Clinical trial · Interventional
Avastin +/- Erlotinib Consolidation Chemotherapy After Carboplatin, Paclitaxel, and Avastin (CTA) Induction Therapy for Advanced Ovarian, Fallopian Tube, Primary Peritoneal Cancer & Papillary Serous or Clear Cell Mullerian Tumors
A Randomized Phase II Trial of Avastin (A) or Avastin and Erlotinib (AE) as First Line Consolidation Chemotherapy After Carboplatin, Paclitaxel, and Avastin (CTA) Induction Therapy for Newly Diagnosed Advanced Ovarian, Fallopian Tube, Primary Peritoneal Cancer & Papillary Serous or Clear Cell Mullerian Tumors
NCT00520013CI-TRIAL-00034018completedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this research study is to evaluate how patients with newly diagnosed advanced ovarian, fallopian tube, primary peritoneal cancer and papillary serous or clear cell mullerian tumors respond to consolidation therapy with Avastin and erlotinib or Avastin alone over 1 year. These drugs have been used in the treatment of other types of cancers and information from those studies suggests that these agents may help to treat the cancers studied here.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Clear Cell Mullerian Tumor | — | UNRESOLVED | — |
| Fallopian Tube Cancer | Malignant Fallopian Tube Neoplasm | ALIAS | 0.90 |
| Ovarian Cancer | Malignant Ovarian Neoplasm | CURATED_EXACT | 0.92 |
| Papillary Serous Mullerian Tumor | — | UNRESOLVED | — |
| Primary Peritoneal Cancer | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| bevacizumab | Drug | Bevacizumab | ALIAS |
| carboplatin | Drug | Carboplatin | ALIAS |
| erlotinib | Drug | Erlotinib | ALIAS |
| paclitaxel | Drug | Paclitaxel | ALIAS |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- carboplatin/paclitaxel/bevacizumab then bevacizumab
- description
- Induction (CTA): Patients received carboplatin IV AUC 5, paclitaxel IV 175 mg/m2 and bevacizumab IV 15 mg/kg on day 1 (+/- 3d) of a 21 day cycle for 6 cycles. Bevacizumab started with cycle 2. Patients with disease progression based on radiographic evaluation after induction could not advance to the randomized consolidation phase. Consolidation (A): Patients received bevacizumab IV 15 mg/kg on day 1 (+/- 3d) of a 21 day cycle for 1 year.
- interventionNames
- Drug: bevacizumab
- Drug: paclitaxel
- Drug: carboplatin
- type
- EXPERIMENTAL
- label
- carboplatin/paclitaxel/bevacizumab then bevacizumab/erlotinib
- description
- Induction (CTA): Patients received carboplatin IV AUC 5, paclitaxel IV 175 mg/m2 and bevacizumab IV 15 mg/kg on day 1 (+/- 3d) of a 21 day cycle for 6 cycles. Bevacizumab started with cycle 2. Patients with disease progression based on radiographic evaluation after induction could not advance to the randomized consolidation phase. Consolidation (AE): Patients received bevacizumab IV 15 mg/kg on day 1 (+/- 3d) of a 21 day cycle and oral erlotinib 150mg daily for 1 year.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 18 years of age and older * Histological diagnosis of epithelial ovarian carcinoma, fallopian tube cancer, primary peritoneal carcinoma, or papillary serous mullerian carcinoma * Previous attempted surgical debulking * Stage III or IV * Willing and able to undergo second look laparoscopy * Performance status 0-1 by ECOG scale * Peripheral neuropathy \< grade 2 * Life expectancy of 6 months or greater Exclusion Criteria: * Patients with clinically significant cardiovascular disease as outlined in the protocol * Neutrophil count \< 1,500/mm3; platelet count \<100,000/m3 * Alkaline phosphatase or bilirubin \> 1.5 x ULN, SGOT \> 5 x ULN * Calculated creatinine clearance \< 50ml/min * Prior chemotherapy or radiotherapy for other malignancy except for the treatment for localized breast cancer greater than five years prior to diagnosis * No more than one cycle of first line chemotherapy with carboplatin and paclitaxel * Inadequate surgical cytoreduction such that interval cytoreductive surgery could materially improve prognosis * Concurrent invasive malignancy * Evidence of bleeding diathesis or coagulopathy * Evidence of tumor involving major blood vessels on any prior CT scans * Surgical wound that has failed to close * Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, or anticipation of need for major surgical procedure during the course of this study * Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to study enrollment * History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to day 0 * Serious non-healing wound, ulcer, or bone fracture * Prior treatment with an anti-angiogenic agent * Any active bleeding * Active psychiatric disease or neurologic symptoms requiring treatment * Presence of central nervous system brain metastases * Proteinuria at screening as demonstrated by criteria in protocol * Dementia or significantly altered mental status that would prohibit the understanding and/or giving of informed consent * Known hypersensitivity to Cremophor EL or any component of Avastin * Active bacterial, viral, or fungal infections * Receiving any other investigational agent * History of gastrointestinal perforation * Prior therapies targeting the epidermal growth factor receptor * Symptoms of bowel obstruction * Dependence on TPN or IV hydration
References
Publications (0)
Data not yet available
No reference posted for this study.