Non-Hodgkin's lymphoma is a heterogeneous group of lymphoproliferative malignancies.
It is the most common hematologic cancer.
The most common subtypes are the diffuse large B-cell and follicular lymphoma. The subtypes are based on the malignant cell's morphology, genetic features, immunohistological characteristics, and stage of maturation.
Comprehensive recommendations on coronavirus disease 2019 (COVID-19) for cancer patients have become available following review of guidelines from 63 national/international oncology societies. [Lancet Oncol 2020, doi: 10.1016/S1470-2045(20)30278-3]
Children with inflammatory bowel disease (IBD) do not appear to have an elevated risk of lymphoma following treatment with anti-tumour necrosis factor (TNF) agents, according to a study presented at the recent Crohn’s and Colitis Congress 2020.
New drug applications approved by US FDA as of 16 - 31 July 2019 which includes New Molecular Entities (NMEs) and new biologics. It does not include Tentative Approvals. Supplemental approvals may have occurred since the original approval date.
A first-in-class immunoglobulin G4 (IgG4) antibody targeting CD47 has demonstrated durable responses when used in combination with rituximab in patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) or indolent lymphoma.
There appears to be a positive and significant link between non-Hodgkin lymphoma risk in Asians and blood concentration of β-hexachlorocyclohexane, an organochloride used in many pesticides, according to a new study.
Antiviral treatment with pegylated interferon and ribavirin leads to a significant reduction in the risk of lymphoma, especially the non-Hodgkin’s type, in patients with chronic hepatitis C virus (HCV) infection, according to a study.
The anti-CD19 chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel has demonstrated high rates of durable responses in adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) in the pivotal international JULIET study.
Lenalidomide, given for 14 days in combination with cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP), has demonstrated acceptable toxicity in the REVAIL study in elderly patients with angioimmunoblastic T-cell lymphoma (AITL), with efficacy results similar to reports from previous studies.
The combination of brentuximab vedotin, cyclophosphamide, doxorubicin, and prednisone (A+CHP) more than doubled progression-free survival (PFS) as well as improved overall survival (OS) in patients with CD30-expressing peripheral T-cell lymphoma compared with a combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP), according to results of the phase III ECHELON-2* trial.
Real-world systemic sequential therapy with regorafenib confers survival benefits in patients with advanced hepatocellular carcinoma (HCC) who failed first-line sorafenib, consistent with previous clinical trial, according to a study in Korea.