Weight-based Dosing for Dense Weekly Paclitaxel and Carboplatin in Overweight Patients w/ Body Surface Area (BSA) > 2.0

Gynecologic Malignancies Clinical Trial

Official title:

A Phase II Trial of Weight-based Dosing for Dense Weekly Paclitaxel and Carboplatin in Overweight Patients With a BSA > 2.0

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02756013
• Other study ID #: CASE13815
• Status: Terminated
• Phase: Phase 2
• Start date: April 20, 2016
• Est. completion date: January 24, 2019

Study information

• Verified date: June 2022
• Source: Case Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the side effects and effectiveness of giving standard paclitaxel chemotherapy in doses based on actual body surface area in combination with standard dosed carboplatin chemotherapy for overweight women.

Description:

Primary Objective The primary objective is to prospectively evaluate the Relative Dose Intensity (RDI) and toxicity of weight-based dose dense weekly paclitaxel and carboplatin in overweight patients with a BSA > 2.0 compared to the Japanese Gynecologic Oncology Group trial (JGOG 2016) during 6 - 9 cycles of chemotherapy.

Secondary Objective(s) The secondary objective is to evaluate progression-free survival in this patient population.

Study Design This is a descriptive study to determine what the relative dose intensity of patients who are overweight with a BSA of greater than 2.0 can achieve.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: January 24, 2019
• Est. primary completion date: August 16, 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with a histologically confirmed or presumed diagnosis of gynecologic malignancy for whom chemotherapy with paclitaxel and carboplatin is planned.

• Body Surface area >2.0

• Patients must have adequate:

• Renal function: Creatinine <1.5 x Institutional upper limits of normal (ULN)

• Bone marrow function:

• Absolute neutrophil count (ANC) = 1,500/mcl. This ANC cannot have been induced or supported by granulocyte colony stimulating factors.

• Platelets = 100,000/mcl.

• Hepatic function:

• Bilirubin = 1.5 x ULN.

• Aspartate aminotransferase (AST) (SGOT) = 2.5 x ULN.

• Alkaline phosphatase = to 2.5 x ULN.

• Neurologic function:

• Neuropathy (sensory and motor) = CTCAE Grade 1.

• Patients must have a Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2.

• Patients must be entered within 12 weeks of diagnosis.

• Subjects must have the ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Patients who have received prior radiotherapy to any portion of the abdominal cavity or pelvis. Prior radiation for localized cancer of the breast, head and neck, or skin is permitted, provided that it was completed more than three years prior to registration, and the patient remains free of recurrent or metastatic disease.

• Patients who have received prior chemotherapy.

• Patients with acute hepatitis or active infection that requires parenteral antibiotics.

• Patients with clinically significant cardiovascular disease. This includes:

• Myocardial infarction or unstable angina < 6 months prior to registration.

• New York Heart Association (NYHA) Grade II or greater congestive heart failure

• Serious cardiac arrhythmia requiring medication. This does not include asymptomatic, atrial fibrillation with controlled ventricular rate.

• Patients who are pregnant or nursing.

• Patients with medical history or conditions not otherwise previously specified which in the opinion of the investigator should exclude participation in this study.

• Patients with known allergy to cremophor or polysorbate 80.

Related Conditions & MeSH terms

• Gynecologic Malignancies
• Overweight

Intervention

Drug:
• Paclitaxel
80mg/m2 IV days 1,8, and 15 every 21 days x 6-9 cycles
• Carboplatin
area under the curve (AUC) 6 IV day 1 every 21 days x 6-9 cycles

Locations

Country	Name	City	State
United States	Cleveland Clinic Taussig Cancer institute, Case Comprehensive Cancer Center	Cleveland	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Case Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Relative Dose Intensity as Measured by Mean Percent of Intended Cycles Completed	Prospective evaluation of the Relative Dose Intensity (RDI) of weight-based dose dense weekly paclitaxel and carboplatin as measured by the average percent of completed treatment cycles out of the intended therapeutic plan	Up to 190 days
Secondary	Number of Participants With Progression-free Survival (PFS)	Progression will be evaluated in this study using the new international criteria proposed by the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1). Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions	every 3 months for up to 2 years, then every 6 months (up to 31 months)