Our Centre provides state-of-the-art services in
haematology and haematological oncology. Our
Haematopathology Laboratory has a wide range of
diagnostic tests available which are essential for modern
management of haematology patients. After making
an accurate diagnosis, optimal treatments are given
promptly to obtain the best clinical outcome possible.
Blood cancers are one of the top ten cancers in Hong
Kong. Every year, over 1,000 new cases are diagnosed.
They include leukaemia, lymphoma and myeloma.
Leukaemia
Leukaemia is the malignancy of white cells. Its causes
are largely unknown. It is occasionally related to
previous chemotherapy or radiation exposure, and
may be preceded by myelodysplastic syndrome or
myeloproliferative disease.
Common Subtypes
- Acute Leukaemia
- Chronic Lymphocytic Leukaemia
- Chronic Myeloid Leukaemia
Acute Leukaemia
Acute myeloid leukemia is more common in adults,
while acute lymphoblastic leukaemia is the commonest
type seen in children and young adults. Symptoms
include anaemia, fever and bleeding, and patients
are more prone to infection. Usually blood tests show
low haemoglobin count, high white cell count and low
platelet count. Leukaemia cells are found in blood and
bone marrow, and they are immature white cells. The
lymph nodes, liver and spleen may be enlarged. In
some cases, the skin and central nervous system may
also be affected.
Diagnosis
- Full blood counts
- Bone marrow biopsy
- Peripheral blood film examination
- Lumbar puncture
- Cytochemical study and immunophenotyping to
define the subtype
- Cytogenetic and molecular genetic studies are essential
Treatment
Intensive chemotherapy is necessary for cure, and
infection must be treated without delay. Supportive
care is also important. Patients may require blood
and platelet transfusions, and haematopoietic
growth factor (e.g. G-CSF) is frequently used for the
disease. Some patients may need an allogeneic bone
marrow transplantation, while gentle chemotherapy is
considered appropriate for the elderly patients. All-trans
retinoic acid and arsenic trioxide are used to treat acute
promyelocytic leukaemia. An unrelated marrow donor
registry is available in Hong Kong, i.e. Hong Kong Bone
Marrow Donor Registry, which is linked to the registries
of Taiwan and the Mainland.
Prognosis
- It is a curable disease for young patients
- Most patients respond well to chemotherapy
- Cure rate may exceed 50% for younger patients
- Survival rate improves with bone marrow transplantation
Chronic Lymphocytic Leukaemia
It is more common among the elderly. While patients are
often asymptomatic initially, some may have enlarged
lymph nodes and spleen. The white cell count is high,
which are mature lymphocytes, and the haemoglobin
and platelet count may be low. The bone marrow is
infiltrated by mature lymphocytes.
Diagnosis
- Full blood counts
- Bone marrow biopsy
- Peripheral blood film examination
- Immunophenotyping to confirm diagnosis
- Cytogenetic and fluorescence in situ hybridization
(FISH) analysis
Treatment
Various combinations of target therapy and
chemotherapy are available:
- Mabthera/Rituximab (anti-CD20 monoclonal antibody)
- Fludarabine
- Cyclophosphamide or Chlorambucil
- Mitoxantrone
- Prednisolone or Dexamethasone
- Bendamustine
- Alemtuzumab/Campath (anti-CD52 monoclonal antibody)
- Bone marrow transplantation is an option for young
patients with relapsed disease
Prognosis
- Good disease control can be achieved in most cases
- Relapses usually respond to retreatment
- FISH tests are useful in determining prognosis
Chronic Myeloid Leukaemia
Chronic myeloid leukaemia is often asymptomatic during
the early phase of the disease. Patients may be quite
young. High white cell counts are noted with increase in
both mature and immature white cells. Platelet count is
also at high level. Spleen is usually enlarged.
Diagnosis
- Full blood counts
- Bone marrow biopsy
- Cytogenetic study showing “Philadelphia
Chromosome”
- Florescence in situ hybridization (FISH) analysis or
polymerase chain reaction to detect bcr-abl translocation
Treatment
- Tyrosine kinase inhibitors (TKI) , e.g. Imatinib, Nilotinib
or Dasatinib
- Long-term therapy is required
- Genetic test monitoring is necessary
Prognosis
- If not properly treated, the disease transforms to
refractory acute leukaemia with an average period of
3 years
- Most patients respond very well to tyrosine kinase
inhibitors and have a long survival period
Common Treatment
Chemotherapy
Most blood cancer patients respond very well to
various combinations of chemotherapy. Chemotherapy
drugs are effective in eradicating rapidly proliferating
cells. As blood cancer cells often grow at a very
high rate, they are more susceptible to the effects of
chemotherapy. Some normal cells in our body also
grow rapidly, e.g. the bone marrow cells. Damages
to the normal cells are responsible for the side
effects, and thus patients must be monitored closely.
Serious infections may complicate low white cell
count and bleeding tendency if the platelet counts
are low. There may also be anaemia. Haematopoietic
growth factor G-CSF may be used. Red cells and
platelet transfusions may be given. Chemotherapy
may be given in our Chemotherapy Centre on either
an outpatient or inpatient basis, depending on the
intensity of the therapy.
Radiotherapy
High-energy radiation is commonly used in cancer
treatment. Blood cancer cells are very sensitive to
radiotherapy, making it an effective treatment for local
control of blood cancers and an adjunct to chemotherapy.
Targeted Therapy
The transformation of normal cells to cancer cells is
the result of many genetic changes. These changes
distinguish cancer cells from normal cells and can
be used as a target for therapy. Either a monoclonal
antibody or a chemical can be used against the target to
inhibit its effects. Mabthera/Rituximab is a monoclonal
antibody commonly used to treat all kinds of B cell
lymphomas, while Imatinib is a chemical drug which is
very effective in treating chronic myeloid leukaemia.
Bone Marrow Transplantation
Bone marrow transplantation is commonly used in
treating various types of blood cancers. It is often the
last hope for patients. There are two main types of
bone marrow transplantation, i.e. autologous transplant
using the patient’s own marrow cells, and allogeneic
transplant using marrow from HLA compatible donors,
who can be a sibling or an unrelated donor. The source
of the marrow cells or haematopoietic stem cells can
be the marrow itself of G-CSF-driven peripheral blood
stem cell or cord blood. A mini transplant can also be
used for elderly patients to minimize the risk.