Distribution of the Homologous Recombination-related (HRR) Genesmutationsand HRD in Breast Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-70
SponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen University

About this trial

This is a cross-sectional and an observational study, investigator-initiated study in HER2-low breast cancer patients. Approximately 255 subjects with HRD (homologous recombination deficiency) assessment will be enrolled in this study to examine the distribution and features of HRD/HRR (homologous recombination repair).

In this study, investigators plan to clarify the frequency of HRR/HRD in Chinese patients with HER2-low breast cancer.

In addition, it is planned to investigate any association between invasive disease-free survival (iDFS)/overall survival (OS) and HRD/HRR in HER2-low breast cancer patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female patients aged 18-70 years with pathologically confirmed HER2-low breast cancer (defined as IHC 2+/ISH- or IHC 1+ per ASCO/CAP guidelines);

ECOG performance status of 0 or 1;

Treatment-naïve operable primary breast cancer with completed homologous recombination deficiency (HRD) assessment;

Disqualifiers

Recurrent or inoperable locally advanced breast cancer;

Bilateral breast cancer;

History of other malignant tumors within the past 5 years;

Incomplete clinical or pathological data.

Trial population

Female patients aged 18-70 years with pathologically confirmed HER2-low breast cancer (defined as IHC 2+/ISH- or IHC 1+ per ASCO/CAP guidelines)

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Standard Management

    Other intervention

    Standard Management

Treatment groups

255 Participants
are divided into 1 treatment group
Group A: Experimental ARM1 intervention

Trial outcomes

Primary outcomes

1

1.To assess the distribution characteristics of mHRR/HRD in breast cancer with low HRE2 expression in Chinese population

the distribution and features of HRD /HRR is evaluated.

Time frame
At the time of 4 weeks after surgery

Secondary outcomes

1

To assess the clinical characteristics between patients with mutations and non-mutation

Association between mutations and non-mutations group in HRD/HRR is assessed.

Time frame
At the time of 4 weeks after surgery
2

To compare the correlation between iDFS/OS and different adjuvant treatment regimens for breast cancer with low HER2 expression

IDFS, was a composite endpoint defined as the time from enrollment until the date of the first occurrence of one of the following events: Ipsilateral invasive breast cancer recurrence (same breast); Ipsilateral (same side of body) local regional invasive breast cancer recurrence (axilla, regional lymph nodes, chest wall, and/or skin); Distant recurrence (evidence of breast cancer in any anatomic site); Death attributable to any cause; Contralateral (opposite side of the body) invasive breast cancer. 3-year Overall survival (OS) was defined as time from date of randomization to death from any cause, otherwise cases were censored at date last known to be alive. Association between IDFS/OS and HRD/HRR information is evaluated.

Time frame
At the time of 36 months after surgery
3

To investigate the HRR/HRD characteristics and clinical characteristics (family history, age pathological feature es, etc.) of breast cancer patients with low HER2 expression

Association between multivariate prognostic factors and survival is evaluated.

Time frame
At the time of 4 weeks after surgery

Other outcomes

Sponsors and contacts

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