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The Role of Early Systematic Best Palliative Care Versus on Request Palliative Care Consultation During Standard Oncologic Treatment for Patients With Advanced Gastric or Pancreatic Cancers: a Randomized, Controlled, Multicenter Trial.

Primary Purpose

Pancreatic Neoplasm, Gastric Neoplasm

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Interventional arm: Early best palliative care
Sponsored by
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Pancreatic Neoplasm focused on measuring gastric neoplasm, pancreatic neoplasm, advanced, palliative care

Eligibility Criteria

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

Inclusion Criteria:

  1. diagnosis of inoperable locally advanced and/or metastatic gastric or pancreatic cancers within the previous eight weeks, any T, any N, M+ or T4 inoperable (neoadjuvant excluded);
  2. patients eligible for chemotherapy and/or new target drugs treatments for metastatic or advanced disease;
  3. ECOG PS 0-2 (Appendix A);
  4. life expectancy >2 months;
  5. both sex;
  6. age ≥18 years;
  7. all ethnic background;
  8. subjects who are, in the opinion of the Investigator, able to understand this study and to cooperate with the study procedures;
  9. written informed consent (Appendix B);
  10. palliative care visit must be performed by a dedicated physician/team different from the medical oncology group.

Exclusion Criteria:

  1. patients already receiving care from the palliative care service;
  2. prior chemotherapy and/or new target drugs treatments for metastatic or advanced disease.

Sites / Locations

  • Palliative Care Clinic IRCCS IRST
  • U.O Oncologia medica
  • S. Donato, Arezzo
  • Centro di Riferimento Oncologico CRO
  • Ospedale degli Infermi,
  • Ospedale Businco, Cagliari
  • Policlinico Universitario, Cagliari
  • ASL AL, Casale Monferrato
  • Irst-Cesena
  • Sant'Anna
  • PO M.Santo, Cosenza
  • Istituti Ospitalieri, Cremona
  • Sant'Anna, Ferrara
  • S.Giovanni Di Dio, Firenze
  • S.Maria Annunziata,
  • E.O. Galliera
  • Aulss 12,
  • Istituto Nazionale Tumori, Milano
  • Ospedale Sacco, Milano
  • S.PAOLO
  • IOV
  • San Matteo
  • Guglielmo da Saliceto
  • Arcispedale S. Maria Nuova
  • Fatebenefratelli,
  • SS Trinità,
  • Gradinego
  • AOP 9, Trapani
  • S. Maria Gruccia, Valdarno
  • AULSS 12, Venezia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Interventional arm

Standard arm

Arm Description

Interventional arm

Standard arm

Outcomes

Primary Outcome Measures

Quality of Life (QoL)
It is the change in the score from T0 (day of enrollment) to T1 (12±3 weeks) on the Trial Outcome Index (TOI) [which is the sum of the scores of specific subscale FACT-Ga or FACT-Hep Functional Assessment of Cancer Therapy-Gastric cancer (FACT-Ga) and Functional Assessment of Cancer Therapy-Hepatobiliary cancers (FACT-Hep) scales, concerning physical symptoms, physical and functional well being].

Secondary Outcome Measures

Hospital Anxiety and Depression Scale (HADS)
Mood will be assessed with the use of Hospital Anxiety and Depression Scale (HADS), which is 14-item instrument composed of two subscales and screens for symptoms of anxiety and depression.
Impact of families satisfaction
The impact of families satisfaction about care will be evaluated by an Italian version of FAMCARE questionnaire.
Overall survival (OS)
It is the time from the date of randomization to the date of death due to any cause.

Full Information

First Posted
November 22, 2013
Last Updated
November 8, 2018
Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
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1. Study Identification

