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Pilot study of early start of chemotherapy after excision of the primary colorectal cancer. (Pearl star 01)

Pilot study of early start of chemotherapy after excision of the primary colorectal cancer. (Pearl star 01) - Pilot study of early start of chemotherapy after excision of the primary colorectal cancer. (Pearl star 01)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004361
Enrollment
5
Registered
2010-10-10
Start date
2010-10-01
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

Colorectal Cancer

Interventions

Oxaliplatin 130mg/m2 i.v. (day1) Bevaciumab 7.5mg/Kg i.v. (day1) Capecitabine2,000mg/m2 p.o.(day1-14) to be repeated every 3 weeks

Sponsors

Department of Gastroenterological Surgery Fukuoka University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Histologically confirmed colorectal cancer 2.Unresectable synchronous liver metastases 3.Resection of primary colorectal cancer 4.No prior chemotherapy and radiotherapy for colorectal cancer 5.Performance Status: 0-1 (ECOG criteria) 6.Age: 20 years to 75 years 7.Vital organ functions are preserved within 7 days prior to entry WBC : >= 3,000 and =< 12,000/mm3 Neutrophil : >=1,500/mm3 Platelet : >= 100,000/mm3 T.bil.: <= 1.5 mg/dl AST,ALT : 2.5 times of normal range in each institute Creatinin : <= upper limit of each institute 8.Signed written informed consent

Exclusion criteria

Exclusion criteria: 1.Prior severe drug allergy 2.Cavity fluid which needs drainage 3.Presence of active infection 4.Symptomatic brain metastases 5.Multiple malignancy within 5 years disease free interval 6.Uncontrolled hypertension 7.Uncontrolled diabetes 8.Peripheral nerve disorder 9.Severe pulmonary disease 10.Significant electrocardiographic abnormality 11.Treatment with anti-platelet drug 12.Chronic systemic treatment of corticosteroid 13.Nursing or pregnant females, or females or males with female partners who are planning to pregnancy 14.Inadequate for study enrollment by the physician

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
Response rate Time to treatment failure Overall survival Progression free survival

Countries

Japan

Contacts

Public ContactYoichiro Yoshida

Fukuoka University School of Medicine Department of Gastroenterological Surgery

yy4160@yahoo.co.jp0928011011

Outcome results

None listed

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