Truthful Information on Chemotherapy and Its Impact on Chemotherapy at the End of Life
HIPPOCRATE
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
2 other identifiers
interventional
123
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2016
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 11, 2015
CompletedFirst Posted
Study publicly available on registry
November 17, 2015
CompletedStudy Start
First participant enrolled
July 15, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 15, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
October 15, 2020
CompletedNovember 20, 2025
September 1, 2025
4.3 years
November 11, 2015
November 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of patients receiving chemotherapy in the last 30 days of life
from date of inclusion until death, assessed up to 1 year
Secondary Outcomes (11)
Patient knowledge of the goals of care assessed by questionnaire
1 month after information
Patient knowledge of the goals of care assessed by questionnaire
6 months after information
Number of survivals
at 1 year
Number of appeals to palliative care
from date of inclusion until death, assessed up to 1 year
Number of onco-palliative meetings
from date of inclusion until death, assessed up to 1 year
- +6 more secondary outcomes
Study Arms (2)
Standard of information
ACTIVE COMPARATORInformation on chemotherapy as done in routine practice following national and international guidelines
Truthful information on chemotherapy risks
EXPERIMENTALInformation on the potential role of anticancer chemotherapy in worsening life-threatening conditions
Interventions
One of two trained oncologist will meet the patient and inform him following an interview-guideline
Eligibility Criteria
You may qualify if:
- stage IV lung cancer, histologically proven
- \> 18 years old
- diagnosed during the last 8 weeks
- systemic therapy indicated
You may not qualify if:
- prior systemic therapy for metastatic disease
- patient has not given its non-objection or not being able to give
- patient unaffiliated or not beneficiary of a social security scheme
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Assistance Publique - Hôpitaux de Parislead
- National Cancer Institute, Francecollaborator
- URC-CIC Paris Descartes Necker Cochincollaborator
Study Sites (1)
Hôpital Cochin
Paris, Paris, 75014, France
Related Publications (1)
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.
PMID: 35802350DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Olivier HUILLARD, MD, PhD
Assistance Publique - Hôpitaux de Paris
- PRINCIPAL INVESTIGATOR
Francois GOLDWASSER, MD, PhD
Assistance Publique - Hôpitaux de Paris
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 11, 2015
First Posted
November 17, 2015
Study Start
July 15, 2016
Primary Completion
October 15, 2020
Study Completion
October 15, 2020
Last Updated
November 20, 2025
Record last verified: 2025-09