The FOCCUS Study: "Focusing on Cancers Chemotherapys' Untreated Symptoms"

Sponsor
Royal Marsden NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT02121626
Collaborator
(none)
248
1
36
6.9

Study Details

Study Description

Brief Summary

The aim of the study is to identify how often gastrointestinal problems interfere with quality of life as a result of treatment for cancer with chemotherapy. We also want to identify the causes for these symptoms and see if simple treatments used for other gastrointestinal conditions could make chemotherapy an easier experience. Chemotherapy for cancer can be hard work for the patient. Often it makes them feel tired. Not infrequently, it can cause a whole range of physical side effects. Probably the most common side effects are those affecting the stomach and bowels. Vomiting used to be a major problem with chemotherapy but research discovered a whole series of new treatments so that severe vomiting from chemotherapy is rarely a problem today. However, patients can develop a whole series of other symptoms during chemotherapy, for example, bloating, wind, diarrhoea, needing to rush to the lavatory and opening the bowels very frequently. The causes for these symptoms have hardly been studied even though they sometimes affect people quite badly. In our specialist gastrointestinal clinic at the Royal Marsden Hospital, over the last 12 years, we have pioneered new methods for dealing with symptoms which affect the bowel after radiotherapy. We would like to extend these methods to people having chemotherapy. We have identified several easily treatable causes for these symptoms after radiotherapy, which previously were often ignored. We believe that some of these causes also occur in people having chemotherapy and if we knew how often they do occur we could focus on improving treatment for affected people. We plan to find out how often 40 stomach and bowel symptoms occur during chemotherapy. In people who are troubled by any or some of these symptoms we will arrange simple series tests which could sort out why these symptoms occur and we will record how they respond to treatment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Chemotherapy (CT) remains an integral part of treatment for many types of cancer often in combination with surgery and/or radiotherapy. In the year March 2011 to April 2012, 1807 patients were referred to the Royal Marsden Hospital (RMH) Gastrointestinal Unit with a new gastro intestinal (GI) cancer of whom 709 were treated with chemotherapy alone or in combination with other long term outcome. GI symptoms are common in patients receiving chemotherapy. They may arise from the tumour, but may also result as a side effect of treatment. They include anorexia, borborygmi, bloating, constipation, diarrhoea, dysphagia, early satiety, frequency of defaecation, incontinence, mucus discharge, nausea, nocturnal defaecation, pain, reflux, regurgitation, steatorrhoea, tenesmus, urgency of defaecation, vomiting, weight loss and wind. Frequently, such symptoms have a significant impact on patients' quality of life. They may also interfere with the delivery of treatment prompting cessation of therapy or dose reduction resulting in sub optimal dosage with a potential impact on morbidity and mortality. Whilst clinicians have long focused on the management of vomiting and pain in cancer patients, less attention has been paid to the incidence, severity or optimal management of other GI symptoms. If the cause of these symptoms can be identified, then appropriate investigations and treatments can be prescribed. The GI Unit has successfully investigated and treated patients with symptoms emerging after radiotherapy. This experience has enabled the team to develop an algorithm for facilitating the investigation and treatment of cancer therapy induced symptoms. The algorithm has recently been shown to be effective in the management of patients with radiation induced bowel injury . In particular, it enables the rapid identification of required investigations and improves the management of symptoms that might otherwise be mislabeled as inevitable consequences of treatment. Five easily treatable causes for GI symptoms have so far been identified:

    • Small bowel bacterial overgrowth

    • Carbohydrate malabsorption

    • Bile acid malabsorption

    • Gastric bile reflux

    • Pancreatic insufficiency

    It is likely that additional causes such as viral infections (eg cytomegalovirus) are more frequent in patients undergoing chemotherapy than currently appreciated.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    248 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The FOCCUS Study: "Focusing on Cancer Chemotherapys' Untreated Symptoms"
    Actual Study Start Date :
    Apr 1, 2014
    Actual Primary Completion Date :
    Jun 1, 2016
    Actual Study Completion Date :
    Apr 1, 2017

    Arms and Interventions

    Arm Intervention/Treatment
    Chemotheraphy Treatement

    The study will be limited to NHS patients to reduce complications associated with the need for additional funding authorisations from private health care providers for algorithm-instigated investigations. It is not envisaged that participation in other studies running within the GI unit at The Royal Marsden Hospital will preclude entry into this study except in the event of those rare studies where the study is specifically measuring toxicity of treatment as the primary end point.

    Outcome Measures

    Primary Outcome Measures

    1. Incidence of new onset GI symptoms per chemotherapy regimen [Every 4 weeks]

    Secondary Outcome Measures

    1. Change in Gastrointestinal Symptom Rating Scale (GSRS) scores [Every 4 weeks]

    2. Change in Vaizey incontinence scores [Every 4 weeks]

    3. Change in Bristol Stool Chart parameters (stool frequency, type, mode) [Every 4 weeks]

    4. Change in Quality of Life scores (FACTG, version 4 questionnaires) [Every 4 weeks]

    5. Change in neurotoxicity scores (FACT/GOGNTX13, version 4) [Every 4 weeks]

    6. Competency (learning outcomes) GI research nurses [Every 2 months]

    7. Identification of genetic profiles which predispose to specific chemotherapy induced toxicities. [1 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients aged 18 years or above able to give informed consent

    • Patients referred to one of the five prescribing consultants described above

    • Patients to be treated within the GI unit at the Royal Marsden Hospital (RMH Chelsea, Sutton or Kingston) with chemotherapy with or without other treatments.

    Exclusion Criteria:
    • Patients aged less than 18 years

    • Patients unable to give informed consent

    • Patients being treated privately

    • Patients on studies with conflicting end-points

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Royal Marsden NHS Foundation Trust London United Kingdom SW3 6JJ

    Sponsors and Collaborators

    • Royal Marsden NHS Foundation Trust

    Investigators

    • Study Chair: Jervoise Andreyev, MBBS, Ph.D, Royal Marsden NHS Foundation Trust
    • Principal Investigator: Linda Wedlake, RD MSc BSc, Royal Marsden NHS Foundation Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Royal Marsden NHS Foundation Trust
    ClinicalTrials.gov Identifier:
    NCT02121626
    Other Study ID Numbers:
    • CCR 3921
    First Posted:
    Apr 23, 2014
    Last Update Posted:
    Nov 22, 2017
    Last Verified:
    Nov 1, 2017

    Study Results

    No Results Posted as of Nov 22, 2017