Skip to content

Neoadjuvant chemotherapy in gastric adenocarcinoma

The effect of neoadjuvant chemotherapy on increasing resectability in patients with locally-advanced gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014053113736N1
Enrollment
60
Registered
2014-06-02
Start date
2012-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Gastric adenocarcinoma. Malignant neoplasm of stomach

Interventions

Intervention 1: Control group: Surgical exploration without neoadjuvant chemotherapy. Intervention 2: Intervention Group Neoadjuvant chemotherapy: - docetaxel 75 mg/m2, IV, 1 hour infusion, day 1 -
Treatment - Surgery
Treatment - Drugs
Control group: Surgical exploration without neoadjuvant chemotherapy
Intervention Group Neoadjuvant chemotherapy: - docetaxel 75 mg/m2, IV, 1 hour infusion, day 1 - cisplatin 75 mg/m2, IV , 2hour infusion, day 1 - 5 FU 750 mg/m2/day, IV continuous infusion, days

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) Age between 18-70 years old 2) Confirmation of gastric adenocarcinoma by endoscopic sampling and histopathological analysis 3) Confirmation of locally-advanced disease by preoperative computed tomography 4) Confirmation of resectability by preoperative computed tomography Exclusion criteria: 1) Ages older than 70 2) Gastric malignancies other than adenocarcinoma 3) Distant metastasis in preoperative assessment 4) Any contraindication to chemotherapy 5) History of previous chemotherapy 6) History of previous radiotherapy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reseactability. Timepoint: Intraoperative (After chemotherapy in case group and after diagnosis in control group). Method of measurement: Intraoperative findings.

Secondary

MeasureTime frame
Local lymph node regression. Timepoint: After neoadjuvant chemotherapy (6 weeks). Method of measurement: Computed tomography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahriyar Hashemzadeh

Tabriz University of Medical Sciences

shahriar_90@yahoo.com+98 41 1334 1317

Outcome results

None listed

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