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A Phase II Study of carboplatin plus paclitaxel for advanced thymic cancer

A Phase II Study of carboplatin plus paclitaxel for advanced thymic cancer - Carboplatin plus paclitaxel for advanced thymic cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001358
Enrollment
40
Registered
2008-09-08
Start date
2008-05-01
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

Thymic cancer

Interventions

Sponsors

West Japan Oncology Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically confirmed thymic carcinoma. 2)Clinically confirmed Masaoka stage III, IVa or IVb not amenable to potentially curative therapy by surgery or radiotherapy. 3)Patients without prior chemotherapy. 4)Recurrence after surgery or radiotherapy but recurrent sites have never been irradiated. 5)Measurable lesion 6)Adult patients (20 years of age or more than 20) 7)Performance status 0-1 8)Adequate organ function 9)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Presence of pleural or pericardial effusion that cannot be controlled by a procedure. 2)Presence of brain tumor with clinical symptoms. 3)Superior vena cava syndrome. 4)Interstitial pneumonitis. 5)Presence of other active malignancy. 6)Acute intercurrent infection or complications 7)History of serious allergy to medical drugs. 8)Uncontrolled psychiatric disease. 9)pregnancy or lactating patients 10)Myasthenia gravis

Design outcomes

Primary

MeasureTime frame
Objective response rate (RECIST criteria)

Secondary

MeasureTime frame
Overall survival, Progression survival, Safety

Countries

Japan

Contacts

Public ContactShinichiro Nakamura

West Japan Oncology Group WJOG datacenter

datacenter@wjog.jp06-6633-7400

Outcome results

None listed

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