Unique Protocol Identification Number
NCT01996540
Brief Title
The Role of Early Systematic Best Palliative Care Versus on Request Palliative Care Consultation During Standard Oncologic Treatment for Patients With Advanced Gastric or Pancreatic Cancers: a Randomized, Controlled, Multicenter Trial.
Official Title
The Role of Early Systematic Best Palliative Care Versus on Request Palliative Care Consultation During Standard Oncologic Treatment for Patients With Advanced Gastric or Pancreatic Cancers: a Randomized, Controlled, Multicenter Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
August 2012 (Actual)
Primary Completion Date
November 2, 2017 (Actual)
Study Completion Date
November 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Title: The role of early systematic best palliative care versus on request palliative care consultation during standard oncologic treatment for patients with advanced gastric or pancreatic cancers: a randomized, controlled, multicenter trial. Description of Study Treatment: Interventional arm Patients will receive standard oncologic care and will be assigned to early systematic best palliative care. They will meet a member of the palliative care team within 2 weeks after enrolment. Thereafter, they shall be visited by a palliative care team member every 2 weeks until death. Patients assigned to this experimental arm will be evaluated if the total of palliative care visits between T0 (day of enrollment) and T1 (12±3 weeks) is ≥3. Palliative care visits and intervention has to be oriented by the General guidelines for palliative care: specific attention will be paid to assessing physical and psychosocial symptoms, establishing goals of care, assisting decision making regarding treatment, and coordinating care on the basis of the individual needs of the patients. The doctor expert in palliative care, with regular visits in the experimental arm, must be a physician dedicated full time to palliative care, that can directly prescribe drugs and other interventions, and with a particular attention to physical, psychological, and spiritual needs. Palliative care doctor must have the possibility to decide about organizational arrangements. He has to perform the palliative care visit according to Temel indications. Standard arm Patients will receive standard oncologic care and will be assigned to on request palliative care consultation. They will be not scheduled to meet with the palliative care service unless a meeting will be requested by the patients, the family, or the oncologist. After the time of evaluation (T1) patients will be followed by the palliative care services as needed. Patient completes QoL (Quality of Life) and mood questionnaires at baseline and at 12 weeks ± 3. Patients will receive standard antineoplastic treatment in both arms of the study according to best clinical practice in each participating centre.
Detailed Description
Title: The role of early systematic best palliative care versus on request palliative care consultation during standard oncologic treatment for patients with advanced gastric or pancreatic cancers: a randomized, controlled, multicenter trial. Short Title/Acronym: Early palliative care Protocol Code: IRST 100.08 Study Design: randomized, controlled, multicenter trial Study Duration: 2 years Number of Subjects: 240 Description of Study Treatment: Interventional arm Patients will receive standard oncologic care and will be assigned to early systematic best palliative care. They will meet a member of the palliative care team within 2 weeks after enrolment. Thereafter, they shall be visited by a palliative care team member every 2 weeks until death. Patients assigned to this experimental arm will be evaluated if the total of palliative care visits between T0 (day of enrollment) and T1 (12±3 weeks) is ≥3. Palliative care visits and intervention has to be oriented by the General guidelines for palliative care: specific attention will be paid to assessing physical and psychosocial symptoms, establishing goals of care, assisting decision making regarding treatment, and coordinating care on the basis of the individual needs of the patients. The doctor expert in palliative care, with regular visits in the experimental arm, must be a physician dedicated full time to palliative care, that can directly prescribe drugs and other interventions, and with a particular attention to physical, psychological, and spiritual needs. Palliative care doctor must have the possibility to decide about organizational arrangements. He has to perform the palliative care visit according to Temel indications. Standard arm Patients will receive standard oncologic care and will be assigned to on request palliative care consultation. They will be not scheduled to meet with the palliative care service unless a meeting will be requested by the patients, the family, or the oncologist. After the time of evaluation (T1) patients will be followed by the palliative care services as