Interview questions Flashcards

1
Q

Explain why you would want to do clinical oncology as a career?

A

Interest in oncology
- MRes
- Clinical attachements
- Work as registrar

Quickly evolving field with many new treatments coming through

Ability to help and impact patients and make meaningful treatments

Follow patients through their treatment and help support them

Team working

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2
Q

Please outline a difficult case you have had to manage

A

GRI case

50 year old admitted with worsening neuropathic right arm pain

Previous visit to ED which on retrospect showed lesion at apex of right lung - awaiting CT thorax

On Ct thorax reported Friday afternoon - showed probable lung malignancy with erosion into T4 body with probably MSCC

Discussions with neurosurgery and oncology

Discussions with husband and wife and breaking bad news

Starting treatment

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3
Q

Please give an example of an mistake you have made and your actions following this

A

During receiving shift on a medical assessment ward a woman was referred in with a history of abdominal pain with a family history of AAA rupture from the rheumatology clinic

I was handed over to chase the report of the CT scan which in the conclusion did not show any evidence of acute coronary syndrome. However in the body for eh report it was noted that the Aorta was enlarged at around 6cm

The following day, the report was amended by the radiology consultant regarding this and advised urgent referral to the vascular service

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4
Q

Please describe a weakness of yours

A

Over critical

Self-confidence

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5
Q

Please give an example showing how you are a team player

A

While working in radiation oncology in NZ, we had a patient undergoing curative chemoradiotherapy for a HNSCC.

In the centre we treated patients for across a wide geographic area, and so some patients stayed in temporary accommodation while completed longer courses of radiotherapy

This patient did not have much family support with her and struggled through treatment with a number of side effects to be expected. She unfortunately did miss a number of fractions because of this.

We would see her regularly to evaluate her symptoms, and worked closely with the nurse specialists, radiotherapy technicians, nurses on the ward, cultural liaison for Maori people in the hospital as well as involving her family with her consent

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6
Q

Please give an example where you showed team leadership

A

Undertaking a respiratory QIP in the inhaler management of COPD to ensure up titration of inhaler therapy to triple therapy inhalers for COPD patients admitted to hospital

Working with pharmacists and more junior staff

Delegating jobs

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7
Q

Please give an example where you showed empathy

A

While covering medical HDU, there were a number of seriously ill patients, often at the ceiling of their care

A 55 year old man, very comorbid with servere LVSD and COPD was admitted from home with necrotising fasciitis, felt that would not be a surgical candidate due to comorbidities and had been having IV antibiotic treatment

Unfortunately was worsening despite this. His wife was with him

Spoke to her of his deterioration with nursing staff present

Offered support and to call his extended family

Offered chaplain

Would check on her throughout the evening

Organised room in the hospital for her to have a bed

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8
Q

Please explain a situation where you had to consent a patient in a vulnerable situation

A

Schizophrenia patient with fungating tumour

Patient in NZ with history of schizophrenia attended with CPN

Not sought medical treatment earlier, had been encouraged by CPN, but had been mistrustful and did not wish to seek advice

At point of referral had a large fumigating breast tumour, for which he had been prescribed a palliative dose of radiotherapy

Explained process and involved CPN
Invited questions
Tried to build rapport

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9
Q

Tell us what you know of the training programme in clinical oncology

A

Enter into ST3 oncology common stem year
- Development of CiPs related to areas of overlap between medical and clinical oncology

Requiring to enrol with the Royal College of Radiologists

Clinical oncology specific ST4-7
- Clinical oncology specific CiPs

Four exams to obtain FRCR (oncology):
- FRCR Part 1 - Oncology - investigation and management of cancer patients, tumour biology, mechanism of cytotoxic drugs, statistics and physics - usually done in ST4
- FRCR Part 2A - radiotherapy and drug therapy - Usually done in ST5-6
- FRCR Part 2B - Usually done in ST5-6

