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Truthful Information on Chemotherapy and Its Impact on Chemotherapy at the End of Life (HIPPOCRATE)

Primary Purpose

Stage IV Lung Cancer

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Truthful information on chemotherapy risks
Standard of information
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Stage IV Lung Cancer focused on measuring Lung cancer, chemotherapy outcome, ethics, information

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • stage IV lung cancer, histologically proven
  • > 18 years old
  • diagnosed during the last 8 weeks
  • systemic therapy indicated

Exclusion Criteria:

  • prior systemic therapy for metastatic disease
  • comorbidity not compatible with the inclusion according to the investigator
  • patient has not given its non-objection or not being able to give
  • patient unaffiliated or not beneficiary of a social security scheme

Sites / Locations

  • Hôpital Cochin

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard of information

Truthful information on chemotherapy risks

Arm Description

Information on chemotherapy as done in routine practice following national and international guidelines

Information on the potential role of anticancer chemotherapy in worsening life-threatening conditions

Outcomes

Primary Outcome Measures

Number of patients receiving chemotherapy in the last 30 days of life

Secondary Outcome Measures

Patient knowledge of the goals of care assessed by questionnaire
Patient knowledge of the goals of care assessed by questionnaire
Number of survivals
Number of appeals to palliative care
Use of palliative care resources
Number of onco-palliative meetings
Number of use of emergency room, intensive care unit and hospice service in the last month of life
Number of unscheduled hospitalizations
Number of chemotherapy cycles received
Number of days spent in acute care
Number of days spent in conventional oncology hospital
Place of death

Full Information

First Posted
November 11, 2015
Last Updated
April 30, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
National Cancer Institute, France, Recherche Clinique Paris Descartes Necker Cochin Sainte Anne
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1. Study Identification

Unique Protocol Identification Number
NCT02606149
Brief Title
Truthful Information on Chemotherapy and Its Impact on Chemotherapy at the End of Life
Acronym
HIPPOCRATE
Official Title
Impact of a Truthful Information Concerning Chemotherapy on Chemotherapy Prescription at the End of Life : a Randomized Controlled Study in Non-curable Lung Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
July 15, 2016 (Actual)
Primary Completion Date
October 15, 2020 (Actual)
Study Completion Date
October 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
National Cancer Institute, France, Recherche Clinique Paris Descartes Necker Cochin Sainte Anne

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with metastatic cancer have a substantial symptom burden and may receive aggressive care at the end of life. There is evidence that the use of chemotherapy near the end of life is not related to its likelihood of providing benefit and the overuse of aggressive anticancer therapies near the end of life may result in more toxicity than clinical benefit. Moreover, proposing new lines of treatment after successive therapeutic failures may be a way of avoiding discussion of prognosis and advance care planning. It has been proposed that systems not providing overly aggressive care near the end of life would be the ones in which less than 10% of patients receive chemotherapy in the last 14 days of life. Presently the first consultation between patient and oncologist is ruled in France by the first "Plan Cancer" and the "Dispositif d'annonce" (announcement planning). Oncologists are supposed to explain the diagnosis of cancer and to present a treatment plan. In routine practice for metastatic non curable cancer patients, chemotherapy is presented as the leading therapy and its side effects are explained. The use of chemotherapy has been associated with the worsening of two major competitive life-threatening conditions for cancer patients: cachexia and thrombo-embolic events. Nevertheless the risk of worsening both those conditions is hardly explained in routine practice. This study proposes to examine in a monocentric interventional prospective randomized trial, the impact of a particular way for the oncologist to present chemotherapy at the diagnosis stage on the easiness of timely chemotherapy interruption at the end of life. The main objective is to determine whether or not the explanation of the potential role of anticancer chemotherapy in worsening life-threatening conditions impacts the proportion of patients receiving chemotherapy in the last 30 days of life compared with usual presentation. Secondary objectives are to determine the impact of this communication strategy on overall survival and other indicators of aggressiveness of care and palliative care resources use. The hypothesis is that the intervention will allow 15% of patients receiving anticancer therapy during the last 30 days of life, as compared to 30% in the control group. The investigators expect that the intervention evaluated in this study will reduce the rate of patients receiving chemotherapy during the last 30 days of life hopefully improving the quality of end of life care. A secondary objective is overall survival and this study will therefore verify that the intervention arm is not associated with poorer overall survival. But more probably investigators expect patients in the intervention arm to have an improved overall survival mainly link to a decrease in harms due to chemotherapy given near the end of life and to better palliative care. In effect the hypothesis is that showing the life-threatening risks associated with chemotherapy and thus reducing for patients the importance of this treatment will leave room for improved palliative care as shown notably by earlier and more frequent referral to palliative care specialists. If this trial is positive, it will prove the capital role of patient-doctor communication in cancer care and that few differences in communication strategy could improve end of life care and maybe even survival. The impact on the oncology community would be major since the intervention could be easily transposed in all practices at no additional cost. It would also emphasize the importance of communication skills and human relationship in the very technical field of medical oncology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stage IV Lung Cancer
Keywords
Lung cancer, chemotherapy outcome, ethics, information

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
123 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of information
Arm Type
Active Comparator
Arm Description
Information on chemotherapy as done in routine practice following national and international guidelines
Arm Title
Truthful information on chemotherapy risks
Arm Type
Experimental
Arm Description
Information on the potential role of anticancer chemotherapy in worsening life-threatening conditions
Intervention Type
Behavioral
Intervention Name(s)
Truthful information on chemotherapy risks
Intervention Description
One of two trained oncologist will meet the patient and inform him following an interview-guideline
Intervention Type
Behavioral
Intervention Name(s)
Standard of information
Primary Outcome Measure Information:
Title
Number of patients receiving chemotherapy in the last 30 days of life
Time Frame
from date of inclusion until death, assessed up to 1 year
Secondary Outcome Measure Information:
Title
Patient knowledge of the goals of care assessed by questionnaire
Time Frame
1 month after information
Title
Patient knowledge of the goals of care assessed by questionnaire
Time Frame
6 months after information
Title
Number of survivals
Time Frame
at 1 year
Title
Number of appeals to palliative care
Description
Use of palliative care resources
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of onco-palliative meetings
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of use of emergency room, intensive care unit and hospice service in the last month of life
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of unscheduled hospitalizations
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of chemotherapy cycles received
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of days spent in acute care
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Number of days spent in conventional oncology hospital
Time Frame
from date of inclusion until death, assessed up to 1 year
Title
Place of death
Time Frame
at death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: stage IV lung cancer, histologically proven > 18 years old diagnosed during the last 8 weeks systemic therapy indicated Exclusion Criteria: prior systemic therapy for metastatic disease comorbidity not compatible with the inclusion according to the investigator patient has not given its non-objection or not being able to give patient unaffiliated or not beneficiary of a social security scheme
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olivier HUILLARD, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Francois GOLDWASSER, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Cochin
City
Paris
ZIP/Postal Code
75014
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
35802350
Citation
Ryan RE, Connolly M, Bradford NK, Henderson S, Herbert A, Schonfeld L, Young J, Bothroyd JI, Henderson A. Interventions for interpersonal communication about end of life care between health practitioners and affected people. Cochrane Database Syst Rev. 2022 Jul 8;7(7):CD013116. doi: 10.1002/14651858.CD013116.pub2.
Results Reference
derived

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Truthful Information on Chemotherapy and Its Impact on Chemotherapy at the End of Life

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