Opinion|Videos|October 28, 2025

Comorbidities, Quality of Life, Efficacy, and Safety in Expanding Subcutaneous Treatment Use

Panelists discuss how subcutaneous checkpoint inhibitors are appropriate for nearly all patients except those with severe cachexia limiting injection sites, with patient conversations emphasizing equivalent efficacy data, safety profiles, quality of life benefits including potential home administration, and the option to maintain IV therapy for patients who prefer their current regimen.

Patient selection for subcutaneous immune checkpoint inhibitors generally includes most individuals receiving cancer treatment, with disease stage, prior therapy, and common comorbidities (diabetes, cardiac conditions) posing no contraindications if patients tolerated intravenous (IV) formulations. The primary limitation involves patients with profound emaciation and cachexia, where identifying suitable subcutaneous injection sites becomes challenging. Otherwise, subcutaneous administration offers particular advantages for patients experiencing difficult venous access, long travel distances, and multiple appointment burdens, or those preferring reduced time in medical settings, with emerging opportunities for home administration as payers begin reimbursing at parity even outside clinical trial settings.

Patient education conversations focus on presenting equivalency data in accessible language, addressing the natural question of whether injections work as effectively as IV infusions. Health care providers review FDA approval studies demonstrating comparable pharmacokinetics, efficacy outcomes including response rates and survival data, and safety profiles showing that adverse effects remain consistent between formulations. Importantly, discussions prepare patients for injection site reactions—a new experience compared with IV therapy—though emphasizing that these reactions typically remain mild and resolve within hours. For patients questioning why they should switch from IV therapy that worked previously, providers respect patient autonomy while highlighting quality of life benefits, including shorter administration time and reduced infusion center requirements.

Implementation approaches vary based on whether patients initiate treatment with subcutaneous formulations or transition from established IV regimens. For treatment-naive patients, presenting both options as equally effective typically generates straightforward acceptance, particularly when emphasizing convenience and avoiding venous access requirements. Converting established patients requires more extensive conversation addressing why changes are being proposed, but clearly conveying quality of life benefits and eliminating line access needs generally overcomes hesitation. Health care systems report minimal hurdles in these discussions when benefits are communicated effectively, with patient teaching materials and open discussions allowing patients and their families to determine what feels best for their circumstances, though most patients readily embrace opportunities avoiding venipuncture and port access while maintaining therapeutic efficacy.

Newsletter

Stay informed on drug updates, treatment guidelines, and pharmacy practice trends—subscribe to Pharmacy Times for weekly clinical insights.


Latest CME