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Haematology & Oncology Prometric exam questions with answers

15 original practice questions written to the Haematology & Oncology exam blueprint, each with the answer and why the other options are wrong. Below them: the Haematology & Oncology exam's format, pass mark and fee at DHA, DOH, SCFHS, QCHP and every other GCC regulator, from their own published rules.

15
Free questions
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GCC regulators
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Regulators covered
12
Questions in the free mock

Quick answer

The Haematology & Oncology exam is 150 MCQs in 3 hours at QCHP (pass mark 65%). Below are 15 original practice questions written to the official blueprint, each with the answer and why the other options are wrong, plus a free 12-question timed mock.

The Haematology & Oncology exam in every GCC country

QCHP publish an exact Haematology & Oncology exam; the others apply one format to every title. Figures come from each regulator's own exam pages - anything not published says so.

Haematology & Oncology licensing exam in every GCC country
RegulatorExamFormatPass markFee per attemptPractise
DHA
Dubai
DHA licensing exam
Regulator-wide format
150 MCQs, 3 hrs50-70%Not publishedDHA questions →
DOH
Abu Dhabi, Al Ain and Al Dhafra
DOH licensing exam
Regulator-wide format
Written + oral/OSCEPass / fail onlyNot publishedDOH questions →
MOHAP
Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah
MOHAP licensing exam
Regulator-wide format
Computer-basedNot publishedNot publishedMOHAP questions →
SHA
Emirate of Sharjah
SHA licensing exam
Regulator-wide format
Set at assessmentNot publishedNot publishedSHA questions →
SCFHS
Kingdom of Saudi Arabia
SCFHS licensing exam
Regulator-wide format
200 MCQs, 240 min500-560 of 800Not publishedSCFHS questions →
QCHP
State of Qatar
Specialist Haematology and Oncology150 MCQs in 3 hours65%Not publishedQCHP questions →
NHRA
Kingdom of Bahrain
NHRA licensing exam
Regulator-wide format
Prometric CBTNot publishedNot publishedNHRA questions →
OMSB
Sultanate of Oman
OMSB licensing exam
Regulator-wide format
Computer-based OC examNot publishedNot publishedOMSB questions →
Kuwait MOH
State of Kuwait
Kuwait MOH licensing exam
Regulator-wide format
150 MCQs, 170 min60-70%Not publishedKuwait MOH questions →

exact exam published for Haematology & Oncology

Pass marks, attempts and fees change - confirm yours on the regulator's exam page before you book.

15 Haematology & Oncology exam questions with answers

Choose your answer first, then open the explanation. The set covers the main blueprint domains at a mix of easy, medium and hard.

  1. Question 1Haemoglobinopathies and Transfusion Medicinemedium

    A young adult with sickle cell disease admitted with a painful crisis develops fever, chest pain, falling oxygen saturation of 89% on air and a new infiltrate on chest radiograph. Besides oxygen and antibiotics, what is the key treatment?

    1. AHigh-dose opioids alone
    2. BBlood transfusion, simple or exchange
    3. CIntravenous furosemide
    4. DStart hydroxyurea immediately
    Show answer and explanation

    Answer: B. Blood transfusion, simple or exchange

    This is acute chest syndrome, a leading cause of death in sickle cell disease. Hypoxia or deterioration is an indication for transfusion, with exchange transfusion for severe disease, alongside oxygen, antibiotics covering atypical organisms, analgesia and incentive spirometry. Hydroxyurea prevents future episodes but does not treat the acute event.

  2. Question 2Haemoglobinopathies and Transfusion Medicinehard

    Which patient most clearly needs irradiated cellular blood components to prevent transfusion-associated graft-versus-host disease?

    1. AA patient with Hodgkin lymphoma
    2. BA patient with iron deficiency anaemia
    3. CA patient with sickle cell trait
    4. DA patient receiving warfarin
    Show answer and explanation

    Answer: A. A patient with Hodgkin lymphoma

    Patients with Hodgkin lymphoma at any stage need irradiated components, as do those treated with purine analogues such as fludarabine and recipients of stem cell transplants. Irradiation inactivates donor lymphocytes that could cause fatal graft-versus-host disease. Iron deficiency, sickle trait and warfarin are not indications.

  3. Question 3Lymphoid Malignancies and Plasma Cell Disordersmedium

    A 68-year-old has a lymphocyte count of 25 x 10^9/L with smudge cells. Flow cytometry shows CD5 and CD23 positive B cells. He has no symptoms, cytopenias or bulky nodes. What is the most appropriate management?

