-Farber Cancer Institute/Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA.
Hemasphere ; 7(2): e826, 2023 Feb.
Article in En | MEDLINE | ID: mdl-36713355
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Hemasphere Year: 2023 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Hemasphere Year: 2023 Document type: Article Affiliation country: United States Country of publication: United States