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Total neoadjuvant multidrug chemotherapy in the management of gastric cancer

The effect of total neoadjuvant multidrug chemotherapy including fluorouracil, leucovorin, oxaliplatin and docetaxel on pathologic complete response resectable locally advanced gastric adenocarcinoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211211053356N1
Enrollment
63
Registered
2022-01-21
Start date
2022-01-21
Completion date
Unknown
Last updated
2022-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric cancer. Malignant neoplasm of stomach, unspecified

Interventions

Intervention group: In total neoadjuvant chemotherapy group, patients will be treated with eight sessions of fluorouracil, leucovorin, oxaliplatin, and docetaxel before surgery. Fluorouracil as a 24-h

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Pathologically confirmed gastric adenocarcinoma in biopsy Perigastric lymph node metastasis in CT scan Resectable primary gastric tumor based on CT scan

Exclusion criteria

Exclusion criteria: Presence of distant metastasis at the presentation Previous history of chemotherapy Previous history of radiotherapy Previous history of malignancy Suffering from uncontrolled diabetes mellitus Suffering from uncontrolled hypertension No consent to enroll

Design outcomes

Primary

MeasureTime frame
Pathologic response. Timepoint: After the intervention and providing the pathologic report of gastrectomy. Method of measurement: Based on report of pathologist.

Secondary

MeasureTime frame
Surgical margin status. Timepoint: After the intervention and providing the pathologic report of gastrectomy. Method of measurement: Based on pathologist report.;Treatment completion rate. Timepoint: During the intervention, every three week. Method of measurement: History taking.;Treatment toxicity. Timepoint: During the intervention, every three week. Method of measurement: history taking.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Golmoradi

Shiraz University of Medical Sciences

mehrdadg239@gmail.com+98 71 3647 4332

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026