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APBI vs Endocrine Therapy for Breast Cancer (CAMERAN Trial)

Phase 2
Recruiting
Led By Dana Casey, MD
Research Sponsored by UNC Lineberger Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Grade 1 or 2 overall tumor grade
Final surgical margins ≥ 2 mm as per APBI criteria
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights

CAMERAN Trial Summary

This trial is testing whether accelerated partial breast irradiation (APBI) is better than endocrine therapy in terms of quality of life for elderly patients with low-risk breast cancer.

Who is the study for?
This trial is for women over 65 with early-stage, low-risk breast cancer (small tumors under 2cm, not aggressive, and no spread to lymph nodes). Participants should be healthy enough for hormone therapy or radiation and have a positive hormone receptor status. They must not have other cancers that could affect the study or serious uncontrolled medical conditions.Check my eligibility
What is being tested?
The CAMERAN study compares two treatments after lumpectomy in older women with low-risk breast cancer: one group receives accelerated partial breast irradiation (APBI) alone, while another gets endocrine therapy alone. The goal is to see which treatment offers better quality of life without compromising disease control.See study design
What are the potential side effects?
Potential side effects from APBI include skin changes like redness and soreness at the treatment site, fatigue, and rare risks associated with radiation. Endocrine therapies may cause hot flashes, mood swings, bone thinning or joint pain.

CAMERAN Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My cancer is at an early stage (grade 1 or 2).
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My cancer surgery removed all visible cancer with at least 2 mm of clear tissue around it.
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My cancer is in the early stage (stage 1).
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My cancer is HER2-negative according to specific guidelines.
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My cancer has not spread to nearby lymph nodes.
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My cancer is at least 10% positive for both estrogen and progesterone receptors.
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I've had surgery to remove part of my breast, possibly with lymph node removal.
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I am a woman aged 65 or older with a new breast cancer diagnosis.

CAMERAN Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Patient reported outcomes assessed by EORTC QLQ-BR45
Patient reported outcomes assessed by European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) C30
Other outcome measures
Disease
Endocrine therapy adherence
Overall survival

CAMERAN Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Accelerated Partial Breast Irradiation (APBI)Experimental Treatment1 Intervention
APBI will consist of 5 fractions of radiation therapy delivered every other day to the lumpectomy cavity.
Group II: Endocrine TherapyActive Control1 Intervention
Endocrine therapy will be chosen by the treating medical oncologist with an aim of 5 years duration, as tolerated by the patient.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Accelerated Partial Breast Irradiation (APBI) targets the lumpectomy cavity with localized radiation, delivering high doses over a short period to destroy any remaining cancer cells while sparing surrounding healthy tissue. This approach minimizes side effects and shortens treatment time, which can improve the patient's quality of life. Endocrine Therapy, on the other hand, involves hormonal modulation to block or lower estrogen levels, as many breast cancers are estrogen receptor-positive and rely on this hormone to grow. By using medications like tamoxifen or aromatase inhibitors, endocrine therapy reduces the risk of cancer recurrence and progression. Both treatments are crucial as they offer effective, targeted options with potentially fewer side effects, enhancing overall outcomes and quality of life for breast cancer patients.
Adjuvant endocrine therapy for premenopausal women with breast cancer.The breast cancer continuum in hormone-receptor-positive breast cancer in postmenopausal women: evolving management options focusing on aromatase inhibitors.

Find a Location

Who is running the clinical trial?

UNC Lineberger Comprehensive Cancer CenterLead Sponsor
354 Previous Clinical Trials
91,383 Total Patients Enrolled
51 Trials studying Breast Cancer
27,896 Patients Enrolled for Breast Cancer
Dana Casey, MDPrincipal InvestigatorUniversity of North Carolina, Chapel Hill
2 Previous Clinical Trials
284 Total Patients Enrolled

Media Library

Accelerated Partial Breast Irradiation (APBI) Clinical Trial Eligibility Overview. Trial Name: NCT05472792 — Phase 2
Breast Cancer Research Study Groups: Endocrine Therapy, Accelerated Partial Breast Irradiation (APBI)
Breast Cancer Clinical Trial 2023: Accelerated Partial Breast Irradiation (APBI) Highlights & Side Effects. Trial Name: NCT05472792 — Phase 2
Accelerated Partial Breast Irradiation (APBI) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05472792 — Phase 2
~53 spots leftby Apr 2027