Literature DB >> 32578065

Radioactive Seed Versus Wire-Guided Localization for Ductal Carcinoma in Situ of the Breast: Comparable Resection Margins.

Marie Colombe Agahozo1, Sofie A M Berghuis2, Esther van den Broek3, Linetta B Koppert4, Inge-Marie Obdeijn5, Carolien H M van Deurzen6.   

Abstract

BACKGROUND: There are currently two widely used methods for preoperative localization of ductal carcinoma in situ (DCIS) of the breast: wire-guided localization (WGL) and radioactive seed localization (RSL). Several studies compared these localization techniques in small cohorts.
OBJECTIVE: The aim of this study was to compare the surgical resection margin status between RSL and WGL in a large national cohort of patients with DCIS. PATIENTS AND METHODS: We included patients from the Dutch Pathology Registry who underwent breast-conserving surgery for DCIS by either RSL (n = 1851) or WGL (n = 2187) between 2009 and 2019. Several clinicopathological characteristics were compared between these two groups, including resection margin status and number of re-excisions.
RESULTS: Patients undergoing RSL were younger (p = 0.014) and were more often diagnosed with a large DCIS (p = 0.013), high grade DCIS (p < 0.001) and comedonecrosis (p < 0.001) compared with patients undergoing WGL. There was no significant difference in resection margin status between both groups (p = 0.089) and the number of re-excisions (p = 0.429). However, in case of re-excision, patients in the RSL group were more often treated with breast-conserving surgery (p = 0.029).
CONCLUSION: In this large national cohort study of patients with DCIS, we demonstrated that there was no difference in resection margin status between both procedures, or in the number of re-excisions, but patients in the RSL group were more often treated with breast-conserving therapy in case of a re-excision.

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Year:  2020        PMID: 32578065      PMCID: PMC7669767          DOI: 10.1245/s10434-020-08744-8

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


Since the introduction and improvement of breast screening by mammography, the detection rate of ductal carcinoma in situ (DCIS) of the breast has increased.1–3 Nowadays, DCIS accounts for approximately 20% of all breast cancers in the screened population.1 The majority of patients with DCIS are treated with surgery, either breast-conserving surgery in combination with radiotherapy, or a mastectomy, depending on the DCIS size and the patients’ preference.3–5 Clinically, DCIS is generally non-palpable and has a diffuse growth pattern, which makes it challenging to estimate the correct size using imaging modalities. In literature, there has been a lack of consensus regarding the most optimal resection margin for patients with DCIS. Several authors used different definitions ranging from ‘no ink on the tumor’ to a 10 mm free margin.6,7 Obviously, extensively positive resection margins are associated with a higher risk for local recurrence, but wide margins (> 10 mm) are more likely to compromise cosmetics, therefore this has to be balanced. In 2016, the Society of Surgical Oncology, the American Society for Radiation Oncology, and the American Society of Clinical Oncology published a consensus guideline for patients with DCIS undergoing breast-conserving surgery with whole-breast irradiation. In this guideline, a margin ≥ 2 mm is proposed as being most optimal for patients with DCIS.8,9 In line with international data, there has been a lack of consensus in The Netherlands regarding the optimal resection margin for DCIS. In The Netherlands, resection margin status for patients with invasive breast cancer is defined as free (no ink on tumor), focally positive (≤ 4 mm ink on tumor), or more than focally positive (> 4 mm ink on tumor).10,11 According to this guideline, invasive breast cancer patients with a focally positive margin undergo a boost of radiation instead of re-excision based on the low local recurrence rate in this group.12 A re-excision is advised in patients with more than focally positive margins based on the increased local recurrence risk. For patients with DCIS, a re-excision was previously advised for patients with positive margins (ink on tumor), although regional differences were present.11 Currently, the Dutch treatment guideline recommends to consider a re-excision for DCIS with a margin < 2 mm, which is consistent with international recommendations.13 In order to achieve optimal resection margins at first surgery, proper preoperative DCIS localization is crucial. There are two widely used techniques for DCIS localization: wire-guided localization (WGL) and radioactive seed localization (RSL).5 In the case of a WGL procedure, single or multiple wire hooks are placed into the lesion and used as a guide to the lesion,14 while in the case of RSL, single or multiple radioactive iodine-I25 seeds are used to mark the lesion.15 Although WGL was historically seen as the gold standard, it has several disadvantages.14–16 The timing of this procedure is dependent on the availability of the radiologist and the surgeon, since the wire hook has to be placed just before surgery. In addition, it causes more discomfort for the patient and may dislocate before or during surgery.14,16 RSL is therefore seen as an attractive alternative;15, 16 it allows more flexibility scheduling the surgery, since it can be placed during a longer period before surgery, and causes less patient discomfort.14,15 However, misplaced seeds can only be surgically removed, and, due to its radioactivity, the introduction of RSL in an institution is a logistical challenge since it requires strict regulation and training of all staff involved.15 In recent years, several studies have compared both localization techniques but the derived results are inconsistent.14,16–18 On the one hand, studies have found comparable results between RSL and WGL in terms of excision margins, resection weight, and the number of re-excisions,16,17 while on the other hand, a lower rate of positive margins and reoperations have been reported for RSL.14,18 However, these studies included small cohorts, usually from one institute, and were not able to demonstrate highly significant differences. In order to present more conclusive results, a large multicenter study including high numbers of patients is required. The aim of this study was to perform a nationwide study, using real-world data, in order to compare the efficacy of WGL versus RSL for patients treated with breast-conserving surgery for DCIS.

