NCT02606149

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
123

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2016

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 11, 2015

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 17, 2015

Completed
8 months until next milestone

Study Start

First participant enrolled

July 15, 2016

Completed
4.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 15, 2020

Completed
Last Updated

November 20, 2025

Status Verified

September 1, 2025

Enrollment Period

4.3 years

First QC Date

November 11, 2015

Last Update Submit

November 17, 2025

Conditions

Keywords

Lung cancerchemotherapy outcomeethicsinformation

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 COMPARATOR

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

Behavioral: Standard of information

Truthful information on chemotherapy risks

EXPERIMENTAL

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

Behavioral: Truthful information on chemotherapy risks

Interventions

One of two trained oncologist will meet the patient and inform him following an interview-guideline

Truthful information on chemotherapy risks
Standard of information

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Hôpital Cochin

Paris, Paris, 75014, France

Location

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.

MeSH Terms

Conditions

Lung Neoplasms

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Olivier HUILLARD, MD, PhD

    Assistance Publique - Hôpitaux de Paris

    STUDY CHAIR
  • Francois GOLDWASSER, MD, PhD

    Assistance Publique - Hôpitaux de Paris

    PRINCIPAL INVESTIGATOR

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

Locations