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Gina Tomaine

News
07/18/2022
Among adults with MM, treatment with lenalidomide, bortezomib, and dexamethasone (RVD) and autologous stem-cell transplantation was associated with longer PFS than RVD alone, according to a phase 3 trial.
Among adults with MM, treatment with lenalidomide, bortezomib, and dexamethasone (RVD) and autologous stem-cell transplantation was associated with longer PFS than RVD alone, according to a phase 3 trial.
Among adults with MM, treatment...
07/18/2022
Oncology
News
09/07/2023
The rituximab biosimilar, SDZ-RTX, combined with a CHOP regimen was effective and well-tolerated as a frontline treatment for patients with diffuse large B-cell lymphoma (DLBCL), according to a real-world study.
The rituximab biosimilar, SDZ-RTX, combined with a CHOP regimen was effective and well-tolerated as a frontline treatment for patients with diffuse large B-cell lymphoma (DLBCL), according to a real-world study.
The rituximab biosimilar,...
09/07/2023
Oncology
News
08/02/2022
Brexucabtagene autoleucel induced durable long-term responses with manageable safety in patients with relapsed/refractory MCL, according to a 3-year follow-up analysis of the ZUMA-2 study.
Brexucabtagene autoleucel induced durable long-term responses with manageable safety in patients with relapsed/refractory MCL, according to a 3-year follow-up analysis of the ZUMA-2 study.
Brexucabtagene autoleucel...
08/02/2022
Oncology
News
11/17/2022
Momelotinib improved symptom responses, transfusion requirements, and spleen responses for symptomatic and anemic myelofibrosis patients previously treated with a JAK inhibitor when compared with danazol, according to the phase 3 MOMENTUM...
Momelotinib improved symptom responses, transfusion requirements, and spleen responses for symptomatic and anemic myelofibrosis patients previously treated with a JAK inhibitor when compared with danazol, according to the phase 3 MOMENTUM...
Momelotinib improved symptom...
11/17/2022
Oncology
News
04/24/2023
On January 19, 2023, the Food and Drug Administration (FDA) approved zanubrutinib for chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). This approval was based on the SEQUOIA and ALPINE trials, respectively. The...
On January 19, 2023, the Food and Drug Administration (FDA) approved zanubrutinib for chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). This approval was based on the SEQUOIA and ALPINE trials, respectively. The...
On January 19, 2023, the Food...
04/24/2023
Journal of Clinical Pathways
News
09/02/2022
Rituximab plus lenalidomide and ibrutinib demonstrated significant clinical activity, manageable safety, and promising survival outcomes both alone and in combination with chemotherapy as a frontline treatment for newly diagnosed DLBCL in the...
Rituximab plus lenalidomide and ibrutinib demonstrated significant clinical activity, manageable safety, and promising survival outcomes both alone and in combination with chemotherapy as a frontline treatment for newly diagnosed DLBCL in the...
Rituximab plus lenalidomide and...
09/02/2022
Oncology
09/23/2022
Study findings show EZH2 mutation status could be a useful biomarker to guide first-line therapy in follicular lymphoma and that ctDNA is a promising tool for identifying patients with this mutation.
Study findings show EZH2 mutation status could be a useful biomarker to guide first-line therapy in follicular lymphoma and that ctDNA is a promising tool for identifying patients with this mutation.
Study findings show EZH2...
09/23/2022
Oncology
News
07/13/2022
Teclistamab, a T-cell–redirecting bispecific antibody, showed promising efficacy in treating patients with triple-class–exposed relapsed or refractory MM, inducing deep and durable responses in a recent study.
Teclistamab, a T-cell–redirecting bispecific antibody, showed promising efficacy in treating patients with triple-class–exposed relapsed or refractory MM, inducing deep and durable responses in a recent study.
Teclistamab, a...
07/13/2022
Oncology
News
07/24/2023
The FDA granted approval to quizartinib for patients with newly diagnosed FLT3/ITD-positive acute myeloid leukemia, as detected by an FDA-approved test.
The FDA granted approval to quizartinib for patients with newly diagnosed FLT3/ITD-positive acute myeloid leukemia, as detected by an FDA-approved test.
The FDA granted approval to...
07/24/2023
Oncology
News
08/02/2022
Ibrutinib added to bendamustine and rituximab followed by rituximab maintenance yields significantly longer PFS vs placebo in older patients with previously untreated MCL, according to findings from the phase 3 SHINE trial.
Ibrutinib added to bendamustine and rituximab followed by rituximab maintenance yields significantly longer PFS vs placebo in older patients with previously untreated MCL, according to findings from the phase 3 SHINE trial.
Ibrutinib added to bendamustine...
08/02/2022
Oncology