Patients and Methods

Data Collection and Patient Cohort

All data were obtained from the Dutch Pathology Registry (PALGA), which is the nationwide registry of pathology reports. Since 2009, Dutch pathologists can use synoptic reporting modules to report the pathological test results for several common tumor types, including breast cancer.19 In these modules, parameters are captured in numerous standardized variables instead of free-text fields, which facilitates the analyses of all reports simultaneously. In this study, synoptic reports of all patients diagnosed with primary DCIS who underwent breast-conserving surgery by either RSL or WSL between 2009 and 2019 in The Netherlands were included. Patients with an invasive component in the initial surgical specimen were excluded from further analysis. Data collection included age at diagnosis, several DCIS characteristics (size, grade, presence of comedonecrosis and microcalcifications), type of surgery, resection margins, and number of re-excisions. If available, the estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) status were also included.

Statistical Analysis

Variables that were described in the data collection were analyzed using the ‘tableone’ package in R (version 3.5.1; The R Foundation for Statistical Computing, Vienna, Austria). To evaluate potential differences between RSL and WGL, statistical analyses were performed; to evaluate whether categorical variables were significantly different between RSL and WGL, or between the different numbers of seeds injected in the RSL group, the Chi-square test was performed; and to evaluate whether the means of the numerical variables were significantly different, analysis of variance (ANOVA) tests were performed. P-values < 0.05 were considered to be significantly different.

Results

Baseline Characteristics

A total of 4038 DCIS patients were included, of whom 2187 were treated by WGL and 1851 were treated by RSL. Overall, the mean age was 60.0 years (standard deviation [SD] 9.25). The mean DCIS size was 1.78 cm (SD 1.45) and the majority of DCIS cases were either intermediate or high grade, accounting for 40.8% and 44.6% of cases, respectively. ER, PR, and HER2 status was not available for the majority of patients. Baseline patient and tumor characteristics of the WGL and RSL groups are described and compared in Table 1. Compared with patients treated with WGL, patients with RSL were slightly younger at the time of treatment (59.6 years vs. 60.3 years; p = 0.014). Regarding the histopathological aspects of DCIS, patients treated with RSL were more often diagnosed with a larger DCIS size (mean diameter 1.84 cm vs. 1.72 cm; p = 0.013), grade 3 DCIS (47.8% vs. 42.0%; p < 0.001), and presence of comedonecrosis (92.1% vs. 79.9%; p < 0.001) compared with the WGL group.
Table 1

Baseline patient and tumor characteristics [n = 4038]

