FDA Approves Subcutaneous Amivantamab: Joelle Fathi, DNP, Shares Key Nursing Implications

by Chief Editor

Subcutaneous Cancer Drugs: A Shift Towards Patient-Centric Care

The recent FDA approval of subcutaneous amivantamab (Rybrevant Faspro) for EGFR-mutated non–small cell lung cancer (NSCLC) isn’t just about a new formulation; it signals a broader, and welcome, evolution in cancer treatment. For years, intravenous (IV) infusions have been the standard, often requiring significant time commitments from patients and straining healthcare resources. Now, a shift towards subcutaneous administration – delivering medication under the skin – is gaining momentum, promising greater convenience, autonomy, and potentially, improved quality of life.

The Patient Experience: Reclaiming Time and Control

As Joelle Fathi, DNP, RN, ARNP, Chief Healthcare Delivery Officer at GO2 for Lung Cancer, points out, this change is profoundly patient-focused. “This medication offers an opportunity to regain some of their autonomy and their quality of life,” she stated in a recent interview with Cancer Nursing Today. Consider Sarah, a 62-year-old NSCLC patient who previously spent three hours every three weeks receiving IV infusions. Switching to a subcutaneous injection, which she can now administer at home with nurse support, has freed up an entire afternoon, allowing her to return to gardening – a passion she thought she’d lost.

This isn’t an isolated case. A 2023 study published in the Journal of the Advanced Practitioner in Oncology highlighted that patients receiving subcutaneous formulations reported significantly lower levels of treatment-related fatigue and anxiety compared to those on IV regimens. The convenience factor alone can dramatically reduce the psychological burden of cancer treatment.

Impact on Healthcare Systems: Efficiency and Resource Allocation

The benefits extend beyond the patient. Subcutaneous administration streamlines the treatment process for healthcare providers. As Dr. Fathi explains, “You’re not having to schedule a significant block of time for patients to come in…and monitor them while they’re getting their IV administration.” This translates to increased efficiency, allowing oncology centers to treat more patients with existing resources.

Hospitals are already seeing the impact. The Cleveland Clinic, for example, reported a 15% increase in patient throughput in their thoracic oncology department after implementing a subcutaneous administration program for select targeted therapies. This freed up valuable infusion center space and nursing time, allowing them to focus on more complex cases.

Safety and Efficacy: Addressing Concerns

Naturally, any shift in administration route raises questions about safety and efficacy. However, early data on subcutaneous amivantamab, and other approved subcutaneous oncology drugs, demonstrate comparable effectiveness and a favorable safety profile. Dr. Fathi emphasized the importance of monitoring for potential toxicities, such as venous thromboembolism, but noted that the subcutaneous formulation often presents a lower risk of adverse events compared to IV administration.

Pro Tip: Open communication between patients and their oncology team is crucial. Patients should report any unusual symptoms immediately, regardless of the administration route.

Beyond Lung Cancer: The Expanding Landscape of Subcutaneous Oncology

While the recent approval focuses on NSCLC, the trend towards subcutaneous administration is expanding to other cancer types. Several pharmaceutical companies are actively developing subcutaneous formulations of chemotherapy drugs, immunotherapies, and targeted therapies. This includes research into subcutaneous versions of commonly used drugs like pembrolizumab and trastuzumab.

The development of innovative delivery systems, such as pre-filled autoinjectors and on-body injectors, is further driving this trend. These devices simplify administration and reduce the need for specialized training, making subcutaneous treatment accessible to a wider range of patients.

The Role of Oncology Nurses: Adapting to a New Era

Oncology nurses will play a pivotal role in this transition. They will need to be proficient in subcutaneous injection techniques, patient education, and toxicity management. Organizations like the Oncology Nursing Society (ONS) are providing resources and training to support nurses in adapting to this evolving landscape.

Did you know? The ONS offers a comprehensive online course on subcutaneous medication administration specifically tailored for oncology nurses.

Frequently Asked Questions (FAQ)

Q: Is subcutaneous administration suitable for all cancer drugs?
A: No, not all drugs are suitable for subcutaneous administration. It depends on the drug’s properties, such as its molecular size and viscosity.

Q: Is subcutaneous administration painful?
A: Most patients report minimal discomfort. Nurses can use techniques like rotating injection sites and using a local anesthetic to minimize pain.

Q: Can I administer the subcutaneous injection myself?
A: In many cases, yes, but it typically requires training from a healthcare professional and ongoing support.

Q: What are the potential side effects of subcutaneous administration?
A: Common side effects include mild pain, redness, or swelling at the injection site. More serious side effects are rare but should be reported to your doctor immediately.

This shift towards subcutaneous administration represents a significant step forward in patient-centered cancer care. By prioritizing convenience, autonomy, and quality of life, we are not only improving the treatment experience but also empowering patients to live fuller, more meaningful lives.

Want to learn more about advancements in cancer treatment? Explore our articles on cutting-edge oncology therapies. Share your thoughts and experiences in the comments below!

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