Lapatinib in Combination With Oral Vinorelbine for Metastatic Breast Cancer
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|ClinicalTrials.gov Identifier: NCT00912275|
Recruitment Status : Unknown
Verified November 2012 by National Taiwan University Hospital.
Recruitment status was: Recruiting
First Posted : June 3, 2009
Last Update Posted : November 16, 2012
Phase I part: to determine the recommended dose, and observe the preliminary response and safety profile of the combination of oral lapatinib with vinorelbine in patients with ErbB2 positive metastatic breast cancer.
Phase II part: to determine the progression free survival, response rate, and to evaluate the safety profile of the combination of oral lapatinib with vinorelbine in patients with ErbB2 positive metastatic breast cancer.
Phase I part has been completed. Phase II part is underway.
|Condition or disease||Intervention/treatment||Phase|
|Metastatic Breast Cancer||Drug: lapatinib plus oral vinorelbine||Phase 1 Phase 2|
This is a phase I/II clinical trial. In phase I part, the primary objective is To determine the recommended dose of the combination of lapatinib with oral vinorelbine in patients with ErbB2 positive metastatic breast cancer. In phase II part, the primary objective is progression free survival of the combination of lapatinib with oral vinorelbine as first line chemotherapy in patients with ErbB2 positive metastatic breast cancer. The secondary objectives are safety profile and the response rate
Lapatinib, an oral inhibitor of EGFR and HER2, have been shown to be an effective treatment in HER2/neu overexpressing metastatic breast cancer patient who refractory herceptin, taxane, and anthracycline treatment. In pre-clinical studies, the highest synergism between anti-Her2 treatment (trastuzumab) and cytotoxics was seen with the platinum compounds and with vinorelbine. The oral vinorelbine has similar efficacy to that of the injection formulation and has demonstrated generally favorable tolerability. We are interested in lapatinib plus oral vinorelbine as 1st line treatment in Her2+ MBC, to which we believe this convenience treatment offer a good response rate with satisfactory life quality.
For phase I part, we plan to use the standard phase I 3-patient cohort (''3 + 3'') design. Up to 18 patients may be enrolled. For phase II part, the expected progression-free survival of the protocol treatment in first line treatment of ErbB2 positive metastatic breast cancer is more than 6 months. With type 1 and type 2 errors of 0.05 and 0.1, respectively, this design calls for 29 patients at the first stage. If 20 or more progression disease is observed after 6 months of treatment, then the study will be terminated. Otherwise, additional 25 patients will be entered at the second stage. The treatment will be rejected if a total of 37 or more progression disease are observed out of 54 patients after 6 months of treatment. With the estimated dropout rate of 10%, 32 patients will be accrued in the first stage and 28 in the second stage.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||78 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Phase I/II Study of Lapatinib in Combination With Oral Vinorelbine for Metastatic Breast Cancer|
|Study Start Date :||May 2009|
|Estimated Primary Completion Date :||December 2013|
|Estimated Study Completion Date :||December 2013|
Experimental: Lapatinib plus Oral Vinorelbine
Oral vinorelbine on day 1 and day 8 q3w plus lapatinib 1000mg/day.
Drug: lapatinib plus oral vinorelbine
Lapatinib -dose level -I, I, II, III 1000mg po daily;dose level IV:1250mg po daily; Oral vinorelbine at the dose level reached on days 1, and 8 of a 21 days cycle. Dose level -I:30mg/m2,I:40mg/m2,II:50mg/m2,III:60mg/m2,IV:60mg/m2,V:80mg/m2
Other Name: Tykerb, Navelbine
- To determine the recommended dose of the combination of oral lapatinib with vinorelbine (phase I part), and progression free survival (phase II part) [ Time Frame: phase I part: 4 months, phase II part: 1 and half years ]
- response rate, safety profile [ Time Frame: 2 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00912275
|Contact: Yen-Shen Lu, M.D. ,Ph.D.||886-2-23123456 ext email@example.com|
|Contact: Ching-Hung Lin, M.D.||886-2-23123456 ext firstname.lastname@example.org|
|Department of Oncology,National Taiwan University Hospital||Recruiting|
|Taipei, Taiwan, 100|
|Contact: Yen-Shen Lu, M.D.,Ph.D 886-2-23123456 ext 7787 email@example.com|
|Contact: Ching-Hung Lin, M.D. 886-2-23123456 ext 7513 firstname.lastname@example.org|
|Principal Investigator: Yen-Shen Lu, M.D.,Ph.D|
|Sub-Investigator: Ching-Hung Lin, M.D.|
|Sub-Investigator: Ching-Jin Chung, M.D.,Ph.D|
|Sub-Investigator: Chiun-Sheng Huang, M.D.,Ph.D|
|Principal Investigator:||Yen-Shen Lu, M.D.,Ph.D||Department of Oncology,National Taiwan University Hospital|