RSLWGLp value
[n = 1851][2187]
Age, years [mean (SD)]59.63 (9.48)60.35 (9.03)0.014
DCIS size, cm [mean (SD)]1.84 (1.52)1.72 (1.38)0.013
No. of seeds
 1920 (49.7)
 2101 (5.5)
 310 (0.5)
 Unknowna820 (44.3)2187 (100)
DCIS grade
 1252 (13.6)295 (13.5)< 0.001
 2698 (37.7)951 (43.5)
 3885 (47.8)919 (42.0)
 Unknowna16 (0.9)22 (1.0)
Comedonecrosis
 Absent68 (3.7)252 (11.5)< 0.001
 Present799 (43.2)1002 (45.8)
 Unknowna984 (53.2)933 (42.7)
Microcalcification
 Absent255 (13.8)302 (13.8)0.214
 Present1012 (54.7)1354 (61.9)
 Unknowna584 (31.6)531 (24.3)
Estrogen receptor
 Negative18 (1.0)15 (0.7)0.356
 Positive37 (2.0)49 (2.2)
 Unknowna1796 (97.0)2123 (97.1)
Progesteron receptor
 Negative26 (1.4)23 (1.1)0.292
 Positive22 (1.2)32 (1.5)
 Unknowna1803 (97.4)2132 (97.5)
HER2 status
 Not amplified3 (0.2)1 (< 0.1)1
 Amplified5 (0.3)2 (0.1)
 Unknowna1843 (99.6)2184 (99.9)

Data are expressed as n (%) unless otherwise specified

RSL radioactive seed localization, WGL wire-guided localization, SD standard deviation, DCIS ductal carcinoma in situ, HER2 human epidermal growth factor receptor

aExcluded from the analysis

Bolded p-values indicate significance

Baseline patient and tumor characteristics [n = 4038] Data are expressed as n (%) unless otherwise specified RSL radioactive seed localization, WGL wire-guided localization, SD standard deviation, DCIS ductal carcinoma in situ, HER2 human epidermal growth factor receptor aExcluded from the analysis Bolded p-values indicate significance

Wire-Guided Localization and Radioactive Seed Localization Have Comparable Surgical Resection Margins

The resection margins are described in Table 2. Overall, around half of the patients had a surgical resection margin ≥ 2 mm, which was not statistically different between the WGL and RSL groups (p = 0.505). In line with this, there was no significant difference in the number of re-excisions between both groups (p = 0.429). In the WGL group, 13.6% of patients underwent a second surgery and 8.8% underwent a third surgery. In the RSL group, 12.6% of patients underwent a second surgery and 7.7% underwent a third surgery. However, patients with a re-excision after RSL more often underwent a breast-conserving surgery compared with the WGL group (69.2% vs. 59.7%; p = 0.029). This resulted in the detection of additional DCIS in 62.8% of patients in both groups. In 1.7% of patients in the WGL group and 2.6% of patients in the RSL group, an invasive component was present in the re-excision material.
Table 2

Surgical resection margin status and additional surgery [n = 4038]

RSL[n = 1851 (45.8%)]WGL[n = 2187 (54.6%)]p value
Resection margins, cm [mean (SD)]0.33 (0.29)0.35 (0.30)0.089
Resection_margins_cat
  < 2 mm984 (53.2)1142 (52.2)0.505
  ≥ 2 mm856 (46.2)1038 (47.5)
 Unknowna11 (0.6)7 (0.3)
Radicality
 Free1451 (78.4)1699 (77.7)0.531
 Focally not radical253 (13.7)314 (14.4)
 More than focally not radical136 (7.3)167 (7.6)
 Unknowna11 (0.6)7 (0.3)
First re-excision
 Yes234 (12.6)296 (13.5)0.429
 No1617 (87.4)1891 (86.5)
Type of first re-excision
 Breast-conserving surgery162 (69.2)176 (59.5)0.029
 Mastectomy72 (30.8)119 (40.2)
 Unknowna01 (0.3)
Findings in first re-excision specimen
 No rest80 (34.2)103 (34.8)0.888
 DCIS147 (62.8)186 (62.8)
 LCIS1 (0.4)2 (0.7)
Invasive carcinoma6 (2.6)5 (1.7)
Second re-excision
 Yes18 (7.7)26 (8.8)0.769
 No216 (92.3)270 (91.2)
Type of second re-excision
 Breast-conserving surgery2 (11.1)2 (7.7)1
 Mastectomy16 (88.9)24 (92.3)
Findings in second re-excision specimen
 DCIS17 (94.4)26 (100.0)0.852
 No rest1 (5.6)0 (0.0)

