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A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy - A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011713
Enrollment
19
Registered
2013-09-12
Start date
2013-09-12
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

Large cell neuroendocrine carcinoma (LCNEC)

Interventions

A combined therapy of Bevacizumab plus Docetaxel

Sponsors

Toho University Omori Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically or Cytlogically confirmed large cell neuroendocrine carcinoma (LCNEC) 2) Stage IIIB/IV or postoperative recurrence 3) Previously treated platinum based chemotherapy 4) Patients aged 20 years or older 5) ECOG performance status of 0-1 6) Measureable region evaluable according to the RECIST(ver.1.1) 7) Adequate organ function 8) Patients who are considered to survive for more than 4 months 9) Written informed consent from the patient

Exclusion criteria

Exclusion criteria: Severe or uncontrollable systemic disease 2) Active infection 3) Active concomitant malignancy 4) Symptomatic brain metastasis 5) Uncontrollable pleural effusion, ascites, or pericardial effusion 6) History of GI perforation 7) Tendency to hemorrhages 8) Pregnancy, breast feeding and suspected pregnancy 9) Invasion to major vessel or cavitations of tumor 10) Uncontrollable hypertension 11) Inappropriate patients for this study judged by the physicians

Design outcomes

Primary

MeasureTime frame
Response rate

Secondary

MeasureTime frame
Overall survival Safety Progression free survival

Countries

Japan

Contacts

Public ContactKazutoshi Isobe

Toho University Omori Medical Center Department of Respiratory Medicine

kazutoshiisobe@aol.com03-3762-4151

Outcome results

None listed

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