Additional file 4: of The CXCR4 antagonist plerixafor enhances the effect of rituximab in diffuse large B-cell lymphoma cell lines

Data used to generate Figure 3. (XLSX 16 kb

MOESM1 of Molecular classification of tissue from a transformed non-Hogkin’s lymphoma case with unexpected long-time remission

Additional file 1. Diagnostic image examinations of the patient case. A) The computed tomography (CT) from the primary lymphoma diagnosis showed retroperitoneal bulk tumor and bilateral hydronephrosis (July 2007). B) A PET/CT was performed after six cycles of R-CHOP and identified a large abdominal residual tumor without FDG (January 2008). C) A routine scan was performed after three months of follow-up and confirmed continues remission (March 2008). D) A control scan was performed six months after therapy showing FDG accumulation in the retroperitoneal residual tumor as well as a palpable cervical tumor (July 2008). After four cycles of rituximab and continues chlorambucil treatment (total 6 months) a status scan was performed and showed a marked reduction of FDG-uptake in the abdominal bulk tumor (November 2008 - data not shown), and repeated as illustrated in E) consistent with continuous complete remission (July 2010) according to the revised response criteria for malignant lymphoma. The superficial process at abdomen in E) was a benign lipoma

MOESM2 of Molecular classification of tissue from a transformed non-Hogkin’s lymphoma case with unexpected long-time remission

Additional file 2. Micro array data files. The Affymetrix .CEL files were deposited at the GEO website under GSE86622. In total, U133 plus 2.0 arrays were performed on 41 DLBCL, 2 tFL and 7 FL patient samples and 3 SNP6.0 arrays were performed on the saliva, primary and relapse tumors on the patient case. Clinical data are registered in the National Clinical Quality Database for Malignant Lymphoma ( http://www.lymphoma.dk )