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10
Q

Tell us of your teaching experience

A

During university:
- SSC with university - anatomy demonstrator for medical/Dental and biomedical students, and clinical skills

Teach the teacher course online

Teaching at hospital:
- ICI with case study of triple M syndrome

Teaching medical students in hospital and online e.g. Haematology and oncology SBAs for medical finals - universities throughout the UK

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11
Q

Tell us the qualities of a good teacher

A

Sets specific and challenging goals
Able to give good quality feedback
Encouraging
Enthusiasm and shows enjoyment in their topic
Adapts the teaching for the students
Involving

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12
Q

Please describe your experiences with QIP/audits

A

QIP in F2:
- Immunisation in <5 year olds

Audit in radiation oncology:
- Treatment with RAI in thyroid cancer - presented at national meeting

Audit of ophthalmology reviews with hydroxychloroquine in a rheumatology department

QIP in resp:
- COPD

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13
Q

Difference between audit and research

A

Audit - Process comparing clinical practice against set standards

Research - Aimed to create new knowledge that can be used to develop new standards of car

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14
Q

Please outline your research experience

A

MRes
Attendance at journal clubs

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15
Q

Please outline why research is important in oncology

A

Evolving medical field, with many new treatments and technologies becoming available

New treatments help with patient survival and outcomes

Example in the ICIs

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16
Q

Please outline your interest in research

A

Know that it is important

Outline reasons you wouldn’t necessarily be involved in research
- Prefer to be patient facing

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17
Q

What is research governance

A

A framework setting out principles of good practice in the management and conduct of health and social care research in the UK

Full guidelines set out in the Health Research Authority document

Principles include safety, competence of the staff undertaking the trial, scientific and ethical conduct, patient, service user and public involvement and integrity quality and transparency

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18
Q

What is evidence based medicine

A

The use of best evidence in making decisions about the care of individual patients, alongside your own clinical expertise and judgement

This is applied to a specific case, taking into account patient values

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19
Q

What are the different levels of evidence available

A

1a. Systematic review or meta-analysis of RCTs

1b. At least one RCT

IIa. At least one well-designed controlled study without randomisation

IIb. At least one well designed quasi-experimental study e.g. cohort study

III Well designed non experimental descriptive studies e.g. comparative studies, correlation studies, case-control studies and case series

IV. expert committee reports, opinions and/or clinical experience of respected authorities

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20
Q

Please outline types of clinical trials

A

Randomised controlled study:
- Two or more study groups followed up over time which differ in interventions. Usually introduction of new therapy in one group with standard of care in other
- Can be blinded with use of placebo and double-blinded in which clinicians do not know where patients have been allocated

Cohort study:
- Follows a group of people over a period of time
- e.g. identifying risk factors over time in a population in who develops cancer

Case-controlled study:
- Looks at people who have a disease and assess against a control group over risk factors developing the disease. Opposite of cohort study
- Quicker and cheaper than cohort studies but often less reliable

Cross-sectional study:
- Carried out at one point in time, or over a short period of time. They find out who has been exposed to a risk factor and who has developed cancer, and see if there is a link.

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21
Q

What is clinical governance

A

Quality assurance process, in which clinicians should be involved to maintain and improve the quality of care that patients receive and ensure that the NHS is accountable to the public

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22
Q

Outline the ethical principles

A

Beneficence - act in patient’s best interest

Non-maleficence - do no harm to patients

Justice

Autonomy

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23
Q

Outline the different stages of clinical trials

A

Pre-clincial trials:
- animal models/ex-vivo/in-vivo/AI assisted

Phase I;
- Tests small number of people with trial drug to ensure safety and identify side effects, and identify dose

Phase II:
- Given to medium size group to identify effectiveness an for safety profiles

Phase III:
- Large groups comparing to gold standard treatment to identify effectiveness

