Blinatumomab for B-cell precursor ALL: From hospital to home

24 Oct 2025
Dr. Carol Cheung
Dr. Carol CheungSpecialist in Haematology & Haematological Oncology
Ms. Kitty Leung
Ms. Kitty LeungClinical pharmacist
Dr. Carol Cheung
Dr. Carol Cheung Specialist in Haematology & Haematological Oncology
Ms. Kitty Leung
Ms. Kitty Leung Clinical pharmacist
Blinatumomab for B-cell precursor ALL: From hospital to home

Blinatumomab, a bispecific T cell–engager antibody administered as a continuous intravenous (IV) infusion, has several indications in B-cell precursor acute lymphoblastic leukaemia (ALL). Traditionally, in Hong Kong, patients receiving blinatumomab are hospitalized for 28-day treatment cycles. In an interview with MIMS Oncology, Dr Carol Cheung, Specialist in Haematology & Haematological Oncology, and clinical pharmacist Ms Kitty Leung shared insights into how a proactive outpatient infusion protocol at a local hospital has enabled patients to receive blinatumomab at home. They discussed how home infusion of blinatumomab works, along with its risks, challenges, and benefits for both patients and healthcare providers.

Evolving role of blinatumomab in ALL
“Blinatumomab has been available in Hong Kong for nearly a decade and has profoundly transformed the treat­ment landscape of ALL. Initially ap­proved for relapsed or refractory [R/R] cases, its role has since expanded to in­clude minimal residual disease [MRD]– positive disease and, more recently, it has become part of frontline consolida­tion therapy. This versatility highlights its relevance across various treatment set­tings. Even in MRD-negative patients, frontline use of blinatumomab has been shown to improve survival outcomes,” noted Cheung. “Furthermore, in Phil­adelphia chromosome [Ph]–positive ALL, there is a growing trend toward potentially eliminating chemotherapy al­together by incorporating blinatumom­ab. For Ph-negative cases, combining multiagent chemotherapy with bli­natumomab as initial therapy has demonstrated remarkable efficacy.” [Blincyto Hong Kong Prescribing In­formation, January 2023; N Engl J Med 2024;391:320-333; J Clin Med 2025;14:2055]

Continuous IV infusion: The need for outpatient options
Blinatumomab is administered via continuous IV infusion over 4 weeks (28 days), followed by a 14-day break, form­ing a 42-day treatment cycle. The total number of cycles is determined by the treating physician, based on indication. In­fusion should be initiated under the super­vision of experienced clinicians. Hospital­ization is generally required for treatment initiation and for subsequent cycles, with the length of hospital stay depending on indication. (Table 1) [Blincyto Hong Kong Prescribing Information, January 2023]

“In Hong Kong, the usual practice has been to hospitalize patients for the entire 28-day treatment cycle due to its inconvenient mode of administration,” Cheung remarked. “This approach, repeated with each cycle, is resource-intensive and burdensome for patients and caregivers, requiring long stays and frequent visits. It creates logistical and emotional challenges, highlighting the need for alternative delivery meth­ods to improve patient comfort and reduce strain on healthcare resources.”

“Therefore, we have introduced an outpatient infusion programme, allow­ing patients to receive blinatumomab at home once their condition is stable,” Cheung added.

Home infusion of blinatumomab: How does it work?
Patient eligibility
“Firstly, we identify patients suitable for home infusion. They should be fit adults with good performance status, support­ive caregivers, and a strong motivation for home infusion,” noted Cheung. “General­ly, we select stable patients with a low risk of developing cytokine release syndrome [CRS]. These patients should live close to the hospital or be able to reach it quickly in case of emergency. Patients and their caregivers need a basic understanding of how to manage outpatient infusion and the ability to operate and care for the pump after education. Motivation and will­ingness are key.”

“Conversely, patients on other IV medications, such as antibiotics, or those with abnormal baseline blood counts, sig­nificant concerns about home infusion, or a high risk of developing CRS are gener­ally not suitable. Ultimately, patient safety and their preference are our top consider­ations,” she continued.

