Annals of Surgical Oncology

, Volume 14, Issue 12, pp 3335–3344

Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic

Authors

  • Bernadette A. M. Heemskerk-Gerritsen
    • Department of Medical Oncology , Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Cecile T. M. Brekelmans
    • Department of Medical Oncology , Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Marian B. E. Menke-Pluymers
    • Department of Surgical Oncology, Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Albert N. van Geel
    • Department of Surgical Oncology, Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Madeleine M. A. Tilanus-Linthorst
    • Department of Surgical Oncology, Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Carina C. M. Bartels
    • Department of Surgical Oncology, Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Murly Tan
    • Department of Psychosocial Care, Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
  • Hanne E. J. Meijers-Heijboer
    • Department of Clinical GeneticsErasmus MC—Daniel den Hoed Cancer Center
    • Department of Clinical GeneticsVrije Universiteit MC
  • Jan G. M. Klijn
    • Department of Medical Oncology , Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
    • Department of Medical Oncology , Family Cancer ClinicErasmus MC—Daniel den Hoed Cancer Center
Open AccessBreast Oncology

DOI: 10.1245/s10434-007-9449-x

Cite this article as:
Heemskerk-Gerritsen, B.A.M., Brekelmans, C.T.M., Menke-Pluymers, M.B.E. et al. Ann Surg Oncol (2007) 14: 3335. doi:10.1245/s10434-007-9449-x

Abstract

Background

BRCA1/2 mutation carriers and women from a hereditary breast(/ovarian) cancer family have a highly increased risk of developing breast cancer (BC). Prophylactic mastectomy (PM) results in the greatest BC risk reduction. Long-term data on the efficacy and sequels of PM are scarce.

Methods

From 358 high-risk women (including 236 BRCA1/2 carriers) undergoing PM between 1994 and 2004, relevant data on the occurrence of BC in relation to PM, complications in relation to breast reconstruction (BR), mutation status, age at PM and preoperative imaging examination results were extracted from the medical records, and analyzed separately for women without (unaffected, n = 177) and with a BC history (affected, n = 181).

Results

No primary BCs occurred after PM (median follow-up 4.5 years). In one previously unaffected woman, metastatic BC was detected almost 4 years after PM (primary BC not found). Median age at PM was younger in unaffected women (P < .001), affected women more frequently were 50% risk carriers (P < .001). Unexpected (pre)malignant changes at PM were found in 3% of the patients (in 5 affected, and 5 unaffected women, respectively). In 49.6% of the women opting for BR one or more complications were registered, totaling 215 complications, leading to 153 surgical interventions (71%). Complications were mainly related to cosmetic outcome (36%) and capsular formation (24%).

Conclusions

The risk of developing a primary BC after PM remains low after longer follow-up. Preoperative imaging and careful histological examination is warranted because of potential unexpected (pre)malignant findings. The high complication rate after breast reconstruction mainly concerns cosmetic issues.

Keywords

BRCA1/2Breast cancerMastectomyPreventionComplicationsUnexpected carcinomas

Women with a germ-line BRCA1 or BRCA2 mutation as well as 50% risk carriers from a hereditary breast(/ovarian) cancer (HB(O)C) family are at increased risk of developing breast and/or ovarian cancer compared with the general population.14 Options to reduce this risk are regular surveillance, chemoprevention, or prophylactic surgery. Prophylactic surgery includes prophylactic mastectomy (PM) and/or prophylactic bilateral salpingo-oophorectomy (PBSO). PM implies either a bilateral prophylactic mastectomy (BPM) in high-risk unaffected women as well as in high-risk women with a history of breast cancer (BC) previously treated with breast conserving therapy (BCT), or a contralateral prophylactic mastectomy (CPM) after a unilateral therapeutic mastectomy. Several studies have shown that PM strongly reduces the risk of developing (contralateral) breast cancer, while PBSO reduces the risk of ovarian as well as primary breast cancer.510 These strategies therefore have commonly been accepted at this moment as risk-reducing strategies for women being at increased risk of HB(O)C.

PM, however, is a drastic and irreversible intervention, and in case of breast reconstruction (BR), is accompanied by a substantial complication rate.11 Further issues of concern with respect to PM include changes in a woman’s body image and self-esteem, changes of sexual function, and in psychological distress.