Phase IV:
- Following approval of medication, long term study of side effects

24
Q

How can you assess capacity

A

Understand

Weigh up risks

Retain

Communicate

25
Q

What are the seven pillars of clinical governance

A

Clinical effectiveness and research
- Evidence based approach
- adopting new guidelines

Audit

Risk management
- Complying with protocols e.g. hand washing
- Learning from mistakes M&M
- Reporting significant adverse events e.g. Datix

Education and training
- CPD
- Exams
- Appraisal

Patient and public involvement

Using information and IT

Staffing and staff management

CARE mnemonic for the top four
PIRATES for all

26
Q

Difference between competence and capacity

A

Competence is a legal judgement

Capacity is a medical judgement

27
Q

Five principles of the Medical Capacity Act

A
  1. Presumption of capacity
  2. Individuals should be supported to make their own decisions
  3. Patients have the right to make what may be deemed as ‘unwise decisions’
  4. Anything done for a patin lacking capacity should be done in their best interests
  5. The less restrictive option should also be used in a patient lacking capacity
28
Q

What is your biggest achievement

A

Presenting at the RANZCR conference in Queenstown NZ

29
Q

Tell me of a recent research article you have read

A

ARANOTE trial - Darolutamide in combination with androgen deprivation in patients with metastatic hormone sensitive prostate cancer

Phase III trial

Darolutamide plus ADT significantly improved rPFS, reducing risk of progression or death by 46% versus placebo

30
Q

What makes you a good team player?

A

Conscientious

Will catch up with team mates regularly

Diligent

31
Q

What makes you a good leader?

A

Able to delegate

Try to take account of team members strengths

Supportive

32
Q

Describe a situation where you showed professional integrity

A

Death certificate on ward 10

Came back from leave and death certificate had not been completed as had to be reported to the procurator fiscal

Cleared in the afternoon prior.

The morning in question family rang up multiple times asking for death certificate to be completed, had to deal with a number of sick patients

During phone call, patients family showing quite a lot of pent up emotion and dissatisfaction with patients care

Apologised for wait, explained wait, and directed towards PALS

Discussed with consultant and completed death certificate

33
Q

how do you handle stress

A

At the time I organise with list and try to prioritise and delegate where possible

Try to plan ahead such as exams or with deadlines

Support from friends

34
Q

What do you like least about this specialty

A

Can be emotionally difficult, following many patients for a long time, and unfortunately some will relapse

There are also some very unlucky patients e.g. 31 fire-fighter with lung cancer with two young children

35
Q

Please explain the clinical oncology curriculum

A

Number of generic and oncology Capabilities in Practise (CIPS)

Generic CIPS can be covered in OCS

Specific oncology in St4-7 years such as brachytherapy, radiotherapy planning, SACT

The scientific basis of cancer and its treatments

Acute oncology presentations

Tumour types - rotation through these in St4-7 years

Emerging technologies e.g. genomics and AI

36
Q

What have you done to demonstrate commitment to specialty

A

Placements throughout the years

Audits in RAI in Palmy

Year as work as a radiation oncology reg
- experience of the department and clinics

37
Q

Take me through your CV

A

Oncology experience:
- F2 experience
- SHO and registrar experience in radiation oncology in NZ - working on oncology wards and in outpatient settings, treatment reviews with radiotherapy patients, consenting to radiotherapy, radiotherapy planning

Academic achievements:
- Distinction in MRes in oncology - research project looking at radioresistance in medulloblastoma

Audits and QIPs:
- RAI audit in NZ, presented at national conference
- Immunisation QIP - two full PDSA cycles, led audit, worked with CSWs, clinical support staff, RNs, GPs, updated practice guidelines, presented locally
- Audit in retinopathy screening in rheumatology - presented locally

Achieved MRCP

Teaching:
- Teaching experience in Uni with SSC in anatomy
- Teaching session - grand round teaching on ICI and with medical students
- teaching the teacher course

