A Phase II Study of Perioperative Paclitaxel in Patients With Gastric Adenocarcinoma and Carcinomatosis or Positive Cytology

NCT ID: NCT05977998

Last Updated: 2025-11-19

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-08
• Study Completion Date: 2030-10-31

Brief Summary

To learn about the effects of paclitaxel and gastrectomy (surgery to remove all or part of the stomach) on improving outcomes in patients with gastric cancer.

Detailed Description

Primary Objectives:

To assess overall survival from the date of diagnosis in subjects with stage IV gastric or gastroesophageal cancer and positive cytology or carcinomatosis after perioperative intraperitoneal paclitaxel and gastrectomy.

Secondary Objectives:

To assess the safety of gastrectomy in subjects with stage IV gastric or gastroesophageal cancer and positive cytology or carcinomatosis undergoing treatment with perioperative intraperitoneal paclitaxel.

Conditions

Carcinomatosis; Gastric Adenocarcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Paclitaxel

Participant will receive paclitaxel every 2 weeks for 6 weeks, and then participants may have a gastrectomy based on what the doctor thinks is in your best interest. You may then receive additional paclitaxel every 2 weeks for 6 weeks.

Group Type: EXPERIMENTAL

Paclitaxel

Intervention Type: DRUG

Given by IP (Intraperitoneal injection)

Dexamethasone

Intervention Type: DRUG

Given by IV (vein)

Diphenhydramine

Intervention Type: DRUG

Given by IV (vein)

Famotidine

Intervention Type: DRUG

Given by IV (vein)

Interventions

Paclitaxel

Given by IP (Intraperitoneal injection)

Intervention Type: DRUG

Dexamethasone

Given by IV (vein)

Intervention Type: DRUG

Diphenhydramine

Given by IV (vein)

Intervention Type: DRUG

Famotidine

Given by IV (vein)

Intervention Type: DRUG

Other Intervention Names

Taxol; Decadron; Benadryl®; Pepcid®

Eligibility Criteria

Inclusion Criteria

1. Age 18 years and above. There will be no upper age restriction. Because no dosing or adverse event data are currently available on the use of intraperitoneal paclitaxel in patients <18 years of age, children are excluded from this study.

2. ECOG performance status ≤ 2 (Karnofsky ≥60%). Appendices 1 and 2.

3. Cytologic or histologic proof of adenocarcinoma of the stomach or gastroesophageal junction.

4. Adequate renal, and bone marrow function:

1. Leukocytes >= 3,000/uL

2. Absolute neutrophil count >= 1,500/uL

3. Platelets >= 60,000/Ul

4. Serum creatinine <= 1.6 mg/dL

5. Distant Metastatic Disease of peritoneum:

1. Positive peritoneal cytology, or

2. Carcinomatosis on diagnostic laparoscopy or laparotomy.

6. Completion of preoperative systemic cytotoxic chemotherapy. Targeted therapy, such as HER2 directed therapy, and immunotherapy, such as PD-1 inhibitors, may be continued.

7. English and non-English speaking patients are eligible.

Exclusion Criteria

1. Distant metastatic disease not limited to the peritoneum such as solid organ metastases to the liver, central nervous system, or lung.

2. Infections such as pneumonia or wound infections that would preclude protocol therapy.

3. Women with a positive urine or serum pregnancy test are excluded from this study; women of childbearing potential (defined as those who are not postmenopausal defined as no menses in greater than or equal to 12 months, have not had a hysterectomy or bilateral salpingo-oophorectomy, do not have ovarian failure, or have not had a surgical sterilization procedure) must agree to refrain from breast-feeding and practice adequate contraception as specified in the informed consent. Adequate contraception consists of oral contraceptive, implantable contraceptives, injectable contraceptives, a double barrier method, or abstinence. Men with reproductive potential must agree to an appropriate method of birth control, including abstinence or double barrier method (diaphragm plus condom).

4. Subjects with unstable angina or New York Heart Association Grade II or greater congestive heart failure.

5. Subjects, such as those with cognitive impairment, deemed unable to comply with study and/or follow-up procedures.

6. Subjects with a known hypersensitivity to protocol systemic chemotherapy that was life-threatening, required hospitalization or prolongation of existing hospitalization, or resulted in persistent or significant disability or incapacity.

7. Previous surgery that would preclude safe cytoreduction and intraperitoneal port placement.

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

Sponsors

M.D. Anderson Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Brian Badgwell, MD

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

M D Anderson Cancer Center

Houston, Texas, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Iqra Rehman, RN

Role: CONTACT

IRehman1@mdanderson.org

713-535-0703

Facility Contacts

Hsiu-Yin Chang, RN

Role: primary

hchang@mdanderson.org

713-745-7335

Provided Documents

Document Type: Informed Consent Form

View Document

Related Links

http://www.mdanderson.org

M D Anderson Cancer Center

Other Identifiers

NCI-2023-05915

Identifier Type: OTHER

Identifier Source: secondary_id

2023-0331

Identifier Type: -

Identifier Source: org_study_id