Diffuse large B-cell lymphoma (DLBCL) is an aggressive non-Hodgkin lymphoma (NHL) and is the most common lymphoid malignancy, accounting for more than 30% of newly diagnosed cases of NHL. 1,2 Diagnosis of DLBCL is made primarily by morphologic and immunohistochemical evaluation of the affected lymphoid tissue. Standard treatment of newly diagnosed DLBCL is anthracycline-based combination chemotherapy plus rituximab (eg, R-CHOP: rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone), which produces long-term remission in the majority of patients, including older patients and patients with advanced stage disease. 3-5 DLBCL can be classified into subgroups based on gene expression profiling (GEP) of tumor tissue (or using immunohistochemistry stains as a proxy for GEP), including the germinal center B-cell (GCB) and activated B-cell (ABC) subtypes, with latter exhibiting an inferior outcome with standard therapy. 6-8 In addition, double-hit lymphomas (DHL)-DLBCL with concurrent rearrangement of MYC and BCL2 and/or BCL6 identified by FISH-and double-expressor lymphoma (DEL)-DLBCL with concurrent expression of the MYC and BCL2 proteins by immunohistochemistry-are subtypes of DLBCL that are associated with poor outcomes after standard therapy. 9-26 Standard treatment for patients with relapsed or refractory DLBCL is non-cross-resistant salvage chemotherapy plus rituximab, followed by high-dose therapy and autologous stem cell transplantation for patients demonstrating chemotherapy-sensitive disease. 27,28 1 | What is considered de novo DLBCL? De novo DLBCL arises in lymphoid tissue without prior history of lymphoma. On the other hand, patients with transformed DLBCL have a prior history of indolent NHL, such as follicular, marginal zone, lymphoplasmacytic lymphoma. Transformed DLBCL has historically been associated with a poor prognosis, though newer data in the rituximab era suggests that outcomes may be improving. Patients with de novo or transformed DLBCL typically present with constitutional symptoms, rapid growth of lymph nodes, elevated lactate dehydrogenase, and can often have involvement of non-nodal sites. Positron emission tomography (PET) scan typically demonstrates increased FDG uptake at sites of involvement by DLBCL (in de novo or transformed disease) as compared to sites of involvement by low-grade lymphoma that tend to have less FDG-avidity. 29 Standard treatment of transformed DLBCL is anthracycline-based chemotherapy plus rituximab, similar to induction regimens for DLBCL. If a patient has had prior exposure to anthracycline-containing chemotherapy as part of treatment for their indolent lymphoma, alternative chemoimmunotherapy should be utilized. Rituximab-containing regimen followed by high-dose chemotherapy (HDT) and autologous stem cell transplantation (ASCT) in patients with transformed lymphoma (TL) showed 3-year overall survival (OS) of over 50%. 30,31
| What are the indications for ASCT in DLBCL?The primary indication for HDT/ASCT in patients with DLBCL is for patients with relapse...