38
Q

What have you done to prepare for clinical oncology

A

Oncology experience
- IP and OP
- Experience with oncology clinics - with consenting patients
- Talking to oncology MDT staff e.g. RTs and nursing staff
- Radiotherapy experience including planning

Discussing with local registrars and consultants
Attended local MDTs and clinics

Audits in thyroid cancer

Looking at the curriculum and exams needed

39
Q

What is involved in clinical oncology training

A

First year in OCS - same training with medical oncology ST3s

4 month rotations in first two years and then repeat in next 2 years

40
Q

Talk me through some part of your CV that you are proud of

A

RAI audit in PN

Audit for patients receiving radioactive iodine for thyroid cancer - comparing to standard set out in the ATA guidelines, identifying that patients have been correctly stratified, received correct dose for RAI, and have been correctly rest ratified following treatment with appropriate post treatment investigations

Identified opportunities to improve on post stratification of patients with investigations as laid out in the ATA guidelines

This was presented at a local multidisciplinary meetings as well as an oral presentation at a national conference in New Zealand to an audience of radiation oncology consultants, registrars and associated specialties

Associated skills:
- Teamwork - working with specialist nursing staff, ward staff, consultant and registrars
- Presentation skills
- Analytical skills

41
Q

A woman with history of breast cancer with recent chemotherapy calls from home through the cancer specialist nurses presenting generally unwell with a temperature

A

Ask for her to come to hospital unit or assessment unit for urgent bloods and assessment

Let staff know that she has had recent chemotherapy and at risk of neutropenia

A-E assessment

Bloods inc FBC and lactate
Blood cultures
CXR
Urine culture
Sputum culture
Flu swab

Start treatment for neutropenic sepsis while awaiting blood results

Escalation status
Alert parent team

Discuss and highlight to senior

42
Q

Patient in chemo unit receiving 5U infusion for a colon cancer has been alerted to you due to SOB, what would you do?

A

Assess in person, abs to check stable

Review notes, PMHx, oncological history, medications, allergies, is this first cycle?, recent oncology clinic letter

Assess A-E

Differentials:
- Allergic reaction
- Infection
- Chemo reaction - coronary vasospasm
- Anaemia
- Progression of disease

Bloods inc FBC and CRP, trop if concerns with chest pain
Blood cultures if pyrexic

Urgent treatment if anaphylaxis as per ALS
Chemo reaction - can slow rates/antihistamine

Alert parent team

43
Q

ON call first week - consent to radical treatment to prostate

A

Seek more information - clarify with nursing/RT staff

Find more information - recent clinic letters, or if staff from the parent team are still present

Discuss with patient and family, find understanding of situation, check not confused

As not able to consent patient to a treatment that I yet do not know, apologise to patient

Notify parent team

Try to arrange appropriate consenting

Postpone start to treatment prior to consenting

44
Q

What do you understand by informed consent

A

Consent given by a patient or proxy for a treatment, for which the intended outcomes, alternatives and potential side effects, especially common or serious side effects have been relayed to the patient

45
Q

Asked to speak to the family of an advanced met HNSCC patient, concerned that he is not getting nutrition and ask about alternative feeding such as PEG

A

Seek more information - read patient notes and recent clinic letters

Discuss with nursing staff and other staff that may know patient e.g. MDT

Check patient’s capacity e.g. check if AWI is in place

Check if ok to discuss with family with patient - whether they would like to discuss in private or together

Check understanding of situation and discuss what they know of alternative feeding methods and what benefits this may gain

Discuss whether this is appropriate - may cause patient harm or distress

If not moving forward - discuss with senior/treating consultant

46
Q

You have been asked to ask patient if they would wish to be consented for a clinical trial

A

Check patient meets the specified basic requirements for the trial

Check patents understanding fo the trial

Information on the trial - what this may involve e.g. treatment, follow up, investigations

If RCT - explain that patient may either receive the trial treatment or placebo, explain that they will also get standard of care so will have some cancer treatment. Clinicians may not know if the patient receives this treatment if double blinded

