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What's the difference between Neulasta and NEUPOGEN?

4 min read

In 2020, over 1.6 million patients in the U.S. were prescribed pegfilgrastim (Neulasta) to help manage the side effects of chemotherapy [1.4.1]. This article answers the question: What's the difference between Neulasta and NEUPOGEN?, exploring two key medications used to prevent infection during cancer treatment.

Quick Summary

Neulasta (pegfilgrastim) is a long-acting drug given once per chemotherapy cycle, while Neupogen (filgrastim) is a short-acting drug requiring daily injections. Both stimulate white blood cell production.

Key Points

  • Core Difference: Neulasta is a long-acting version of Neupogen due to a process called pegylation, which extends its half-life [1.2.2, 1.4.3].

  • Dosing Frequency: Neulasta requires only a single injection per chemotherapy cycle, whereas Neupogen must be injected daily [1.2.1].

  • Active Ingredients: Neulasta's active ingredient is pegfilgrastim, while Neupogen's is filgrastim [1.2.2].

  • Mechanism of Action: Both drugs are Granulocyte Colony-Stimulating Factors (G-CSFs) that stimulate the bone marrow to produce more infection-fighting white blood cells (neutrophils) [1.4.1].

  • Primary Use: They are used to reduce the risk of infection in cancer patients receiving chemotherapy that suppresses bone marrow function [1.2.1, 1.2.2].

  • Common Side Effect: The most common side effect for both medications is bone pain, resulting from the stimulation of bone marrow [1.5.1, 1.5.6].

  • Cost & Biosimilars: Both are expensive, but lower-cost biosimilar versions are available for both Neulasta (e.g., Udenyca, Fulphila) and Neupogen (e.g., Zarxio) [1.2.1, 1.5.2].

In This Article

Understanding Neutropenia and G-CSF Medications

Chemotherapy is a cornerstone of cancer treatment, but it targets all rapidly dividing cells, not just cancerous ones [1.2.1]. This includes healthy white blood cells, particularly neutrophils, which are the body's primary defense against bacterial infections. A significant drop in these cells leads to a condition called neutropenia, increasing a patient's risk of developing serious infections [1.2.1]. Neutropenia typically occurs 7 to 12 days after a chemotherapy session [1.2.1].

To counteract this, doctors prescribe medications known as Granulocyte Colony-Stimulating Factors (G-CSFs). Neulasta and NEUPOGEN are two of the most common brand-name G-CSFs [1.4.1]. Both are man-made versions of a natural protein that stimulates the bone marrow to produce more neutrophils, thereby reducing the risk of infection and a complication called febrile neutropenia (neutropenia with a fever) [1.2.2, 1.4.1]. These medications bind to receptors on hematopoietic stem cells in the bone marrow, prompting them to proliferate and differentiate into mature neutrophils [1.4.2, 1.4.4].

The Core Difference: Pegylation and Half-Life

The fundamental difference between Neulasta and NEUPOGEN lies in their molecular structure and, consequently, their duration of action. NEUPOGEN's active ingredient is filgrastim [1.2.2]. Neulasta's active ingredient is pegfilgrastim, which is created by attaching a polyethylene glycol (PEG) molecule to filgrastim in a process called pegylation [1.4.3].

This single molecular addition dramatically changes how the drug behaves in the body. The PEG molecule makes pegfilgrastim much larger, slowing its clearance from the body primarily through the kidneys [1.4.7]. This results in a significantly longer half-life. Neulasta has a half-life of up to 80 hours, whereas NEUPOGEN's half-life is around 3.5 to 5.8 hours [1.5.2, 1.4.5]. Because Neulasta lasts much longer, it's considered a long-acting medication, while NEUPOGEN is short-acting [1.2.1].

Dosing and Administration: Convenience vs. Flexibility

The difference in half-life directly impacts the dosing schedule, which is often the most significant factor for patients and healthcare providers.

  • Neulasta (pegfilgrastim): Due to its long-acting nature, Neulasta is administered as a single 6 mg subcutaneous injection once per chemotherapy cycle [1.2.2]. It is typically given 24 hours after the chemotherapy dose and should not be given within the 14 days before the next round [1.2.1]. This convenience of a single shot is a major advantage, especially for patients who wish to avoid daily injections [1.3.4]. An on-body injector (Neulasta Onpro) is also available, which automatically delivers the dose about 27 hours after being applied by a healthcare provider [1.6.6].
  • NEUPOGEN (filgrastim): As a short-acting drug, NEUPOGEN requires daily subcutaneous injections [1.2.2]. Treatment usually starts 24 hours after chemotherapy and continues for up to two weeks, or until the absolute neutrophil count (ANC) reaches a safe level [1.2.1]. While less convenient, this daily regimen allows for more flexibility and closer management of the patient's neutrophil levels [1.2.2].

