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Surgery : BC Cancer Agency

 lancezwl 2010-05-16

Surgery

 

Published: Thursday, May 03, 2007

  1. Indications for mastectomy versus breast conserving surgery
  2. Optimal surgical margins
  3. Guidelines for re-excision and boost following breast conserving surgery
  4. Recommendations for axillary dissection for breast cancer surgery
  5. Sentinel lymph node biopsy
  6. Recommendations for sentinel lymph node biopsy
  7. Types of breast reconstruction
  8. Potential contraindications to breast reconstruction
  9. Advantages of breast reconstruction
  10. Recommendations for adjuvant cancer treatments following immediate breast reconstruction
  11. Breast prosthesis and how to help a patient obtain one

1. Indications for mastectomy versus breast conserving surgery

  • For patients with stage I or II breast cancer, breast conserving surgery (BCS) followed by radiotherapy is generally recommended. In the absence of special reasons for selecting mastectomy, the choice between BCS and mastectomy can be based on the patient’s circumstances and personal preferences
  • Mastectomy should be considered in the presence of any of the following:
    • Factors that increase the risk of local recurrence such as extensive malignant-type calcifications visible on the mammogram, multiple primary tumours or failure to obtain tumour-free margins
    • Physical disabilities that preclude lying flat or abducting the arm, for radiotherapy treatment. Pregnancy in the first or second trimester, previous irradiation of the breast, or conditions such as systemic lupus erythematosus or scleroderma
    • Large tumour size in proportion to breast size
    • The patient’s clear preference for mastectomy
  • The following factors are not contraindications for BCS:
    • The presence of a centrally located tumour mass
    • Axillary lymph-node involvement
    • The presence of breast implants
  • In some cases, preoperative chemotherapy can shrink a large primary tumour and allow for BCS
  • Before deciding between BCS and mastectomy, the physician must make a full and balanced presentation to the patient concerning the pros and cons of these procedures
  • Whenever an open biopsy is performed on the basis of even modest suspicion of carcinoma, the procedure should be, in effect, a lumpectomy, using wide local excision of the intact tumour surrounded by a cuff of tumour-free tissue (determined by palpation and visual inspection)
  • The following recommendations should be observed to provide optimum clinical and cosmetic results:
    • Tumour-involved margins should be revised
    • Separate incisions should be used for removal of the primary tumour and for the axillary dissection except when these coincide anatomically
    • Curvilinear incisions, concentric with the areolar margin, or transverse incisions are recommended over radial incisions
    • Drains and approximation sutures should not be used in the breast parenchyma
  • All patients treated by partial mastectomy and axillary dissection should have a post-surgical consultation with a radiation oncologist regarding radiation to the breast. Some patients may also require radiation to the axilla1

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2. Optimal surgical margins

It is important to obtain negative resection margins at the time of surgery (tumour > 2 mm from an inked margin) for all patients with invasive disease or DCIS.2 Invasive or in situ disease at the margin is treated in the same manner. A positive margin is defined as tumour touching ink and (or transected tumour), a close margin is margin < 2 mm and anything in-between (Table 1).

Even with pathologically negative margins, 25% to 40% of women treated with partial mastectomy alone (without radiation) will recur in the breast within five to ten years of follow up.2

Table 1. Biopsy: Margins of Resection

Negative and positive "margins" or "margins of resection" (the distance between the tumour and the edge of the tissue).

A: cancer cells

B: normal tissue

C: ink marking the edge

Diagram of negative margins and positive margins sourced with permission from www.

Table content sourced with permission from www.

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3. Guidelines for re-excision and boost following breast conserving surgery

Re-excision to obtain negative margins is recommended for patients with close or positive margins. If a margin is <2 mm and re-excision is declined or inappropriate, a radiation boost to the tumour bed is recommended. Re-excision should be more strongly recommended where the risk of ipsilateral breast tumour recurrence (IBTR) is high and systemic risk is low3, for example:

Margin <2 mm and:3

  • extensive intraductal component present;
  • age < 50;
  • histology of LCIS or invasive lobular carcinoma;
  • lymphatic invasion present;
  • no systemic therapy given;
  • at multiple sites;
  • margin status unknown;
  • tumour touching inked margin at any site; or
  • pure ductal carcinoma in situ.

When the deep margin is positive, and the surgeon has dissected down to fascia, then a boost should be given. Patients with close or positive margins who decline re-excision should be advised that the risk of IBTR is increased. The relative risks/ benefits of re-excision vs. boost in the context of local control and cosmesis should be discussed.3

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4. Recommendations for axillary dissection for breast cancer surgery

  • Removal and pathological examination of axillary lymph nodes should be standard procedure for patients with early, invasive breast cancer
  • For accurate staging and to reduce the risk of recurrence in the axilla, level 1 and level 2 nodes should be removed (Table 2)
  • Patients should be made fully aware of the frequency and severity of the potential complications of axillary dissection
  • Irradiation of the axilla should carried out with caution after axillary dissection
  • Omission of axillary dissection may be considered when the risk of axillary metastasis is very low or when knowledge of node status will have no influence on therapy
  • Patients should be offered the opportunity to participate in clinical trials whenever possible4
Table 2. Axillary Lymph Nodes

Lymph node areas adjacent to breast area.

