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http://bit.ly/2q8duxM
These guidelines are very important in cardiac surgery. Tranfusion triggers, perfusion interventions,blood salvage,blood products all are described in great detail.
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http://bit.ly/2q8duxM
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Therapeutic Monoclonal Antibodies and Blood Transfusion.pdf
1. Therapeutic monoclonal
antibodies & blood transfusion
Essential information for hospital transfusion
laboratories, transfusion practitioners &
haematology clinical teams
2. Background
• Targeted therapeutic monoclonal antibodies are used to treat
patients with myeloma and other haematological malignancies.
• It is likely that these patients will need regular transfusion support.
• Depending on the nature of the monoclonal antibody, these drugs
may interfere with pre-transfusion testing.
• The use of these targeted monoclonal antibody therapies is
increasing, as promising clinical trials lead to their administration
in routine clinical practice.
3. Which drugs are involved?
Anti-CD38 (Daratumumab / Darzalex for multiple myeloma)
–NICE technology appraisal, completed March 2018.
There are other drugs currently undergoing trials and you may also
encounter these:
Anti-CD47 (CAMELLIA for acute myeloid leukaemia and
myelodysplastic syndrome)
– Trial due to complete January 2019
Anti-CD38 (Isatuximab for multiple myeloma)
– Currently 19 trials listed
– Phase III clinical trials in the UK as combination therapy
– Currently collecting data on interference with testing. Follow
protocol for Daratumumab patients.
4. CAMELLIA overview
• CAMELLIA (anti-CD47) is a monoclonal antibody used to treat acute
myeloid leukaemia and myelodysplastic syndrome.
• CD47 is widely expressed on human tissues and red cells.
• CD47 acts as a marker of self, a "Do not eat me" signal for healthy tissue.
• Blocking of CD47 on the surface of Red Blood Cell (RBC) with the use of
targeted monoclonal antibodies decreases the protective signal and
increases the phagocytosis of circulating RBCs by macrophages in the
spleen.
• Increased phagocytosis by splenic macrophages is clinically manifested
with indices of extravascular haemolysis.
5. CAMELLIA overview
• RBCs express high levels of CD47
• Treatment with anti-CD47 is likely to cause anomalous grouping results
• If after treatment, the ABO group cannot be concluded, group O red cells
may be required for transfusion
• In patients who are DAT positive, adsorption studies can allow
satisfactory antibody detection / identification in many cases.
6. Daratumumab overview
• Daratumumab is a human monoclonal antibody for the treatment of multiple
myeloma.
• Daratumumab binds to CD38, a protein that is ubiquitously expressed on
myeloma and lymphoma cells but expressed at low levels on normal lymphoid
and myeloid cells.
• CD38 is also expressed at low levels on red blood cells (RBCs).
• To date, no clinically significant haemolysis has been observed in patients
receiving 16 mg/kg Daratumumab. Continuous monitoring will be performed in
clinical studies and post-marketing safety data.
• Among a cohort of 46 patients receiving Daratumumab at a dose of 16 mg/kg
and requiring RBC and whole blood transfusions (135 transfusions received),
no transfusion reactions have occurred.
Daratumumab binds to
CD38 on RBCs
CD38
Daratumumab
• Approval of Daratumumab by NICE has
lead to an increase in the routine clinical
use of Daratumumab.
7. • Daratumumab is a human
monoclonal antibody.
• Daratumumab binds to CD38, a
protein expressed at low levels on
red blood cells (RBCs).
• Daratumumab may mask the
detection of antibodies in the
patient’s serum. This interferes
with compatibility tests, including
the antibody screening and
crossmatching that are part of a
routine pre-transfusion work up.
Daratumumab results in a
false positive antibody screen
8. Recommendations for serological
testing - 1
• Prior to commencing monoclonal antibody therapy, it is
recommended to undertake the following testing:
– Baseline ABO and D group and antibody screen, and
antibody identification if required
– Direct antiglobulin test (DAT )
– Undertake phenotype/genotype Rh CcDEe, MNSs, Kk, Jka,
Jkb, Fya and Fyb groups.
9. Recommendations for serological
testing - 2
• Once Daratumumab (anti-CD38) therapy commenced
– ABO and D type by normal methods
– DAT may be positive (or negative)
– The antibody screen / identification will be positive due to
interference by the drug
– The effect can persist for up to 6 months after treatment.
• Once CAMELLIA (anti-CD47) therapy commenced
– ABO and D type as per normal method. If the ABO group cannot be
concluded, group O red cells may be required for transfusion
– In patients who have are DAT positive, adsorption studies can allow
satisfactory antibody detection / identification in many cases.
