TY - JOUR
T1 - Diffuse large B-cell lymphoma involving osseous sites
T2 - utility of response assessment by PET/CT and good long-term outcomes
AU - Ghione, Paola
AU - Ahsanuddin, Salma
AU - Luttwak, Efrat
AU - Varela, Sabela Bobillo
AU - Nakajima, Reiko
AU - Michaud, Laure
AU - Gupta, Kanika
AU - Navitski, Anastasia
AU - Straus, David
AU - Palomba, M. Lia
AU - Moskowitz, Alison
AU - Noy, Ariela
AU - Hamlin, Paul
AU - Matasar, Matthew
AU - Kumar, Anita
AU - Falchi, Lorenzo
AU - Yahalom, Joachim
AU - Horwitz, Steven
AU - Zelenetz, Andrew
AU - Younes, Anas
AU - Salles, Gilles
AU - Schöder, Heiko
AU - Joffe, Erel
N1 - Publisher Copyright:
©2024 Ferrata Storti Foundation.
PY - 2024/1
Y1 - 2024/1
N2 - Osseous involvement by diffuse large B-cell lymphoma (DLBCL-bone) is a heterogeneous disease. There is limited data regarding response assessment by positron emission tomography with fluorodeoxyglucose, which may demonstrate residual avidity despite a complete response. We analyzed clinical data of patients with newly diagnosed DLBCL and identified all cases with DLBCL-bone. End of treatment scans were reviewed by two independent experts classifying osseous lesions into Deauville (DV) ≤3; DV ≥4, or reactive uptake in the bone marrow (M), site of fracture (F) or surgery (S). We compared outcomes of DLBCL-bone to other extranodal sites (EN) matched on International Prognotic Index features and regimen. Of 1,860 patients with DLBCL (bone 16%; EN 45%; nodal 39%), 41% had localized disease and 59% advanced. Only 9% (n=27) of patients with initial bone involvement had residual fluorodeoxyglucose avidity at the osseous site. In half of these cases, the uptake was attributed to F/S/M, and of the remaining 13, only two were truly refractory (both with persistent disease at other sites). Overall survival and progression-free survival (PFS) were found to be similar for early-stage nodal DLBCL and DLBCL-bone, but inferior in EN-DLBCL. Advanced-stage disease involving the bone had a similar 5-year PFS to nodal disease and EN-DLBCL. After matching for International Prognotic Index and treatment regiments, PFS between bone and other EN sites was similar. Osseous involvement in DLBCL does not portend a worse prognosis. End of treatment DV ≥4 can be expected in 5-10% of cases, but in the absence of other signs of refractory disease, may be followed expectantly.
AB - Osseous involvement by diffuse large B-cell lymphoma (DLBCL-bone) is a heterogeneous disease. There is limited data regarding response assessment by positron emission tomography with fluorodeoxyglucose, which may demonstrate residual avidity despite a complete response. We analyzed clinical data of patients with newly diagnosed DLBCL and identified all cases with DLBCL-bone. End of treatment scans were reviewed by two independent experts classifying osseous lesions into Deauville (DV) ≤3; DV ≥4, or reactive uptake in the bone marrow (M), site of fracture (F) or surgery (S). We compared outcomes of DLBCL-bone to other extranodal sites (EN) matched on International Prognotic Index features and regimen. Of 1,860 patients with DLBCL (bone 16%; EN 45%; nodal 39%), 41% had localized disease and 59% advanced. Only 9% (n=27) of patients with initial bone involvement had residual fluorodeoxyglucose avidity at the osseous site. In half of these cases, the uptake was attributed to F/S/M, and of the remaining 13, only two were truly refractory (both with persistent disease at other sites). Overall survival and progression-free survival (PFS) were found to be similar for early-stage nodal DLBCL and DLBCL-bone, but inferior in EN-DLBCL. Advanced-stage disease involving the bone had a similar 5-year PFS to nodal disease and EN-DLBCL. After matching for International Prognotic Index and treatment regiments, PFS between bone and other EN sites was similar. Osseous involvement in DLBCL does not portend a worse prognosis. End of treatment DV ≥4 can be expected in 5-10% of cases, but in the absence of other signs of refractory disease, may be followed expectantly.
UR - http://www.scopus.com/inward/record.url?scp=85181852786&partnerID=8YFLogxK
U2 - 10.3324/haematol.2022.282643
DO - 10.3324/haematol.2022.282643
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C2 - 37646672
AN - SCOPUS:85181852786
SN - 0390-6078
VL - 109
SP - 200
EP - 208
JO - Haematologica
JF - Haematologica
IS - 1
ER -