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Acute Oncology Service at UHL
Helen Guyatt
Acute Oncology CNS
Dr Eleni Karapanagiotou
Medical Oncologist
Acute Oncology: a new subspecialty in
Oncology developed from reports
• NCEPOD report
• NPSA report
• Cancer peer reviews
Systematic approach to deal with
cancer-related emergencies
Acute Oncology Service (AOS)
• Development of acute oncology
teams in every hospital with an
ED/acute admitting beds
• Access to oncology review within
24hrs of admission
• Clear guidance on management of
Neutropaenic sepsis
Metastatic cord compression
MMP CMT teaching Feb 2012 4
For better, for worse
Inclusion criteria
• Patients aged 16 years or
over
• Solid tumours or
haematological
malignancies
• Received chemotherapy,
monoclonal antibodies or
immunotherapy during the
study period
• Died within 30 days of
receiving treatment
Main Outcomes
• 2% of pts died within 30 days of SACT
• 86% of pts received SACT with
palliative intent .
• 30-40% mortality from sepsis alone !
Room for improvement
• Decision to treat
• Process of care
– Prescribing, dispensing and administration of SACT
• Communication
– Patient information, medical records
• SACT toxicity
– Admission, assessment and treatment
– Management of neutropenic sepsis
– Urgent recognition and appropriate treatment of MSCC
• End of life decisions
Uurgent referral to
ED
communication
Oncology and GPb
Acute Oncology Service (AOS)
Development of acute oncology
teams in every hospital with an
ED/acute admitting beds
Access to oncology review within
24hrs of admission
Clear guidance on management of
Neutropenic sepsis
Metastatic cord compression
Components of Acute Oncology Service
AOS
Fast-
track
clinics
CUP
pathway24/7
telephone
advice
Neutropenic
sepsis
MSCC
pathway
Flagging
system
AOT
Management
protocols
Training
Aims of an Acute Oncology Service
 Better communication between treating teams
 Increased patient safety
 Prevention of unnecessary admissions
 Reduced length of stay
 Minimised unnecessary investigations
 To improve patient experience
 Appropriate and prompt referrals to other specialties
/ hospitals as required
The Acute Oncology Team at UHL
Managerial structure:
Dr Naheed Mir, Lead for Cancer Services
Julie Baker, Lead Macmillan Nurse
Clinical Structure:
Dr Eleni Karapanagiotou, Medical Oncologist
Dr Dan Smith, Clinical Oncologist
Helen Guyatt, AOS CNS
Dian Welch, Administrator
AOS: dealing with treatment related-complications
Systemic treatment-related:
• Neutropenic sepsis
• Uncontrolled nausea and vomiting
• Extravasation injury
• Acute hypersensitivity reactions
including anaphylactic shock
• Complications associated with venous
access devices
• Uncontrolled diarrhoea
• Uncontrolled mucositis
• Hypomagnesaemia
Radiotherapy-related
• Acute skin reactions
• Uncontrolled nausea and vomiting
• Uncontrolled diarrhoea
• Uncontrolled mucositis
• Acute radiation pneumonitis
• Acute cerebral/other CNS, oedema
AOS: dealing with cancer-related complications
Presentations as caused directly by malignant disease and presenting as an
urgent acute problem
• Pleural effusion
• Pericardial effusion
• Lymphangitis carcinomatosa
• Superior mediastinal obstruction syndrome, including superior vena
caval obstruction
• Abdominal ascites
• Hypercalcaemia
• Spinal cord compression including MSCC
• Cerebral space occupying lesion(s)
Growing AOS in UHL
• AOS reviews on average 41 patients per
month at UHL site.
• 855 patients seen between 06/13 - 02/15.
0
20
40
60
80
No. of patients seen by AOS
Referrals to AOS
• Referrals are made via fax, email and phone
calls.
• Referrals from A+E, Admitting medical and
surgical teams, Cancer CNS, Community
palliative care teams, Other AOS teams.
AOS: specific areas of interest
• Cancer of unknown primary
• Neutropenic sepsis
• MSCC
Carcinoma of unknown primary (CUP)
• Confirmed carcinoma of unknown primary
origin (CUP): Metastatic epithelial or neuro-
endocrine malignancy identified on the basis
of final histology, with no primary site
detected despite a selected initial screen of
investigations, specialist review, and further
specialised investigations as appropriate.
