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  1. OncLive® On Air
  2. S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD
S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

OncLive® On Air · Jul 9, 2026

Nivolumab + AVD is the new standard for advanced Hodgkin lymphoma, offering superior efficacy (91% 3-yr PFS) and better quality of life.

Nivolumab+AVD Improves Hodgkin Lymphoma Patient Quality of Life by Reducing Neuropathy

The S1826 study showed nivolumab+AVD is better tolerated than the previous standard, brentuximab vedotin+AVD. It causes less peripheral neuropathy, fewer infections, and reduces the need for growth factors, leading to less bone pain and better patient-reported quality of life.

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD thumbnail

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

OncLive® On Air·5 days ago

Nivolumab+AVD Simplifies Hodgkin Lymphoma Treatment By Benefiting All Patient Subgroups

Data from the SWOG 1826 trial shows that nivolumab+AVD improves progression-free survival across all evaluated subgroups, including by age, disease stage, and risk score. This broad efficacy simplifies clinical decision-making, establishing it as a new standard for advanced-stage disease.

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD thumbnail

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

OncLive® On Air·5 days ago

Oncologists' Experience with Nivolumab in Solid Tumors Eases its Adoption for Lymphoma

The adoption of nivolumab+AVD in community oncology is streamlined because practitioners are already experienced with managing immune-related adverse events from using checkpoint inhibitors in various solid tumors. This existing familiarity flattens the learning curve for this new lymphoma regimen.

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD thumbnail

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

OncLive® On Air·5 days ago

Hodgkin Lymphoma Research Shifts to De-escalation Using ctDNA-Guided Therapy

With remission rates for advanced-stage Hodgkin lymphoma now exceeding 90%, the next research focus is on personalizing and reducing treatment intensity. Future trials will use tools like circulating tumor DNA (ctDNA) to identify patients who can receive less chemotherapy or need adapted therapy.

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD thumbnail

S17 Ep48: FDA Approval Insights: Nivolumab Plus AVD for Untreated Classical Hodgkin Lymphoma: With Alex Herrera, MD

OncLive® On Air·5 days ago