Carboplatin Plus Docetaxel With Day 2 Pegylated G-CSF (Neulasta®) in Patients With Advanced Stage Ovarian Carcinoma

Ovarian Cancer Clinical Trial

Official title:

Phase II Trial of Carboplatin Plus Docetaxel With Day 2 Pegylated G-CSF (Neulasta®) in the Front-line Treatment of Patients With Advanced Stage Ovarian Carcinoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02469116
• Other study ID #: 05-1023
• Status: Terminated
• Phase: Phase 2
• First received: June 1, 2015
• Last updated: June 8, 2015
• Start date: January 2006
• Est. completion date: March 2010

Study information

• Verified date: June 2015
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

In this study the investigators will be using an AUC of 6 based on creatinine clearance using the Carboplatin dosing formula used for Gynecologic Oncology Group protocols.

Given that myelosuppression was significant using the docetaxel dose of 75 mg/m*2 in the SCOTROC trial, the prophylactic use of pegylated G-CSF in this Phase II trial is warranted. The expectation would be that patients will be able to receive their cycles in a more timely fashion, with less delays, thereby allowing for improved outcomes and decreased hospitalizations due to myelosuppression.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 18
• Est. completion date: March 2010
• Est. primary completion date: August 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed newly diagnosed Stage III/IV epithelial ovarian or primary peritoneal carcinoma at time of initial diagnosis

• Treatment must start within 8 weeks of surgery

• Subjects may be measurable per RECIST criteria or evaluable for disease response by CA125. Evaluable CA 125 levels are defined as an elevated CA125 pre operatively which either remains elevated post-operatively or normalizes after surgery

• No prior chemotherapy or radiation therapy

• Age = 18

• Performance Status must be = 2 (ECOG)

• Peripheral neuropathy: must be = grade 1

• Hematologic (minimal values)

• Absolute neutrophil count = 1,500/mm3

• Hemoglobin = 8.0 g/dl

• Platelet count = 100,000/mm3

• Hepatic

*Total Bilirubin = ULN

• AST and ALT and Alkaline Phosphatase must be within the range allowing for eligibility.

• If alkaline phosphatase is = ULN and AST or ALT is >5x ULN then the patient is not eligible

• If alkaline phosphatase is >1x but =2.5 x the ULN and the AST or ALT is >1.5x the ULN then the patient is not eligible

• If alkaline phosphatase is >2.5x but =5x the ULN and the AST or ALT is >1x the ULN then the patient is not eligible

• If alkaline phosphatase is >5x the ULN then the patient is not eligible

• Renal: Creatinine (serum) less than or equal to 1.5 ULN, CTC grade 1.

• Women of childbearing potential must have a negative pregnancy test and must be willing to consent to using effective contraception while on treatment and for at least 3 months thereafter.

PT/PTT = 1.5 x's ULN

Exclusion Criteria:

• Patients with a history of severe hypersensitivity reaction to Docetaxel or other drugs formulated with polysorbate 80.

• Women who are pregnant or breast-feeding.

• Patients who have signs of infection or who have not recovered from the effects of recent surgery

• Patients with a performance status of 3 or 4

• Patients with a second malignancy within past 5 years other than non-melanoma skin carcinoma.

• Patients who have received prior myelosuppressive chemotherapy or XRT.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Drug:
• Docetaxel

• Carboplatin

• Pegylated G-CSF

Locations

Country	Name	City	State
United States	Washington University School of Medicine	St. Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Washington University School of Medicine	Sanofi

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of grade 3-4 neutropenia as measured by CTCAE Version 3		Through 30 days after completion of treatment (approximately 22 weeks)	Yes
Secondary	Efficacy of regimen as measured by CA-125 response	Progression is defined as one of the following: Patients with elevated CA-125 pretreatment and normalization of CA-125 must show evidence of CA-125 = twice the upper limit of normal on two occasions at least one week apart; Patients with elevated CA-125 pretreatment which never normalizes must show evidence of CA-125 = 2 times the nadir value OR > 50% increase from the nadir on two occasions at least one week apart,; Patients with CA-125 in the normal range pretreatment must show evidence of CA-125 = two times the upper limit of normal on two occasions at least one week apart.; Complete response is defined as a CA-125 value <13 confirmed on two occasions at least 2 weeks apart.; Partial Response is defined as a reduction of at least 50% from the original elevated CA-125 value (original value must have been > 50), confirmed on two occasions at least 2 weeks apart.; Stable Disease is defined as not meeting one of the above criteria.	Completion of follow-up (up to 41 months, follow-up ranged from 8 months up to 41 months)	No
Secondary	Time to progression (TTP)	Progressive disease is at least a 20% increase in the sum of LD of target lesions taking as references the smallest sum LD or the appearance of new lesions within 8 weeks of study entry. Unequivocal progression of existing non-target lesions, other than pleural effusions without cytological proof of neoplastic origin, in the opinion of the treating physician within 8 weeks of study entry is also considered increasing disease (in this circumstance an explanation must be provided). In the case where the ONLY target lesion is a solitary pelvic mass measured by physical exam, which is not radiographically measurable, a 50% increase in the LD is required.	Completion of follow-up (up to 41 months, follow-up ranged from 8 months up to 41 months)	No
Secondary	Overall survival (OS)	Overall Survival is the observed length of life from entry into the study to death or the date of last contact	Completion of follow-up (up to 41 months, follow-up ranged from 8 months up to 41 months)	No
Secondary	Progression-free survival (PFS)	-Progression-Free Survival is the period from study entry until disease progression, death or date of last contact.	Completion of follow-up (up to 41 months, follow-up ranged from 8 months up to 41 months)	No
Secondary	Quality of life (QoL) as measured by FACT-O assessment tool	The FACT-O questionnaire consists of a Physical Well-Being Section, Social/Family Well-Being Section, Emotional Well-Being Section, Functional Well-Being Section, and Additional Concerns Section; Answers range from "Not at all" to "Very Much" with 0 = not at all and 4 = very much	Completion of follow-up (up to 41 months, follow-up ranged from 8 months up to 41 months)	No

External Links

•   Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine