Preparation for candidates sitting:
SCFHS•DHA•DOH•QCHP•KMOH•NHRA
Oncology Question Bank
800 questions•8 mock exams•6 months
Practice with exam-style questions, detailed rationales, timed mock exams, and tracking that shows your weak topics.
- Mapped to the blueprint — Every question sits under an official outline heading — not a scraped MCQ dump.
- A rationale on every answer — Why the key is right, and why each distractor was written to tempt you.
- Timed mock exams — Same clock, same length, same question style as the real sitting.
- One bank, several authorities — Valid preparation for the regulators listed on this page.
3,578 practitioners have studied with this bank
Written as preparation for
Sample questions
Same stem length, same distractor style, same rationale you get inside the bank.
Free — no payment, no account
Read the Oncology Question Bank sample questions
1.According to the NIH 2014 consensus criteria, which clinical finding is sufficient on its own to establish a diagnosis of chronic graft-versus-host disease?
- A.Maculopapular erythematous rash
- B.Raised serum bilirubin
- C.Diarrhoea with anorexia and weight loss
- D.Lichen planus–like changes of the oral mucosaCorrect
Why: The NIH 2014 criteria distinguish 'diagnostic' signs, which are sufficient to establish chronic GVHD, from 'distinctive' signs, which require biopsy or other confirmation. Diagnostic features include poikiloderma, lichen planus–like, sclerotic, morphea-like or lichen sclerosus–like skin changes; lichen planus–like oral changes; genital lichen planus–like or vaginal scarring; oesophageal web or stricture; bronchiolitis obliterans diagnosed by lung biopsy; and fasciitis or joint contractures. Maculopapular rash, diarrhoea, anorexia and hyperbilirubinaemia are common to acute and chronic GVHD and cannot establish chronic GVHD alone. The diagnosis is based on clinical features, not on the time since transplantation. Pearl: xerostomia, nail dystrophy and keratoconjunctivitis sicca are distinctive but not diagnostic features.
2.An 81-year-old man has a 6 cm ulcerated basal cell carcinoma at the medial canthus invading the orbit. Curative surgery would require orbital exenteration, which he declines, and the multidisciplinary team considers radiotherapy inappropriate. There are no distant metastases. What is the most appropriate systemic treatment?
- A.Cemiplimab
- B.Imatinib
- C.Carboplatin plus paclitaxel
- D.VismodegibCorrect
Why: More than 90% of BCCs have activated hedgehog signalling, usually through PTCH1 loss or SMO mutation. Hedgehog pathway inhibitors (vismodegib or sonidegib) inhibit Smoothened and are first-line systemic therapy for locally advanced BCC not amenable to surgery or radiotherapy; in ERIVANCE, vismodegib achieved an objective response rate of about 43–60% in locally advanced disease. Cemiplimab is approved for patients who progress on or are intolerant of hedgehog inhibitors. Platinum-taxane chemotherapy has limited evidence and more toxicity. Imatinib has no established role. Pearl: common hedgehog inhibitor adverse effects are muscle spasms, dysgeusia, alopecia and weight loss; the drugs are teratogenic.
3.A 63-year-old woman with multiple myeloma has received monthly IV zoledronic acid for 3 years. Ten weeks after a lower molar extraction she has pain and an area of exposed, necrotic bone in the mandible at the extraction site that has not healed. She has never received head and neck radiotherapy. What is the most likely diagnosis?
- A.Osteoradionecrosis of the mandible
- B.Medication-related jaw osteonecrosisCorrect
- C.Plasmacytoma involving the mandible
- D.Alveolar osteitis (dry socket)
Why: The AAOMS 2022 definition of medication-related osteonecrosis of the jaw (MRONJ) requires current or previous treatment with an antiresorptive (bisphosphonate or denosumab) or antiangiogenic agent, exposed bone or bone probeable through a fistula in the maxillofacial region persisting for more than 8 weeks, and no history of jaw radiotherapy or obvious metastatic disease of the jaw. High-dose, prolonged IV bisphosphonate therapy and dental extraction are the main risk factors. Osteoradionecrosis requires prior radiotherapy. Dry socket occurs within days of extraction and resolves within weeks. Plasmacytoma presents as a lytic mass rather than exposed necrotic bone. Pearl: management is conservative (antiseptic rinses, antibiotics, limited debridement), and dental work should ideally be completed before antiresorptive therapy.