At the Rotterdam Family Cancer Clinic, 35–51% of women carrying a BRCA1 or BRCA2 mutation opt for either bilateral or contralateral PM.12,13 For women who are contemplating this intervention, it is imperative to have reliable data on the outcomes of PM in a well-defined cohort to make a good informed decision and to minimize postoperative feelings of deception. At the Rotterdam Family Cancer Clinic there is ample and long-term experience with sufficient numbers of women undergoing PM. We previously reported data concerning the occurrence of breast cancer after BPM in unaffected women with a proven BRCA1/2 mutation,5,14 complications of PM with breast reconstruction,11,15 and psychological aspects of PM in combination with BR.16

In the current analysis, we report on an extended series with longer follow-up of women having undergone a PM at the Rotterdam Family Cancer Clinic because of either a proven BRCA1/2 mutation or a genetic susceptibility (50% risk carriers from a HB(O)C family). Our study sample was large enough to discriminate between unaffected women and women with a history of BC (affected). Special attention is paid to the prevalence of (pre)malignant lesions in prophylactically removed mastectomy specimens. Further, we report on the postoperative complications of PM in combination with breast reconstruction.

PATIENTS AND METHODS

As of the start of the Rotterdam Family Cancer Clinic in 1991, PM and/or PBSO are being discussed as risk-reducing strategies with women at increased risk of hereditary BC and/or ovarian cancer. In early years, PM was discussed with BRCA1/2 mutation carriers as well as with women from a HB(O)C family without a proven mutation (so-called 50% risk carriers), and applied for unaffected as well as affected (with a history of breast cancer) women. Due to the development of more advanced mutation-detection methods enabling the performance of a complete gene mutation screen, there has been a shift in more recent years to discuss the option of PM only with identified mutation carriers. Before 1996, the decision to undergo a PM and/or PBSO was discussed individually by the doctor and the woman in question. As of 1996, women opting for either PM and/or PBSO are additionally discussed in the multidisciplinary Committee on Hereditary Tumors. For this purpose, institutional guidelines concerning the surveillance schedule and indications regarding PM/PBSO have been further elaborated and implemented as of 2000, which were updated as knowledge progressed and more evidence-based data became available.

Before 2000, no additional examinations were performed before PM, irrespective of the individual situation (unaffected/affected; mutation/50% risk carrier). Women were seen biannually for physical examination, while a mammography was performed annually. As of 2000, institutional guidelines from the working party on hereditary tumors recommended to perform clinical breast examination (CBE) and imaging examination within 3 months prior to PM, to minimize the risk of finding unexpected malignant changes at PM. At first, imaging examination consisted of either mammography or magnetic resonance imaging (MRI) scan, while more recently MRI has been preferred. Breast ultrasound (US) and, if necessary, fine-needle aspiration cytology (FNAC) are additionally performed in case lesions are found at CBE or one of the imaging examinations. Further, the guidelines recommend the discussion of the case in the multidisciplinary Committee on Hereditary Tumors and a standard visit with a psychologist. For affected women, the guidelines are extended with dissemination investigations to rule out recurrent or distant breast cancer activity (chest x-ray, liver ultrasound, bone scan, liver functions and determination of Ca15.3/Ca125). Where women with a history of ovarian cancer were previously eligible for PM, at the moment this is not discussed anymore in this setting, because the prognosis is mainly dictated by the ovarian cancer. In the sample, these women were classified as “unaffected,” unless they also had a history of BC.

To evaluate the short-term and long-term medical effects of prophylactic surgery in high-risk women, a combined retrospective and prospective, longitudinal study was activated at our institution, including all genetically susceptible women who had opted for prophylactic surgery (either PM and/or PBSO). Women were informed by oral and written information and were asked for written consent. The protocol was approved by the institutional review board (project EMC-DDHK 98-15).

