VEGF Trap and Docetaxel in Treating Patients With Persistent or Recurrent Ovarian Epithelial Cancer, Primary Peritoneal Cancer, or Fallopian Tube Cancer

NCT00436501 | Completed Phase 1 Results

• 3 other identifiers: NCI-2009-002182006-0329P50CA083639
• Study Type: interventional
• Target: 58
• Locations: 1 country
• Sites: 2

Brief Summary

This phase I/II trial is studying the side effects and best dose of VEGF Trap when given together with docetaxel and to see how well they work in treating patients with persistent or recurrent ovarian epithelial cancer, primary peritoneal cancer, or fallopian tube cancer. VEGF Trap may stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving VEGF Trap together with docetaxel may kill more tumor cells

Conditions

Fallopian Tube Cancer; Malignant Tumor of Peritoneum; Recurrent Ovarian Epithelial Cancer

Keywords

primary peritoneal cavity cancer; Ovarian Epithelial Cancer; Peritoneal Cancer; Fallopian Tube Cancer; VEGF Trap; aflibercept; vascular endothelial growth factor trap; Zaltrap; docetaxel; RP 56976; Taxotere; TXT

Outcome Measures

Primary Outcomes (5)

• Maximum Tolerated Dose of VEGF Trap (Phase I)

  Escalating dose levels of VEGF Trap were administered intravenously over three dose levels (2, 4, or 6 mg/kg; one dose every 21 days) to identify the maximum tolerated dose (MTD). The MTD is defined as the highest dose level below which 2 or more patients encounter a dose limiting toxicity (DLT), graded according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0. MTD established on absence of observed DLT(s) in either cycle 0 (single agent) or cycle 1 (combination therapy) of any given dose level.

  21 day cycle, up to 3 cycles

• Number of Participants With Clinical Response (Partial Response or Complete Response) According to the Response Evaluation Criteria in Solid Tumors (RECIST)

  Frequency of clinical response (partial response or complete response) according to the Response Evaluation Criteria in Solid Tumors (RECIST). Complete Response (CR): Disappearance all target lesions; Partial Response (PR): \>/= 30% decrease in sum of longest diameter (LD) of target lesions, reference baseline sum LD; Progressive Disease (PD): \>/= 20% increase in sum of LD of target lesions, reference smallest sum LD recorded since treatment started or appearance of 1+ new lesions; Stable Disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, reference smallest sum LD since treatment started.

  Up to 6 months

• Median Overall Survival (OS) (Phase II)

  Overall survival was defined from the date of study entry until death or date of last contact. Median survival time points calculated in the method of Kaplan-Meier. Standard RECIST criteria followed to evaluate response and progression, and all documented responses required confirmation by imaging, examination, or both, no sooner than 4 weeks after the initial documentation of response. In the absence of new symptoms, response assessment consistently done after two additional cycles of therapy.

  Time from start of treatment to time of progression, assessed up to 6 years.

• Overall Objective Response Rate According to RECIST (Phase II)

  The percentage of participants in the Phase II arm with an objective response defined as a measurable response according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.0. Standard RECIST criteria were followed to evaluate response and progression. All documented responses were required to undergo confirmation by imaging, examination, or both, no sooner than 4 weeks after the initial documentation of response. In the absence of new symptoms, this response assessment was consistently done after two additional cycles of therapy.

  Up to 6 months

• Median Progression-Free Survival (PFS) (Phase II)

  Progression-Free Survival was calculated from study entry until documented disease, death or date of last contact.

  Time from start of treatment to time of progression, assessed up to 6 years.

Secondary Outcomes (3)

• Overall Median Duration of Response (Phase II)

  Response assessed following treatment (every 3 weeks), up to 6 years. Study duration January 2007 to May 2013.

• Number of Participants With Treatment-related Adverse Effects as Assessed by NCI CTCAE v3.0 (Phase II)

  Up to 6 years

• Number of Participants With PFS (Phase II)

  6 months

Study Arms (2)

Treatment (VEGF Trap, Docetaxel)

EXPERIMENTAL

Phase I (closed to accrual as of 3/14/2008): Patients receive VEGF Trap IV over 1 hour on day 1 of course 1. Patients then receive VEGF Trap IV over 1 hour and docetaxel IV over 1 hour on day 1 in all subsequent courses. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of VEGF Trap until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 or 6 patients experience dose-limiting toxicity.