    1. AStart a BTK inhibitor now
    2. BStart chemoimmunotherapy now
    3. CRefer for allogeneic transplant
    4. DActive monitoring without treatment
    Show answer and explanation

    Answer: D. Active monitoring without treatment

    Early-stage asymptomatic chronic lymphocytic leukaemia is managed by watch and wait, as early treatment has not improved survival. Treatment is indicated for active disease such as progressive marrow failure, symptomatic nodes or spleen, constitutional symptoms or rapid lymphocyte doubling. Transplant is reserved for selected high-risk relapsed disease.

  4. Question 4Myeloid Malignanciesmedium

    A 40-year-old has bleeding gums, a low fibrinogen, raised D-dimer and abnormal promyelocytes with multiple Auer rods on the blood film. What is the most important immediate step?

    1. AWait for genetic confirmation before any treatment
    2. BStart all-trans retinoic acid at once
    3. CGive heparin to treat the coagulopathy
    4. DPerform an urgent splenectomy
    Show answer and explanation

    Answer: B. Start all-trans retinoic acid at once

    Suspected acute promyelocytic leukaemia is an emergency because of life-threatening coagulopathy. All-trans retinoic acid should start as soon as the diagnosis is suspected, without waiting for PML-RARA confirmation, together with aggressive blood product support. Early deaths are mainly from haemorrhage.

  5. Question 5Red Cell Disorders and Anaemiaseasy

    A 34-year-old woman with heavy periods has haemoglobin 92 g/L, MCV 71 fL and a normal CRP. Which single test best confirms iron deficiency?

    1. ASerum ferritin
    2. BSerum iron
    3. CHaemoglobin electrophoresis
    4. DReticulocyte count
    Show answer and explanation

    Answer: A. Serum ferritin

    A low serum ferritin is the most specific test for iron deficiency, especially when inflammation is absent. Serum iron fluctuates widely and is unreliable alone. Haemoglobin electrophoresis is used for suspected thalassaemia when ferritin is normal.

  6. Question 6Myeloid Malignanciesmedium

    On day 8 of all-trans retinoic acid for acute promyelocytic leukaemia, a patient develops fever, weight gain, breathlessness and pulmonary infiltrates. What is the most appropriate treatment?

    1. ADexamethasone 10 mg twice daily
    2. BBroad-spectrum antibiotics only
    3. CDouble the dose of retinoic acid
    4. DIntravenous furosemide only
    Show answer and explanation

    Answer: A. Dexamethasone 10 mg twice daily

    These features suggest differentiation syndrome, which is treated promptly with dexamethasone 10 mg twice daily, with temporary interruption of the differentiating agent if severe. Antibiotics may be given if infection is possible but do not treat the syndrome. Increasing retinoic acid would worsen it.

  7. Question 7Solid Tumour Oncologyhard

    A man has orchidectomy for a testicular mass, and histology reports pure seminoma. His serum AFP is clearly raised. How should this be interpreted?

    1. AIt is typical of pure seminoma
    2. BIt suggests a hepatoma unrelated to the testis
    3. CIt indicates non-seminomatous elements
    4. DIt is a laboratory error to be ignored
    Show answer and explanation

    Answer: C. It indicates non-seminomatous elements

    Pure seminoma does not produce AFP, so a raised AFP indicates non-seminomatous elements such as yolk sac tumour, and the patient should be managed as non-seminomatous germ cell tumour. Beta-hCG can be mildly raised in seminoma. Other causes of raised AFP should be excluded, but the result should not be ignored.

  8. Question 8Systemic Anticancer Therapy and Supportive Careeasy

    Ten days after chemotherapy, a patient has a temperature of 38.5 degrees Celsius and a neutrophil count of 0.3 x 10^9/L. He is haemodynamically stable. What is the most important immediate action?

    1. AWait for blood culture results before treating
    2. BGive oral paracetamol and review in 4 hours
    3. CStart empirical IV broad-spectrum antibiotics within 1 hour
    4. DGive granulocyte colony-stimulating factor only
    Show answer and explanation

    Answer: C. Start empirical IV broad-spectrum antibiotics within 1 hour

    Neutropenic sepsis is a medical emergency, and empirical intravenous broad-spectrum antibiotics such as piperacillin-tazobactam should be given within 1 hour of presentation after cultures are taken. Delay increases mortality. G-CSF is not a substitute for antibiotics.

