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NCT Number: NCT07344597

Prospective Comparative Study of Hypofractionated Adjuvant Radiotherapy in 2 Virsus 3 Weeks in Breast Cancer

To compare the efficacy and safety of two hypofractionated adjuvant radiotherapy regimens 34 Gy in 10

fractions versus 40.05 Gy in 15 fractions in patients with breast cancer treated at the South Egypt Cancer

Institute.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Assuit

Asyut, Egypt

About this study

Female breast cancer (BC) has been the leading cause of cancer morbidity and mortality among women in the

majority of countries for decades. In 2020, there were an estimated 2.3 million new cases and 685,000 deaths

from female BC worldwide, which accounted for one in four cancer cases and one in six cancer deaths among

women.

u For women with newly diagnosed, non-metastatic breast cancer, treatment consists of a multidisciplinary

approach that involves input from surgery, radiation oncology, and medical oncology. The objective of adjuvant

radiation therapy (RT) is to eradicate any tumor deposits remaining following surgery for patients treated by

either breast-conserving surgery or mastectomy . Doing so reduces risk of locoregional recurrence and improves

breast cancer-specific and overall survivals.

u A historical regimen of 25-28 fractions over 6 weeks was adopted for radiotherapy (RT) following breast-

conserving surgery (BCS) and total mastectomy. An early assumption that breast cancer cell lines might be more

sensitive to fractional doses than acute skin reactions and other squamous carcinomas lead to development of the

hypofractionated RT (HypoRT) approach, which elevated fractional dose up to 3 Gy with reduced total

dose/fractions, for obtaining radiobiological equivalence to a traditional regimen of 50-50.4 Gy in 25-28

fractions.

u Recently, the American Society of Radiation Oncology released a task force guideline recommending

hypofractionated radiotherapy for all women of any age whether they had received chemotherapy or not ,Their

evidence-based recommendations were supported by studies from Canada and the United Kingdom.

u Benefits of HypoRT include both, radiobiologic advantages and reduced length of treatment courses, for

improving healthcare resources and patient convenience. Consequently, HypoRT has been widely adopted

worldwide based on a series of randomized clinical trials .

u Recently, HypoRT over 3 weeks and with shorter courses of 5 fractions have been recommended in treatment

guidelines.

u Regarding clinical outcomes of a 2-week fractionation schedule , it was observed that acute and late effects were

acceptable with control rates similar to those reported in other trials with hypofractionation,Based

on these findings we started a trial to compare a 3-week radiotherapy schedule with a 2-week schedule .

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female patients aged ≥18 years.

Female or male patients with invasive carcinoma of the breast.

Complete microscopic excision of primary tumor.

Undergoing breast-conserving surgery (BCS) or modified radical mastectomy (MRM).

≥ Axillary lymph nodes dissected.

T1_4pN0_3M0 disease.

Neoadjuvant or adjuvant CTH .

Signed informed consent and able to comply with follow up.

Exclusion criteria

  • Evidence of distant metastases.

Past history of malignancy.

Prior radiotherapy to the chest region

Simultaneous malignancy (except non-melanoma skin cancer or in situ cervical carcinoma)

Connective tissue diseases (e.g., lupus erythematosus, scleroderma)

Pregnancy or lactation

Treatment and study plan

Radiotherapy

Device

Hypofractionated Adjuvant Radiotherapy in 2 versus 3 Weeks of Breast Cancer and effect skin toxicity and over all survival

Primary outcomes

  1. Disease free survival analyzed from the date of diagnosis.

    Time frame: through study completion, an average of 1 year

    local control was defined as absence of disease in the irradiated areas.recurrence were categorized as local(breast or surgical bed), regional(lymphatic drainage of axillary, supraclavicular fossa or internal mammary chain),or distant (metastasis),and any associayion of these

Secondary outcomes

  1. Assessment of Acute Skin Toxicity

    Time frame: From start of radiotherapy through 3 months after completion of radiotherapy

    Acute toxicities will be assessed according to RTOG criteria. The most severe toxicity presented will be reported.

  2. Assessment of Late Skin Toxicity

    Time frame: From 3 months after completion of radiotherapy through study completion, an average of 1 year

    Late toxicities will be assessed according to RTOG criteria. The most severe toxicity presented will be reported.

Study contacts

Contact information is provided by the study sponsor or research team.

SALWA SHAWKY BAKEET

CONTACT

[email protected]

+2001154224860

samir shehata mohamed, professor

CONTACT

[email protected]

01222302375

Sponsors and collaborators

Lead sponsor

Salwa Shawky Bakeet Ali

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 15, 2026
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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