Explain this is absolutely up to the patient, and if patient does not wish to enter trial will still get cancer treatment. Explain that they can drop out of the trial at any time

Involve trial nurses and give trial patient information

47
Q

You are approached by a family of the patient in the corridor, they have asked you not to give bad news if there shows signs of progression on a recent CT

A

Question of autonomy

Explain to family in general terms that for any scan results if the patient wishes to know and has capacity then they have the right to know but ask if there were any specific reasons that they did not want the patient to know e.g. low mood

Read patient notes and overview of history and acquaint myself with scan results

Have patient in consultation, and ask whether they would prefer for this to be by themselves or with family present

Go over understanding of treatment so far

Ask whether patient would like to know results of scans - warning shot if wishes to know and negative results

Ideally have specialist nurse present - identify how patient feels and discuss next options in treatment

48
Q

Call from 17.30 with signs of cord compression

A

Gain patient information, read notes scans

Contact patient and arrange urgent assessment

Identify if having any pain

Discuss with neurosurgery if surgical route an option - particularly if new diagnosis, no prior biopsy sample, good PS

If any signs of instability ensure log rolling patient

Start high dose steroids and PPI

QDS BMs

May need titration of diabetic meds if has underlying DM

Discuss with on call consultant re urgent radiotherapy

Alert parent team - may need discussion on current treatments and discuss next line treatments

49
Q

You are called to review a patient that has arrived at chemotherapy treatment and is very confused

A

Get information from nurses

Information on patient - clinic notes, previous admissions, GP summary and recent medications

History and A-E assessment:
- May need collateral
- Assess for baseline
- PMHx
- Meds and allergies
- Recent oncological history

Bloods:
- Na, Ca, CRP, FBC
- Urine dip
- Blood cultures if spiking

Explain will need to delay chemotherapy as cannot give consent and may be unwell

Dx:
- Hyponatraemia
- Hypercalcaemia
- Drugs e.g. opioids
- Delirium
- Infection
- Disease progression e.g. brain mets

50
Q

Tell me about the curriculum and exams

A

New curriculum implemented in 2021, updated 2023

ST4-5 will do 4 month rotations in a number of different tumour types, will then repeat these in ST6-7

Within the Royal College of Radiologists

Competency based

Generic CiPs - develop in OCS in ST3 year

Then further 4 years of training with ST4-7 years - will focus on development of clinical oncology specific CiPs

3 exams:
- Part one, needed to progress to St5 level - usually sat in St4
- - Comprised of 4 parts, clinical pharmacology, cancer biology and radiobiology, medical statistics and physics

  • Part 2A and B - written paper and practical exams respectively
    • Usually sat in St5-6 year
51
Q

What is needed for curriculum

A

Number of different methods to show competency

CBD, Mini-CEx, DORPS, ACAT, MCR, MSF, Teaching observation

2x QIPATs expected to be done within ST4-7

52
Q

Tell me about developments in clinical oncology

A

Exciting research driven specialty
- Many new treatment in oncology
- Immunotherapy
- Mutation based treatment e.g. TKI

Arc based models - complex 3D treatment +/- nodes with various doses of radiotherapy

VMAT (volume modulated arc therapy) and IMRT

SABR - Gamma knife

Proton beam radiotherapy

53
Q

Can you tell me of any trials that have made a difference in the treatment of clinical oncology patients

A

FAST-Forward trial

Published in the Lancet

Showed non-inferiority with hypo-fractionation in adjuvant radiotherapy for breast cancer with 26Gy in 5# vs 40Gy in 15# in early breast cancer with similar side effect profile

Benefit for patients - not needing extensive longer treatments, which they may have to traveller or spend time away from family

Reduced time for machines and so allows increased slots for other patients

54
Q

Underperforming colleague

55
Q

Chemo prescribing error

56
Q

Patient with brain mets that are still driving