Efficacy and Clinical Use

Both medications are highly effective at reducing the incidence and duration of severe neutropenia [1.2.1]. Studies have shown that a single dose of Neulasta is comparable in efficacy and safety to multiple daily injections of NEUPOGEN for preventing febrile neutropenia [1.3.3]. The choice between them often comes down to the specific chemotherapy regimen, patient convenience, cost, and provider preference [1.2.2]. While Neulasta's single-dose schedule is often favored, NEUPOGEN's flexibility can be beneficial in certain treatment plans [1.2.2]. Neupogen also has broader approved applications, including for patients undergoing bone marrow transplants and peripheral blood progenitor cell collection [1.2.2].

Side-by-Side Comparison

Feature Neulasta (pegfilgrastim) NEUPOGEN (filgrastim)
Active Ingredient Pegfilgrastim Filgrastim [1.2.2]
Mechanism Long-acting G-CSF due to pegylation [1.2.1, 1.2.2] Short-acting G-CSF [1.2.1]
Half-Life Up to 80 hours [1.5.2] ~3.5-5.8 hours [1.5.2, 1.4.5]
Dosing Schedule One subcutaneous injection per chemo cycle [1.2.2] Daily subcutaneous injections for several days [1.2.1]
Common Side Effect Bone pain, muscle pain [1.5.1, 1.5.4] Bone pain [1.5.1, 1.5.7]
FDA Approval January 31, 2002 [1.5.2] February 20, 1991 [1.5.2]

Side Effects and Safety Profile

The side effect profiles for Neulasta and NEUPOGEN are very similar, which is expected since they share the same core mechanism [1.5.1]. The most commonly reported side effect for both is mild to moderate bone pain, often described as an aching in the bones or muscles [1.5.1, 1.5.6]. This occurs because the medications are actively stimulating the bone marrow [1.2.2].

Other potential side effects include:

  • Nausea and vomiting [1.5.3]
  • Headache [1.5.3]
  • Fatigue [1.5.1]
  • Injection site reactions (redness, swelling) [1.5.3]

Serious, though rare, side effects for both drugs include splenic rupture, acute respiratory distress syndrome (ARDS), and serious allergic reactions [1.5.1, 1.3.9]. Patients with sickle cell disorders may be at risk for a sickle cell crisis [1.5.1].

Cost and Biosimilars

Both Neulasta and NEUPOGEN are expensive specialty medications. Without insurance, a single injection of brand-name Neulasta can cost thousands of dollars, while a course of brand-name NEUPOGEN can also be very costly [1.6.9].

Fortunately, lower-cost alternatives called biosimilars are available for both drugs [1.2.1]. A biosimilar is a biological product that is highly similar to and has no clinically meaningful differences from an existing FDA-approved reference product.

  • Neulasta (pegfilgrastim) biosimilars include brands like Fulphila, Udenyca, and Ziextenzo [1.5.2].
  • NEUPOGEN (filgrastim) biosimilars include Zarxio and Nivestym [1.5.2].

These biosimilars offer comparable efficacy at a potentially reduced cost, making treatment more accessible [1.2.2].

Conclusion

The primary difference between Neulasta and NEUPOGEN is their duration of action, dictated by the pegylation of Neulasta's active ingredient. This leads to Neulasta being a convenient, single-dose-per-cycle medication, while NEUPOGEN offers a more flexible, daily-dosing regimen. Both are effective colony-stimulating factors used to prevent dangerous drops in white blood cells during chemotherapy. The choice between them depends on a variety of factors including the specific cancer treatment, patient preference for dosing frequency, and cost considerations, which now include the availability of multiple biosimilars for both medications. Patients should discuss with their healthcare provider which option is most appropriate for their specific situation.

For more detailed information from a primary source, you can visit the manufacturer's website: Why Neulasta® (pegfilgrastim) Onpro

Frequently Asked Questions

Neulasta isn't necessarily 'stronger,' but it is longer-acting. A single dose of Neulasta (pegfilgrastim) has been shown to be as effective as multiple daily doses of Neupogen (filgrastim) in preventing neutropenia [1.3.3].

Neulasta is 'pegylated,' meaning a molecule is attached to the drug that makes it last much longer in the body. It has a half-life of up to 80 hours, compared to about 3.5-5.8 hours for Neupogen, so a single dose is sufficient for the entire cycle [1.5.2, 1.2.1].

The most common side effect for both Neulasta and Neupogen is bone pain. This happens because the medication stimulates the bone marrow to rapidly produce new white blood cells [1.5.1, 1.5.6].

These medications are generally not used together in standard chemotherapy support. Your doctor will prescribe one or the other based on your specific treatment plan. In some specific clinical situations, like stem cell mobilization, they might be used in sequence [1.3.8].

While there are no 'generic' versions in the traditional sense, there are FDA-approved 'biosimilars' for both drugs. Biosimilars like Zarxio (for Neupogen) and Udenyca (for Neulasta) are highly similar, have no clinically meaningful differences, and can be a more affordable option [1.2.1, 1.2.2].

The Neulasta Onpro is a wearable, on-body injector. After chemotherapy, a healthcare provider applies it to the patient's skin, and it is designed to automatically deliver the Neulasta dose approximately 27 hours later, reducing the need for a return visit to the clinic [1.6.6].

Both medications are typically administered at least 24 hours after a chemotherapy dose. They should not be given in the 14 days leading up to a chemotherapy dose [1.2.1, 1.4.3].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.