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Gina Tomaine

News
09/20/2022
Busulfan plus cyclophosphamide demonstrated noninferior efficiency and safety compared with total body irradiation plus cyclophosphamide for adult patients with standard-risk B-cell ALL in a phase 3 trial.
Busulfan plus cyclophosphamide demonstrated noninferior efficiency and safety compared with total body irradiation plus cyclophosphamide for adult patients with standard-risk B-cell ALL in a phase 3 trial.
Busulfan plus cyclophosphamide...
09/20/2022
Oncology
News
11/14/2022
Parallel testing of both tissue and liquid biopsy samples detects a higher frequency of EZH2 mutations in patients with follicular lymphoma, with significant clinical implications, according to a recent study.
Parallel testing of both tissue and liquid biopsy samples detects a higher frequency of EZH2 mutations in patients with follicular lymphoma, with significant clinical implications, according to a recent study.
Parallel testing of both tissue...
11/14/2022
Oncology
News
11/15/2022
Benefits associated with venetoclax-rituximab on the phase 3 MURANO trial were maintained at 3 years following treatment cessation in patients with relapsed/refractory CLL, according to an update published in Blood.
Benefits associated with venetoclax-rituximab on the phase 3 MURANO trial were maintained at 3 years following treatment cessation in patients with relapsed/refractory CLL, according to an update published in Blood.
Benefits associated with...
11/15/2022
Oncology
News
09/08/2023
Luspatercept demonstrated multiple clinical benefits for ESA-naive patients with transfusion-dependent lower-risk MDS, including hemoglobin increases and transfusion-burden decreases, according to research presented at the SOHO 2023 Annual...
Luspatercept demonstrated multiple clinical benefits for ESA-naive patients with transfusion-dependent lower-risk MDS, including hemoglobin increases and transfusion-burden decreases, according to research presented at the SOHO 2023 Annual...
Luspatercept demonstrated...
09/08/2023
Oncology
News
08/17/2022
For patients with early stage unfavorable Hodgkin lymphoma, brentuximab vedotin combined with AVD was associated with an improved rate of PET negativity vs standard ABVD in a phase 2 trial.
For patients with early stage unfavorable Hodgkin lymphoma, brentuximab vedotin combined with AVD was associated with an improved rate of PET negativity vs standard ABVD in a phase 2 trial.
For patients with early stage...
08/17/2022
Oncology
News
11/17/2022
CD20-CD3 bispecific antibody odronextamab showed a manageable safety profile and encouraging preliminary activity in heavily pretreated patients with B-cell non-Hodgkin lymphoma, according to a recent phase 1 study.
CD20-CD3 bispecific antibody odronextamab showed a manageable safety profile and encouraging preliminary activity in heavily pretreated patients with B-cell non-Hodgkin lymphoma, according to a recent phase 1 study.
CD20-CD3 bispecific antibody...
11/17/2022
Oncology
News
08/25/2022
The FDA granted expedited approval to ibrutinib for pediatric patients with chronic GVHD after failure of 1 or more lines of systemic therapy.
The FDA granted expedited approval to ibrutinib for pediatric patients with chronic GVHD after failure of 1 or more lines of systemic therapy.
The FDA granted expedited...
08/25/2022
Oncology
News
07/10/2023
Switching from reference trastuzumab to biosimilar trastuzumab may not have a significant effect on the frequency of infusion reaction expression or the occurrence of cardiac dysfunction among patients with HER2-positive breast cancer.
Switching from reference trastuzumab to biosimilar trastuzumab may not have a significant effect on the frequency of infusion reaction expression or the occurrence of cardiac dysfunction among patients with HER2-positive breast cancer.
Switching from reference...
07/10/2023
Oncology
News
11/17/2022
The FDA granted approval to brentuximab vedotin in combination with doxorubicin, vincristine, etoposide, prednisone, and cyclophosphamide for pediatric patients 2 years of age and older with previously untreated high-risk classical Hodgkin...
The FDA granted approval to brentuximab vedotin in combination with doxorubicin, vincristine, etoposide, prednisone, and cyclophosphamide for pediatric patients 2 years of age and older with previously untreated high-risk classical Hodgkin...
The FDA granted approval to...
11/17/2022
Oncology
News
09/28/2023
Tacrolimus plus a reduced-dose of methotrexate combined with mycophenolate for GVHD prevention demonstrated a more favorable toxicity profile compared with the standard-of-care, according to a phase 3 trial.
Tacrolimus plus a reduced-dose of methotrexate combined with mycophenolate for GVHD prevention demonstrated a more favorable toxicity profile compared with the standard-of-care, according to a phase 3 trial.
Tacrolimus plus a reduced-dose...
09/28/2023
Oncology