TY - JOUR TI - Positron emission tomography after response to rituximab-CHOP in primary mediastinal large B-cell lymphoma: impact on outcomes and radiotherapy strategies AU - Vassilakopoulos, T.P. AU - Papageorgiou, S.G. AU - Angelopoulou, M.K. AU - Chatziioannou, S. AU - Prassopoulos, V. AU - Karakatsanis, S. AU - Arapaki, M. AU - Mellios, Z. AU - Sachanas, S. AU - Kalpadakis, C. AU - Katodritou, E. AU - Leonidopoulou, T. AU - Kotsianidis, I. AU - Hatzimichael, E. AU - Kotsopoulou, M. AU - Dimou, M. AU - Variamis, E. AU - Boutsis, D. AU - Terpos, E. AU - Michali, E. AU - Karianakis, G. AU - Tsirkinidis, P. AU - Vadikolia, C. AU - Poziopoulos, C. AU - Pigaditou, A. AU - Vrakidou, E. AU - Siakantaris, M.P. AU - Kyrtsonis, M.-C. AU - Symeonidis, A. AU - Anargyrou, K. AU - Papaioannou, M. AU - Chatziharissi, E. AU - Vervessou, E. AU - Tsirogianni, M. AU - Palassopoulou, M. AU - Gainaru, G. AU - Mainta, C. AU - Tsirigotis, P. AU - Assimakopoulou, T. AU - Konstantinidou, P. AU - Papadaki, H. AU - Dimopoulos, M.-A. AU - Pappa, V. AU - Karmiris, T. AU - Roussou, P. AU - Datseris, I. AU - Panayiotidis, P. AU - Konstantopoulos, K. AU - Pangalis, G.A. AU - Rondogianni, P. JO - Annals of Hematology PY - 2021 VL - 100 TODO - 9 SP - 2279-2292 PB - Springer Science and Business Media Deutschland GmbH SN - 0939-5555, 1432-0584 TODO - 10.1007/s00277-021-04421-2 TODO - cyclophosphamide plus doxorubicin plus prednisolone plus rituximab plus vincristine; antineoplastic agent; cyclophosphamide; doxorubicin; prednisone; R-CHOP protocol; rituximab; vincristine, adolescent; adult; aged; Article; cancer prognosis; cancer radiotherapy; cancer recurrence; female; human; large cell lymphoma; major clinical study; male; mediastinum cancer; positron emission tomography-computed tomography; primary tumor; radiation dose; retrospective study; treatment outcome; diagnostic imaging; diffuse large B cell lymphoma; mediastinum tumor; middle aged; young adult, Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Cyclophosphamide; Doxorubicin; Female; Humans; Lymphoma, Large B-Cell, Diffuse; Male; Mediastinal Neoplasms; Middle Aged; Positron Emission Tomography Computed Tomography; Prednisone; Retrospective Studies; Rituximab; Treatment Outcome; Vincristine; Young Adult TODO - End-of-treatment (EoT) PET/CT is used as a guide to omit radiotherapy (RT) patients with primary mediastinal large B-cell lymphoma (PMBCL). We present the mature and extended results of a retrospective study evaluating the prognostic significance of EoT-PET/CT after adequate response to R-CHOP. Among 231 consecutive PMLBCL patients, 182 underwent EoT-PET/CT and were evaluated according to the Deauville 5-point scale (D5PS) criteria. Freedom from progression (FFP) was measured from the time of PET/CT examination. Among 182 patients, 72 (40%) had D5PS score 1 (D5PSS-1), 33 (18%) had 2, 28 (15%) had 3, 29 (16%) had 4, and 20 (11%) had 5. The 5-year FFP was 97, 94, 92, 82, and 44% for D5PSS-1, D5PSS-2, D5PSS-3, D5PSS-4, and D5PSS-5, respectively. Among 105 patients with unequivocally negative PET/CT (D5PSS-1/D5PSS-2), 49 (47%) received RT (median dose 3420 cGy) and 56 (53%) did not with relapses in 0/49 vs. 4/56 patients (2 mediastinum and 2 isolated CNS relapses).The 5-year FFP for those who received RT or not was 100% versus 96%, when isolated CNS relapses were censored (p = 0.159). Among D5PSS-3 patients (27/28 irradiated-median dose 3600 cGy), the 5-year FFP was 92%. The 5-year FFP for D5PSS-4 and D5PSS-5 was 82 and 44%; 44/49 patients received RT (median dose 4000 and 4400 cGy for D5PSS-4 and D5PSS-5). Our study supports the omission of RT in a sizeable fraction of PET/CT-negative patients and definitely discourages salvage chemotherapy and ASCT in patients with PMLBCL who conventionally respond to R-CHOP, solely based on PET/CT positivity in the absence of documented progressive or multifocal disease. The persistence of positive PET/CT with D5PSS < 5 after consolidative RT should not trigger the initiation of further salvage chemotherapy in the absence of conventionally defined PD. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature. ER -