Drug: docetaxel; Biological: ziv-aflibercept; Other: laboratory biomarker analysis; Other: pharmacological study

Phase II Treatment (VEGF Trap, Docetaxel)

EXPERIMENTAL

Phase II (opened to accrual as of 5/9/2008): Patients receive VEGF Trap at the MTD determined in phase I and docetaxel as in phase I. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Drug: docetaxel; Biological: ziv-aflibercept

Interventions

docetaxel DRUG

25 mg/m\^2 given intravenously (IV) over 1 hour (+/- 10 minutes) following VEGF Trap every 3 weeks starting cycle 1 (21 day cycles)

Also known as: RP 56976, Taxotere, TXT

Phase II Treatment (VEGF Trap, Docetaxel); Treatment (VEGF Trap, Docetaxel)

ziv-aflibercept BIOLOGICAL

Starting dose 2 mg/kg given IV Cycle 0. Phase I Group: Every 3 weeks beginning with Cycle 0 (Completed 03/14/2008); Phase II Group: Every 3 weeks starting cycle 1 (Opened 05/09/2008).

Also known as: aflibercept, vascular endothelial growth factor trap, VEGF Trap, Zaltrap

Phase II Treatment (VEGF Trap, Docetaxel); Treatment (VEGF Trap, Docetaxel)

laboratory biomarker analysis OTHER

Correlative studies

Treatment (VEGF Trap, Docetaxel)

pharmacological study OTHER

Correlative studies

Also known as: pharmacological studies

Treatment (VEGF Trap, Docetaxel)

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

Criteria: * Histologically confirmed ovarian epithelial, primary peritoneal, or fallopian tube cancer: Persistent or recurrent disease * Measurable disease, defined as \>= 1 unidimensionally measurable lesion \>= 20 mm by conventional techniques: * Must have \>= 1 target lesion to assess response; * Tumors within a previously irradiated field are considered nontarget lesions * Must have received 1 prior platinum-based chemotherapy regimen (for primary disease) containing carboplatin, cisplatin, or other organoplatinum compound: Initial treatment may have included any of the following: * High-dose therapy; * Consolidation therapy; * Extended therapy administered after surgical or nonsurgical assessment * AND Must have received 1 prior platinum-based chemotherapy regimen (for primary disease) containing carboplatin, cisplatin, or other organoplatinum compound: One additional cytotoxic regimen for recurrent or persistent disease allowed * No history or evidence of CNS disease, including primary brain tumor or brain metastases * Zubrod performance status 0-2 (0-1 for patients who received 2 prior regimens \[taxane and/or platinum regimens are counted separately\]) * Absolute neutrophil count \>= 1,500/mm\^3 * Platelet count \>= 100,000/mm\^3 * Hemoglobin \>= 9 g/dL * Bilirubin normal * aspartate aminotransferase / alanine aminotransferase (AST/ALT) \< 2.5 times upper limit of normal (ULN) * Creatinine \< 1.5 times ULN OR creatinine clearance \> 60 mL/min * Prothrombin Time (PT)/international normalized ratio (INR) \< 1.5 OR in-range INR 2-3 (if patient is on a stable dose of therapeutic warfarin or low molecular weight heparin) * PTT \< 1.2 times control * Urine protein:creatinine ratio \< 1 * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception during and for at least 6 months after completion of study treatment * No active infection requiring antibiotics * No sensory and motor neuropathy \>= grade 2 * No history of allergic reactions attributed to compounds of similar chemical or biologic composition to VEGF Trap, Magnevist, or fludeoxyglucose F 18 * No history of allergic reaction to paclitaxel or docetaxel or to products mixed in Cremophor EL or Tween 80 * No active bleeding or pathologic condition that would carry a high risk of bleeding, including any of the following: Known bleeding disorder; Coagulopathy; Peptic ulcer disease; Diverticulitis; Tumor involving major vessels * No active and/or untreated pulmonary embolism, deep vein thrombosis, or other thromboembolic event (i.e., any condition associated with aberrant clotting or migration of an induced clot) * No history or evidence of other CNS disease, including any of the following: Seizures not controlled with standard medical therapy; Cerebrovascular accident; Transient ischemic attack; Subarachnoid hemorrhage within the past 6 months * No clinically significant cardiovascular disease, including any of the following: Uncontrolled hypertension (i.e., systolic blood pressure \[BP\] \> 150 mm Hg or diastolic BP \> 100 mm Hg; systolic BP \> 180 mm Hg and diastolic BP \< 90 mm Hg OR diastolic BP \> 90 mm Hg on \>= 2 measurements within the past 3 months); Myocardial infarction; Coronary or peripheral artery bypass graft * No clinically significant cardiovascular disease, including any of the following: New York Heart association class III or IV congestive heart failure; Serious cardiac arrhythmia requiring medication; Peripheral vascular disease \>= grade 2; Unstable angina within the past 6 months; Clinically significant peripheral artery disease (e.g., claudication) within the past 6 months * No known hypersensitivity to Chinese hamster ovary cell products or other recombinant human or humanized antibodies * Able to undergo an MRI scan: No claustrophobia; No implanted devices or metallic foreign bodies not compatible with MRI (e.g., ferromagnetic implants or pacemakers); No known history of allergic reaction to gadolinium contrast agents * No other invasive malignancy within the past 5 years except nonmelanoma skin cancer * No significant traumatic injury within the past 28 days * Recovered from prior therapy to NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0 grade =\< 1: Alopecia allowed * No prior VEGF Trap * No prior cancer treatment that would preclude study treatment * Prior paclitaxel allowed * Prior docetaxel for primary or recurrent disease allowed provided the following criteria are met: No disease progression during therapy; No disease relapse within 3 months of completing therapy; No persistent disease at the completion of primary therapy * More than 7 days since prior placement of a vascular access device or core biopsy * At least 1 week since prior hormonal therapy for the malignant tumor * At least 4 weeks since other prior therapy, including immunologic agents (6 weeks for nitrosoureas or mitomycin C) * More than 28 days since prior major surgery, open biopsy, dental extraction, or other dental surgery/procedure resulting in an open wound * No concurrent major surgery * No concurrent combination antiretroviral therapy for HIV-positive patients * No other concurrent anticancer therapy * No other concurrent investigational agents * No concurrent hematopoietic growth factors during course 1 of phase I * Concurrent hormone replacement therapy allowed * White blood count (WBC) \>= 3,000/mm\^3

