TY - JOUR
T1 - Clinical characteristics of interim-PET negative patients with a positive end PET from the prospective HD08-01 FIL study
AU - Rigacci, Luigi
AU - Puccini, Benedetta
AU - Broccoli, Alessandro
AU - Dona, Manjola
AU - Gotti, Manuel
AU - Evangelista, Andrea
AU - Santoro, Armando
AU - Bonfichi, Maurizio
AU - Re, Alessandro
AU - Spina, Michele
AU - Botto, Barbara
AU - Pulsoni, Alessandro
AU - Pagani, Chiara
AU - Stelitano, Caterina
AU - Salvi, Flavia
AU - Nassi, Luca
AU - Mannelli, Lara
AU - Kovalchuk, Sofia
AU - Gioia, Daniela
AU - Zinzani, Pier Luigi
PY - 2020/2
Y1 - 2020/2
N2 - FDG-positron emission tomography (PET) performed early during therapy in advanced Hodgkin lymphoma patients has been confirmed as being important for progression-free survival. A group of patients with a negative interim-PET (i-PET) showed a positive end induction PET (e-PET). The aim of this study was to evaluate the clinical characteristics of patients with a positive e-PET as a secondary end point of the HD0801 study. A total of 519 patients with advanced-stage de novo Hodgkin lymphoma received initial treatment and underwent an i-PET. Patients with negative results continued the standard treatment. i-PET negative patients were then evaluated for response with an e-PET and those patients found to have a positive one were also then given a salvage therapy. Among 409 i-PET negative, 16 interrupted the therapy, 393 patients were evaluated with an e-PET, and 39 were positive. Sixteen out of 39 underwent a diagnostic biopsy and 15 were confirmed as HD. Seventeen out of 39 e-PET were reviewed according to the Deauville Score and, in sixteen, it was confirmed positive (10 DS 5, 6 DS 4). With the exception of high LDH value at diagnosis (p = 0.01; HR 95% CI 1.18-4.89), no clinical characteristics were significantly different in comparison with e-PET negative patients. Positive e-PET after a negative i-PET has a worse outcome when compared with i-PET positive patients salvaged with therapy intensification. It was not possible to identify clinical characteristics associated with a positive e-PET.
AB - FDG-positron emission tomography (PET) performed early during therapy in advanced Hodgkin lymphoma patients has been confirmed as being important for progression-free survival. A group of patients with a negative interim-PET (i-PET) showed a positive end induction PET (e-PET). The aim of this study was to evaluate the clinical characteristics of patients with a positive e-PET as a secondary end point of the HD0801 study. A total of 519 patients with advanced-stage de novo Hodgkin lymphoma received initial treatment and underwent an i-PET. Patients with negative results continued the standard treatment. i-PET negative patients were then evaluated for response with an e-PET and those patients found to have a positive one were also then given a salvage therapy. Among 409 i-PET negative, 16 interrupted the therapy, 393 patients were evaluated with an e-PET, and 39 were positive. Sixteen out of 39 underwent a diagnostic biopsy and 15 were confirmed as HD. Seventeen out of 39 e-PET were reviewed according to the Deauville Score and, in sixteen, it was confirmed positive (10 DS 5, 6 DS 4). With the exception of high LDH value at diagnosis (p = 0.01; HR 95% CI 1.18-4.89), no clinical characteristics were significantly different in comparison with e-PET negative patients. Positive e-PET after a negative i-PET has a worse outcome when compared with i-PET positive patients salvaged with therapy intensification. It was not possible to identify clinical characteristics associated with a positive e-PET.
KW - Adult
KW - Antineoplastic Combined Chemotherapy Protocols/administration & dosage
KW - Autografts
KW - Bleomycin/administration & dosage
KW - Dacarbazine/administration & dosage
KW - Disease-Free Survival
KW - Doxorubicin/administration & dosage
KW - Female
KW - Fluorodeoxyglucose F18/administration & dosage
KW - Hodgkin Disease/diagnostic imaging
KW - Humans
KW - Male
KW - Positron-Emission Tomography
KW - Prospective Studies
KW - Stem Cell Transplantation
KW - Survival Rate
KW - Vinblastine/administration & dosage
U2 - 10.1007/s00277-019-03889-3
DO - 10.1007/s00277-019-03889-3
M3 - Article
C2 - 31872361
VL - 99
SP - 283
EP - 291
JO - Ann. Hematol.
JF - Ann. Hematol.
SN - 0939-5555
IS - 2
ER -