4.A 58-year-old woman with bulky chronic lymphocytic leukaemia on day 2 of chemoimmunotherapy develops palpitations. Potassium is 7.1 mmol/L, and the ECG shows peaked T waves and widening of the QRS complex. What is the most appropriate immediate treatment?
- A.IV calcium gluconateCorrect
- B.Urgent haemodialysis
- C.Oral sodium polystyrene sulfonate
- D.IV furosemide
Why: Hyperkalaemia with ECG changes is a medical emergency. IV calcium gluconate (e.g., 10 mL of 10% solution over several minutes) stabilises the cardiac membrane within minutes, although it does not lower serum potassium. It should be followed immediately by measures that shift potassium intracellularly (IV insulin with glucose, nebulised salbutamol) and then remove it. Oral sodium polystyrene sulfonate acts over hours and is unsuitable as immediate therapy. Furosemide is slow and ineffective with oliguric TLS-related kidney injury. Haemodialysis may be required for refractory hyperkalaemia in TLS but cannot be arranged quickly enough to be the first measure. Pearl: in TLS, repeat potassium every 4–6 hours.
5.A 79-year-old immunocompetent man has a recurrent 8 cm cutaneous squamous cell carcinoma of the scalp with skull invasion. He has previously had surgery and radiotherapy to the area, and the tumour board deems further surgery or radiotherapy not feasible with curative intent. He has ECOG 1 and no autoimmune disease. What is the most appropriate systemic treatment?
- A.Vismodegib
- B.CemiplimabCorrect
- C.Cetuximab
- D.Dabrafenib plus trametinib
Why: Cutaneous SCC has one of the highest tumour mutational burdens, driven by UV damage, and is highly responsive to PD-1 blockade. Cemiplimab produced objective responses in about 45–50% of locally advanced or metastatic cSCC not amenable to curative surgery or radiotherapy, with durable responses, and pembrolizumab is also approved; NCCN lists anti-PD-1 therapy as preferred first-line systemic treatment. Cetuximab has lower, shorter responses and is reserved for patients unsuitable for immunotherapy. Vismodegib targets the hedgehog pathway in BCC. BRAF/MEK inhibitors have no role in cSCC. Pearl: in solid-organ transplant recipients, PD-1 inhibitors carry a high risk of allograft rejection.
6.A 58-year-old man with metastatic colorectal cancer receiving FOLFOX reports that during his last 2-hour oxaliplatin infusion he developed jaw tightness, a sensation of difficulty swallowing and breathing, and tingling fingers, worsened by drinking cold water. During the episode SpO₂ was 98%, with no stridor, wheeze, rash or hypotension, and symptoms resolved within hours. What is the most appropriate modification for the next cycle?
- A.Administer oxaliplatin by a 12-step desensitisation protocol
- B.Give calcium and magnesium infusions before and after oxaliplatin
- C.Extend the oxaliplatin infusion from 2 to 6 hoursCorrect
- D.Permanently discontinue oxaliplatin as an anaphylactic reaction
Why: This is acute oxaliplatin neurotoxicity with pharyngolaryngeal dysaesthesia: transient, cold-triggered paraesthesias and a subjective feeling of throat tightness without objective airway compromise, affecting most patients to some degree. It reflects oxalate-related prolongation of voltage-gated sodium channel opening in peripheral nerves. Management is reassurance, avoiding cold exposure, and prolonging the infusion to 6 hours, which lowers peak concentration and reduces recurrence. Normal saturation and the absence of stridor, rash or hypotension distinguish it from hypersensitivity, so discontinuation or desensitisation is not warranted. Calcium–magnesium infusions failed to reduce oxaliplatin neurotoxicity in the phase III N08CB trial and are not recommended by ASCO. Pearl: this acute syndrome is distinct from cumulative sensory neuropathy.
