RecruitingPhase 3NCT06998758

Megestrol Acetate in Improving Neoadjuvant Chemotherapy-Related Weight Loss in Locally Advanced CRC

Megestrol Acetate in Improving Neoadjuvant Chemotherapy-Related Weight Loss in Patients With Locally Advanced Colorectal Cancer: A Multicenter Randomized Controlled Clinical Trial


Sponsor

Sixth Affiliated Hospital, Sun Yat-sen University

Enrollment

60 participants

Start Date

Nov 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Cancer-associated anorexia, a debilitating condition characterized by progressive appetite loss in oncology patients, contributes to pancytopenia, sarcopenia, and adipose tissue depletion. Megestrol acetate (MA) improves appetite and promotes weight gain through multiple mechanisms, playing a crucial role in the nutritional management of cancer patients. Total mesorectal excision (TME) following neoadjuvant chemotherapy has become the standard treatment strategy for patients with locally advanced colorectal cancer (LACRC). Despite its oncological benefits, neoadjuvant chemotherapy frequently induces grade ≥2 gastrointestinal toxicities (including nausea, emesis, and diarrhea) that exacerbate malnutrition through appetite suppression and negative energy balance. Previous studies have demonstrated that combining MA with first-line maintenance chemotherapy in patients with metastatic colorectal cancer significantly improves appetite, increases body weight, enhances quality of life, and improves prognosis. However, the safety and efficacy of MA during the neoadjuvant treatment phase of LACRC remain unclear. This multicenter, randomized controlled clinical trial aims to evaluate the effects of MA on chemotherapy--related weight loss, anorexia, nutritional status, and chemotherapy tolerance in patients with LACRC undergoing neoadjuvant chemotherapy. Additionally, this study will assess the safety profile of MA in this clinical setting.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding megestrol acetate — a medication that stimulates appetite and helps maintain weight — can prevent significant weight loss in patients with locally advanced colorectal cancer who are receiving chemotherapy (mFOLFOX6) before surgery. **You may be eligible if...** - You are between 18 and 75 years old - You have confirmed colorectal adenocarcinoma with locally advanced disease (Stage cTxN1-2M0) - Your cancer shows a specific molecular feature (pMMR or MSS status) - You are scheduled to receive mFOLFOX6 neoadjuvant chemotherapy - Your ECOG performance status is 0 or 1 **You may NOT be eligible if...** - You have a history of heart rhythm problems, heart attack, or severe heart failure - You have HIV infection or active hepatitis B or C - You have poorly controlled high blood pressure - You have previously received chemotherapy - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMegestrol Acetate

Oral megestrol acetate at 625 mg/day is given from the beginning to the end of neoadjuvant chemotherapy.


Locations(1)

The Sixth Affiliated Hospital of Sun-Yat sen University

Guangzhou, Guangdong, China

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NCT06998758


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