Assessing Cachexia Status in Pakistani Cancer Patients Using the Mini-CASCO Score
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 140
- Locations
- 1
- Primary Endpoint
- Change in cachexia severity measured by the Mini-CASCO composite score
Study Overview
Brief Summary
In this parallel, two-arm randomized controlled trial (RCT), 140 female patients with advanced-stage breast cancer and clinical features of cachexia will be randomized using block-stratified allocation into an intervention group (n = 70) and a control group (n = 70). The intervention group will receive standard oncological care along with personalized dietary counseling and monthly nutritional monitoring for six months, whereas the control group will receive standard care alone. The severity of cachexia will be assessed at baseline and follow-up using the Mini-CASCO tool, which will evaluate five domains: body composition, inflammatory-metabolic profile (C-reactive protein, serum albumin, hemoglobin, absolute lymphocyte count), physical performance (Eastern Cooperative Oncology Group [ECOG] status), anorexia (Simplified Nutritional Appetite Questionnaire [SNAQ]), and quality of life (European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 [EORTC QLQ-C30]).
Detailed Description
This randomized controlled trial evaluates the impact of individualized dietary counseling with ongoing nutritional monitoring on cancer cachexia severity in women with advanced breast cancer. Cancer cachexia is a multifactorial syndrome characterized by muscle wasting, anorexia, inflammation, and reduced functional status, significantly impairing quality of life and treatment tolerance. Despite its clinical relevance, targeted interventions for cachexia remain underutilized in routine oncology care.
The study is designed as a two-arm, parallel-group trial comparing standard oncological care alone with standard care plus a tailored nutritional intervention. The intervention is structured to address energy and protein intake requirements using individualized plans developed by a clinical dietitian. It incorporates scheduled nutritional counseling sessions, structured adherence monitoring through food logs and checklists, and reinforcement strategies including light physical activity promotion and psychosocial support.
To ensure methodological rigor, the study employs block-stratified randomization with concealed allocation using opaque, sealed envelopes. While blinding of participants and care providers is not feasible due to the nature of the intervention, outcome assessors and data analysts will be blinded to minimize bias. The primary outcome-change in cachexia severity over six months-will be evaluated using a validated multidimensional tool that captures clinical, functional, and patient-reported parameters.
Data will be entered into a secure, password-protected database with built-in quality control processes, including double data entry and discrepancy checks. Missing data will be handled using multiple imputation under the assumption of missing at random. Statistical analyses will be conducted on an intention-to-treat basis, with appropriate covariate adjustment and effect size reporting.
This trial is expected to provide practical evidence on the feasibility and effectiveness of structured, individualized nutritional interventions as part of supportive oncology care in resource-constrained settings.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 20 Years to 60 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Female patients aged 20 to 60 years
- •Histologically confirmed advanced breast cancer
- •Documented unintentional weight loss of ≥5% over the past 6 months
- •Hemoglobin level <12 g/dL or average daily energy intake <1500 kcal/day
- •Ability to provide written and verbal informed consent
Exclusion Criteria
- •Malnutrition due to non-cancer causes (e.g., chronic starvation, eating disorders)
- •Presence of chronic gastrointestinal or endocrine disorders affecting nutritional status (e.g., Crohn's disease, Cushing's syndrome)
- •Current pregnancy or lactation
- •Concurrent diagnosis of another malignancy
- •Any condition that, in the opinion of the investigator, may interfere with study participation or outcomes (e.g., severe psychiatric illness, cognitive impairment)
Arms & Interventions
Standard Oncological Care + Tailored Dietary Counseling + Nutritional Monitoring
Participants in the intervention group will receive:
Standard oncological care (including chemotherapy and other routine cancer treatments) plus
Individualized dietary counseling: Tailored nutrition plans developed by a clinical dietitian based on energy (25-30 kcal/kg/day) and protein (1.2-1.5 g/kg/day) needs, adjusted for clinical status, dietary tolerance, and treatment side effects.
Regular nutritional monitoring: Counseling sessions every 15-21 days over a period of six months.
Dietary adherence tracking: Using structured food records and goal adherence checklists.
Light physical activity guidance: Encouragement to engage in low-intensity activity appropriate to patient capacity.
Psychosocial support: Sessions with a certified clinical psychologist to address emotional distress, fatigue, and anorexia.
Adherence criteria: Defined as attending ≥75% of sessions and meeting ≥80% of dietary goals.
Intervention: Standard Oncological Care + Tailored Dietary Counseling + Nutritional Monitoring (Behavioral)
Standard Oncological Care
Participants in this group will receive standard oncological care only, including chemotherapy and other routine cancer treatments, without additional dietary or psychosocial interventions.
Intervention: Standard Oncological Care + Tailored Dietary Counseling + Nutritional Monitoring (Behavioral)
Outcomes
Primary Outcomes
Change in cachexia severity measured by the Mini-CASCO composite score
Time Frame: From baseline to 6 months
The primary outcome will be the change in cachexia severity from baseline to six months, measured using Mini-CASCO, which includes: Body Composition (40%): Body weight and lean body mass assessed by digital scale and BIA. Inflammatory/Metabolic/Immune Status (20%): CRP, albumin, hemoglobin, and lymphocyte count. Physical Performance (15%): ECOG scale, handgrip strength, stair climbing, and fatigue assessments. Anorexia (15%): SNAQ scores, 24-hour recall, and food frequency questionnaires. The Mini-Cancer Cachexia Score (Mini-CASCO) is a validated multidimensional scoring system that assesses cancer cachexia severity using five domains: body composition, inflammation/metabolism, physical performance, anorexia, and quality of life. The total score ranges from 0 to 100, with higher scores indicating more severe cachexia.
Secondary Outcomes
- Change in Quality of Life (EORTC QLQ-C30, Urdu version)(From baseline to 6 months)
- Change in Body Weight(From baseline to 6 months)
- Change in ECOG Performance Status(From baseline to 6 months)
- Change in SNAQ Score (Simplified Nutritional Appetite Questionnaire)(From baseline to 6 months)
- Change in Lean Body Mass(From baseline to 6 months)
- Change in C-Reactive Protein (CRP)(From baseline to 6 months)
Investigators
Junaid Jamshed
Clinical Research Coordinator
Pakistan Society of Pediatric Oncology