Oncology III Flashcards
What the patient tells us
- About themselves
- About there mental state
- Co-morbidities
- Medication
- Support
Toxicity the questions we should be asking
- Duration vs Severity
- Single vs Multiple
- Visible vs Invisible
- Preventable vs Manageable
Signs and symptoms of anaphylaxis

Anaphylactic reaction pathway
- ABCDE (Airway Breathing Circulation Disability Exposure) =>
- Diagnosis: Acute onset of illness, life-threatening airway/breathing/circulation problems =>
- Call for help: Lie patient flat, raise patient legs =>
- Adernaline =>
- When skills and equipment available
- Establish airway, high O2 flow, IV fluid challenge, Chlorphenamine, hydrocortisone
- MONITOR: Pulse, ECG, BP
Extravasation is
- The leakage of one drug from its intended compartment of delivery into one or more adjacent compartments
- It has a number of euphemisms- infiltration, tissuing, displacement- but at the end of the day they are all the same injury
- It is a complex interaction of factors
- It is a whole spectrum of reactions from a pre-extravasation syndrome to a complete necrotic breakdown of tissue
- It is an oncological parenteral therapy emergency
Difficult to diagnose, varied and unpredictable development & outcome

Factors known to be involved
- Patient
- Practical
- Personnel
- Pharmacological
- An individual extravasation injury will be a mix of all of the above
- Some factors are causative of injuries whilst others are contributory too it
Basis of treatment
- ALWAYS
- Aspirate
- Palliate the immediate symptoms
- THEN
- Localise and Neutralise- followed by
- Dilute and spread
- For established or missed extravasations
- treat as for other ulcerated tissue- de-bride and granulate
There should be a national protocol for the treatment of extravasation, and a standard approach to antidotes

Chemotherapy-induced N&V (CINV)
- Can lead to serious complications
- Dehydration
- Malnutrition
- Electrolyte disturbance
- May result in delay, dose reduction or discontinuation of SACT
- Effective management is an important part of patient care
Risk factors
- Gender
- Age
- Chemotherapy (previous treatments)
- History of lifestyle
Emetogenic risk with SACT
- CINV is complex
- Main risk factors
- SACT emetogenic potential
- SACT categorised for emetic risk
- Minimal (0-10%)
- Low (10-30%)
- Moderate (>30-90%)
- High (90%)
Types of N+V associated with chemotherapy
- Acute vomiting
- Occurs within 24 hrs of SACT, peaks after 5-6 hours
- Delayed N&V
- >24hrs post SACT, lasts 3-7 days
- Anticipatory N&V
- Conditioned response; associated poor control previously
- Breakthrough N&V
- CINV despite prophylaxis
- Refractory vomiting
- CINV despite interventions, recurs in subsequent cycles
Antiemetic prophylaxis for chemotherapy-induced N&V

Emetic reflex
Neurotransmitters: targeting key pathways
- DA
- Histamine
- 5-HT
- Endorphins
- Substance P
- GABA
- Cannabinoids
- ACh
CINV classification & examples of anti-emetics
- Acute- 5-HT3 receptor anatagonist, metoclopramide, dexamethasone
- Delayed- dexamethasone, NK1-blocker
- Breakthrough- Metoclopramide, cyclizine
- Anticipatory- lorazepam
- Refractory- Levomepromazine, NK1-blocker, nabilone
MRHA advice- domperidone, metoclopramide, ondansetron
-
Domperidone (May 2014): cardiac side effects inc. QT prolongation
- Lowest effective dose (30mg) for the shortest possible time (max 48hrs)
-
Metoclopramide (Aug 2013): neurological effects
- Maximum 30mg/24 hours (or o.5mg/kg)
- Short term use; upto 5-days; IV slow over >3mins
-
Onsansetron (July 2013); QT prolongation, cardiac arrhythmia
- Max dose restrictions for CINV
- <75yrs 16mg
- >75yrs 8mg
- 15 minute infusion
- Repeat doses (at least 4hr intervals)
- Max dose restrictions for CINV
Overview of guidelines for acute N&V

Risking factors- summary
Oral mucositis

Effect of radiation on oral mucositis

Treatment of oral mucositis

Why do we give chemotherapy every 3 weeks
Neutropenia

Predisposing factors
- Infectious complications are a major cause of morbidity and mortality in cancer patients
- 8% mortality in patients admitted with febrile neutropenic episodes
- Predisposing factors include
- Neutropenia
- Loss of cell-mediated and humoral immunity
- Disruption of skin or mucosal barriers
Predisposing factors- neutropenia

Prevention of infection
- Protective isolation
- Good oral hygiene
- Antimicrobial prophylaxis
- Anti-bacterial (inc gut decontamination)
- Anti-fungal
- Anti-viral- surveillance of viral load
- Neutropenic diet
Diagnosis of febrile neutropenia
- Definition vary
- Temp >38’C
- Neut- <0.5 x109/L or <1x109/L and falling
- Usual inflammatory signs of infection often absent due to lack of neutrophils
- Caution- patients in septicaemic shock may present with tachycardia, hypotension and no fever
Management of febrile neutropenia
- Investigations
- Take history
- Clinical examination
- Peripheral and Hickman line blood cultures
- FBC, U&E
- Sputum, MSU, Stool, swab sites of infection
- Chest X-ray and nasopharyngeal aspirate if necessary
- Most crucial factor is prompt initiation of antibiotics
Treatment schedule
- Tazocin monotherapy unless significant hypotension (diastolic BP <60 mmHg) or septic shock- then add gentamycin
- Vancomycin only if obvious line infection and/or severe mucositis
- Reassess at 48 hours, if significant isolate amend therapy
Antibiotic prophylaxis- quinolones
- Two large trials and a meta-analysis published in 2005
- Gafter-Gvilli A et al. Ann Intern med 2005; 142: 979-95
- Bucaneve G et al
- Cullen M et al
- Meta-analysis: Decrease mortality risk cf placebo or no treatment
- Both studies included solid tumour & lymphoma patients
- Bucaneve et al: higher risk group (inc autos, acute leukaemia)
- Cullen: decrease febrile episodes, probable infection, hospitalisation
- Bucaneve: decrease clinically significant bacterial infections, including G-ve rod bacteraemias
Effect of antimicrobial prophylaxis on the rate of and time of infection

Antibiotic prophylaxis- other
- Co-trimoxazole (960mg M/W/F0 recommended as prophylaxis if significant T-cell immunosuppression
- E.g. fludarabine, cladribine, alemtuzumab, ciclosporin, corticosteroids
- Dapsone
- Penicillin V (500mg BD) post-transplant
Antifungal prophylaxis

Antiviral prophylaxis
- Low risk patients do not require aciclovir prophylaxis (unless prior HSV)
- Aciclovir prophylaxis for intermediate/high risk patients (HSV)
- Historically, high dose aciclovir used in high risk patients to prevent VZV/CMV, alternatives ganciclovir, foscarnet or cidofovir
- HSV- Herpes Simplex Virus
- VZV- Vermicelli-Zoster Virus
- CMV- CytoMegaloVirus