<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mark T</submitter><funding>NCI NIH HHS</funding><pagination>654-60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3626496</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>143(5)</volume><pubmed_abstract>The M-protein is the major reference measure for response in multiple myeloma (MM) and its correct interpretation is key to clinical management. The emergence of oligoclonal banding is recognized as a benign finding in the postautologous stem cell transplantation setting (ASCT) for MM but its significance during non-myeloablative therapy is unknown. In a study of the immunomodulatory combination BiRD, (lenalidomide and dexamethasone with clarithromycin), we frequently detected the emergence of mono- and oligo-clonal immunoglobulins unrelated to the baseline diagnostic M-protein. The new M-proteins seen on serum immunofixation electrophoresis were clearly different in either heavy or light chain component(s) from the original M-spike protein and were termed atypical serum immunofixation pat</pubmed_abstract><journal>British journal of haematology</journal><pubmed_title>Atypical serum immunofixation patterns frequently emerge in immunomodulatory therapy and are associated with a high degree of response in multiple myeloma.</pubmed_title><pmcid>PMC3626496</pmcid><funding_grant_id>K23 CA109260</funding_grant_id><funding_grant_id>K23 CA109260-01</funding_grant_id><pubmed_authors>Agrawal YP</pubmed_authors><pubmed_authors>Lent R</pubmed_authors><pubmed_authors>Pearse RN</pubmed_authors><pubmed_authors>Furman RR</pubmed_authors><pubmed_authors>Christos PJ</pubmed_authors><pubmed_authors>Matthew S</pubmed_authors><pubmed_authors>Lee JW</pubmed_authors><pubmed_authors>Cesarman E</pubmed_authors><pubmed_authors>Mark T</pubmed_authors><pubmed_authors>Coleman M</pubmed_authors><pubmed_authors>Wang YL</pubmed_authors><pubmed_authors>Niesvizky R</pubmed_authors><pubmed_authors>Chen-Kiang S</pubmed_authors><pubmed_authors>Mazumdar M</pubmed_authors><pubmed_authors>Ely S</pubmed_authors><pubmed_authors>Leonard JP</pubmed_authors><pubmed_authors>Jayabalan D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atypical serum immunofixation patterns frequently emerge in immunomodulatory therapy and are associated with a high degree of response in multiple myeloma.</name><description>The M-protein is the major reference measure for response in multiple myeloma (MM) and its correct interpretation is key to clinical management. The emergence of oligoclonal banding is recognized as a benign finding in the postautologous stem cell transplantation setting (ASCT) for MM but its significance during non-myeloablative therapy is unknown. In a study of the immunomodulatory combination BiRD, (lenalidomide and dexamethasone with clarithromycin), we frequently detected the emergence of mono- and oligo-clonal immunoglobulins unrelated to the baseline diagnostic M-protein. The new M-proteins seen on serum immunofixation electrophoresis were clearly different in either heavy or light chain component(s) from the original M-spike protein and were termed atypical serum immunofixation pat</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Dec</publication><modification>2025-04-03T23:57:54.966Z</modification><creation>2019-03-27T01:07:25Z</creation></dates><accession>S-EPMC3626496</accession><cross_references><pubmed>18950461</pubmed><doi>10.1111/j.1365-2141.2008.07374.x</doi></cross_references></HashMap>