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Docetaxel, cisplatin and S-1 (DCS) combination chemotherapy for gastric cancer patients with peritoneal metastasis: retrospective study

Docetaxel, cisplatin and S-1 (DCS) combination chemotherapy for gastric cancer patients with peritoneal metastasis: retrospective study - DCS combination chemotherapy for gastric cancer patients with peritoneal metastasis: retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000025464
Enrollment
37
Registered
2016-12-28
Start date
2016-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gastric cancer

Interventions

None listed

Sponsors

Sapporo Medical University School of Medicine, Department of Medical Oncology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) had a histologically proven gastric adenocarcinoma (2) had a performance status (PS) of 0-2 on the Eastern Cooperative Oncology Group scale (3) aged 20-80 years (4) received DCS as first-line therapy for either metastatic or unresectable disease, with PM confirmed by image diagnosis such as computed tomography (CT), macroscopic evaluation or cytology (5) no prior chemotherapy other than adjuvant chemotherapy, which was required to have been completed 6 months before enrollment (6) received no other concomitant targeted therapy, such as trastuzumab (7) had documented follow-up with a physician and a radiographic tumor evaluation (8) showed adequate bone marrow, liver, and renal function (9) no other serious medical conditions (10) life expectancy 3 months (11) not pregnant or breast-feeding (12) provided written, informed consent.

Exclusion criteria

Exclusion criteria: (1)Patients with active double cancer (2) Any other patients who are regarded as unsuitable for this study by the investigators

Design outcomes

Primary

MeasureTime frame
Overall survival

Secondary

MeasureTime frame
Response rate Progression-free survival Adverse events Drug exposure

Countries

Japan

Contacts

Public ContactHiroyuki Ohnuma

Sapporo Medical University School of Medicine Department of Medical Oncology

ohnuma@sapmed.ac.jp011-611-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026