Data are expressed as n (%) unless otherwise specified

RSL radioactive seed localization, WGL wire-guided localization, SD standard deviation, DCIS ductal carcinoma in situ, LCIS lobular carcinoma in situ

aExcluded from the analysis

Bolded p-values indicate significance

Surgical resection margin status and additional surgery [n = 4038] Data are expressed as n (%) unless otherwise specified RSL radioactive seed localization, WGL wire-guided localization, SD standard deviation, DCIS ductal carcinoma in situ, LCIS lobular carcinoma in situ aExcluded from the analysis Bolded p-values indicate significance

Number of Seeds and Clinicopathological Characteristics

The association between the number of seeds and clinicopathological characteristics is depicted in Table 3. Overall, the majority of cases (89.2%) were localized by one seed. There was a significant association between the number of seeds and age at diagnosis; a single seed was associated with older age at diagnosis (p = 0.017). In addition, single seed localization was associated with a smaller DCIS diameter (p < 0.001) and the highest percentage of patients with a resection margin ≥ 2.0 mm (p = 0.001) compared with multiple seed localization. However, there was no significant difference in the number of patients undergoing a re-excision (p = 0.161).
Table 3

Clinicopathological characteristics according to the number of seeds [n = 1031]a

Single seed[n = 920 (89.2%)]Multiple seeds (two or three)[n = 111 (10.8%)]p value
Age, years [mean (SD)]59.44 (9.33)57.16 (10.39)0.017
DCIS size, cm [mean (SD)]1.70 (1.37)3.03 (2.14)< 0.001
Resection margins, cm [mean (SD)]0.36 (0.30)0.25 (0.24)0.002
Resection_margins_cat
 < 2 mm448 (48.7)73 (65.8)0.001
 ≥ 2 mm469 (51.0)37 (33.3)
 Unknown3 (0.3)1 (0.1)
Radicality
 Free731 (79.5)88 (79.3)0.574
 Focally not radical123 (13.4)12 (10.8)
 More than focally not radical63 (6.8)10 (9.0)
 Unknownb3 (0.3)1 (0.9)
First re-excision
 Yes110 (12.0)19 (17.1)0.161
 No810 (88.0)92 (82.9)

Data are expressed as n (%) unless otherwise specified

SD standard deviation, DCIS ductal carcinoma in situ

aOnly patients with a known number of seeds were included

bExcluded from the analysis

Bolded p-values indicate significance

Clinicopathological characteristics according to the number of seeds [n = 1031]a Data are expressed as n (%) unless otherwise specified SD standard deviation, DCIS ductal carcinoma in situ aOnly patients with a known number of seeds were included bExcluded from the analysis Bolded p-values indicate significance Subgroup analysis was performed by comparing the use of one seed versus more than one seed in patients with a large DCIS (> 3 cm) [Table 4]. The use of multiple seeds was associated with a larger DCIS diameter (p = 0.002) and higher rate of radicality (free versus focally irradical versus more than focally irradical; p = 0.025). However, there was no association between the number of seeds and the categorical resection margins (< 2 mm vs. ≥ 2; p = 1)
Table 4

Clinicopathological characteristics of patients with large DCIS according to the number of seeds [n = 210]a

