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  1. OncLive® On Air
  2. S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH
S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH

S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH

OncLive® On Air · Jul 28, 2026

FDA approves Sacituzumab Govitecan + Pembrolizumab for first-line PD-L1+ metastatic TNBC, a major advance for this hard-to-treat cancer.

NCCN Guideline Updates Drive Cancer Drug Adoption By Triggering Insurance Coverage

FDA approval is only the first hurdle for new cancer therapies. Inclusion in NCCN guidelines as a preferred regimen is the critical next step. This update validates a treatment's practice-changing potential and, more pragmatically, serves as a key signal for insurance companies to provide reimbursement.

S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH thumbnail

S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH

OncLive® On Air·7 days ago

Sacituzumab Plus Pembrolizumab Combination Shows No Additive Toxicity in TNBC Treatment

This new combination therapy for triple-negative breast cancer showed no increased toxicity compared to its individual components. Surprisingly, immune-related side effects were numerically lower than in the standard chemotherapy-immunotherapy arm, highlighting a favorable safety profile that is crucial for patient management.

S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH thumbnail

S17 Ep64: FDA Approval Insights: First-Line Sacituzumab Govitecan Plus Pembrolizumab for PD-L1+ TNBC: With Sara M. Tolaney, MD, MPH

OncLive® On Air·7 days ago