needed. Patient completes QoL (Quality of Life) and mood questionnaires at baseline and at 12 weeks ± 3. Patients will receive standard antineoplastic treatment in both arms of the study according to best clinical practice in each participating centre. Primary Objective: To assess the effects on quality of life and clinical symptoms of introducing early systematic palliative care versus on request palliative care consultation during standard oncological care on quality of life. Secondary Objectives: To assess the impact of early palliative care on symptom burden and mood. To assess the impact of families satisfaction about care. To compare the use of health services, including anticancer therapy, medication prescriptions, referral to hospice, hospital admissions, emergency department visits, and the location of death between study arms. To compare overall survival. Statistical Methodology: Primary endpoint is the change in the score from T0 to T1 on the Trial Outcome Index (TOI), which is the sum of the scores of specific subscale FACT-Ga or FACT-Hep concerning physical symptoms, and physical and functional well being. Secondary endpoints are the change in the percentage of patients with anxiety and/or depression form T0 to T1 on the Mood questionnaire; the impact of families satisfaction about care; the use of health services, including anticancer therapy, medication prescriptions, referral to hospice, hospital admissions, emergency department visits, and the location of death between study arms; the overall survival. For each type of cancer (gastric or pancreatic), we estimate that with 120 patients the study would have 80% power to detect a significant between-group difference in the change in the TOI score from T0 to T1, with a medium effect size of 0.5 standard deviation. A total of 240 patients will be enrolled.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasm, Gastric Neoplasm
Keywords
gastric neoplasm, pancreatic neoplasm, advanced, palliative care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
394 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Interventional arm
Arm Type
Experimental
Arm Description
Interventional arm
Arm Title
Standard arm
Arm Type
No Intervention
Arm Description
Standard arm
Intervention Type
Other
Intervention Name(s)
Interventional arm: Early best palliative care
Other Intervention Name(s)
Early best palliative care
Intervention Description
Patients will receive standard oncologic care and will be assigned to early systematic best palliative care. They will meet a member of the palliative care team within 2 weeks after enrolment. Thereafter, they shall be visited by a palliative care team member every 2 weeks until death.
Primary Outcome Measure Information:
Title
Quality of Life (QoL)
Description
It is the change in the score from T0 (day of enrollment) to T1 (12±3 weeks) on the Trial Outcome Index (TOI) [which is the sum of the scores of specific subscale FACT-Ga or FACT-Hep Functional Assessment of Cancer Therapy-Gastric cancer (FACT-Ga) and Functional Assessment of Cancer Therapy-Hepatobiliary cancers (FACT-Hep) scales, concerning physical symptoms, physical and functional well being].
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Hospital Anxiety and Depression Scale (HADS)
Description
Mood will be assessed with the use of Hospital Anxiety and Depression Scale (HADS), which is 14-item instrument composed of two subscales and screens for symptoms of anxiety and depression.
Time Frame
24 months
Title
Impact of families satisfaction
Description
The impact of families satisfaction about care will be evaluated by an Italian version of FAMCARE questionnaire.
Time Frame
24 months
Title
Overall survival (OS)
Description
It is the time from the date of randomization to the date of death due to any cause.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of inoperable locally advanced and/or metastatic gastric or pancreatic cancers within the previous eight weeks, any T, any N, M+ or T4 inoperable (neoadjuvant excluded); patients eligible for chemotherapy and/or new target drugs treatments for metastatic or advanced disease; ECOG PS 0-2 (Appendix A); life expectancy >2 months; both sex; age ≥18 years; all ethnic background; subjects who are, in the opinion of the Investigator, able to understand this study and to cooperate with the study procedures; written informed consent (Appendix B); palliative care visit must be performed by a dedicated physician/team different from the medical oncology group. Exclusion Criteria: patients already receiving care from the palliative care service; prior chemotherapy and/or new target drugs treatments for metastatic or advanced disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marco Maltoni, MD
Organizational Affiliation
IRST IRCCS, Meldola
Official's Role
Principal Investigator
Facility Information:
Facility Name
Palliative Care Clinic IRCCS IRST
City
Meldola
State/Province
FC
ZIP/Postal Code
47014
Country
Italy
Facility Name