• Around 4% of all cancers
CUP: diagnostic algorithm
Patient identified:
Previous cancer diagnosis which may
explain metastatic disease e.g.
relapsed breast, colorectal, lung
cancer
If suspected primary identifiable, refer to
relevant team for further work-up and
diagnosis eg: suspected lung primary
refer to chest physician
AOS NOT INVOLVED IN 2WW
REFERRALS!! No
Yes
Involve AOS
Collaboration between AOS and medical/surgical team to assess fitness for investigation
and treatment, with imaging and biopsy arranged as indicated
 with multiple lung metastases
 with multiple liver metastases
 with multiple bone metastases
 with single/ multiple nodal stations involved
 with multiple brain metastases
When to stop investigations?
Perform investigations only if:
• the results are likely to affect a treatment decision
Eg are they fit for any treatment. Involve AOS/palliative care
• the patient understands why the investigations are being carried out
• the patient understands the potential benefits and risks of
investigation and treatment and
• − the patient is prepared to accept treatment
CUP: clinical management
Specific subset of CUP:
Women with peritoneal papillary
serous carcinoma
Women with adenocarcinoma
involving axillary LN
SCC involving cervical LN
Neuro-endocrine CUP
CUP of a single location
Specific treatment according to presumed primary
Patient with suspected carcinoma of unknown primary
Exclude a non-CUP neoplasm:
Non-epithelial cancer (lymphoma, sarcoma,
melanoma)
Extragonadal germ-cell tumour
Non-specific subset of CUP
Discuss treatment options based on PS
and prognosis
UHL links to GSTT
CUP MDM
CUP: a case presentation
A fit 84 yo lady (LA) presents with bilateral neck lymphadenopathy
 Head and neck examination: -ve
 LN excision biopsy: adenocarcinoma
CK7+ve, CK20-ve, EMA+ve, TTF-1 -ve, thyroglobulin -ve, ER-ve
 CT TAP: Bilateral neck and SCF LN and Rt axilla LN
!AOS
Mammogram and US: -ve
Discuss at MDM: not further investigations required
CONFIRMED CUP
Discuss treatment
CUP CASES IN UHL
• 18 Patients linked to GSTT CUP MDM since
June 2013 with suspected CUP.
• 8 of these Patients confirmed CUP
Neutropenic sepsis
Neutropenic sepsis MUST be treated quickly (within 60 mins)
 haematology and oncology patients
 recent chemotherapy or immunosuppressant drugs WITHIN 6/52
 any patient who is pyrexial (38ºC) or clinically septic and neutrophil count of
<0.5 x 109/L
1. History –has patient been on chemotherapy and how long ago?
2. Examine –Urgent bloods (FBC, Cultures), TPR, ports for infection,
3. Action –get Antibiotics prescribed (do not wait for bloods)
4. Treat –Antibiotics +? Fluids within 60 minutes of arrival
The interval between patient's arrival and commencement of antibiotic
treatment (‘door-to-needle time') should not exceed 1 hour!!!
Neutropenic sepsis: Abx
No penicillin allergy
• Piperacillin/tazobactam
4.5 g QDS
Mild penicillin allergy
• Ceftriaxone 2g IV OD
• Gentamicin IV OD
Severe penicillin allergy
• Teicoplanin 400mg
IV(If> 70 Kg give
6mg/Kg every 12 h for 3
doses then OD
• Gentamicin
• ± Ciprofloxacin 400mg
IV BD
* NEUTROPENIC SEPSIS GUIDELINES AVAILABLE ON INTRANET
Risk assessment: MASCC score
Characteristic Yes No Point score
Burden of illness
*No or mild symptoms (not interfering with
daily routine)
5
*Moderate symptoms (patient uncomfortable
and symptoms influencing daily routine)
3
*Severe symptoms (severly limiting daily
activity)
0
Does patient have hypotension (Systolic
<90mmHg)
0 5
Does patient have chronic obstructive
pulmonary disease
0 4
Does patient have a solid tumor or no previous
fungal infection in haematological tumor
4 0
Outpatient status at time of presentation 3 0
Is the patient dehydrated or requiring IV fluids 0 3
Aged <60 years 2 0
Total MASCC score
Neutropenic sepsis: risk assessment
Criteria Yes No
1 MASCC score < 21
2 Profound neutropenia (ANC ≤ 100cells/mm3) anticipated to extend >7 day
3 Severe mucositis that interferes with swallowing
4 Severe diarrhoea
5 New-onset neurological changes
6 Intravascular catheter related infection
7 New pulmonary infiltrate or hypoxaemia
8 Hepatic insufficiency (aminotransferase levels > 5 × normal values)
9 Renal insufficiency (eGFR <30ml/min or on dialysis)
NO to all these criteria will put the patient in a low risk category
Consider de-escalation of antimicrobials.