Single seed[n = 156 (74.3%)]Multiple seeds (two or three)[54 (25.7%)]p value
Age, years [mean (SD)]60.17 (9.60)58.07 (10.71)0.18
DCIS size [mean (SD)]4.05 (1.24)4.73 (1.62)0.002
Resection margins [mean (SD)]0.19 (0.20)0.17 (0.17)0.561
Resection margin categories
 < 2 mm130 (83.3)44 (81.5)1
 ≥ 2 mm25 (29.1)9 (22.0)
 Unknownb1 (0.6)1 (1.9)
Radicality
 Free86 (55.1)41 (75.9)0.025
 Focally not radical41 (26.3)5 (9.3)
 More than focally not radical28 (17.9)7 (13.0)
 Unknownb1 (0.6)1 (1.9)
First re-excision
 Yes44 (28.2)11 (20.4)0.343
 No112 (71.8)43 (79.6)

Data are expressed as n (%) unless otherwise specified

DCIS ductal carcinoma in situ, SD standard deviation

aOnly patients with large DCIS (> 3 cm) with a known number of seeds were included

bExcluded from the analysis

Bolded p-values indicate significance

Clinicopathological characteristics of patients with large DCIS according to the number of seeds [n = 210]a Data are expressed as n (%) unless otherwise specified DCIS ductal carcinoma in situ, SD standard deviation aOnly patients with large DCIS (> 3 cm) with a known number of seeds were included bExcluded from the analysis Bolded p-values indicate significance

Discussion

The WGL method has historically been used as the gold standard for preoperative localization of non-palpable breast tumors; however, in recent years, RSL has been considered to be an attractive alternative for WGL since it offers more flexibility in scheduling the surgery and is more patient-friendly.15 Several, generally small, previous studies compared both methods regarding their surgical outcome, but the derived results were non-consistent.14,16–18 In this large, population-based cohort study we compared the efficacy of WGL and RSL in patients with DCIS undergoing breast-conserving surgery. This study demonstrated that preoperative localization with RSL was more frequently performed in patients who were younger, were diagnosed with a large or high-grade DCIS, or had a DCIS with comedonecrosis. We hypothesize that these differences may be related to an unequal use of these techniques within different hospitals, since the localization technique is an institutional policy and not a patient-dependent choice. Academic hospitals and specialized cancer centers are potentially more likely to use RSL compared with general hospitals, and these centers attract younger patients, whom generally have a higher rate of high-grade lesions compared with older patients. However, the clinical relevance of these differences, which are relatively limited but statistically significant in this large series, is unclear. When comparing both methods, there was no difference in the surgical resection margins or the number of re-excisions. This is in line with the majority of the studies, which demonstrated equally successful excision rates between RSL and WGL.14,16,17 However, one previous study suggested significant superiority of RSL over WGL based on 169 patients (p = 0.048).18 In our study, we observed that in case of a re-excision, patients in the RSL group were more often treated with breast-conserving surgery compared with the WGL group. Potential explanations for this difference could be that these patients are slightly younger. Another hypothesis is that the volume of the initial surgical specimen in patients treated with RSL could be smaller compared with WGL, due to a more accurate localization. Lastly, we also showed that in terms of RSL, the use of a single seed is associated with a smaller DCIS diameter, which consequently results in a larger resection margin. In our subgroup analysis restricted to patients with extensive DCIS (≥ 3 cm), we demonstrated that the use of multiple seeds was associated with a higher rate of radicality. This is in line with a recent study that also suggested superiority of multiple seeds over a single seed in patients with extensive DCIS (lesions ≥ 3 cm).20 Overall, our study included a large, national cohort of patients receiving breast-conserving surgery for DCIS with either WGL or RSL, using real-world data. However, it also has several limitations. Our data used for this analysis, did not contain information regarding the weight or size of the excision specimen. Removal of large excision specimens obviously decreases the rate of positive margins.14 The weight of the specimen would provide more information regarding the interpretation of the resection margins and postoperative cosmetics. Additionally, data regarding the method of marker placement (ultrasound-guided or guided by mammography), the number of wires, and the use of intraoperative examination of the specimen and oncoplastic surgery were also lacking, which could have influenced the results. Furthermore, the location of the (involved) margin was not included in the data, which could affect the decision to perform re-excision, i.e. dorsal-involved margins can be less suitable for re-excision, since there might not be any more breast tissue to remove. In addition, we included patients over a period of 10 years, during which the treatment guidelines have changed. Since WGL was used more frequently in the beginning of this period and RSL more frequently towards the end of this period, this could have influenced the re-excision rates. Another limitation is the lack of clinical follow-up data regarding local recurrence, due to the fact that synoptic reporting only began in 2009. Finally, as mentioned above, the localization technique is not a patient-driven choice but an institutional policy, which could have biased our findings.

