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Completed

NCT Number: NCT00165256

Wide Excision Alone as Treatment for Ductal Carcinoma in Situ of The Breast

The purpose of this study is to determine if wide excision (surgical removal) alone is adequate treatment for small, grade 1 or 2 ductal carcinoma in situ (DCIS) of the breast.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

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About this study

  • Patients with DCIS are usually treated with the combination of breast-conserving surgery and radiation therapy or breast-conserving surgery alone. The purpose of this study is to evaluate whether localized low- or intermediate-grade DCIS, diagnosed with modern mammography and careful pathologic evaluation, could be treated with wide excision alone (omission of radiation therapy) and result in acceptably low local recurrence rates.
  • Follow-up consists of physical examinations at least every 6 months by the surgeon or radiation oncologist. Mammograms of the affected breast will be obtained every 6 months for 5 years and then annually. Mammograms of the unaffected breast will be performed annually.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients must have high quality mammogram including magnification views of the area containing suspicious calcifications.
  • A specimen radiograph is required. If the specimen radiograph does not assure removal of all suspicious microcalcifications, a post-operative mammogram showing removal of all suspicious calcifications is required.
  • The clinical extent of DCIS must be less than or equal to 2.5 cm.
  • Grade 1 or 2 DCIS; patients with lobular carcinoma-in-situ (LCIS) in addition to DCIS in the breast are eligible. Negative margins are not required on the LCIS.
  • Patients must undergo a wide excision. A re-excision after the initial biopsy might be needed. Complete resection of the area of DCIS with a histologic margin of at least 1 cm must be achieved.
  • Patients must be enrolled on this protocol within 3 months of the last surgical procedure.

Exclusion criteria

  • Patients with invasive carcinoma including microinvasive disease
  • Carcinoma found in the sampled lymph nodes if axillary dissection is done
  • Patients with nipple discharge
  • Patients with adjuvant chemotherapy or Tamoxifen
  • Patients with a history of prior malignancies other than squamous or basal cell carcinoma of the skin, or carcinoma in situ of the cervix.
  • Patients with a history of ipsilateral or contralateral breast carcinoma or DCIS or simultaneous bilateral DCIS.

Treatment and study plan

observation

Other

Wide excision of DCIS and a minimum of 1cm histologically negative margin of breast tissue

Primary outcomes

  1. To determine if patients with DCIS can be effectively treated with wide excision alone.

    Time frame: TBD-survivorship

    Using information gathered from follow-up physical examinations and mammography to check for recurrence (DCIS or invasive carcinoma in the breast), DCIS patients treated with wide excision alone will be evaluated.

Secondary outcomes

  1. To explore whether patients with grade 2 DCIS have a higher breast recurrence than patients with grade 1 DCIS.

    Time frame: TBD-survivorship

    Using information gathered from follow-up physical examinations and mammography, the exploration of breast recurrences between grade 2 DCIS and grade 1 DCIS patients will be evaluated.

Sponsors and collaborators

Lead sponsor

Dana-Farber Cancer Institute

Other

Collaborators

  • Beth Israel Deaconess Medical Center
  • Brigham and Women's Hospital
  • Massachusetts General Hospital

Registry information

Official study title

Wide Excision Alone for DCIS-Grades 1 and 2

Important dates

Study start
1995
Primary completion
2022
Study completion
2026
First posted
Sep 14, 2005
Registry last updated
Jun 29, 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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