AOS UHL: neutropenic sepsis cases
Door to needle times for suspected neutropenic
sepsis 02/14 – 02/15
0
0.5
1
1.5
2
2.5
Feb-14
Mar-14
Apr-14
May-14
Jun-14
Jul-14
Aug-14
Sep-14
Oct-14
Nov-14
Dec-14
Jan-15
Feb-15
Time in hours
Time in hours
Chemotherapy-related-diarrhoea
Grade 1 Grade 2 Grade 3 Grade 4
2-3 BM 4-6 BM 7-9 BM >10BM
↑in stoma output ↑↑ in stoma
output
↑↑↑in stoma
output
↑↑↑↑in stoma
output
Moderate cramping Severe cramping Grossly bloody
diarrhoea
Nocturnal stools Nocturnal stools,
interfering with
ADL
Parental support
Check:
What chemotherapy?: capecitabine/irinotecan/erlotinib/ipilimumab
When?
RT? (abdomen?)
Observations: temperature, pulse, BP, RR O2
Investigations: FBC, U&E, CRP, stool sample
Chemotherapy-related-diarrhoea: treatment
Action:
Stop chemotherapy
Start fluids
Start loperamide
Consider codeine phosphate
Diet advise
STOP:
Wait for C&S if:
• Recent hospitalization
• Recent AB
• Bloody diarrhoea
• Recent travelling abroad
•History of contact of
diarrhoea
INFORM AOS!!
MSCC: a neurosurgical/
radiotherapy emergency
• Step by step protocols in place for all the
Trusts
• Clinical presentation/imaging
protocols/immediate Rx
• Virtual Case discussion with radiologist/
surgeon/ clinical radiologist
• Determine spinal stability of patients for
nursing/transfer
MSCC: pathway
Suspected MSCC
Patient with prior diagnosis of cancer or unknown primary with symptoms
suggestive of spinal metastases/MSCC:
•Severe intractable progressive pain- especially in thoracic region
•New spinal nerve root pain( burning, shooting, causing numbness)
•Altered sensation and/or reduced power in limbs
•Bladder and/or bowel disturbance( i.e. new onset of incontinence)
Follow the MSCC protocol
MSCC: pathway
Symptoms suggestive of
spinal metastasis or MSCC
WITH
Neurological symptoms
Contact MSCC coordinator
immediately.
Urgent MRI within 24
hours.
Transfer MRI/CT images to
MSCC centre for urgent
review. Fax referral form to
MSCC centre
Symptoms suggestive of
spinal metastasis or MSCC
WITHOUT new
neurological symptoms
MRI within 7 days
Contact MSCC coordinator
immediately within 24 hrs
of MRI scan.
Nonspecific lower back pain
Locally managed standard
backcare (outside remit of
MSCC Guidelines)
Continue frequent
observation to monitor
symptom progression. If
symptoms persist or
progress refer
Contact Network Metastatic Spinal Cord Compression Team at Kings College Hospital
Telephone: 02032995468 Fax Referrals: 020 3299 4197
Patient discussed with the on-call Clinical Advisor (Consultant neuro-surgeon/Clinical
Oncologist/Radiologist. CONFIRMED MSCC
Network MSCC coordinator feeds back to referrer and initiates treatment plan
SURGERY RADIOTHERAPY
Discussion with AOS and
treating oncologists
(histology needed, first
presentation, prognosis)
MSCC: case presentation
Aug 2012: A 41 yo female (TS) presented with back pain
gradually worsening 2/12
Previous diagnosis of Rt breast cancer in 2006
Histology: IDC, ER+ve, HER2+ve
Treatment: neoadjuvant chemotherapy (ECX4 followed by DX4),
WLE + AC, RT, adjuvant trastuzumab and Tamoxifen
MSCC: radiological findings
Walking affected
Rt lower limb numbness
Rt limb: Motor power 4/5
Dexamethasone 8mg bd
Urgent MRI
MSCC pathway activated
NS: NOT for surgery
Urgent RT
MSCC cases in UHL
• 15 patients seen in UHL with impending and
confirmed MSCC between 06/13 – 04/15
• 14 patients received Radiotherapy at GSTT
• 1 patient transferred to KCH for surgery
Food for thought….
