Original Investigation

To clip or not to clip the breast tumor bed? A retrospective look at the geographic miss index and normal tissue index of 110 patients with breast cancer

10.4274/jtgga.2016.0222

  • Florian Ebner
  • Nikolaus de Gregorio
  • Andreas Rempen
  • Peter Mohr
  • Amelie de Gregorio
  • Achim Wöckel
  • Wolfgang Janni
  • Gerlo Witucki

Received Date: 21.12.2016 Accepted Date: 16.03.2017 J Turk Ger Gynecol Assoc 2017;18(2):67-71 PMID: 28400348

Objective:

Planning of breast radiation for patients with breast conserving surgery often relies on clinical markers such as scars. Lately, surgical clips have been used to identify the tumor location. The purpose of this study was to evaluate the geographic miss index (GMI) and the normal tissue index (NTI) for the electron boost in breast cancer treatment plans with and without surgical clips.

Material and Methods:

A retrospective descriptive study of 110 consecutive post-surgical patients who underwent breast-conserving treatment in early breast cancer, in which the clinical treatment field with the radiologic (clipped) field were compared and GMI/NTI for the electron boost were calculated respectively.

Results:

The average clinical field was 100 mm (range, 100-120 mm) and the clipped field was 90 mm (range, 80-100 mm). The average GMI was 11.3% (range, 0-44%), and the average NTI was 27.5% (range, 0-54%). The GMI and NTI were reduced through the use of intra-surgically placed clips.

Conclusion:

The impact of local tumor control on the survival of patients with breast cancer is also influenced by the precision of radiotherapy. Additionally, patients demand an appealing cosmetic result. This makes “clinical” markers such as scars unreliable for radiotherapy planning. A simple way of identifying the tissue at risk is by intra-surgical clipping of the tumor bed. Our results show that the use of surgical clips can reduce the diameter of the radiotherapy field and increase the accuracy of radiotherapy planning. With the placement of surgical clips, more tissue at risk is included in the radiotherapy field. Less normal tissue receives radiotherapy with the use of surgical clips.

Keywords: Breast cancer, clips, radiotherapy, geographic miss index, normal tissue index, boost, reduction

Introduction

Wide local excision is the current surgical treatment for most early breast cancers. With the oncologic benefit taken for granted, the cosmetic results are becoming more important (1). In today’s practice, surgeons 'hide' scars around the areola, laterally in the lower axilla or underneath the breast. Guidelines recommend that breast conserving surgery is accompanied by whole breast irradiation. The benefit of guideline-adherent radiotherapy has been clearly demonstrated (2-5); however, clinical 'landmarks' (i.e. scars) for radiotherapy treatment planning are becoming less reliable. Therefore, the use of surgical clips has been discussed in the last decade (6-9). Though practical, the use of clips has not been established routinely in some centers, as such proof for the dosimetric advantage is still pending. To estimate the accuracy of radiotherapy treatment, the geographic miss index (GMI) and the normal tissue index (NTI) for the electron boost are used (Figure 1). Ideally, the GMI and the NTI should be as low as possible.


Material and Methods

Between November 2008 and December 2010, 110 patients with breast cancer who underwent breast conserving surgery with intra-mammary clips and axillary lymph node dissection (ALND) or sentinel node biopsy (SNB) were treated at the Breast Centre Radiotherapy Department with Adjuvant Radiotherapy.

To determine the GMI and NTI in our Breast Cancer Centre, we retrospectively analyzed the radiotherapy treatment plans of 110 patients who underwent breast conserving surgery followed by radiotherapy between 2008 and 2010.

Statistical analysis

GMI is defined as the percentage of the radiologically-defined field (RF) that is not predicted using clinical landmarks [shared field=SF; GMI=(RF-SF)/RF]. This area represents tissue within the tumor bed, at high risk of local recurrence, which would not have been included in a clinically-marked electron boost field. NTI measures the percentage of the clinically-marked field (CF) that is not part of the RF ('simulation' field'), which receives high-dose treatment [NTI=(CF-SF)/CF].

In our standard surgical protocol, at least three clips are inserted at the margins of the excision cavity and additionally in areas of tumor extension. The volume that the clips cover encloses the former tumor volume. The walls of the excision cavity are approximated at the time of surgery.

