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Spots Global Cancer Trial Database for Gemcitabine + Carboplatin in Breast Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Gemcitabine + Carboplatin in Breast Cancer

Official Title: Gemcitabine Plus Carboplatin in Patients With Pretreated Metastatic Breast Cancer

Study ID: NCT00450762

Conditions

Breast Cancer

Study Description

Brief Summary: The rational for this trial is given by the knowledge that gemcitabine acts as a potent inhibitor of DNA repair and therefore may prevent adequate repair of platin-induced DNA damage. Gemcitabine is an excellent choice for combination therapy by its unique mechanism of action and favourable toxicity profile. The combination of gemcitabine and cisplatin was shown to be effective in several trials, producing response rates of 30-52 % in patients with pretreated metastatic breast cancer. To improve on tolerability and handling of the regime carboplatin may be the more appropriate choice for treatment. The mechanism of action of carboplatin is very similar to that of cisplatin. The rational for combining gemcitabine and carboplatin is based on their single-agent activities in metastatic breast cancer, the activity of this combination in other malignancies and on the fact that carboplatin has demonstrated efficacy comparable with cisplatin in several tumor types.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Contact Details

Name: Volker Heinemann, MD

Affiliation: University of Munich - Klinikum Grosshadern

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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