• No established pathway between AOS and GP practices
• AOS inpatient service
• Not enough AOS resources as yet
• Established pathways still work between GPs and ED/2ww

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Aos gp 24.04.15

  • 1. Acute Oncology Service at UHL Helen Guyatt Acute Oncology CNS Dr Eleni Karapanagiotou Medical Oncologist
  • 2. Acute Oncology: a new subspecialty in Oncology developed from reports • NCEPOD report • NPSA report • Cancer peer reviews Systematic approach to deal with cancer-related emergencies
  • 3. Acute Oncology Service (AOS) • Development of acute oncology teams in every hospital with an ED/acute admitting beds • Access to oncology review within 24hrs of admission • Clear guidance on management of Neutropaenic sepsis Metastatic cord compression
  • 4. MMP CMT teaching Feb 2012 4 For better, for worse Inclusion criteria • Patients aged 16 years or over • Solid tumours or haematological malignancies • Received chemotherapy, monoclonal antibodies or immunotherapy during the study period • Died within 30 days of receiving treatment Main Outcomes • 2% of pts died within 30 days of SACT • 86% of pts received SACT with palliative intent . • 30-40% mortality from sepsis alone !
  • 5. Room for improvement • Decision to treat • Process of care – Prescribing, dispensing and administration of SACT • Communication – Patient information, medical records • SACT toxicity – Admission, assessment and treatment – Management of neutropenic sepsis – Urgent recognition and appropriate treatment of MSCC • End of life decisions Uurgent referral to ED communication Oncology and GPb
  • 6. Acute Oncology Service (AOS) Development of acute oncology teams in every hospital with an ED/acute admitting beds Access to oncology review within 24hrs of admission Clear guidance on management of Neutropenic sepsis Metastatic cord compression
  • 7. Components of Acute Oncology Service AOS Fast- track clinics CUP pathway24/7 telephone advice Neutropenic sepsis MSCC pathway Flagging system AOT Management protocols Training
  • 8. Aims of an Acute Oncology Service  Better communication between treating teams  Increased patient safety  Prevention of unnecessary admissions  Reduced length of stay  Minimised unnecessary investigations  To improve patient experience  Appropriate and prompt referrals to other specialties / hospitals as required
  • 9. The Acute Oncology Team at UHL Managerial structure: Dr Naheed Mir, Lead for Cancer Services Julie Baker, Lead Macmillan Nurse Clinical Structure: Dr Eleni Karapanagiotou, Medical Oncologist Dr Dan Smith, Clinical Oncologist Helen Guyatt, AOS CNS Dian Welch, Administrator
  • 10. AOS: dealing with treatment related-complications Systemic treatment-related: • Neutropenic sepsis • Uncontrolled nausea and vomiting • Extravasation injury • Acute hypersensitivity reactions including anaphylactic shock • Complications associated with venous access devices • Uncontrolled diarrhoea • Uncontrolled mucositis • Hypomagnesaemia Radiotherapy-related • Acute skin reactions • Uncontrolled nausea and vomiting • Uncontrolled diarrhoea • Uncontrolled mucositis • Acute radiation pneumonitis • Acute cerebral/other CNS, oedema
  • 11. AOS: dealing with cancer-related complications Presentations as caused directly by malignant disease and presenting as an urgent acute problem • Pleural effusion • Pericardial effusion • Lymphangitis carcinomatosa • Superior mediastinal obstruction syndrome, including superior vena caval obstruction • Abdominal ascites • Hypercalcaemia • Spinal cord compression including MSCC • Cerebral space occupying lesion(s)
  • 12. Growing AOS in UHL • AOS reviews on average 41 patients per month at UHL site. • 855 patients seen between 06/13 - 02/15. 0 20 40 60 80 No. of patients seen by AOS
  • 13. Referrals to AOS • Referrals are made via fax, email and phone calls. • Referrals from A+E, Admitting medical and surgical teams, Cancer CNS, Community palliative care teams, Other AOS teams.