Descriptive statistics were calculated with SPSS for Windows (IBM Corp. Released 2010. IBM SPSS Statistics for Windows, Version 19.0. Armonk, NY: IBM Corp) and are given as means, standard deviation (SD), minimum (Min) and maximum (Max).

Radiation therapy

External beam radiotherapy was planned four to six weeks after completion of chemotherapy or surgery, depending on the clinical situation. Postoperative radiation is given by using a linear accelerator (Elekta Precise) from two (up to four) opposed tangential breast fields, thereby providing a cumulative radiation dose of 50 Gy photons as recommended by the International Commission on Radiation Units&Measurement (10). Mixed energies of 6- and 10-MV photons were used in patients with large breasts. The therapy was administered over a five-week period using 2-Gy daily fractions and a wedge compensator to achieve a uniform dose. The planned target volume encompassed the entire ipsilateral breast. Photon radiation of the entire breast was followed by an electron boost, usually delivering an additional dose of 10 Gy, also in 2-Gy daily fractions.

Clinical markers (scar, memory of patient, hematoma) were used to plan a clinical field area for the electron boost. A 100-mm diameter metal ring was then placed on the breast. X-ray imaging was used to show the clips. On a treatment plan simulation, the clips were outlined and a 30-mm margin was added. The RF ring was then placed around this window. The diameter was taken and the GMI and NTI were calculated.

The study is a descriptive study for standard treatment and did not require ethical approval.


Results

A total of 110 consecutive patients who underwent breast conserving surgery were included in the study. The average age was 58 years (28-87 years). The average tumor diameter was known in 97.3% of cases. One patient had a complete remission under neoadjuvant treatment and two patients’ final histology data were missing from the database. The diameters ranged from 3 to 52 mm (average 19 mm). After surgery, 75 patients were classified as T1, 31 as T2, two patients had a T4b, and a further two had ductal carcinoma in situ (DCIS). All patients completed the surgical treatment prior to radiotherapy. Ninety-three patients had positive hormone receptors (16 negative) and 19 had herceptin receptor over expression (86 negative, five unknown; further details are provided in Table 1).

The average follow-up was 41 months (30-57 months). One patient had a local recurrence, two had local and distant recurrence, and two had distant recurrences. Of these patients, two died of a tumor-related cause (distant metastasis). One patient died unrelated to the tumor diagnosis (traffic accident). One patient was diagnosed as having contra lateral breast cancer after 47 months. One hundred six patients had hormone therapy +/- chemotherapy. Two patients had a large (>50 mm), high-grade DCIS and therefore hormonal or chemotherapy was not recommended. No further treatment information was available for two cases. After excluding these 4 patients from further analysis, the average clinical field was 100 mm (range, 100-120 mm) and the radiologic field was 90 mm (range, 80-100 mm). The average GMI was 11.3% (range, 0-44%), and the average NTI was 27.5% (range, 0-54%) (see Table 2).


Discussion

Local disease control is associated with overall survival (11). Efforts have been made to reduce the rate of local recurrence with surgical, systemic therapy, and radiotherapy (12). The influence of systemic therapy on local and distant recurrence has been accepted (13, 14). The surgical resection margin has also been identified as a marker for recurrence rates and the influence of boost radiation (15, 16). The accuracy of the boost can be judged by the GMI and NTI. These indices measure the accuracy of radiotherapy towards the tumor bed. Traditionally, the surgical scar has been used to locate the tumor bed, but breast surgeons and radiation oncologists (17) are becoming more and more concerned about the cosmetic results of their surgery. This results in a scar being a very poor clinical marker for tumor location (6, 18). Patients memory regarding the tumour location is also variable. Fifteen (14%) of our patients had a GMI of 25% or more. This number was lower than the GMI published by Harrington et al. (19). One of the reasons might be the surgical technique of placing the incision immediately over the tumor, which is the common approach of our breast surgeons. Harrington et al. (19) published a GMI depending on the margins between 32.9% (1-cm margin) and 18.6% (3-cm margin) and gave an NTI between 14.6% and 9.7%. Kirby et al. (20) had a GMI of 37% and an NTI of 9%. Twenty-seven cases had a GMI of 0%, meaning that the 'simulation' field was completely covered by the clinical field. With a smaller diameter, the radiologic field resulted in more accurate targeting. In our case series, the NTI was 0% in two patients, with an NTI on average of 27.5%. This shows that even with a good clinical field, one third of high-risk tissue might be missed.