Timing for transition
“In adult patients, hospitalization for ≥9 days during the first cycle is recom­mended for R/R ALL. In other settings, shorter durations are often sufficient,” said Cheung. (Table 1) “The initial hospital stay is crucial, even when outpatient treat­ment is planned, as it allows close moni­toring of adverse events [AEs], especially during the initial phase of the first cycle, when conditions like CRS or neurologi­cal toxicity are most likely to occur,” she explained. “To ensure safety, we usually keep patients in-hospital for close moni­toring during this period.”

“If clinically relevant AEs occur and treatment is interrupted at any point, blinatumomab should be restarted at 9 mcg/day. We typically monitor patients closely for ≥7 days until they reach the full dose of 28 mcg/day and show no signs of recurring toxicity before discharge,” Cheung continued.

“Hospital stays also offer patients the opportunity to receive training via videos, demonstrations and hands-on practice in managing the infusion pump and re­sponding to potential issues,” Cheung added. “The frontline healthcare team must ensure that patients are confident and competent in handling the pump and recognizing warning signs before autho­rizing discharge.”

“Generally, if the first cycle is tolerat­ed well without significant AEs, a patient is less likely to encounter major issues in subsequent cycles. These patients may require only 2–3 days of hospitalization for the second and later cycles, and some stable patients may even go home after 1–2 days. This timing is highlyindividual­ized depending on each patient’s condi­tion and ability to manage the treatment safely,” she shared.

Delivering blinatumomab at home
“When a patient’s condition is sta­ble, treatment can be continued at home using a small, portable IV infusion pump and an admixed infusion bag containing blinatumomab, reconstituted by a phar­macist in aseptic conditions,” Leung and Cheung explained. “Infusion bags are available for 7-day [1-week] infusion, as well as 1-day [24-hour], 2-day [48-hour], 3-day [72-hour] and 4-day [96-hour] infusions.”

“In our practice, we usually dispense the 7-day infusion bags for outpatient use. The drug in the infusion bag is delivered via the ambulatory pump at a constant, preset flow rate that cannot be modified by anyone except the supplier,” Leung continued. “The pump is programmable, lockable, non-elastomeric, and equipped with an alarm that alerts if drug delivery is interrupted.”

Patient education and supplies
“Before discharge, patients receive training via videos and demonstrations during hospitalization. They practice oper­ating the ambulatory pump with their 7-day infusion bag to build confidence,” said Cheung. “Trained nurses then complete a checklist to ensure patients can manage

home infusion independently. Patients are also provided with a booklet contain­ing instructions, a diary, and frequently asked questions for troubleshooting. They use the diary to record daily body temperature and perform handwrit­ing assessments, such as writing their home address, to monitor for drug-related toxicity. They are also encour­aged to note alarms or unusual symp­toms to discuss with their healthcare team during their next hospital visit.”

Tables 2 and 3 list detailed reminders on daily management and when to seek medical assistance.


“Each patient receives a purposeful­ly designed backpack to carry the infu­sion bag while commuting, along with an extra battery for the infusion pump and a power cord for use between vis­its. A spillage kit is also provided in case of drug leakage, and a double clamp is provided for the infusion line,” Leung added.

Safety monitoring and management
“Fever is a common sign of CRS, oc­curring in more than half of our patients receiving blinatumomab. Neurological toxicity is also frequently observed,” Cheung remarked. “Premedication with steroids, such as dexamethasone, ad­ministered 1 hour before each cycle, can help prevent these toxicities. Patients with high tumour burden are considered high-risk and have an increased likelihood of CRS and neurological side effects. In such cases, cytoreduction prior to starting blinatumomab may be necessary. A step-up dosing regimen, beginning at 9 mcg/ day and escalating to 28 mcg/day after 7 days, along with premedication before each escalation, may also mitigate the risk of toxicity.” [Blincyto Hong Kong Prescrib­ing Information, January 2023]

“During hospitalization, vital signs should be monitored very closely during the initial days of treatment to detect early signs of CRS. Blood tests are performed 3–4 times daily to check for markers of tumour lysis syndrome, liver and renal function, haematological pa­rameters, and coagulation profile. Pa­tients should perform daily handwriting assessments to monitor for any signs of neurological toxicity. Blood oxygen lev­els should also be regularly checked,” Cheung highlighted.