U.O Oncologia medica
City
Lugo
State/Province
RA
ZIP/Postal Code
48022
Country
Italy
Facility Name
S. Donato, Arezzo
City
Arezzo
Country
Italy
Facility Name
Centro di Riferimento Oncologico CRO
City
Aviano
Country
Italy
Facility Name
Ospedale degli Infermi,
City
Biella
Country
Italy
Facility Name
Ospedale Businco, Cagliari
City
Cagliari
Country
Italy
Facility Name
Policlinico Universitario, Cagliari
City
Cagliari
Country
Italy
Facility Name
ASL AL, Casale Monferrato
City
Casale Monferrato
Country
Italy
Facility Name
Irst-Cesena
City
Cesena
Country
Italy
Facility Name
Sant'Anna
City
Como
Country
Italy
Facility Name
PO M.Santo, Cosenza
City
Cosenza
Country
Italy
Facility Name
Istituti Ospitalieri, Cremona
City
Cremona
Country
Italy
Facility Name
Sant'Anna, Ferrara
City
Ferrara
Country
Italy
Facility Name
S.Giovanni Di Dio, Firenze
City
Firenze
Country
Italy
Facility Name
S.Maria Annunziata,
City
Firenze
Country
Italy
Facility Name
E.O. Galliera
City
Genova
Country
Italy
Facility Name
Aulss 12,
City
Mestre
Country
Italy
Facility Name
Istituto Nazionale Tumori, Milano
City
Milano
Country
Italy
Facility Name
Ospedale Sacco, Milano
City
Milano
Country
Italy
Facility Name
S.PAOLO
City
Milano
Country
Italy
Facility Name
IOV
City
Padova
Country
Italy
Facility Name
San Matteo
City
Pavia
Country
Italy
Facility Name
Guglielmo da Saliceto
City
Piacenza
Country
Italy
Facility Name
Arcispedale S. Maria Nuova
City
Reggio Emilia
Country
Italy
Facility Name
Fatebenefratelli,
City
Roma
Country
Italy
Facility Name
SS Trinità,
City
Sora - Frosinone
Country
Italy
Facility Name
Gradinego
City
Torino
Country
Italy
Facility Name
AOP 9, Trapani
City
Trapani
Country
Italy
Facility Name
S. Maria Gruccia, Valdarno
City
Valdarno
Country
Italy
Facility Name
AULSS 12, Venezia
City
Venezia
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
30357555
Citation
Scarpi E, Dall'Agata M, Zagonel V, Gamucci T, Berte R, Sansoni E, Amaducci E, Broglia CM, Alquati S, Garetto F, Schiavon S, Quadrini S, Orlandi E, Casadei Gardini A, Ruscelli S, Ferrari D, Pino MS, Bortolussi R, Negri F, Stragliotto S, Narducci F, Valgiusti M, Farolfi A, Nanni O, Rossi R, Maltoni M; Early Palliative Care Italian Study Group (EPCISG). Systematic vs. on-demand early palliative care in gastric cancer patients: a randomized clinical trial assessing patient and healthcare service outcomes. Support Care Cancer. 2019 Jul;27(7):2425-2434. doi: 10.1007/s00520-018-4517-2. Epub 2018 Oct 24.
Results Reference
derived
PubMed Identifier
27821313
Citation
Maltoni M, Scarpi E, Dall'Agata M, Schiavon S, Biasini C, Codeca C, Broglia CM, Sansoni E, Bortolussi R, Garetto F, Fioretto L, Cattaneo MT, Giacobino A, Luzzani M, Luchena G, Alquati S, Quadrini S, Zagonel V, Cavanna L, Ferrari D, Pedrazzoli P, Frassineti GL, Galiano A, Casadei Gardini A, Monti M, Nanni O; Early Palliative Care Italian Study Group (EPCISG). Systematic versus on-demand early palliative care: A randomised clinical trial assessing quality of care and treatment aggressiveness near the end of life. Eur J Cancer. 2016 Dec;69:110-118. doi: 10.1016/j.ejca.2016.10.004. Epub 2016 Nov 4. Erratum In: Eur J Cancer. 2017 Feb;72 :272-273.
Results Reference
derived
PubMed Identifier
27472648
Citation
Maltoni M, Scarpi E, Dall'Agata M, Zagonel V, Berte R, Ferrari D, Broglia CM, Bortolussi R, Trentin L, Valgiusti M, Pini S, Farolfi A, Casadei Gardini A, Nanni O, Amadori D; Early Palliative Care Italian Study Group (EPCISG). Systematic versus on-demand early palliative care: results from a multicentre, randomised clinical trial. Eur J Cancer. 2016 Sep;65:61-8. doi: 10.1016/j.ejca.2016.06.007. Epub 2016 Jul 26.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
study publication
Available IPD/Information URL
https://www.ncbi.nlm.nih.gov/pubmed/27472648
Available IPD/Information Comments
Maltoni M et al Systematic versus on-demand early palliative care: results from a multicentre, randomised clinical trial. Eur J Cancer 2016 Sep;65:61-8
Available IPD/Information Type
study publication
Available IPD/Information URL
https://www.ncbi.nlm.nih.gov/pubmed/27821313
Available IPD/Information Comments
Maltoni M et al Systematic versus on-demand early palliative care: A randomised clinical trial assessing quality of care and treatment aggressiveness near the end of life. Eur J Cancer 2016 Dec;69:110-118.
Available IPD/Information Type
study publication
Available IPD/Information URL
https://doi.org/10.1007/s00520-018-4517-2
Available IPD/Information Comments
Scarpi E. et al Systematic vs. on-demand early palliative care in gastric cancer patients: a randomized clinical trial assessing patient and healthcare service outcomes

Learn more about this trial

The Role of Early Systematic Best Palliative Care Versus on Request Palliative Care Consultation During Standard Oncologic Treatment for Patients With Advanced Gastric or Pancreatic Cancers: a Randomized, Controlled, Multicenter Trial.

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