Effect of Multi-modal Intervention Care on Cachexia in Patients With Advanced Cancer Compared to Conventional Management (MIRACLE)

Kil Yeon Lee

Status and phase

Unknown

Phase 2

Conditions

Precachexia

Gastric Cancer

Biliary Tract Cancer

Cachexia

Lung Cancer

Pancreatic Cancer

Colorectal Cancer

Treatments

Combination Product: Multi-modal intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04907864

KHMC-HUMANITAS-01

Details and patient eligibility

About

Background

Cancer Cachexia (CC) is a multi-factorial process characterized by progressive weight loss, muscle mass and fat tissue wasting, and adversely affecting their quality of life and survival in patients with advanced stage of cancer.

Megestrol acetate (MA), which can help maintain body weight in advanced cancer patients, has not been proven to be effective in improving quality of life or lean body mass. Furthermore, its use is often limited due to various adverse event such as Cushing syndrome, adrenal insufficiency, or thromboembolic risk.

CC has a complex and multi-factorial pathophysiology, and there is no established standard treatment.

Hypothesis CC is irreversible once it occurs and is also difficult to suppress its progression with any single treatment modality.

The investigators hypothesized that a multi-modal intervention comprised of anti-inflammation, omega-3-fatty acids, oral nutritional supplement with counselling by nutritionist, physical exercise, psychiatric intervention as well as Bojungikki-tang which mediates immune-modulation and reverse both of chronic inflammation and wasting condition as a complementary and alternative medicine (CAM) could prevent the development of CC or improve the CC in advanced cancer patients during chemotherapy compared to those who received usual supportive.

Full description

[PICOT] Population: Patients with recurrent or metastatic solid cancer (gastric, colorectal, pancreas, biliary tract and lung)

Intervention: Multimodal treatment

Comparison: Conventional palliative care

Outcome: Change of total lean body mass, Change of handgrip strength Time: 12 weeks of study period for each subject during the first- or second-line palliative chemotherapy

Enrollment

112 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients over 19 years of age
Patients diagnosed with gastrointestinal (stomach, esophageal, direct colon, liver, pancreatic biliary tract) cancer and lung cancer
Patients receiving first- or second-line palliative chemotherapy
ECOG PS 0-2
Patients who were classified as normal, precachexia or cachexia according to the cachexia classification criteria
- Normal: Neither pre-cachexia Nor cachexia
- Precachexia: Weight loss ≤5%, Anorexia or glucose intolerance in last 6 months
- Cachexia: Weight loss >5%, or BMI <20 with weight loss >2% in last 6 months
Adequate organ functions

Exclusion criteria

Patients with history of heart failure or currently being treated for heart failure
Patients with SBP of 160 mmHg or higher or DBP of 100 mmHg or higher despite antihypertensive medication
Patients with or have a history of bronchial asthma
Patients with bowel obstruction
Patients who have taken appetite stimulants or anabolic or anti-catabolic agents (eg. Megestrol acetate, progestational agents, etc.) within 30 days prior to the study enrollment
Patients who received steroid treatment (> 10 mg/d prednisolone or equivalent) within 3 months prior to the study enrollment
Patients who have taken nonsteroidal anti-inflammatory drugs or aspirin continuously for more than 1 week
Patients with problems with taking non-steroidal anti-inflammatory drugs (NSAIDs) or those with uncontrolled diabetes due to digestive system diseases (gastric ulcer, gastrointestinal bleeding, etc.)
Patients who are pregnant or breastfeeding, who have not used proper contraception (oral, injection, infusion or hormonal contraceptive methods, intrauterine devices and blocking methods)
Patients who are taking anticoagulants (e.g. warfarin or heparin)
Patients who have difficulty in oral administration
Patients who have a history of hypersensitivity reactions such as asthma, hives, or allergic reactions to drugs containing ibuprofen, aspirin, and other nonsteroidal anti-inflammatory drugs (including COX-2 inhibitors)
Patients who showed clinically significant hypersensitivity reactions to investigational products