Alisertib for Breast Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether adding alisertib, a new potential drug, to regular treatments can combat HR+/HER2+ breast cancer, which involves proteins that promote cancer growth. Researchers aim to determine if alisertib can block these proteins and identify genetic markers indicating its effectiveness. Participants will continue their usual treatment while taking alisertib. The trial seeks individuals with HR+/HER2+ breast cancer who have undergone chemotherapy and are currently on other cancer-fighting medications. As a Phase 2 trial, this research focuses on assessing the treatment's effectiveness in an initial, smaller group of participants.
Is there any evidence suggesting that alisertib is likely to be safe for humans?
Research has shown that alisertib, when combined with other treatments, offers potential benefits but also presents some safety concerns. In earlier studies, the most common serious side effects included low levels of white blood cells (neutropenia and leukopenia) and low red blood cell count (anemia), affecting many patients. For instance, one study found that 84.8% of patients taking paclitaxel and alisertib together experienced serious side effects. However, other research indicated that alisertib was generally well tolerated, with common but less severe side effects such as mouth inflammation (stomatitis).
The mid-phase trial for breast cancer testing alisertib suggests some evidence of safety exists, but further research is necessary to fully understand all potential risks and benefits.12345Why do researchers think this study treatment might be promising for breast cancer?
Alisertib is unique because it targets a specific protein called Aurora A kinase, which plays a crucial role in cell division and is often overactive in cancer cells. Unlike traditional chemotherapy treatments for breast cancer that broadly attack dividing cells, alisertib offers a more targeted approach that could potentially lead to fewer side effects. Researchers are excited about alisertib because its specific mechanism might enhance the effectiveness of standard treatments, potentially improving outcomes for patients with breast cancer.
What evidence suggests that alisertib might be an effective treatment for breast cancer?
Research suggests that alisertib may help treat certain types of breast cancer. In this trial, participants will receive alisertib alongside the standard of care. Studies have shown that when combined with other treatments, alisertib led to a reduction in tumor size in about 1 in 5 patients. Additionally, it has been linked to slowing cancer progression for approximately 5.4 to 5.6 months. While side effects, such as a decrease in white blood cells, can occur, these early findings indicate that alisertib could be effective for HR+/HER2+ breast cancer.14567
Who Is on the Research Team?
Kari Wisinski, MD
Principal Investigator
University of Wisconsin, Madison
Are You a Good Fit for This Trial?
This trial is for people with advanced breast cancer that tests positive for both hormone receptors (HR+) and HER2. Participants should be adults who are able to receive additional treatment alongside their usual care.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive alisertib in addition to standard of care endocrine therapy and HER2-targeted therapy
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Alisertib
Trial Overview
The study is testing if adding a drug called alisertib to standard treatments can help treat HR+/HER2+ breast cancer. All participants will get alisertib along with their regular therapy.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants receive alisertib in addition to usual care
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Wisconsin, Madison
Lead Sponsor
Citations
ALISertib in combination with endocrine therapy in patients ...
Alisertib had activity in phase 1 and 2 trials, including objective response rates (ORRs) of 19.6–20% and median progression-free survival (PFS ...
2.
onclive.com
onclive.com/view/alisertib-induces-early-signals-of-efficacy-in-endocrine-resistant-breast-cancerAlisertib Induces Early Signals of Efficacy in Endocrine- ...
Common grade 3 or higher adverse effects that were associated with alisertib included neutropenia (41.8%) and anemia (13.2%). “Further ...
Evaluation of Alisertib Alone or Combined With Fulvestrant ...
The ORR was not significantly improved by the addition of fulvestrant to alisertib, with an ORR of approximately 20.0% for both regimens.
4.
cancernetwork.com
cancernetwork.com/view/despite-lack-of-efficacy-alisertib-shows-meaningful-activity-in-breast-cancerDespite Lack of Efficacy, Alisertib Shows 'Meaningful' ...
The 1-year overall survival (OS) rate was 75.1% (95% CI, 63.4%-89.0%), and the estimated median OS was 22.7 months (95% CI, 18.4-not estimable ...
Study Details | NCT02860000 | Alisertib With or Without ...
Alisertib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Hormone therapy using fulvestrant may fight breast cancer
6.
onclive.com
onclive.com/view/alisertib-plus-endocrine-therapy-is-under-evaluation-in-hr-her2-negative-metastatic-breast-cancerAlisertib Plus Endocrine Therapy Is Under Evaluation in ...
Regarding safety, the most common grade 3 or higher adverse effects (AEs) reported during TBCRC041 included neutropenia, anemia, and leukopenia.
Efficacy and Safety of Weekly Paclitaxel With or Without ...
Grade 3 or 4 adverse events occurred in 56 patients (84.8%) receiving paclitaxel plus alisertib vs 34 patients (48.6%) receiving paclitaxel ...
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