A: pectoralis major muscle

B: axillary lymph nodes: levels I

C: axillary lymph nodes: levels II

D: axillary lymph nodes: levels III

E: supraclavicular lymph nodes

F: internal mammary lymph nodes

Image of axillary lymph nodes sourced with permission from www.

Table content sourced with permission from www.

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5. Sentinel lymph node biopsy

Sentinel lymph node biopsy is a diagnostic procedure used to determine whether a breast cancer has metastasized to axillary lymph nodes. A sentinel lymph node biopsy requires the removal of only one to three lymph nodes. If the sentinel nodes do not contain cancer cells, this may eliminate the need to remove additional axillary lymph nodes.

The sentinel lymph node procedure entails the injection of a small dose of a low-level radioactive tracer called technetium-99 into the breast in the region of the patient’s tumour at least two hours before surgery. At the time of surgery, a blue dye is also injected to help visually track the location of the sentinel node during the operation. After injection of the blue dye, the surgeon uses a hand held gamma ray counter to detect the radioactive tracer and locate the sentinel node. Once the area has been pinpointed, the surgeon will make a small incision (usually one-half inch) and remove the sentinel node(s) for a pathologist to examine under a microscope. The blue dye provides additional visual confirmation of the sentinel node’s location during surgical removal.5

Sometimes, lymphoscintigraphy will be used after injecting the technetium-99 before surgery. Since the uptake of the technetium-99 by cancerous lymph nodes is sometimes different than the uptake by normal lymph nodes, these nuclear medicine images may also help show which lymph nodes are cancerous.5

In facilities that offer intraoperative consultation and imprint histology, the pathologist performs a quick touch prep H&E test to provide preliminary information regarding sentinel node metastases. If this test comes back positive, the surgeon will proceed with axillary dissection. If the touch prep H&E test comes back negative, the surgeon will proceed as per established guidelines as previously discussed with the patient. A complete sentinel node assessment will be performed post-surgery to provide complete pathology of the nodes.5

Table 3. Injection of Blue Dye for Sentinel Node Biopsy

Blue dye draining away from lumpectomy site, within lymphatic channels, towards the axilla.

A: blue dye in lumpectomy site

B: axillary lymph nodes: levels I

C: axillary lymph nodes: levels II

D: axillary lymph nodes: levels III

E: large lymphatic channels

F: small lymphatic channels

G: sentinel lymph nodes taking up dye

Image of Blue dye draining away from lumpectomy site, within lymphatic channels, towards the axilla, sourced with permission from www.

Table content sourced with permission from www.

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6. Recommendations for sentinel lymph node biopsy

  • Axillary dissection is the standard of care for the surgical staging of operable breast cancer
  • Centres that elect to perform sentinel lymph node biopsy for breast cancer patients require a multidisciplinary approach, coordinating the efforts of radiology, surgery and pathology divisions
  • Appropriate training and skills development for participants from each division is mandatory
  • If a patient requests or is offered SLN biopsy, the benefits and risks as well as what is and is not known about the procedure should be outlined
  • Patients should be informed of the number of SLN biopsies performed by the surgeon and the surgeon’s success rate with the procedure, as determined by the identification of the SLN and the false-negative rate (the presence of tumour cells in the axillary nodes when the SLN biopsy result is negative)
  • Before surgeons replace axillary dissection by SLN biopsy as the staging procedure at their institution, they should:
    • familiarize themselves with the literature on the topic and the techniques needed to perform the procedure'
    • follow a defined protocol for all three aspects of the procedure (nuclear medicine, surgery, pathology); and
    • perform backup axillary dissection until an acceptable success rate (as determined by the identification of the SLN and the false-negative rate) is achieved
  • A surgeon who performs breast cancer surgery infrequently should not perform SLN biopsy
  • All patients should undergo level 1 and level 2 axillary dissection if the sentinel node(s) are reported positive for malignancy, if the surgeon is unable to identify a sentinel node or as part of the surgeon’s training and validation process
  • Indications for SLN biopsy include women with T1 and T2 breast cancers
  • SLN biopsy is contraindicated in women who have clinically palpable nodes, locally advanced breast cancer, multifocal tumours, previous breast surgery, previous irradiation of the breast, adverse reactions to vital dyes and inability for the patient to give consent
  • Staining of tissue sections with hematoxylin and eosin (H&E), and not immunohistochemical analysis for cytokeratin, should determine adjuvant therapy
  • Sterile technique should be used for invasive breast imaging and surgical removal of the sentinel lymph node
  • A combined technique for sentinel node imaging using radiotracer (37 Mbq of 99mTc Sulphur Colloid) and 5ml of 1% Isosulfan blue dye maximizes detection rates
  • Radiotracer and isosulfan injections should be given peritumourally within 1 cm of the cancer or biopsy cavity
  • An option of using a subdermal injection of contrast has been found to increase detection of sentinel nodes
  • Preoperative sentinel node imaging in the nuclear medicine department has been found to assist surgeons to successfully identify sentinel node(s) intraoperatively
  • Standardized documentation and data collection is necessary from all departments (radiology, surgery, pathology) for the determination of institutional and surgeon specific case volume, sentinel node identification rate and false negative rate
  • Participation in randomized clinical trials is encouraged5,6