Conclusions

Whereas previous studies mainly focused on invasive breast cancer, this study is the first to include a large national cohort using real-world data on patients with DCIS. We have shown that RSL and WGL have comparable resection margins and number of re-excisions. However, in the case of a re-excision, patients in the RSL group were more often treated with breast-conserving surgery compared with the WGL group.
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Authors:  E Senkus; S Kyriakides; S Ohno; F Penault-Llorca; P Poortmans; E Rutgers; S Zackrisson; F Cardoso
Journal:  Ann Oncol       Date:  2015-09       Impact factor: 32.976

Review 2.  Breast conservation in ductal carcinoma in situ (DCIS): what defines optimal margins?

Authors:  Michael S Toss; Sarah E Pinder; Andrew R Green; Jeremy Thomas; David A L Morgan; John F R Robertson; Ian O Ellis; Emad A Rakha
Journal:  Histopathology       Date:  2016-12-20       Impact factor: 5.087

Review 3.  Is DCIS breast cancer, and how do I treat it?

Authors:  N Bijker; M Donker; J Wesseling; G J den Heeten; E J Th Rutgers
Journal:  Curr Treat Options Oncol       Date:  2013-03

4.  Focally positive margins in breast conserving surgery: Predictors, residual disease, and local recurrence.

Authors:  E L Vos; J Gaal; C Verhoef; K Brouwer; C H M van Deurzen; L B Koppert
Journal:  Eur J Surg Oncol       Date:  2017-06-23       Impact factor: 4.424

5.  Overall survival in patients with a re-excision following breast conserving surgery compared to those without in a large population-based cohort.

Authors:  Elvira L Vos; Agnes Jager; Cornelis Verhoef; Adri C Voogd; Linetta B Koppert
Journal:  Eur J Cancer       Date:  2014-12-27       Impact factor: 9.162

6.  Radioactive seed localization compared with wire-guided localization of non-palpable breast carcinoma in breast conservation surgery- the first experience in the United Kingdom.

Authors:  Robert Milligan; Andrew Pieri; Adam Critchley; Richard Peace; Tom Lennard; J M O'Donoghue; Rachel Howitt; Stewart Nicholson; Henry Cain; George Petrides; Nidhi Sibal
Journal:  Br J Radiol       Date:  2017-11-16       Impact factor: 3.039

Review 7.  Margins in breast cancer: How much is enough?

Authors:  Melissa Pilewskie; Monica Morrow
Journal:  Cancer       Date:  2018-01-16       Impact factor: 6.860

8.  Effect of three decades of screening mammography on breast-cancer incidence.

Authors:  Archie Bleyer; H Gilbert Welch
Journal:  N Engl J Med       Date:  2012-11-22       Impact factor: 91.245

Review 9.  Ductal carcinoma in situ: to treat or not to treat, that is the question.

Authors:  Maartje van Seijen; Esther H Lips; Alastair M Thompson; Serena Nik-Zainal; Andrew Futreal; E Shelley Hwang; Ellen Verschuur; Joanna Lane; Jos Jonkers; Daniel W Rea; Jelle Wesseling
Journal:  Br J Cancer       Date:  2019-07-09       Impact factor: 7.640

Review 10.  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.

Authors:  Monica Morrow; Kimberly J Van Zee; Lawrence J Solin; Nehmat Houssami; Mariana Chavez-MacGregor; Jay R Harris; Janet Horton; Shelley Hwang; Peggy L Johnson; M Luke Marinovich; Stuart J Schnitt; Irene Wapnir; Meena S Moran
Journal:  Ann Surg Oncol       Date:  2016-08-15       Impact factor: 5.344

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