10. Treat reagent RBCs with DTT or locally validated methods
• Treat reagent RBCs with dithiothreitol (DTT) to disrupt daratumumab binding, thus
allowing antibody screening or cross-matching to be performed; (Chapuy et al. 2015)
Alternative locally validated methods can also be used.
• Blood components for transfusion are identified for daratumumab-treated patients, after
using DTT-treated reagent RBCs for antibody screening.
• Since the Kell blood group antigens are also sensitive to DTT treatment, units should be
supplied which are matched for K- or k- patients, based on their phenotype or genotype,
after ruling out or identifying alloantibodies using DTT-treated RBCs.
Management of interference with
blood compatibility testing by Daratumumab
11. Provision of blood
• Elective and non urgent transfusion - Provide ABO extended Rh
and K compatible units after ruling out or identifying
alloantibodies using DTT-treated reagent RBCs.
• Irradiated blood components should be provided where
required.
• If blood needed urgently can provide ABO extended Rh and K
compatible pending further serological testing.
• In an absolute emergency - Uncrossmatched, ABO and D
compatible RBC units should be administered as per local
hospital transfusion laboratory practice.
12. How to prevent blood transfusion
delays – communication cascade
13. Cascade the following key messages to
hospital clinical teams
• To ensure that your patient receives a timely transfusion, send a group
and screen sample prior to starting daratumumab and inform the blood
bank that the patient is to commence daratumumab therapy.
• Inform shared care hospital
• Extended phenotyping/genotyping is recommended prior to
starting daratumumab.
• If patients have already commenced daratumumab therapy it is essential
to inform the blood bank.
• Specific techniques will be required for blood compatibility testing and
blood component selection with likely referral to the NHSBT Red Cell
Immunology (RCI) reference lab.
• This communication is essential to avoid delays in transfusion.
14. Inform the patient - provide a Patient Card
• Advise patients that they should carry their Patient ID Card for 6 months after
the treatment has ended.
• Patient ID Card information includes
– The name of the patient
– If they are no longer taking daratumumab, the date they stopped treatment
– Their blood type (A, B, AB, O, RhD+, RhD-) before starting daratumumab
– Their antibody screen results before starting daratumumab.
Before starting daratumumab my blood test results collected on
______ / ______ / _______ were:
DD MM YYYY
Blood type: □ A □ B □ AB □ O □ RhD+ □ RhD-
Antibody screen was:
□ Negative □ Positive for the following antibodies:
_____________________________________________________
Other: ________________________________________________
Contact details of institution where the blood tests were performed:
______________________________________________________
Daratumumab PATIENTS: Provide this card to healthcare providers
BEFORE blood transfusion and carry it for 6 months after treatment
has ended. For further information, please refer to the Patient
Information Leaflet
Patient ID Card for DARATUMUMAB
Name: __________________________________________________
I am taking the following medication:
Daratumumab antibody product for the treatment of Multiple Myeloma
I stopped taking this medication on ____ / ____ / ______
DD MM YYYY
15. Action needed – effective communication
• Effective communication is essential between the following to
ensure appropriate care and to avoid delays in transfusion:
– Patients
– Hospital consultants, trainees and nurses treating patients or
covering on call
– Hospital transfusion laboratories
– Shared care hospitals
– NHS Blood and Transplant Red Cell Immunohaematology (RCI)
laboratories.
• Complete the contact details of the institution where the blood tests
were performed on the patient card, it is especially useful in
emergency situations.
16. Further information
• The following information has been approved by the MHRA
in accordance with their guidelines.
Healthcare Professional materials:
https://www.medicines.org.uk/emc/RMM.539.pdf
Patient Card:
https://www.medicines.org.uk/emc/RMM.540.pdf
Blood Bank:
https://www.medicines.org.uk/emc/RMM.545.pdf
17. References
1. British Society for Haematology: Addendum to the Pre-
Transfusion Compatibility Procedures in Blood Transfusion
Laboratories, 2017 www.b-s-h.org.uk
2. Darzalex® UK Summary of Product Characteristics. 2017
3. Chapuy CI, et al. Transfusion. 2015;55(6 Pt 2):1545-1554
4. Albeniz I, et al. Hematology. 2007;12(5):409-414
5. Mehta K, et al. FASEB J. 1996;10(12):1408-1417
6. Zocchi E, et al. Biochem Biophys Res Commun.
1993;196(3):1459-1465
7. Westhoff CM, Reid ME. 2004;20(1):37-49
8. National Cancer Drugs Fund (CDF) List. (2018) Available at:
https://www.england.nhs.uk/wp-content/uploads/2017/04/national-
cdf-list-v1-68.pdf