Skip to content

Combination chemotherapy with gemcitabine plus oxaliplatin in patients with refractory germ cell cancer

Combination chemotherapy with gemcitabine plus oxaliplatin in patients with refractory germ cell cancer - chemotherapy with gemcitabine plus oxaliplatin for refractory germ cell cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017471
Enrollment
10
Registered
2015-05-08
Start date
2014-09-17
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

germ cell cancer

Interventions

Combination chemotherapy with gemcitabine, oxaliplatin and paclitaxel

Sponsors

Department of Urology, Tohoku University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1.Patients had to present with histologically confirmed germcell tumors. 2.Refractory was defined as incomplete reduction or elevation of serum tumor marker, or increase in the product of perpendicular diameters for any lesion or the appearance of any new lesions during chemotherapy.Relapse was defined as elevation of serum tumor marker after normalization, or the appearance of any new lesions after disappearance of all evidence of disease. 3. Patients wererequired to have a performance status less than 22 before registration of this study. Additional eligibility criteria included adequate major organ function, defined as a lneutrocyte count of 1000,/mm3, a thrombocyte count of 50,000/mm3, serum creatinine level less than 1.5 times the upper limit of normaland a liver enzyme level less than 2.5 times the upper limit of normal.

Exclusion criteria

Exclusion criteria: 1.patient with symptomatic interstitial pneumonia 2.patient with grade 3 or 4 cardiac insufficiency with NYHA classification 3.patient with severe infection 4.patient with severe comorbidity 5.patient with severe allergy 6.patient with active another malignancy

Design outcomes

Primary

MeasureTime frame
response rate

Secondary

MeasureTime frame
median survival time, progression free survival

Countries

Japan

Contacts

Public ContactShigeyuki Yamada

Tohoku University Graduate School of Medicine Department of Urology

shige-yamada@uro.med.tohoku.ac.jp+81-22-717-7278

Outcome results

None listed

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