Olanzapine Improves the Chemotherapy Tolerance of Advanced Gastric Cancer

NCT ID: NCT03575637

Last Updated: 2018-07-03

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-31
• Study Completion Date: 2021-06-30

Brief Summary

To explore whether adding olanzapine to paclitaxel chemotherapy could improve chemotherapy tolerance and improve patient quality of life and prolong treatment failure time (TTF) in advanced gastric cancer after failure of first-line chemotherapy.

This is a multi-center prospective randomized controlled open clinical study. Patients will formally be enrolled after they had been screened and signed informed consent. Baseline examinations will be started after entry into the group. Those who meet the criteria for inclusion and exclusion were dynamically randomized at 1: 1. The experimental group will receive olanzapine and paclitaxel until treatment failure and the control group will receive paclitaxel until treatment failure.

Conditions

Gastric Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Olanzapine intervention group

Patients who have failed first-line treatment of advanced gastric cancer receive second-line treatment with paclitaxel regimen and olanzapine 5 mg QD.

Group Type: EXPERIMENTAL

Olanzapine

Intervention Type: DRUG

Patients who have failed first-line treatment of advanced gastric cancer receive second-line treatment with paclitaxel regimen and olanzapine 5 mg QD.

Control group

Patients who have failed first-line treatment of advanced gastric cancer receive second-line treatment with paclitaxel regimen.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Olanzapine

Patients who have failed first-line treatment of advanced gastric cancer receive second-line treatment with paclitaxel regimen and olanzapine 5 mg QD.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Sign written informed consent;

2. Age more than 18 years of age;

3. Histologically confirmed adenocarcinoma of the stomach or gastroesophageal junction;

4. Locally advanced recurrent or metastatic disease;

5. Have received systemic first-line chemotherapy and confirmed first-line treatment failure (platinum combined with fluorouracils);

6. Subjects' baseline blood routine and biochemical indicators meet the following criteria Hemoglobin ≥90g/L The absolute neutrophil count (ANC) is ≥1.5×10^9/L. Platelets ≥100×10^9/L ALT, AST ≤ 2.5 times the normal upper limit, ≤ 5 times the normal upper limit (with liver metastasis) ALP≤2.5 times normal upper limit, ≤ 5 times normal upper limit (with liver or bone metastases) Serum total bilirubin <1.5 times normal upper limit Serum creatinine <1.5 times normal upper limit Serum albumin ≥30g/L

7. KPS score ≥ 60 points;

8. Life expectancy ≥ 3 months.

Exclusion Criteria

1. Does not meet the above selection criteria;

2. The first-line treatment uses paclitaxel-based drugs;

3. Pregnancy and lactation women;

4. Allergies to research drugs or people with metabolic disorders;

5. History of organ transplantation (including bone marrow autologous transplantation and peripheral stem cell transplantation);

6. Those who have been receiving systemic steroids for a long period of time (Note: Short-term users may be discontinued >2 weeks for inclusion);

7. Brain metastasis;

8. With severe infections need treatment;

9. Accompanied by dysphagia active peptic ulcer complete or incomplete intestinal obstruction active gastrointestinal bleeding perforation etc;

10. Severe liver diseases (such as liver cirrhosis etc.) kidney disease respiratory diseases or chronic diseases such as diabetes high blood pressure that cannot be controlled;

11. Having other malignant tumors within 5 years except non-melanoma skin cancer and cervical cancer in situ;

12. Heart disease with markedly abnormal electrocardiogram or clinical symptoms such as congestive heart failure marked coronary heart disease uncontrolled arrhythmia high blood pressure or previous myocardial infarction within 12 months or cardiac function Class III or IV.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Peking University

OTHER

Sponsor Role: lead

Responsible Party

Shen Lin

Department of Gastrointestinal oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Shen Lin

Role: PRINCIPAL_INVESTIGATOR

Peking University Cancer Hospital & Institute

Locations

Peking University Cancer Hospital & Institute

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Shen Lin

Role: CONTACT

goodjf@163.com

88156561

Facility Contacts

Shen Lin

Role: primary

Other Identifiers

Olanzapine

Identifier Type: -

Identifier Source: org_study_id