Overview

Short-Course Chemoradiotherapy Followed by Chemotherapy for the Treatment of Resectable Gastric Adenocarcinoma

Status:
Recruiting
Trial end date:
2027-12-31
Target enrollment:
0
Participant gender:
All
Summary
This phase Ib trial investigates the side effects and how well a shorter course of chemotherapy and radiation treatment (chemoradiotherapy) for 2 weeks instead of 5 weeks followed by standard chemotherapy works in treating patients with gastric cancer who are scheduled to have treatment and then surgery to remove the tumor. Chemotherapy drugs, such as capecitabine and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Radiation therapy uses high energy sources to kill tumor cells and shrink tumors. Giving short-course chemo-radiotherapy before chemotherapy and surgery may help to control the disease.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Capecitabine
Fluorouracil
Criteria
Inclusion Criteria:

- Eastern Cooperative Oncology Group (ECOG) performance status =< 2

- Patients with a biopsy-confirmed diagnosis of adenocarcinoma of the stomach

- No evidence of distant metastatic disease based on standard of care preoperative
imaging evaluation

- Evidence of T2 stage or greater primary tumor, or any T stage with node positive
disease based on endoscopic ultrasound or standard of care imaging

- Leukocytes >= 3,000/ul

- Absolute neutrophil count >= 1,500/ul

- Platelets >= 60,000/UI

- Glomerular filtration rate >= 60 mL/min/1.73 m^2. The estimated glomerular filtration
rate (eGFR) is calculated using the Chronic Kidney Disease Epidemiology Collaboration
(CKD-EPI) equation. The eGFR declines with age. eGFR < 60 mL/min/1.73 m2 is considered
as "decreased". This equation should only be used for patients 18 and older. According
to the National Kidney Foundation's Kidney Disease Outcome Quality Initiative (KDOQI)
classification and 2012 Kidney Disease Improving Global Outcomes (KDIGO) Clinical
Practice Guideline, the stage of CKD should be categorized based on estimated GFR

Exclusion Criteria:

- Presence of metastatic disease on staging with standard of care imaging, with or
without diagnostic laparoscopy. Subjects not able to undergo staging laparoscopy due
to previous surgery will not be excluded from this trial, and the determination of
absence of metastatic disease will be decided solely on imaging consistent with our
current standard of care

- Patients with known malabsorption syndromes or a lack of physical integrity of the
upper gastrointestinal tract

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

- Women with a positive urine or serum pregnancy test are excluded from this study;
women of childbearing potential (defined as those who have not undergone a
hysterectomy or who have not been postmenopausal for at least 12 consecutive months)
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, barrier methods,
or abstinence. Contraception for males consists of barrier methods or abstinence

- Subjects with unstable angina or New York Heart Association grade II or greater
congestive heart failure

- Subjects deemed unable to comply with study and/or follow-up procedures

- 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

- Prior radiotherapy to the same field

- Comorbid conditions (examples - collagen vascular diseases, certain genetic conditions
that predispose to secondary malignancies) that are prohibitive to preoperative
therapy, or contraindications to radiotherapy