7.Which measure is recommended by MASCC/ISOO guidelines to prevent oral mucositis in patients receiving bolus 5-fluorouracil chemotherapy?
- A.Sucralfate mouthwash four times daily
- B.Palifermin injection before each chemotherapy cycle
- C.Oral cryotherapy with ice chips for 30 minutesCorrect
- D.Chlorhexidine mouthwash four times daily
Why: Oral cryotherapy (holding ice chips in the mouth starting shortly before and continuing for about 30 minutes during bolus 5-FU administration) causes local vasoconstriction, reducing delivery of the short half-life drug to the oral mucosa. MASCC/ISOO 2020 guidelines recommend it for bolus 5-FU and for high-dose melphalan conditioning. The guidelines recommend against chlorhexidine and sucralfate mouthwashes for mucositis prevention because of lack of efficacy. Palifermin, a keratinocyte growth factor, is recommended for patients with haematological malignancies receiving high-dose chemotherapy and total body irradiation before autologous stem cell transplantation, not for standard 5-FU regimens. Pearl: avoid cryotherapy with oxaliplatin because it triggers cold-induced dysaesthesia.
8.A 24-year-old man presents with cough and chest pain. CT shows a 9-cm anterior mediastinal mass and enlarged retroperitoneal lymph nodes. Serum beta-hCG is 2,500 IU/L and AFP is 350 ng/mL. Testicular ultrasound is normal. Biopsy shows poorly differentiated carcinoma, and FISH demonstrates isochromosome 12p. What is the most appropriate treatment?
- A.Carboplatin-paclitaxel as for unfavourable carcinoma of unknown primary
- B.Primary surgical resection of the mediastinal mass
- C.Cisplatin-based germ cell tumor chemotherapyCorrect
- D.Definitive radiotherapy to the mediastinum
Why: A young man with midline (mediastinal and retroperitoneal) disease, markedly raised AFP and hCG, and isochromosome 12p, the genetic hallmark of germ cell tumors, has an extragonadal nonseminomatous germ cell tumor, a favourable subset of carcinoma of unknown primary that is potentially curable. Primary mediastinal nonseminomatous germ cell tumors are classified as poor risk by IGCCCG and are treated with four cycles of cisplatin-based chemotherapy (BEP or VIP; VIP is often preferred to avoid bleomycin lung toxicity before thoracic surgery), followed by resection of residual masses. Empirical carboplatin-paclitaxel is inferior for this chemosensitive tumor. Radiotherapy is not curative for nonseminomatous disease, and upfront surgery is inappropriate with elevated markers and metastatic spread. Pearl: mediastinal NSGCT is associated with Klinefelter syndrome and hematological malignancies.
9.According to WHO CNS5 (2021), which molecular combination defines oligodendroglioma?
- A.IDH mutation with 1p/19q codeletionCorrect
- B.IDH wildtype with EGFR amplification
- C.H3 K27M mutation with ATRX loss
- D.IDH mutation with ATRX loss and TP53 mutation
Why: Oligodendroglioma is defined by the combination of an IDH1 or IDH2 mutation and whole-arm codeletion of chromosomes 1p and 19q; these tumours also typically have TERT promoter mutations and retain nuclear ATRX. They are graded as CNS WHO grade 2 or 3 and carry the most favourable prognosis among diffuse gliomas, with high chemosensitivity. IDH mutation with ATRX loss and TP53 mutation characterises astrocytoma, IDH-mutant. IDH-wildtype tumours with EGFR amplification are glioblastoma in adults. H3 K27M mutation defines diffuse midline glioma, H3 K27-altered. Pearl: ATRX loss and 1p/19q codeletion are mutually exclusive, so ATRX loss makes oligodendroglioma unlikely.
