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Gina Tomaine

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
News
08/17/2022
For patients with classical Hodgkin lymphoma, first-line treatment with brentuximab vedotin plus AVD resulted in a significantly lower risk of death by 41% vs standard ABVD at 6 years, according to results from the ECHELON-1 trial.
For patients with classical Hodgkin lymphoma, first-line treatment with brentuximab vedotin plus AVD resulted in a significantly lower risk of death by 41% vs standard ABVD at 6 years, according to results from the ECHELON-1 trial.
For patients with classical...
08/17/2022
Oncology
News
01/20/2023
On January 19, 2023, the FDA approved zanubrutinib for chronic lymphocytic leukemia or small lymphocytic lymphoma.
On January 19, 2023, the FDA approved zanubrutinib for chronic lymphocytic leukemia or small lymphocytic lymphoma.
On January 19, 2023, the FDA...
01/20/2023
Oncology
News
09/30/2022
Bendamustine is an effective lymphodepletion regimen before tisagenlecleucel in patients with refractory/relapsed large B-cell lymphomas, according to a recent study.
Bendamustine is an effective lymphodepletion regimen before tisagenlecleucel in patients with refractory/relapsed large B-cell lymphomas, according to a recent study.
Bendamustine is an effective...
09/30/2022
Oncology
News
07/10/2023
In a phase 3 study, biosimilar candidate TAB008 was found to be similar to reference bevacizumab in terms of efficacy and safety for patients with locally advanced, metastatic EGFR wild-type non-squamous non-small cell lung cancer.
In a phase 3 study, biosimilar candidate TAB008 was found to be similar to reference bevacizumab in terms of efficacy and safety for patients with locally advanced, metastatic EGFR wild-type non-squamous non-small cell lung cancer.
In a phase 3 study, biosimilar...
07/10/2023
Oncology