In addition to the above discussion of GMI and NTI, which is based on 2D radiographs, clips offer a further advantage. The dose distribution of the electron boost can be calculated on the basis of computerized tomography (CT) images and 3D planning software. The visibility of the clips allows to select the optimum electron energy that is high enough to cover the clips, but as low as possible to minimize the dose in the lung.

The German Society of Radiooncology practical guidelines for radiotherapy of Breast Cancer I (21) gave the option of placing intra-operative clips, and additionally using presurgical mammography and CT-scans or ultrasound to locate the tumor bed. In the current version, no recommendation is published (22). The S3 guidelines recommend the use of intra surgical clips (13).

One of the limitations of our study is the use of 'classic' external beam radiotherapy. Though it is still commonly in use, the forefront in radiotherapy is shorter treatment protocols, intra-surgical radiation and others (23). Also, it needs to be considered that the intention of the paper was not to provide information on disease-free survival even though the number of patients was fair, but to show the necessity of marking the tumor bed with clips in order to make radiotherapy more precise. The follow-up time was only adequate for early relapses.

Our data clearly demonstrate that with the use of clips in CT radiotherapy planning, the diameter of the field can be reduced by 10 mm on average while increasing the accuracy of the radiotherapy treatment compared with clinical placement with a larger diameter. We think that this can be stated even with such a small case series. Despite this, the common use of intra-surgical clips is not yet established.

Ethics Committee Approval: Ethics committee approval was not needed according to the ethics committee of the university Heidelberg as the study is a retrospective analysis of existing treatment data.

Informed Consent: Written informed consent was obtained from patients who participated in this study.

Peer-review: Externally and internally peer-reviewed.

Author Contributions: Concept – G.W., A.R., F.E.; Design – P.M., G.W., A.R., F.E.; Supervision – A.W., A.R., G.W.; Materials – P.M., A.R., F.E.; Data Collection and/or Processing – A.D., N.D., F.E.; Analysis and/or Interpretation – J.W., F.E., N.D., A.W.; Literature Review – F.E., A.D.; Writer – F.E., G.W.; Critical Review – A.R., J.W., A.W.

Conflict of Interest: No conflict of interest is declared by the authors.

Financial Disclosure: The authors declared that this study received no financial support.