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7. Types of breast reconstruction

  • Autologous – this refers to the use of a patient’s own tissue only (abdominal tissue (TRAM flap) or latisimus muscle) (Table 4 and 5)
  • Non-autologous – this means that some form of breast implant is used as part of the reconstruction (Table 6 and 7)
  • Immediate – at the same time as mastectomy
  • Delayed – at any time following mastectomy

The reconstruction may include the breast mound alone or also the nipple-areola complex. It is also possible for women to have delayed reconstruction following mastectomy with a combination of implant and tissue reconstruction or for women with significant cosmetic deficit following breast conserving surgery to have delayed reconstruction with implant and/or tissue reconstruction.

For immediate reconstruction, the general surgeon performs the mastectomy at the same time the plastic surgeon reconstructs the breast. For delayed reconstruction, the plastic surgeon should be in close contact with the general surgeon who performed the original mastectomy for details of the patient's previous treatment and prognosis.

Reduction mammoplasty of the other breast may be considered to retain symmetry. The remaining breast is at increased risk for malignancy with the risk probably greatest for patients who have lobular carcinoma or a significant family history. Some patients may be candidates for, or may choose to have, contralateral total mastectomy with bilateral reconstruction rather than simple reduction mammoplasty on the contralateral side.7

Table 4. TRAM Flap Breast Reconstruction - Preparation

Woman after mastectomy, showing trans-rectus abdominis muscle (TRAM) and surrounding tissues, in preparation for reconstruction.

A: mastectomy site

B: right trans rectus abdominis muscle

C: left trans rectus abdominal muscle

D: segment of abdominal tissues: skin and fat, to be transferred along with muscle to create the new breast

Image of Woman after mastectomy, showing trans-rectus abdominis muscle (TRAM) and surrounding tissues, in preparation for reconstruction, sourced with permission from www.

Table content sourced with permission from www.

Table 5. Latissimus Muscle in New Location

Woman with latissimus dorsi muscle swung forward to re-create the new breast.

A: latissimus dorsi muscle in new location to re-create breast.

Image of Woman with latissimus dorsi muscle swung forward to re-create the new breast, sourced with permission from www.

Table content sourced with permission from www.

Table 6. Unfilled Tissue Expander

Side view of breast area with unfilled tissue expander in place.

A: tissue expander – unfilled

B: port

C: catheter

D: syringe

E: ribs

F: pectoralis major muscle

G: Other muscles of the chest wall (three lines to one letter)

Image of Side view of breast area with unfilled tissue expander in place, sourced with permission from www.

Table content sourced with permission from www.

Table 7. Filled Tissue Expander

Side view of breast area with filled tissue expander in place.

A: tissue expander – filled

B: port

C: catheter

D: syringe

E: ribs

F: pectoralis major muscle

G: other muscles of the chest wall (three lines to one letter)

Image of Side view of breast area with filled tissue expander in place, sourced with permission from www.

Table content sourced with permission from www.

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8. Potential contraindications to breast reconstruction

  • Severe lung disease
  • Advanced diabetes
  • Recent heart attack
  • Heavy smokers
  • Metastatic disease
  • Those whose emotions, motivation or personal circumstances make it difficult for them to cope with additional surgery and healing

9. Advantages of breast reconstruction

In terms of body image and emotional state, the advantages of immediate breast reconstruction are well documented. However, there are many patients who have no interest in breast reconstruction, but it is reasonable for the surgeon or the oncologist to discuss its availability with all women. Any patient contemplating reconstruction should recognize that the goal of reconstruction is for a good body image while fully clothed. A reconstructed breast will not look like or feel like a natural breast.7

To learn more about breast reconstruction options, decision-making, pre- and post-op care and follow-up, review the material on the UBC Breast Reconstruction Program.