“If CRS or neurological toxicity occurs during treatment, management should follow international guidelines. For low-grade fever, observation and symptom­atic relief are typically sufficient. However, if a patient develops high-grade fever, with or without haemodynamic instabil­ity or increased oxygen requirements, steroids are indicated,” Cheung advised. “Treatment may be interrupted if a patient experiences grade ≥3 clinically relevant AEs. Re-premedication is recommended before resuming blinatumomab after an interruption >4 hours.”

Potential risks and challenges
Logistics and supply
“Reconstitution of blinatumomab is performed after pharmacists receive a drug order from nurses in the ward. Since the shelf life of the reconstituted drug is limited under room temperature, mini­mizing the time between reconstitution and administration is essential to prevent treatment delays and reduce drug wast­age. Therefore, effective communication between nursing staff and pharmacists is crucial,” emphasized Leung.

Bag preparation and priming
“Pharmacists use specific techniques and follow procedures outlined in the prescribing information to prepare the 7-day infusion bags. The stabilizer and saline are combined in an empty bag and gently swirled—avoiding vigorous shaking — before adding the reconsti­tuted drug. It is also important that the pump cassettes and IV tubing are com­patible: the IV tubing must be polyolefin, diethylhexylphthalate [DEHP]-free poly­vinyl chloride [PVC] or ethylene vinyl ac­etate [EVA],” pointed out Leung. “The IV line must be primed with the prepared solution by trained nursing staff. Each 7-day bag contains about 9 mL of excess volume to allow for the priming.” [www.Blincytohcp.com/dosing/preparation]

Risk of drug interruptions
“Drug interruptions are particu­larly concerning, given the high cost and short shelf life of blinatumomab, as well as the potential need for re-priming, which can cause drug shortfalls on the 7th day due to insufficient excess vol­ume,” noted Cheung. “Therefore, re-priming should be limited. Selecting stable patients with a low risk of developing CRS is essen­tial to minimize the risk of interruptions.”

Drug delivery when volume is low
“Due to limited excess volume, the pump may encounter difficulties at the end of the 7-day regimen, such as drug shortfalls from re-priming or air bubbles in the tubing, leading to frequent alarms or the need for tubing tapping,” Leung noted. “In most cases, scheduled bag replacements are timed carefully to mini­mize such issues.”

Other technical issues and troubleshooting
“The pump alarm indicates technical issues, such as air bubbles in the tubing or flow irregularity. Patients can follow troubleshooting instructions, such as gently tapping the tubing if air bubbles or flow irregularities trigger the alarm, to resolve these minor problems, advised Leung, “If issues persist, they should re­turn to the hospital promptly to seek help from nursing staff.”

Real-world experience
“In our hospital, approximately 60–70 percent of blinatumomab infusion cases are managed as outpatients. Over the past 2 years, >20 cycles have been suc­cessfully administered in outpatient set­ting. Few minor issues were encountered, mainly air bubbles or tubing problems, which were promptly resolved by trained nursing staff. During this period, only one patient sought medical attention for fever during home infusion,” shared Cheung.

“Our frontline nursing team plays a vital role as the primary contact for pa­tients experiencing infusion issues at home. Patients can call immediately whenever issues arise, and their concerns are triaged for further management.”

“Overall, patients are highly satisfied with staying at home for infusions. The approach is highly personalized — some patients continue with hospital stays, while others have 7-day home infusions or shorter 24- or 48-hour in-hospital in­fusions before transitioning to the 7-day home-based regimen. This flexibility al­lows our patients to receive the regimen that is most suitable for their needs,” Cheung concluded.


This educational material is supported by Amgen. The views and opinions expressed are those of the individual faculty member and are intended for healthcare professional educational purpose only.
SC-HKG-AMG103-00112 Sept 2025

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