Halfway - how are you scoring?

Test yourself under real exam conditions

The free 12-question mock is timed and scored against the pass mark, domain by domain, so you see exactly where you are losing marks. The full Haematology & Oncology bank has 3 full-length papers (about 450 questions) for AED 289, one-time.

  1. Question 9Red Cell Disorders and Anaemiasmedium

    A 70-year-old has macrocytic anaemia, numb feet and impaired vibration sense. Both serum B12 and folate are low. What is the correct order of replacement?

    1. AFolic acid first, then B12 after 2 weeks
    2. BFolic acid alone, as neuropathy is unrelated
    3. CStart B12 before or with folic acid
    4. DOral iron first, then both vitamins
    Show answer and explanation

    Answer: C. Start B12 before or with folic acid

    When both are deficient, B12 should be started before or together with folic acid, because folate alone can correct the anaemia while allowing neurological damage such as subacute combined degeneration to progress. Neurological signs indicate the need for intensive intramuscular B12. Iron is not indicated without iron deficiency.

  2. Question 10Red Cell Disorders and Anaemiasmedium

    A patient with active rheumatoid arthritis has normocytic anaemia, ferritin 450 micrograms/L, low transferrin saturation and raised CRP. What mechanism mainly explains the anaemia?

    1. ARaised hepcidin restricting iron release
    2. BAutoimmune destruction of red cells
    3. CLoss of iron from the gut
    4. DDeficient erythropoietin from kidney failure
    Show answer and explanation

    Answer: A. Raised hepcidin restricting iron release

    In anaemia of inflammation, cytokines such as IL-6 increase hepcidin, which blocks iron release from macrophages and gut absorption, giving low transferrin saturation with normal or high ferritin. Gut iron loss would give a low ferritin. Haemolysis would raise reticulocytes and bilirubin.

  3. Question 11Solid Tumour Oncologymedium

    A non-smoker has metastatic lung adenocarcinoma with an EGFR exon 19 deletion. What is the preferred first-line systemic treatment?

    1. APlatinum doublet chemotherapy
    2. BPembrolizumab monotherapy
    3. COsimertinib
    4. DCrizotinib
    Show answer and explanation

    Answer: C. Osimertinib

    Osimertinib, a third-generation EGFR tyrosine kinase inhibitor, improved survival over earlier EGFR inhibitors in first-line treatment of EGFR-mutant NSCLC. Immunotherapy alone is less effective in EGFR-mutant disease. Crizotinib targets ALK and ROS1 rearrangements.

  4. Question 12Solid Tumour Oncologymedium

    A postmenopausal woman with ER-positive early breast cancer is starting adjuvant letrozole. Which baseline assessment is most important?

    1. ABone mineral density scan
    2. BRetinal examination
    3. CAudiometry
    4. DPulmonary function tests
    Show answer and explanation

    Answer: A. Bone mineral density scan

    Aromatase inhibitors lower oestrogen further and accelerate bone loss, so baseline bone density assessment, calcium and vitamin D, and bisphosphonates where indicated are recommended. Tamoxifen has different risks, including thromboembolism and endometrial cancer. Audiometry relates to platinum drugs.

  5. Question 13Stem Cell Transplantation and Professional Practicemedium

    Three weeks after allogeneic stem cell transplant, a patient develops a rash on the palms and soles, diarrhoea and raised bilirubin. Which condition do these three organ systems most suggest?

    1. AAcute graft-versus-host disease
    2. BEngraftment failure
    3. CCytomegalovirus retinitis
    4. DVeno-occlusive disease alone
    Show answer and explanation

    Answer: A. Acute graft-versus-host disease

    Acute graft-versus-host disease classically affects the skin, gastrointestinal tract and liver, with rash often starting on the palms and soles. Veno-occlusive disease causes jaundice, painful hepatomegaly and fluid retention but not the rash and diarrhoea. Biopsy and exclusion of infection support the diagnosis before systemic steroids.

  6. Question 14Systemic Anticancer Therapy and Supportive Caremedium

    Which chemotherapy drug is best known for cumulative dose-related cardiomyopathy, so that lifetime dose must be recorded?

