» Articles » PMID: 37646672

Diffuse Large B-cell Lymphoma Involving Osseous Sites: Utility of Response Assessment by PET/CT and Good Longterm Outcomes

Abstract

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.

Citing Articles

Comparison of Cox regression and generalized Cox regression models to machine learning in predicting survival of children with diffuse large B-cell lymphoma.

Qin J, Zhu X, Chen X, Sang W, Jin Y Transl Cancer Res. 2024; 13(7):3370-3381.

PMID: 39145065 PMC: 11319973. DOI: 10.21037/tcr-23-2358.

References
1.
Messina C, Christie D, Zucca E, Gospodarowicz M, Ferreri A . Primary and secondary bone lymphomas. Cancer Treat Rev. 2015; 41(3):235-46. DOI: 10.1016/j.ctrv.2015.02.001. View

2.
Muller A, Dreyling M, Roeder F, Baur-Melnyk A, Knosel T, Klein A . Primary bone lymphoma: Clinical presentation and therapeutic considerations. J Bone Oncol. 2020; 25:100326. PMC: 7554647. DOI: 10.1016/j.jbo.2020.100326. View

3.
Vitolo U, Seymour J, Martelli M, Illerhaus G, Illidge T, Zucca E . Extranodal diffuse large B-cell lymphoma (DLBCL) and primary mediastinal B-cell lymphoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016; 27(suppl 5):v91-v102. DOI: 10.1093/annonc/mdw175. View

4.
Meignan M, Gallamini A, Haioun C . Report on the First International Workshop on Interim-PET-Scan in Lymphoma. Leuk Lymphoma. 2009; 50(8):1257-60. DOI: 10.1080/10428190903040048. View

5.
Micallef I, Maurer M, Wiseman G, Nikcevich D, Kurtin P, Cannon M . Epratuzumab with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy in patients with previously untreated diffuse large B-cell lymphoma. Blood. 2011; 118(15):4053-61. PMC: 3204728. DOI: 10.1182/blood-2011-02-336990. View