Effect of Geriatric Intervention in Frail Patients with Gastric, Biliary, and Pancreatic Cancer Receiving Palliative Chemotherapy
NCT ID: NCT06040801
Last Updated: 2025-02-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
138 participants
INTERVENTIONAL
2021-12-01
2026-07-31
Brief Summary
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Although the benefit of palliative chemotherapy seems to be the same for elderly and young cancer patients in clinical study, elderly patients are less frequently treated with chemotherapy or treated with suboptimal dosage. Elderly patients do not receive palliative chemotherapy because concerns of elder age, comorbidity, poor performance, lack of social/economic support and worry about treatment toxicities.
The increase in life expectancy of the general population resulted in an increase in the number of elderly patients with cancers referred for palliative chemotherapy. Overtreatment may result in high mortality due to disregard of the aging patients' frailty; on the other hand, under-treatment resulting from over-concern regarding their ability to tolerate treatment, may compromise the survival outcome. Therefore, the appropriately selection of geriatric cancer patients for palliative chemotherapy has to be addressed urgently.
Frailty is a progressive decline of physiological reserve leading to multiple functional disability and increases vulnerability to subsequent morbidity and mortality. Frailty is associated with treatment toxicity, chemotherapy tolerance, and survival outcome in clinical oncology. Recent randomized study reported geriatric intervention significantly improved chemotherapy tolerance in elderly patients. Therefore, the American Cancer Association has recommended routine geriatric assessment and intervention in oncogeriatric patients upon providing antitumor treatments. However, the effect of geriatric intervention on chemotherapy tolerance is seldom in Taiwan.
This study is an open, randomized, prospective trial to evaluate the effect of geriatric intervention on chemotherapy tolerance in patients with unresectable gastric, biliary, and pancreatic cancer. All patients with receive frailty assessment within 7 days before initiation of first cycle palliative chemotherapy followed by geriatric intervention. The study aim is to compare for chemotherapy tolerance, treatment-related toxicity, and quality of life after completion 3 months chemotherapy treatment course between frail and non-frail patients. This study also aims to explore the effect of geriatric intervention of treatment tolerance, treatment-related toxicity, and quality of life in frail patients with gastric, biliary, and pancreatic cancer receiving palliative chemotherapy.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Frail group
All patients receive a frailty assessment within 7 days before initiating the first cycle of palliative chemotherapy, followed by geriatric intervention. Patients exhibiting impairments in at least two dimensions are considered frail. The frail group will receive management and recommendations based on the specific impairment domain.
Frailty intervention measures
Providing management and recommendations based on the specific impairment domain.
Assessment domain:
* Functional status
* Nutrition
* Comorbidity
* Mobility/Falls
* Mood
* Cognition
* Polypharmacy
* Social support.
Non-frail group
All patients receive a frailty assessment within 7 days before initiating the first cycle of palliative chemotherapy, followed by geriatric intervention. Patients exhibiting impairments in at least two dimensions are considered frail. The non-frail group will not receive additional interventions, but the clinical physicians will still provide appropriate treatment based on the patient's condition.
No interventions assigned to this group
Interventions
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Frailty intervention measures
Providing management and recommendations based on the specific impairment domain.
Assessment domain:
* Functional status
* Nutrition
* Comorbidity
* Mobility/Falls
* Mood
* Cognition
* Polypharmacy
* Social support.
Eligibility Criteria
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Inclusion Criteria
* The patient must sign the informed consent form.
* Estimated survival period of more than 3 months.
* Conscious and able to communicate verbally or in writing, and willing to cooperate with invasive procedures.
Exclusion Criteria
* Patients receiving concurrent other anticancer treatments (radiation or surgery).
* Patients with multiple types of cancer requiring simultaneous treatment.
* Patients who have previously participated in this study during a prior chemotherapy regimen.
65 Years
ALL
No
Sponsors
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Chang Gung Memorial Hospital
OTHER
Responsible Party
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Locations
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Chang Gung Memorial Hospital
Taoyuan District, Taiwan, Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CMRPG3L1611
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
202002181B0A3
Identifier Type: -
Identifier Source: org_study_id
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