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• National Cancer Institute (NCI): lead

Study Sites (2)

M D Anderson Cancer Center

Houston, Texas, 77030, United States

Location

University of Virginia Health System

Charlottesville, Virginia, 22903, United States

Location

Related Publications (1)

• Coleman RL, Duska LR, Ramirez PT, Heymach JV, Kamat AA, Modesitt SC, Schmeler KM, Iyer RB, Garcia ME, Miller DL, Jackson EF, Ng CS, Kundra V, Jaffe R, Sood AK. Phase 1-2 study of docetaxel plus aflibercept in patients with recurrent ovarian, primary peritoneal, or fallopian tube cancer. Lancet Oncol. 2011 Nov;12(12):1109-17. doi: 10.1016/S1470-2045(11)70244-3. Epub 2011 Oct 10.

  PMID: 21992853 DERIVED

Related Links

• The University of Texas MD Anderson Cancer Center Official Website

MeSH Terms

Conditions

Fallopian Tube Neoplasms; Carcinoma, Ovarian Epithelial

Interventions

Docetaxel; aflibercept

Condition Hierarchy (Ancestors)

Genital Neoplasms, Female; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Fallopian Tube Diseases; Adnexal Diseases; Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases; Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Ovarian Neoplasms; Endocrine Gland Neoplasms; Ovarian Diseases; Endocrine System Diseases; Gonadal Disorders

Intervention Hierarchy (Ancestors)

Taxoids; Cyclodecanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Hydrocarbons; Organic Chemicals; Diterpenes; Terpenes

Results Point of Contact

• Title: Robert Coleman, MD / Professor
• Organization: UT MD Anderson Cancer Center, Office of Multicenter Clinical Research

RColeman@mdanderson.org

Study Officials

• Robert Coleman

  M.D. Anderson Cancer Center

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: LTE60
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: NIH
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 15, 2007
• First Posted: February 19, 2007
• Study Start: January 1, 2007
• Primary Completion: March 1, 2011
• Study Completion: November 1, 2012
• Last Updated: February 26, 2019
• Results First Posted: March 11, 2015

Record last verified: 2019-02

Locations

US (2)