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Systemic Anti Cancer Therapy Study

June 2006 to July 2006
Publication date: 12th November 2008

Background
This study will examine the process of care of all patients who die within 30 days of systemic anti-cancer therapy (SACT), sphygmomanometer looking for areas where their care might have been improved. It will not concentrate solely on those patients whose death may have been treatment-related.

This work is supported by the Joint Collegiate Council for Oncology (JCCO), a joint group between the Royal College of Radiologists and Royal College of Physicians; and the Joint Specialty Committee (JSC) for Medical Oncology at the Royal College of Physicians.

Originally it was proposed that the study would focus on those patients in which it was thought that the toxic effects of the patient’s therapy contributed to their death. Whilst this is an extremely important group of patients to study, it would only be possible to identify this cohort of patients following close examination of individual sets of case notes. As stated above, the study will include all patients who die within 30 days of systemic anti-cancer therapy and will therefore include many patients who die from progressive disease as well as those who suffer iatrogenic disease. Patient management should adhere to guidelines and standards, which aim to reduce risk. This expanded study will enable NCEPOD to obtain a large dataset on patient care from which to identify remedial factors and make meaningful recommendations.

The 30 day period will be defined as 30 days from Day 1 of the SACT cycle immediately prior to death. If SACT is given continuously - 30 days from the date of the last prescription.

A pilot study, with voluntary participation, was conducted in September 2006. Data was collected retrospectively on all patients that received SACT in April 2006 (i.e. Day 1 of a cycle in April) and died 30 days afterwards. However, for those that did not have electronic systems to enable quick and easy data retrieval, we suggested pharmacy data of drug administration was collected prospectively from 1st September 2006 to 30th September 2006 inclusive, with data collected on any deaths occurring within 30 days from the end of September.

The main study commenced in February 2007. A starter pack with local reporter instructions, organisational questionnaire, protocol, specialty codes, ICD-10 codes, and case note extract requirements, was posted to all local reporters on 19th February 2007. The data collection spreadsheet was emailed to all local reporters on 20th February 2007. Please note that intravesical treatment is included in our SACT definition.

The protocol has been approved by the Expert Group and NCEPOD Steering Group and is available to download here.

We can only accept data for the study submitted using our master spreadsheet for the study. For submitting data the spreadsheet can be downloaded here.

Deadlines:

  • Return of spreadsheets was: 7th December 2007
  • Return of Organisational questionnaires: 20th January 2008
  • Final return of clinical questionnaires: 25th March 2008

Further questions about the study may be directed to: cancertherapies@ncepod.org.uk


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Frequently Asked Questions

When did the main study start?
The main study has now commenced. Hospitals/Centres/
Units will be asked to supply details of patients that received SACT in June and July 2006 and they will also be asked for all death data regardless of disease or disorder for the months of June, July and August 2006.
I would like to read the protocol - could you send me a copy?
Yes. All hospital/units/centres will be asked to take part regardless of whether or not they treat patients with SACT as NCEPOD need all death data from all hospitals for this study.
Is participation in this study mandatory?
Yes. All hospital/units/centres will be asked to take part regardless of whether or not they treat patients with SACT as NCEPOD need all death data from all hospitals for this study.
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