
Patient Satisfaction, Comfort Level, and Operational Benefits of SubQ Immune Checkpoint Inhibitors
Panelists discuss how subcutaneous formulations provide operational benefits through increased patient satisfaction, reduced chair time allowing higher patient throughput, cost savings from eliminated intravenous (IV) supplies and reduced infusion duration, improved nursing satisfaction from avoiding difficult venous access procedures, and potential for dedicated injection clinics or bays that free up traditional infusion center capacity.
Episodes in this series

Patient Satisfaction and Operational Efficiency Benefits
Patient satisfaction represents a critical driver for subcutaneous checkpoint inhibitor adoption beyond pure drug revenue considerations. The immediate positive patient response upon receiving subcutaneous injections and rapid discharge creates measurable satisfaction improvements that influence institutional reputation and patient preference for care centers. Operationally, freeing infusion chairs from lengthy checkpoint inhibitor appointments increases overall patient throughput capacity, allowing treatment of more patients without physical facility expansion. Innovative scheduling models emerge, including potential weekend subcutaneous injection clinics after provider clearance, expanding access beyond traditional weekday infusion center hours. These granular operational improvements accumulate substantially across institutional operations.
Cost savings extend beyond chair time to encompass multiple supply chain elements. Subcutaneous administration eliminates costs for Huber needles for port access, IV tubing, infusion pumps, and saline flush solutions. When aggregated across all immunotherapy administrations institution-wide, these seemingly minor per-patient savings generate significant annual cost reductions. More importantly, reducing checkpoint inhibitor infusion appointments to brief injection visits liberates chair capacity for patients requiring more complex combination chemotherapy regimens or longer infusion times, optimizing resource use without infrastructure investment. The financial implications prove uniformly positive: Reduced chair time translates directly to cost savings while enabling higher chair turnover and expanded infusion service capacity.
Multidisciplinary team perspectives on subcutaneous adoption show universal enthusiasm. Nursing staff, particularly nurse managers focused on maximizing staffing efficiency and minimizing patient wait times, strongly support subcutaneous options. Experienced infusion nurses who witness patient distress during repeated difficult venipunctures—the anxiety escalating with first, second, and third attempts—recognize the profound impact on patient-nurse interactions and patient pain. This emotional burden on nursing staff correlates with their eagerness for effective subcutaneous alternatives. Staff nurse satisfaction parallels patient satisfaction improvements, both vital metrics for thriving cancer center cultures. Advanced practice providers and nurse managers alike advocate for expanding subcutaneous medication availability. As subcutaneous product volume increases across therapeutic areas (anti-HER2 agents including trastuzumab, pertuzumab coformulations, anti-CD38 therapies, and now checkpoint inhibitors), infusion centers may require dedicated injection rooms or sections, though not necessarily exclusive spaces. Adoption of wearable devices or standardized injection pumps applicable across multiple subcutaneous products could further streamline administration as volume scales, building on experience gained transitioning multiple antibody classes to subcutaneous delivery over recent years.