Gen Surg SAQs · breast
Extensive high-grade DCIS on core biopsy — upgrade consent, 2 mm margins, sentinel-node choice, radiotherapy and endocrine plan
Fellowship SAQ on DCIS: one-in-four upgrade rule with predictors, 2 mm margin standard, sentinel node with conservation-versus-mastectomy logic, B-17/EORTC radiotherapy numbers, B-24/UK/ANZ endocrine halves, and COMET-fenced surveillance counsel.
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Prompt
A 58-year-old woman has screen-detected grouped calcifications spanning 28 mm. Stereotactic 14-gauge core biopsy shows high-grade ductal carcinoma in situ with comedonecrosis; the area is palpably thickened. (A) Consent her for the upgrade risk, state your surgical plan including margins and the sentinel-node decision, and justify each. (4 marks) (B) Lay out the radiotherapy and endocrine evidence for her lesion, with the exact trial numbers and doses. (3 marks) (C) She asks about avoiding surgery after reading about monitoring trials. Fence the surveillance conversation honestly and set her follow-up. (3 marks)
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Model answer
(A) Upgrade consent and surgical plan (4 marks)
- Quote the upgrade rule before anything else: about one in four core-biopsy DCIS diagnoses (25.9% pooled) prove invasive at excision — and her lesion carries nearly every predictor: 14-gauge sampling, high grade, 28 mm span, palpable thickening.[10]
- Plan complete excision to the 2 mm standard with whole-breast irradiation in view: negative margins halve recurrence against ink on DCIS, 2 mm minimises it, wider clearance adds nothing — while under-2 mm negativity alone never mandates mastectomy.[9]
- Sentinel-node decision follows the operation, not the anxiety: with planned conservation, no sentinel surgery (ASCO reserves it for mastectomy); if extent forces mastectomy, stage the axilla at the same operation because the window closes.[11]
- Her 28 mm span makes mastectomy a legitimate branch of the same consent — size predicts both mastectomy and upstaging — with clip placement, imaging-pathology correlation and multidisciplinary review either way.[9][10]
(B) Radiotherapy and endocrine evidence (3 marks)
- Radiotherapy: B-17 cut invasive ipsilateral tumours from 13.4 to 3.9% with lumpectomy plus 50 Gy, all subgroups benefiting; EORTC at 15 years lifted recurrence-free 69 to 82% — with no survival difference (BCSS HR 1.07, OS HR 1.02), so consent local control, not rescue.[1][4]
- Endocrine therapy: B-24 (tamoxifen 20 mg daily for 5 years with lumpectomy plus radiation) cut 5-year events 8.2 versus 13.4%, holding even with involved margins and comedonecrosis; UK/ANZ confirms fewer local and contralateral events with the same 20 mg dose.[2][5]
- Name the limit both halves share: treatment cuts local events with no survival effect — her high-grade, extensive disease argues for maximal local treatment, not for promising what radiation and tamoxifen cannot deliver.[17]
(C) Surveillance fence and follow-up (3 marks)
- She fails every surveillance fence: COMET enrolled hormone-receptor-positive grade 1-2 disease, and her high-grade, 28 mm, palpable lesion is the opposite population — monitoring trials do not cover her.[13]
- Add the two quantitative fences: LORIS-eligible women still had 6.0% 10-year invasive recurrence without radiation, and one in five core non-high-grade DCIS cases hides invasion at excision — her higher-risk profile starts from worse.[16]
- Grade sets her clock: invasive recurrence arrives at 76 months from high-grade disease (against 131 for low grade), with recurrence at 180 months doubling that at 60 — so follow-up is annual mammography for a decade, not short reassurance.[18]
References11ShowHide
- [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]Fisher B, et al. Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial. Lancet, 1999.PMID 10376613
- [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
- [5]Cuzick J, et al. Effect of tamoxifen and radiotherapy in women with locally excised ductal carcinoma in situ: long-term results from the UK/ANZ DCIS trial. Lancet Oncol, 2011.PMID 21145284
- [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
- [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
- [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
- [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
- [16]Pilewskie M, et al. Women with Low-Risk DCIS Eligible for the LORIS Trial After Complete Surgical Excision: How Low Is Their Risk After Standard Therapy? Ann Surg Oncol, 2016.PMID 27766556
- [17]Delaloge S, et al. Ductal carcinoma in situ of the breast: finding the balance between overtreatment and undertreatment. Lancet, 2024.PMID 38735296
- [18]Wallis MG, et al. The effect of DCIS grade on rate, type and time to recurrence after 15 years of follow-up of screen-detected DCIS. Br J Cancer, 2012.PMID 22516949