  • 14. AOS: specific areas of interest • Cancer of unknown primary • Neutropenic sepsis • MSCC
  • 15. Carcinoma of unknown primary (CUP) • Confirmed carcinoma of unknown primary origin (CUP): Metastatic epithelial or neuro- endocrine malignancy identified on the basis of final histology, with no primary site detected despite a selected initial screen of investigations, specialist review, and further specialised investigations as appropriate. • Around 4% of all cancers
  • 16. CUP: diagnostic algorithm Patient identified: Previous cancer diagnosis which may explain metastatic disease e.g. relapsed breast, colorectal, lung cancer If suspected primary identifiable, refer to relevant team for further work-up and diagnosis eg: suspected lung primary refer to chest physician AOS NOT INVOLVED IN 2WW REFERRALS!! No Yes Involve AOS Collaboration between AOS and medical/surgical team to assess fitness for investigation and treatment, with imaging and biopsy arranged as indicated  with multiple lung metastases  with multiple liver metastases  with multiple bone metastases  with single/ multiple nodal stations involved  with multiple brain metastases
  • 17. When to stop investigations? Perform investigations only if: • the results are likely to affect a treatment decision Eg are they fit for any treatment. Involve AOS/palliative care • the patient understands why the investigations are being carried out • the patient understands the potential benefits and risks of investigation and treatment and • − the patient is prepared to accept treatment
  • 18. CUP: clinical management Specific subset of CUP: Women with peritoneal papillary serous carcinoma Women with adenocarcinoma involving axillary LN SCC involving cervical LN Neuro-endocrine CUP CUP of a single location Specific treatment according to presumed primary Patient with suspected carcinoma of unknown primary Exclude a non-CUP neoplasm: Non-epithelial cancer (lymphoma, sarcoma, melanoma) Extragonadal germ-cell tumour Non-specific subset of CUP Discuss treatment options based on PS and prognosis UHL links to GSTT CUP MDM
  • 19. CUP: a case presentation A fit 84 yo lady (LA) presents with bilateral neck lymphadenopathy  Head and neck examination: -ve  LN excision biopsy: adenocarcinoma CK7+ve, CK20-ve, EMA+ve, TTF-1 -ve, thyroglobulin -ve, ER-ve  CT TAP: Bilateral neck and SCF LN and Rt axilla LN !AOS Mammogram and US: -ve Discuss at MDM: not further investigations required CONFIRMED CUP Discuss treatment
  • 20. CUP CASES IN UHL • 18 Patients linked to GSTT CUP MDM since June 2013 with suspected CUP. • 8 of these Patients confirmed CUP
  • 21. Neutropenic sepsis Neutropenic sepsis MUST be treated quickly (within 60 mins)  haematology and oncology patients  recent chemotherapy or immunosuppressant drugs WITHIN 6/52  any patient who is pyrexial (38ºC) or clinically septic and neutrophil count of <0.5 x 109/L 1. History –has patient been on chemotherapy and how long ago? 2. Examine –Urgent bloods (FBC, Cultures), TPR, ports for infection, 3. Action –get Antibiotics prescribed (do not wait for bloods) 4. Treat –Antibiotics +? Fluids within 60 minutes of arrival The interval between patient's arrival and commencement of antibiotic treatment (‘door-to-needle time') should not exceed 1 hour!!!
  • 22. Neutropenic sepsis: Abx No penicillin allergy • Piperacillin/tazobactam 4.5 g QDS Mild penicillin allergy • Ceftriaxone 2g IV OD • Gentamicin IV OD Severe penicillin allergy • Teicoplanin 400mg IV(If> 70 Kg give 6mg/Kg every 12 h for 3 doses then OD • Gentamicin • ± Ciprofloxacin 400mg IV BD * NEUTROPENIC SEPSIS GUIDELINES AVAILABLE ON INTRANET
  • 23. Risk assessment: MASCC score Characteristic Yes No Point score Burden of illness *No or mild symptoms (not interfering with daily routine) 5 *Moderate symptoms (patient uncomfortable and symptoms influencing daily routine) 3 *Severe symptoms (severly limiting daily activity) 0 Does patient have hypotension (Systolic <90mmHg) 0 5 Does patient have chronic obstructive pulmonary disease 0 4 Does patient have a solid tumor or no previous fungal infection in haematological tumor 4 0 Outpatient status at time of presentation 3 0 Is the patient dehydrated or requiring IV fluids 0 3 Aged <60 years 2 0 Total MASCC score
  • 24. Neutropenic sepsis: risk assessment Criteria Yes No 1 MASCC score < 21 2 Profound neutropenia (ANC ≤ 100cells/mm3) anticipated to extend >7 day 3 Severe mucositis that interferes with swallowing 4 Severe diarrhoea 5 New-onset neurological changes 6 Intravascular catheter related infection 7 New pulmonary infiltrate or hypoxaemia 8 Hepatic insufficiency (aminotransferase levels > 5 × normal values) 9 Renal insufficiency (eGFR <30ml/min or on dialysis) NO to all these criteria will put the patient in a low risk category Consider de-escalation of antimicrobials.
