Cancer Clinical Trial
Official title:
An Exploratory Assessment of the Cost Impact of Managing GI Consequences of Cancer Treatment Outside of a Specialist Clinic
An estimated 90,000 patients are suffering from long term gastrointestinal problems after
cancer treatments, and whilst the National Cancer Survivorship Initiative have been working
to develop specific pathways of care, these pathways lack in both specialised tariff funding
and awareness. This study aims to assess the economic and personal impact on patients
suffering from stomach and/or bowel problems after cancer treatment prior to referral to the
Gastrointestinal and Nutrition Team (GIANT) at the Royal Marsden Hospital. All patients
referred to the GIANT service (including private patients but excluding re referrals) will be
offered participation in the study.
The study will consist of a 9 page patient retrospective questionnaire, asking questions
about investigations and medications prescribed over the past year, as well as costs and
methods of trying to treat their symptoms themselves, and the personal cost to themselves of
their symptoms through loss of work and emotional impact. As this questionnaire asks patients
questions about the past year, and thus can be difficult to answer accurately, patient
answers will be validated for reliability by sending a 1 page questionnaire to their GP
asking the same questions about clinic visits concerning stomach/bowel problems,
investigations and medications prescribed in the past year. Once this data is collected from
the participants, and the study has finished, the average cost of clinical interventions,
economic impact, and personal impact, will be calculated.
The results from this study will be useful in helping to show the economic burden of GI
symptoms, and will provide evidence as to the economic benefit of specialised clinics for the
consequences of cancer treatment; highlighting the need for a nationally recognised algorithm
for management.
The number of people who survive cancer has tripled in the past 30 years; however, chronic
physical consequences of treatment for cancer adversely affect the quality of life of 20-25%
of survivors. The largest group of patients reporting debilitating chronic side effects are
those treated with radiotherapy alone or in combination with other treatments for pelvic
cancer. Gastrointestinal symptoms are the most common chronic physical side effects reported,
and have the greatest effect on daily activity. Overall, 50% of patients report that that
their gastrointestinal symptoms affect their quality of life, and 20-40% state that this
effect is moderate or severe. Such problems include chronic faecal incontinence (up to 60% of
patients) after radiotherapy for prostate or rectal cancer (53, 54), and chronic loose stool
(47%), defaecatory urgency (29%), or chronic abdominal pain (17%) after radiotherapy for
gynecological cancer.
In 2010, the UK National Cancer Survivorship Initiative Vision challenged professionals to
develop new models of care for patients because "the needs of cancer survivors are not being
met, that being 'cured' of cancer does not necessarily equate with being well and that
chronic consequences of treatment can have a devastating impact on daily life". The National
Cancer Survivorship Initiative accepts that currently there is limited access to specialist
services, despite an estimated 90,000 people in the UK experiencing long-term
gastrointestinal problems as a consequence of cancer treatment. Furthermore, recent surveys
of clinical oncologists and gastroenterologists concur with this sentiment, highlighting a
lack of available expertise; with two UK audits of gastroenterology consultants and
oncologists demonstrating no improvement in provision of specialist services between 2003 to
2010. Whilst NHS Improvement has developed stratified pathways of care, the Roadmap for
Recovery report created recently by the Anthony Nolan Bone Marrow Transplant charity
underlined the ongoing issue of lack of specialised commissioning of services for complex
consequences of cancer treatment. It is estimated that £40 million (DoH) is wasted annually
in futile and dangerous treatments for Pelvic Radiation Disease alone; academic estimates
suggest this is closer to £80 million . Furthermore the incapacitating affects of GI symptoms
leads to both loss of productivity and huge social costs. Currently there is no NHS tariff
payable for GI consequences of cancer treatment; however the mean cost per completed episode
of care by the GIANT (Gastrointestinal and Nutrition Team) service was calculated, amounting
to an average cost of £1563 per patient. This can be compared to a tariff of £14,800 per
woman treated with chemo-radiation for cervical cancer, and a cost in excess of £45,000 for a
person with rectal cancer treated with long course chemo-radiation followed by surgery and
adjuvant chemotherapy. With specialist clinics lacking, it can be assumed that the majority
of people living with GI consequences of cancer treatment are being treated by their GPs;
however, the Quality and Outcomes Framework by which GP Surgeries are measured and awarded
financial incentives includes no domain or measure for gastrointestinal problems; and there
have been no studies into the cost of managing patients with GI problems as a consequence of
cancer treatment outside of the GIANT service. This exploratory study is a step in this
direction.
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