10.A 55-year-old woman who has never smoked undergoes CT of the chest after a road traffic accident. There is an incidental solitary 4-mm smooth solid nodule in the right lower lobe. She has no history of malignancy or immunosuppression. According to the Fleischner Society 2017 guidelines, what is the most appropriate management of the nodule?
- A.Repeat chest CT in 3 months
- B.FDG PET-CT
- C.No routine follow-up imagingCorrect
- D.CT-guided percutaneous biopsy
Why: For an incidental single solid nodule smaller than 6 mm in a low-risk patient, the Fleischner Society 2017 guidelines recommend no routine follow-up, because the malignancy risk is below 1%. In high-risk patients an optional CT at 12 months may be considered. PET-CT is unreliable below about 8 mm owing to limited spatial resolution, and biopsy of a 4-mm nodule is neither feasible nor justified. Short-interval CT at 3 months is reserved for larger (>8 mm) nodules. Pearl: Fleischner guidelines do not apply to lung cancer screening (use Lung-RADS), patients younger than 35 years, or patients with known cancer or immunosuppression.
Why candidates choose this bank
Written like the exam
Single-best-answer items in the exam's own phrasing and length — clinical vignette first, then the lead-in question.
Rationales, not answer keys
Each explanation says why the key is correct and why the other options were built to look correct.
Full-length timed papers
Complete papers under the real clock, scored by topic so you can see where the marks leaked.
Weak-topic tracking
Your dashboard ranks topics by accuracy and pushes the weakest ones back into your next session.
Updated with the blueprint
When the authority revises the outline, the bank is revised. Updates are free for your whole term.
Built for gaps in the day
Works on phone, tablet and desktop; progress syncs, so ten minutes between patients still counts.
About this bank
What the Oncology Question Bank covers
Built for physicians preparing for the Oncology licensing exam with the Saudi Commission for Health Specialties (SCFHS), the Dubai Health Authority (DHA), the Department of Health Abu Dhabi (DOH, formerly HAAD) or the Qatar Council for Healthcare Practitioners (QCHP).
What the bank covers
The questions follow the areas an oncology licensing exam draws on:
- Tumour biology, screening, diagnosis and staging
- Principles of systemic therapy and its toxicities
- Principles of radiotherapy
- Oncological emergencies
- Common solid tumours and haematological malignancies
- Supportive, palliative and end-of-life care
How you practise
Every question is multiple choice in the style of the exam, and every answer comes with an explanation of why it is right — so a wrong answer teaches you something instead of just costing a mark. Questions are grouped into quizzes you can work through in order, and each one runs on your phone, tablet or laptop.
Access
Your access runs for six months from the day you buy, long enough to work through the whole bank and revise it again before exam day.
Available exams
8 timed mock exams
60 minutes each • 70% target score
| Mock | Questions | Time | Action |
|---|---|---|---|
| Quiz 1Free sample — 10 questions | 100 | 60 min | See sample questions |
| Quiz 2 | 100 | 60 min | Included with full access |
| Quiz 3 | 100 | 60 min | Included with full access |
| Quiz 4 | 100 | 60 min | Included with full access |
| Quiz 5 | 100 | 60 min | Included with full access |
| Quiz 6 | 100 | 60 min | Included with full access |
Your 4-step preparation plan
Subscribe
One payment, account live in under a minute.
Sit a baseline mock
A timed paper on day one. You need a real score before you build a plan.
Drill your weak topics
Work the lowest-scoring topics until they move.
Rehearse the real thing
A full timed mock in the final week, so exam-day pressure is already familiar.
Frequently asked questions
Related banks
Your exam date is already set. Your preparation should be too.
Start on the free questions above, or take the full bank today.