  • 25. AOS UHL: neutropenic sepsis cases Door to needle times for suspected neutropenic sepsis 02/14 – 02/15 0 0.5 1 1.5 2 2.5 Feb-14 Mar-14 Apr-14 May-14 Jun-14 Jul-14 Aug-14 Sep-14 Oct-14 Nov-14 Dec-14 Jan-15 Feb-15 Time in hours Time in hours
  • 26. Chemotherapy-related-diarrhoea Grade 1 Grade 2 Grade 3 Grade 4 2-3 BM 4-6 BM 7-9 BM >10BM ↑in stoma output ↑↑ in stoma output ↑↑↑in stoma output ↑↑↑↑in stoma output Moderate cramping Severe cramping Grossly bloody diarrhoea Nocturnal stools Nocturnal stools, interfering with ADL Parental support Check: What chemotherapy?: capecitabine/irinotecan/erlotinib/ipilimumab When? RT? (abdomen?) Observations: temperature, pulse, BP, RR O2 Investigations: FBC, U&E, CRP, stool sample
  • 27. Chemotherapy-related-diarrhoea: treatment Action: Stop chemotherapy Start fluids Start loperamide Consider codeine phosphate Diet advise STOP: Wait for C&S if: • Recent hospitalization • Recent AB • Bloody diarrhoea • Recent travelling abroad •History of contact of diarrhoea INFORM AOS!!
  • 28. MSCC: a neurosurgical/ radiotherapy emergency • Step by step protocols in place for all the Trusts • Clinical presentation/imaging protocols/immediate Rx • Virtual Case discussion with radiologist/ surgeon/ clinical radiologist • Determine spinal stability of patients for nursing/transfer
  • 29. MSCC: pathway Suspected MSCC Patient with prior diagnosis of cancer or unknown primary with symptoms suggestive of spinal metastases/MSCC: •Severe intractable progressive pain- especially in thoracic region •New spinal nerve root pain( burning, shooting, causing numbness) •Altered sensation and/or reduced power in limbs •Bladder and/or bowel disturbance( i.e. new onset of incontinence) Follow the MSCC protocol
  • 30. MSCC: pathway Symptoms suggestive of spinal metastasis or MSCC WITH Neurological symptoms Contact MSCC coordinator immediately. Urgent MRI within 24 hours. Transfer MRI/CT images to MSCC centre for urgent review. Fax referral form to MSCC centre Symptoms suggestive of spinal metastasis or MSCC WITHOUT new neurological symptoms MRI within 7 days Contact MSCC coordinator immediately within 24 hrs of MRI scan. Nonspecific lower back pain Locally managed standard backcare (outside remit of MSCC Guidelines) Continue frequent observation to monitor symptom progression. If symptoms persist or progress refer Contact Network Metastatic Spinal Cord Compression Team at Kings College Hospital Telephone: 02032995468 Fax Referrals: 020 3299 4197 Patient discussed with the on-call Clinical Advisor (Consultant neuro-surgeon/Clinical Oncologist/Radiologist. CONFIRMED MSCC Network MSCC coordinator feeds back to referrer and initiates treatment plan SURGERY RADIOTHERAPY Discussion with AOS and treating oncologists (histology needed, first presentation, prognosis)
  • 31. MSCC: case presentation Aug 2012: A 41 yo female (TS) presented with back pain gradually worsening 2/12 Previous diagnosis of Rt breast cancer in 2006 Histology: IDC, ER+ve, HER2+ve Treatment: neoadjuvant chemotherapy (ECX4 followed by DX4), WLE + AC, RT, adjuvant trastuzumab and Tamoxifen
  • 32. MSCC: radiological findings Walking affected Rt lower limb numbness Rt limb: Motor power 4/5 Dexamethasone 8mg bd Urgent MRI MSCC pathway activated NS: NOT for surgery Urgent RT
  • 33. MSCC cases in UHL • 15 patients seen in UHL with impending and confirmed MSCC between 06/13 – 04/15 • 14 patients received Radiotherapy at GSTT • 1 patient transferred to KCH for surgery
  • 34. Food for thought…. • No established pathway between AOS and GP practices • AOS inpatient service • Not enough AOS resources as yet • Established pathways still work between GPs and ED/2ww

Notes de l'éditeur

  1. NCEPOD: national confidential enquiry into patient outcome and death
  2. EMA: epithelial membrane antigen: for epithelial tumours