Orlistat Overcoming Third-generation EGFR-TKI Resistance (OOTER)

Clinical Study on the Safety and Efficacy of Orlistat in Third-generation EGFR-TKI Resistance

EGFR mutation positivity accounts for 50% of lung adenocarcinoma cases. Multiple clinical trials, represented by FLAURA, AENEAS, and FURLONG studies, have confirmed that third-generation EGFR-TKI can provide significant benefits to patients with EGFR sensitive mutations and has become the first-line preferred treatment for EGFR mutation positive NSCLC, with a median PFS of around 19 and OS of around 38 months. These large-scale Phase III studies have confirmed the excellent efficacy of third-generation EGFR-TKI in EGFR mutation positive patients. However, regardless of the targeted drug, resistance will occur within less than 2 years. Blood test data for first-line treatment with osimertinib showed that the most common forms of resistance were secondary MET amplification (20%), EGFR C797S mutation (8%), PIK3CA, Her-2 amplification, and so on. The mechanism of resistance is complex and has many factors. Currently, for the treatment of third-generation EGFR-TKI resistance, the IMPOWER150 and ORIENTAL31 treatment modes are commonly used. Although the combination of these four drugs has good efficacy, the side effects are significant. Some patients are unwilling to undergo chemotherapy due to physical problems and hope to continue taking targeted drugs orally. Orlistat is a long-acting and potent specific gastrointestinal lipase inhibitor that can directly block the absorption of body fat. It is commonly used for weight loss in clinical practice and is relatively inexpensive. Our project team found in vitro and in vivo data that orlistat can effectively promote sensitivity to osimertinib. The combination of orlistat and osimertinib can overcome osimertinib resistance without significant toxic side effects. For patients who are unwilling to undergo chemotherapy and require continued oral targeted therapy, the investigators attempted to add orlistat to see if it can improve resistance.

Study Overview

• Status: Not yet recruiting
• Conditions: Lung Adenocarcinoma; Osimertinib
• Intervention / Treatment: Drug: Orlistat 120 mg

• Study Type: Interventional
• Enrollment (Estimated): 36
• Phase: Phase 2

Contacts and Locations

• Study Contact: Name: Ping Peng, PhD; Phone Number: 008613429818576; Email: pengpingtj@163.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Previously received three generations of systemic TKI treatment and developed resistance (including Axitinib, Amitinib, Fumatinib, Bevatinib, Lazetinib, etc.);
2. General condition score ECOG 0-2 points;
3. Expected survival period of more than 3 months;

4. Laboratory examination:

   ① WBC≥3.5×109／L，ANC≥1.5×109／L，PLT≥80×109／L， Hb≥90g/L；

   ② Blood BUN and creatinine are within 1.5 times the upper limit of normal values;

   ③ TBIL ≤ 1.5 times the upper limit of normal value;

   ④ ALT and AST ≤ 2.5 times the upper limit of normal values; Patients with liver metastasis should not exceed 5 times the upper limit of normal values;

   ⑤ Normal coagulation function (PT, APTT within 1.5 times the upper limit of normal range).

5. The patient requests to continue taking targeted drugs orally
6. Voluntarily sign the informed consent form, with expected compliance.

Exclusion Criteria:

1. Suffering from serious medical diseases, including serious heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, serious infection, and active gastrointestinal ulcer;
2. A large amount of pleural and pericardial effusion requires immediate treatment;
3. Brain metastases with clinical symptoms;
4. Pregnant or lactating women;
5. The patient is able to tolerate chemotherapy and is willing to accept it

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: orlistat group; For patients who are resistant to osimertinib and require continued oral administration of targeted drugs, we will add orlistat	Drug: Orlistat 120 mg; Orlistat 120 mg po tid

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
ORR	Overall response rate (ORR) was defined as the combination of CR and PR.	At the end of cycle 3 (each cycle is 21 days)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Safety (Rate of grade 3 and higher grade treatment-related adverse events)	Adverse events will be evaluated and recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 5.0)	From date of treatment allocation until treatment completion 30 days

Collaborators and Investigators

• Sponsor: Ping Peng
• Collaborators: Hubei Cancer Hospital

Study record dates

Study Major Dates

• Study Start (Estimated): February 16, 2025
• Primary Completion (Estimated): May 15, 2025
• Study Completion (Estimated): November 15, 2025

Study Registration Dates

• First Submitted: February 3, 2025
• First Submitted That Met QC Criteria: February 8, 2025
• First Posted (Actual): March 25, 2025

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: February 10, 2025
• Last Verified: February 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Site; Neoplasms; Neoplasms by Histologic Type; Neoplasms, Glandular and Epithelial; Adenocarcinoma; Respiratory Tract Neoplasms; Thoracic Neoplasms; Lung Neoplasms; Carcinoma; Adenocarcinoma of Lung; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Anti-Obesity Agents; Lipid Regulating Agents; Orlistat
• Other Study ID Numbers: EGFR-TKI resistance study

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No