1.    Ciammella P, Podgornii A, Galeandro M, Micera R, Ramundo D, Palmieri T, et al. Toxicity and cosmetic outcome of hypofractionated whole-breast radiotherapy: predictive clinical and dosimetric factors. Radiat Oncol 2014; 9: 97.
2.    Hancke K, Denkinger MD, König J, Kurzeder C, Wöckel A, Herr D, et al. Standard treatment of female patients with breast cancer decreases substantially for women aged 70 years and older: A German clinical cohort study. Ann Oncol 2010; 21: 748-53.
3.    Schwentner L, Wolters R, Koretz K, Wischnewsky MB, Kreienberg R, Rottscholl R, et al. Triple-negative breast cancer: the impact of guideline-adherent adjuvant treatment on survival--a retrospective multi-centre cohort study. Breast Cancer Res Treat 2012; 132: 1073-80.
4.    Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, et al. Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med 2002; 347: 1233-41.
5.    Fiorentino A, Mazzola R, Ricchetti F, Giaj Levra N, Fersino S, Naccarato S, et al. Intensity modulated radiation therapy with simultaneous integrated boost in early breast cancer irradiation. Report of feasibility and preliminary toxicity. Cancer Radiothér 2015; 19: 289-94.
6.    Hansen CJ, de Winton E, Guglani S, Vamvakas E, Willis D, Chua BH. Target localisation for tumour bed radiotherapy in early breast cancer. J Med Imaging Radiat Oncol 2012; 56: 452-7.
7.    Benda RK, Yasuda G, Sethi A, Gabram SG, Hinerman RW, Mendenhall NP. Breast boost: are we missing the target? Cancer 2003; 97: 905-9.
8.    Thomassin-Naggara I, Lalonde L, David J, Darai E, Uzan S, Trop I. A plea for the biopsy marker: how, why and why not clipping after breast biopsy? Breast Cancer Res Treat 2012; 132: 881-93.
9.    Witucki G, Degregorio N, Rempen A, Schwentner L, Bottke D, Janni W, et al. Evaluation of Sentinel Lymph Node Dose Distribution in 3D Conformal Radiotherapy Techniques in 67 pN0 Breast Cancer Patients. Int J Breast Cancer 2015; 2015: 539842.
10.    The international commission on radiation units and measurements. J ICRU 2010;10:NP.
11.    Clarke M, Collins R, Darby S, Davies C, Elphinstone P, Evans E, et al. Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomised trials. Lancet 2005; 366: 2087-106.
12.    Genebes C, Chand ME, Gal J, Gautier M, Raoust I, Ihrai T, et al. Accelerated partial breast irradiation in the elderly: 5-year results of high-dose rate multi-catheter brachytherapy. Radiat Oncol 2014; 9: 115.
13.    Kreienberg R, Kopp I, Albert US, Bartsch HH, Beckmann MW, Berg D, et al. Interdisziplinäre S3-Leitlinie und Nachsorge des Leitlinie. Ger Cancer Soc 2012; 7: 32-45.
14.    Kaufmann M, von Minckwitz G, Bergh J, Conte PF, Darby S, Eiermann W, et al. Breakthroughs in research and treatment of early breast cancer: an overview of the last three decades. Arch Gynecol Obstet 2013; 288: 1203-12.
15.    Bartelink H, Horiot JC, Poortmans PM, Struikmans H, Van den Bogaert W, Fourquet A, et al. Impact of a higher radiation dose on local control and survival in breast-conserving therapy of early breast cancer: 10-year results of the randomized boost versus no boost EORTC 22881-10882 trial. J Clin Oncol 2007; 25: 3259-65.
16.    Jones HA, Antonini N, Hart AA, Peterse JL, Horiot JC, Collin F, et al. Impact of pathological characteristics on local relapse after breast-conserving therapy: a subgroup analysis of the EORTC boost versus no boost trial. J Clin Oncol 2009; 27: 4939-47.
17.    Piroth MD. (Risks of unfavorable cosmetic and toxicity after percutaneous accelerated partial breast irradiation (APBI). Interim analysis from the Canadian RAPID trial). Strahlenther Onkol 2013; 189: 1054-5.
18.    Denham JW, Sillar RW, Clarke D. Boost Dosage to the Excision Site Following Conservative Surgery for Breast Cancer: It’s Easy to Miss! Clin Oncol (R Cool Radiol) 1991; 3: 257-61.
19.    Harrington KJ, Harrison M, Bayle P, Evans K, Dunn PA, Lambert H, et al. Surgical clips in planning the electron boost in breast cancer: a qualitative and quantitave evaluation. Int J Radiat Oncol Biol Phys 1996; 34: 579-84.
20.    Kirby AM, Evans PM, Nerurkar AY, Desai SS, Krupa J, Devalia H, et al. How does knowledge of three-dimensional excision margins following breast conservation surgery impact upon clinical target volume definition for partial-breast radiotherapy? Radiother Oncol 2010; 94: 292-9.
21.    Sautter-Bihl ML, Budach W, Dunst J, Feyer P, Haase W, Harms W, et al. DEGRO practical guidelines for radiotherapy of breast cancer I: breast-conserving therapy. Strahlenther Onkol 2007; 183: 661-6.
22.    Sedlmayer F, Sautter-Bihl ML, Budach W, Dunst J, Fastner G, Feyer P, et al. DEGRO practical guidelines: radiotherapy of breast cancer I: radiotherapy following breast conserving therapy for invasive breast cancer. Strahlenther Onkol 2013; 189: 825-33.
23.    Akhtari M, Teh BS. Accelerated partial breast irradiation: Advances and controversies. Chin J Cancer 2016; 35: 31.