    1. AVincristine
    2. BDoxorubicin
    3. CCisplatin
    4. DMethotrexate
    Show answer and explanation

    Answer: B. Doxorubicin

    Anthracyclines such as doxorubicin cause cardiomyopathy whose risk rises with cumulative dose, so lifetime exposure is tracked and cardiac function monitored. Vincristine causes neuropathy and cisplatin nephrotoxicity and ototoxicity. Methotrexate toxicity includes mucositis and myelosuppression.

  7. Question 15Systemic Anticancer Therapy and Supportive Caremedium

    A patient is to receive high-dose cisplatin. Which antiemetic combination is recommended as prophylaxis for this highly emetogenic regimen?

    1. AMetoclopramide and domperidone as needed
    2. BOndansetron and dexamethasone only
    3. CDexamethasone and lorazepam only
    4. DNK1 and 5-HT3 antagonists, dexamethasone, olanzapine
    Show answer and explanation

    Answer: D. NK1 and 5-HT3 antagonists, dexamethasone, olanzapine

    For highly emetogenic chemotherapy such as cisplatin, guidelines recommend a four-drug regimen combining an NK1 receptor antagonist, a 5-HT3 antagonist, dexamethasone and olanzapine. Single agents give poor control of acute and delayed vomiting. Uncontrolled vomiting can cause dehydration and worsen cisplatin nephrotoxicity.

What the Haematology & Oncology exam covers

The blueprint groups questions into these domains. Weight your revision the same way - the heavier domains carry more of your score.

Red Cell Disorders and Anaemias

~14%

Iron deficiency and anaemia of inflammation · Vitamin B12 and folate deficiency · Autoimmune haemolytic anaemia

Haemoglobinopathies and Transfusion Medicine

~12%

Sickle cell disease · Thalassaemia trait and major · ABO incompatibility and acute haemolytic reactions

Haemostasis and Thrombosis

~14%

Interpretation of PT, APTT and mixing studies · Haemophilia A and B · Von Willebrand disease

Myeloid Malignancies

~10%

Acute myeloid leukaemia · Acute promyelocytic leukaemia and differentiation syndrome · Chronic myeloid leukaemia and TKI monitoring

Lymphoid Malignancies and Plasma Cell Disorders

~12%

Hodgkin lymphoma · Diffuse large B-cell lymphoma and anti-CD20 therapy · Burkitt and other high-grade lymphomas

Solid Tumour Oncology

~16%

Breast cancer · HER2-targeted therapy and cardiac monitoring · Colorectal cancer

Systemic Anticancer Therapy and Supportive Care

~10%

Neutropenic sepsis management · Chemotherapy toxicities · Antiemetic prophylaxis by emetic risk

Oncological Emergencies

~7%

Metastatic spinal cord compression · Tumour lysis syndrome · Hypercalcaemia of malignancy

Stem Cell Transplantation and Professional Practice

~5%

Indications for autologous and allogeneic transplant · Graft-versus-host disease · Infection prophylaxis after transplant

How to answer these questions

1

Read the last line of the stem first, then the vignette: you will know whether it asks for a diagnosis, the next investigation or the next step in management.

2

"Most appropriate next step" means the next thing you would actually do, in order - stabilise, then confirm, then treat.

3

Specialist papers lean on current international guidelines; when an option sounds outdated, it usually is.

4

Aim to score comfortably above your regulator's pass mark - 10 to 15 points of margin - on timed, full-length practice before you book.

Haematology & Oncology exam questions: FAQs

How many questions are in the Haematology & Oncology Prometric exam?
It depends on the regulator: QCHP 150 MCQs in 3 hours. The full table above lists every GCC regulator.
What is the pass mark for the Haematology & Oncology exam?
QCHP: 65%. Pass marks are set exam by exam, so use your own regulator's figure.
Are these real exam questions?
No. Regulators do not release their papers, and anything sold as a leaked paper is unofficial and risky to rely on. These are original questions written to the official exam blueprint, at the level and in the style of the real exam, each with a worked explanation.
Is the Haematology & Oncology exam the same in every GCC country?
The clinical content is broadly similar because the exams test the same safe practice, but the format, length, pass mark, attempts and fees differ by regulator. Prepare on the content once, then check your regulator's exact rules before you book.
How should I use these questions?
Answer each one before opening the explanation, and note why each wrong option is wrong. Then take the free 12-question timed mock to see your score against the pass mark, and move to full-length papers when you score comfortably above it.

Last reviewed September 2026. Questions are original and written to the published exam blueprint; they are not taken from any real paper.

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