Clinical trial

Phase II Study Of Carboplatin Plus Paclitaxel Treatment Of Advanced Thymoma Or Thymic Carcinoma

Name
CDR0000068461
Description
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one chemotherapy drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of carboplatin combined with paclitaxel in treating patients who have advanced thymoma.
Trial arms
Trial start
2001-06-19
Estimated PCD
2008-11-01
Trial end
2012-08-01
Status
Completed
Phase
Early phase I
Treatment
carboplatin
Dosed to AUC of 6.0, given IV over 30 minutes day 1 of a 21-day cycle, for up to 6 cycles
Arms:
Paclitaxel plus Carboplatin
Other names:
CBDCA, Paraplatin, JM-8, NSC # 241240
paclitaxel
225 mg/m2 given by intravenous (IV) infusion over 3 hours on day 1 of a 21-day cycle, for up to 6 cycles
Arms:
Paclitaxel plus Carboplatin
Other names:
Taxol, NSC #125973
Size
46
Primary endpoint
Best Overall Response by RECIST Criteria (Version 1.0)
Assessed every 2 cycles (6 weeks)
Eligibility criteria
Inclusion Criteria: * Histologically confirmed invasive, recurrent, or metastatic thymoma or thymic carcinoma not amenable to potentially curative therapy by surgery * Extensive disease (distant disease, pleural disease, pulmonary with or without mediastinal disease, or recurrent progressive disease in site of prior radiotherapy) * Advanced limited disease allowed if ineligible for primary radiotherapy or surgery * Measurable disease * Age 18 and over * ECOG Performance Status 0-1 * Granulocyte count at least 1,500 cells/mm\^3 * Platelet count at least 100,000 cells/mm\^3 * Bilirubin no greater than 1.5 mg/dL * Creatinine no greater than 2.0 mg/dL * Concurrent corticosteroids for myasthenia gravis or other chronic conditions allowed Exclusion Criteria: * Acute concurrent complications such as infection or post-surgical complications * Other prior malignancy within the past 5 years unless curatively treated with no evidence of recurrence * Pregnant or nursing. A negative pregnancy test was required, and fertile patients must use effective contraception * Prior chemotherapy for metastatic disease. Prior preoperative or adjuvant chemotherapy allowed if disease-free survival prior to recurrence was more than 1 year
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 46, 'type': 'ACTUAL'}}
Updated at
2023-06-29

1 organization

2 drugs

2 indications

Indication
Thymoma
Drug
AN0025