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Invasive Breast Cancer clinical trials

View clinical trials related to Invasive Breast Cancer.

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NCT ID: NCT02773784 Completed - Clinical trials for Invasive Breast Cancer

Comparison of CNB and Surgical Specimens for ER, PgR, HER2 Status and Ki67 Index in Invasive Breast Cancer.

Start date: September 2014
Phase:
Study type: Observational

- This is a prospective, single-center, non-randomized, non-controlled study. - The estrogen receptor (ER), progesterone receptor (PgR), HER2 status and Ki67 index of CNB specimen are critical biomarkers for making neoadjuvant therapy strategy in invasive breast cancer. The concordance of these biomarkers between CNB and surgical specimen was varied in previous retrospective reports. The aim of this study is to determine the discordance of these biomarkers between CNB and surgical specimen and the influence of making treatment strategy by the discordance.

NCT ID: NCT02333890 Recruiting - Breast Cancer Clinical Trials

A Phase 2 Randomized, Double-blind Trial Evaluating the Effects of Chloroquine in Breast Cancer

CUBiC
Start date: July 2015
Phase: Phase 2
Study type: Interventional

Chloroquine (CQ) is a well known, well tolerated medication that has been used for many years traditionally for arthritis, lupus, and malaria. It has anti-inflammatory properties but is often the drug of choice for arthritis and malaria due to its few side effects. Recently, laboratory investigations have proven that CQ may potentially have anti-cancer properties, by inhibiting a process which allows cancers such as breast cancer to continue to grow (a process known as "autophagy"). Therefore, this study will look at how well CQ can inhibit the growth of breast cancers in patients while waiting for surgery.

NCT ID: NCT02244580 Completed - Clinical trials for Invasive Breast Cancer

Re-Evaluation of Tumor Samples From Women With Breast Cancer With the in Vitro Diagnostic Kit "MammaTyperTM"

Start date: August 2014
Phase: N/A
Study type: Interventional

This is a prospective examination of tumor material of breast cancer patients randomized into the FinHer-trial (= (= Comparison of vinorelbine and docetaxel and trastuzumab as adjuvant treatments of breast cancer patients wirh a high risk of cancer recurrence). The formalin-fixed, paraffin-embedded tissue samples will be analysed for Estrogen receptor 1 (ESR1), progesterone receptor (PgR), Human epidermal growth factor receptor 2 (HER2) and Antigen Ki-67 (Ki-67) with the molecular in vitro diagnostic kit MammaTyperâ„¢. According to the new subtyping the 5 year Distant disease free survival (DDFS) and Overall survival (OS) will be re-evaluated.

NCT ID: NCT02190227 Completed - Clinical trials for Invasive Breast Cancer

RNA Disruption Assay (RDA) Response Prediction in Neoadjuvant Chemotherapy Breast Cancer Treatment

Start date: May 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the optimal time to use the Tumor RNA Disruption Assay (RDA) as a predictor of pathological complete response (pCR) in patients with breast cancer treated with neoadjuvant chemotherapy. This is important because the earlier non-responders are identified, the greater is the impact of reducing side effects of ineffective treatments. The study hypothesis is that the RDA score will accurately predict for tumor response after one cycle of chemotherapy.

NCT ID: NCT02077569 Completed - Clinical trials for Invasive Breast Cancer

AKT Inhibitor in Oestrogen Positive Breast Cancer

STAKT
Start date: January 2014
Phase: Phase 2
Study type: Interventional

To compare the effect of four and a half days treatment of a range of doses of AZD5363 on selected markers of the AKT pathway and anti-proliferation compared with placebo in oestrogen receptor positive breast cancers. To assess the tolerability of four and a half days treatment of AZD5363.

NCT ID: NCT02022202 Active, not recruiting - Clinical trials for Invasive Breast Cancer

Breast Cancer Genome Guided Therapy Study (BEAUTY)

BEAUTY
Start date: February 2013
Phase:
Study type: Observational

The purpose of this research study is to better understand the reasons why or why not breast cancers are destroyed by standard chemotherapy. This information will be used to develop new and better cancer therapies.

NCT ID: NCT01934335 Terminated - Clinical trials for Invasive Breast Cancer

Effect of Vandetanib on Cellular Markers in Invasive Breast Cancer

Start date: October 2013
Phase: Phase 2
Study type: Interventional

The purpose of this project is to examine whether treatment with vandetanib has an effect on the tumor cells in breast cancer by examining tissue markers.

NCT ID: NCT01916837 Completed - Clinical trials for Invasive Breast Cancer

Genomic Grade Index (GGI): Feasibility in Routine Practice and Impact on Treatment Decisions in Early Breast Cancer

Start date: February 2010
Phase: N/A
Study type: Observational

In this prospective study the investigators sought to evaluate the feasibility of using the genomic signature - Genomic Grade Index (GGI) - in routine clinical practice and its impact on treatment recommendations.

NCT ID: NCT01856543 Completed - Clinical trials for Invasive Breast Cancer

Mometasone Furoate 0.1% Versus Eucerin on Moderate to Severe Skin Toxicities in Breast Cancer Patients Receiving Postmastectomy Radiation

Start date: May 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to find out if the effect of mometasone furoate is any different from Eucerin in decreasing the severity of redness of the skin during irradiation, preventing the skin from peeling, or reducing the amount of irritation the patient reports during treatment.

NCT ID: NCT01815476 Completed - Clinical trials for Invasive Breast Cancer

The Prone Breast Radiation Therapy Trial

Start date: May 4, 2013
Phase: N/A
Study type: Interventional

Participants undergoing radiation after breast conserving surgery for an early breast cancer (either Ductal Carcinoma In Situ (DCIS), or Early Stage Invasive breast cancer), and are at increased risk of developing a skin reaction because of their large breast size. After breast conserving surgery (also known as a 'lumpectomy'), women with either DCIS or early stage invasive breast cancer receive radiation to the breast to decrease the risk of cancer recurrence. Breast radiation is usually done with women lying on their back ("supine"). Some women develop temporary breakdown of the skin (moist desquamation). This skin reaction can be painful and has been linked to long term side effects such as chronic pain and decreased quality of life. This study is being done because women with large breasts have higher rates of skin breakdown (called 'moist desquamation') and breast pain during and shortly after radiation therapy is complete. It is unclear if such skin reactions and pain would be improved by alternating treatment position - namely lying on your belly ("prone") during their radiation treatment.