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A study of HIPEC plus apatinib and S-1 conversion therapy for gastric cancer with positive exfoliative cancer cells

A study of HIPEC plus apatinib and S-1 conversion therapy for gastric cancer with positive exfoliative cancer cells

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014817
Enrollment
Unknown
Registered
2018-02-07
Start date
2018-02-05
Completion date
Unknown
Last updated
2018-02-12

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

Conditions

gastric cancer

Interventions

Experimental:apatinib, paclitaxel, S-1

Sponsors

Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Untreated (e.g. chemotherapy, radiotherapy and other antitumor therapy); 2. Aged 18 to 70 years old; 3. Man or female (except pregnant and lactating women); 4. Has been confirmed to with gastric adenocarcinoma; 5. Proven gastric cancer of T stage was T3 and T4, and no distant metastasis was observed. The exfoliative cancer cells detection in peritoneal washes was positive; 6. Blood cell count has to meet the following certeria: WBC=3.5×10^9/L; ANC=1.5×10^9/L; PLT=100×10^9/L; HB=90g/L; 7. Liver/kidney function has to meet the following certeria: ALT and AST=2.5 ULN; TBIL<1.5 ULN; Serum creatinine =1.5 ULN; 8. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1; 9. Participants were willing to join in this study, good adherence and written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with other malignant tumors within 5 years; 2. Metastasis was found to be visible to the naked eye; 3. It has serious or uncontrolled heart diseases and infections (Including atrial fibrillation, angina pectoris, cardiac insufficiency, ejection fraction less than 50%, poor-controlled hypertension and so on); 4. History of psychiatric drugs abuse and can't quit or patients with mental disorders; 5. Patients with severe or uncontrollable mental illness; 6. Patients with tendency of gastrointestinal bleeding, including the following: a local active ulcerative lesions, and defecate occult blood (+ +).Has melena and hematemesis in two months; 7. Pregnant or lactating women; 8. It have serious harm to the patient's safety or affect the patients who have completed the research. 9. The researchers think inappropriate.

Design outcomes

Primary

MeasureTime frame
R0-resection rate;

Secondary

MeasureTime frame
Conversion to negative rate;Overall survival (OS) of 3, 5 years;Progression free survival (PFS) of 3, 5 years;safety;

Countries

China

Contacts

Public ContactQun Zhao

Fourth Hospital of Hebei Medical University

Zhaoqun516@126.com+86 13930162111

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 17, 2026