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Gen Surg Vivasbreast

Gen Surg Vivas · breast

New DCIS on core biopsy — upgrade, margins, radiation, axilla, endocrine choice and the patient who wants surveillance

Fellowship viva on DCIS surgical decision-making: upgrade predictors, 2 mm margins, B-17/EORTC radiotherapy with no survival effect, B-24/IBIS-II endocrine choice, sentinel-node discipline by operation, and COMET-fenced surveillance counsel.

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FRACSFRCS(Gen Surg)ABSFRCSC
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FRACSFRCS(Gen Surg)ABSFRCSC
Prompt
A 54-year-old woman with screen-detected calcifications has core-biopsy DCIS. Talk me through the upgrade risk, your excision and margin plan, whether she needs radiation and endocrine therapy, what you do with the axilla, and how you answer when she asks about monitoring instead of surgery.

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Examiner prompts with model answers

Upgrade first — the number that opens consent. About one in four core-biopsy DCIS diagnoses (25.9% across 52 studies) prove invasive at excision — so the excision may change the diagnosis, and the plan must survive that change.[10]

Grade the predictors, not just the diagnosis. 14-gauge devices, high grade, size over 20 mm, BI-RADS 4-5, mass pattern and palpability raise upgrade risk — read her mammogram and core details as a probability, not a label.[10]

Margins — the 2 mm answer with its evidence base. Excise to 2 mm with whole-breast irradiation: negative margins halve recurrence against ink on DCIS, 2 mm minimises it, wider adds nothing — from 20 studies and 7883 patients, with fewer re-excisions as the service dividend.[9]

Radiation — halves recurrence, never survival. B-17 cut invasive ipsilateral tumours 13.4 to 3.9% with 50 Gy; EORTC at 15 years lifted recurrence-free 69 to 82% with no survival difference — consent local control, and name the invasive-recurrence survival penalty (BCSS HR 17.66) as the reason control still matters.[1][4]

Axilla by operation. Conservation means no sentinel biopsy; mastectomy means offer it — ASCO reaffirmed without change, the Dutch cohort validates omission (2% metastases in pure DCIS, delayed biopsy retrievable), and no pure-DCIS patient in Alberta had a positive sentinel node.[11][12]

Endocrine choice in receptor-positive disease. Tamoxifen 20 mg daily for 5 years is the default; anastrozole 1 mg daily is the non-inferior alternative (67 versus 77 recurrences, superiority not shown) for the postmenopausal woman with a tamoxifen contraindication — chosen on toxicity, not efficacy.[8]

The surveillance question — fenced, not dismissed. COMET randomised low-risk hormone-receptor-positive grade 1-2 DCIS to 6-monthly monitoring versus surgery: 4.2 versus 5.9% invasive at 2 years, non-inferior — but median follow-up is 36.9 months against a 60-month peak, so monitoring is evaluated, not established, and high-grade or extensive disease never enters the conversation.[13]

Close with the pair. 15 to 25% of diagnoses, most never progress; treatment cuts local events with no survival effect — so the answer is shared decision-making for personalised treatment, with annual mammography for a decade whatever she chooses.[17]

References9ShowHide
  1. [1]Fisher B, et al. Lumpectomy and radiation therapy for the treatment of intraductal breast cancer: findings from National Surgical Adjuvant Breast and Bowel Project B-17. J Clin Oncol, 1998.PMID 9469327
  2. [4]Donker M, et al. Breast-conserving treatment with or without radiotherapy in ductal carcinoma In Situ: 15-year recurrence rates and outcome after a recurrence, from the EORTC 10853 randomized phase III trial. J Clin Oncol, 2013.PMID 24043739
  3. [8]Forbes JF, et al. Anastrozole versus tamoxifen for the prevention of locoregional and contralateral breast cancer in postmenopausal women with locally excised ductal carcinoma in situ (IBIS-II DCIS): a double-blind, randomised controlled trial. Lancet, 2016.PMID 26686313
  4. [9]Morrow M, et al. Society of Surgical Oncology-American Society for Radiation Oncology-American Society of Clinical Oncology Consensus Guideline on Margins for Breast-Conserving Surgery With Whole-Breast Irradiation in Ductal Carcinoma In Situ. J Clin Oncol, 2016.PMID 27528719
  5. [10]Brennan ME, et al. Ductal carcinoma in situ at core-needle biopsy: meta-analysis of underestimation and predictors of invasive breast cancer. Radiology, 2011.PMID 21493791
  6. [11]Lyman GH, et al. Sentinel Lymph Node Biopsy for Patients With Early-Stage Breast Cancer: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol, 2017.PMID 27937089
  7. [12]van Roozendaal LM, et al. Sentinel lymph node biopsy can be omitted in DCIS patients treated with breast conserving therapy. Breast Cancer Res Treat, 2016.PMID 27083179
  8. [13]Hwang ES, et al. Active Monitoring With or Without Endocrine Therapy for Low-Risk Ductal Carcinoma In Situ: The COMET Randomized Clinical Trial. JAMA, 2025.PMID 39665585
  9. [17]Delaloge S, et al. Ductal carcinoma in situ of the breast: finding the balance between overtreatment and undertreatment. Lancet, 2024.PMID 38735296
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