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10. Recommendations for adjuvant cancer treatments following immediate breast reconstruction

Breast reconstruction following mastectomy for cancer does not adversely affect the prognosis or the physician's ability to follow the patient for metastatic disease.7

There is no documented increase in local or regional recurrence associated with immediate reconstruction nor is there a delay in the recognition of local or regional recurrence when it does develop. As well, no survival difference can be identified in patients who have undergone immediate reconstruction. Hence, in terms of tumour control, there are no patients in whom the procedure is specifically contraindicated.7

Post-operative radiotherapy, when indicated, may be given in the usual way. There may be some adverse effects in terms of capsular fibrosis around implants. Tissue flaps should not be adversely affected.7

It is possible that post-operative complications may be increased if extensive tissue transfer is carried out and this in turn may delay the start of adjuvant chemotherapy. A review of the literature does not suggest that this is a significant problem in centres where this type of procedure is done frequently. The complication rate does not appear to be higher than that for mastectomy alone.7

Generally, there does not appear to be any contraindication to immediate reconstruction in terms of adjuvant treatment and patient outcomes. However, operating time for autologous reconstruction is significantly longer than for regular breast surgery. This, combined with challenges in coordinating both a general surgeon and plastic surgeon's operating schedules, can add to the surgical wait time.7

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11. Breast prosthesis and how to help a patient obtain one

Not all women are interested in breast reconstruction following mastectomy. Some choose to wear an external breast prosthesis in their bra or bathing suit to give the appearance of a natural breast. There are many types and levels of quality of breast prostheses on the market. Prostheses can be made of light, fluffy cotton, foam, or silicone gel.

Temporary “fluffy” breast forms are available free of charge for women who have had a mastectomy or for women with significant deficit after breast conserving surgery. These can be worn immediately after surgery, if desired, to fill out their clothing. Temporary forms can be obtained through most hospitals, local Canadian Cancer Society offices or by calling the Cancer Information Service line at 1.888.939.3333.

Permanent external breast forms can be fitted four to six weeks after mastectomy, when the incision line is healed, there is no infection, and swelling has dissipated. A woman should also be emotionally ready for a fitting. A physician prescription is required for financial reimbursement if a woman purchases a breast form and mastectomy bra.

Wearing a permanent prosthesis can help with posture changes and back issues that can result from having a breast removed. Partial breast shapers are available for women who have had breast conserving surgeries and can be placed in the bra to replace lost tissue and balance the figure.

Permanent external breast forms can be purchased through specialty stores who often have trained fitters. Financial assistance toward the purchase of permanent breast prosthesis is available through a variety of sources. Patients should contact the appropriate source to see what is covered by their plan.

  • Some private insurance extended benefit plans
  • Pharmacare
  • Ministry of Social Services and Housing
  • Canadian Cancer Society's Breast Prosthesis Bank. Call 1.888.939.3333
  • Private insurance

The Canadian Cancer Society has a Breast Prosthesis Bank (BPB) that offers gently used or end of the line bras and prosthesis free of charge to women with limited financial means. Patients should call the Cancer Information Service at 1.888.939.3333 to find a Breast Prosthesis Bank in their community or to arrange for prosthesis to be mailed to them.

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References:

1. Clinical practice guidelines for the care and treatment of breast cancer, Guideline 3: Mastectomy or lumpectomy? The choice of operation for clinical stages I and II breast cancer, Rev. July 23, 2002, © 2006 CMA Media Inc. or its licensors.

2. BC Cancer Agency (http://www.bccancer.). Vancouver (BC): 2006. (cited Sep 22, 2006). Available from: BC Cancer Agency's Cancer Management Guidelines -> Breast -> Management

3. BC Cancer Agency (http://www.bccancer.). Vancouver (BC): 2006. (cited Sep 22, 2006). Available from: BC Cancer Agency's Cancer Management Guidelines -> Breast -> Management

4. Clinical practice guidelines for the care and treatment of breast cancer, Guideline 4: Axillary dissection (2001 decision: no update required) © 2006 CMA Media Inc. or its licensors.

5. BC Cancer Agency (http://www.bccancer.). Vancouver (BC): 2006. (cited Sep 22, 2006). Available from: http://www.bccancer./NR/rdonlyres/169A6C64-24C3-4D5E-9828-BB3F4FBC2BC7/17503/BreastSLNGuidelineFeb2006.pdf

6. Clinical practice guidelines for the care and treatment of breast cancer, Guideline 13: Sentinel lymph node biopsy,July 24, 2001, © 2006 CMA Media Inc. or its licensors.

7. BC Cancer Agency (http://www.bccancer.). Vancouver (BC): 2006. (cited Sep 22, 2006). Available from: BC Cancer Agency's Cancer Management Guidelines -> Breast -> Management

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