Surgical Technique

At our institute, the oncological and plastic surgeon perform the PM and BR as a team. During the operation, the patient is under general anesthesia in a half-supine position. A skin-sparing mastectomy is performed through a vertical, peri-areolar incision, which extends from just above the nipple down the submammary fold. The breast tissue, including the superficial fascia (creating thin skin flaps), the axillary tail, the inframammary fold, the nipple-areolar complex, and the fascia of the pectoral muscle are removed. In case of immediate breast reconstruction, either a subpectoral silicone implant is inserted in a pocket created below the pectoral muscles in a one-stage procedure, or autologeous tissue is used. Autologeous reconstruction encompasses a broad range of procedures incorporating the patient’s own tissues to recreate the breast. The transverse rectus abdomis myocutaneous (TRAM) flap and latissimus dorsi flap are two standard myocutaneous flaps used for breast reconstruction. More recent modifications to the traditional techniques led to the use of the deep inferior epigastric perforator (DIEP) flap. Nipple reconstruction is offered after 6 months and consists of three small transposition flaps; the areola is mimicked by tattooing the desired skin color. Breast reconstruction is not always performed in the same operation as the mastectomy; the techniques for these delayed reconstructions, however, are as described previously.

Microscopic Examination of Mastectomy Specimens

As of 1995, a standard procedure has been followed for meticulous microscopic examination of prophylactically removed mastectomy specimens to rule out the presence of “occult” (microscopic) malignant alterations. The protocol prescribes that mastectomy specimens are cut into slices of 0.5–1 cm thickness, whereby each slice is carefully inspected and palpated for abnormalities. Standard, three randomly selected parenchymal tissue samples from each quadrant and a transverse section through the nipple are submitted for histology, in addition to samples of all visible or palpable abnormalities. Further, three samples from each quadrant of the mastectomy specimens are snap frozen for the tissue bank. Radiographic examination of breast tissue specimens is not performed on a routine basis.

Study Design

The current study included all women at increased risk of hereditary BC, according to previously described criteria,17 who underwent prophylactic bilateral or contralateral mastectomy between January 1, 1994 until December 31, 2004. Of our study cohort 310 women (86.6%) underwent PM at our clinic, while 48 women (13.4%) were treated elsewhere, e.g., due to a waiting list at our clinic, or the fact that previous surgery was performed elsewhere. The latter women were only eligible for this analysis if the follow-up after PM took place at our clinic, and a copy of the pathology report was available. In general, DNA testing was performed before the prophylactic surgery, although some women choose for prophylactic surgery without or irrespective of DNA testing. DNA analysis was performed according to standard procedures, as has been previously described.18,19 DNA testing was not an inclusion criterion for participation in the study. Proven noncarriers from a family BRCA mutation were excluded from the study.

Relevant data were extracted from the hospital records. For each woman, including deceased women, the following information was obtained: date of birth, death, and PM, performance (yes/no) and type of breast reconstruction, PBSO, diagnosis of breast and/or ovarian cancer, mutation status, duration of follow-up after PM (end date being either the date of death or the date of last clinic visit in case of loss to follow-up, or the end date of this study, i.e. December 31, 2004), and type and number of complications after breast reconstruction. Regarding the latter, we distinguished between early (within 6 weeks) and late postoperative complications (after 6 weeks). Early complications consisted of infection, necrosis, bleeding, and luxation of the prosthesis. Late complications were divided in surgical complications (such as capsular formation, infection, necrosis, and luxation of the prosthesis), and complaints related to cosmetic outcome (such as poor symmetry and dog ears). Nipple reconstruction is regarded as part of the breast reconstruction and therefore has not been registered as a cosmetic complication. A computerized database (MS-Access) was used to process the data. Data were entered retrospectively as well as prospectively after each clinic visit.

Statistical Analysis

Descriptive statistics (median, range, and frequency) were computed. When appropriate, statistical significance testing between relevant subgroups was performed using the chi-square test for categorical variables and a t-test for continuous variables. A P value of less then .05 was considered statistically significant.

RESULTS

Study Population

In Table 1 the characteristics of the women who underwent a PM are shown. A total of 358 women, with a median follow-up after PM of 4.5 years, fulfilled the study eligibility criteria, consisting of 181 (50.6%) women with a history of breast cancer (affected women), and 177 (49.4%) women without a history of BC (unaffected women). A total of 236 (65.9%) women were BRCA1/2 mutation carriers, while the other 122 women (34.1%) were 50% risk carriers from a HB(O)C family. The unaffected group mainly consisted of BRCA1/2 mutation carriers as compared with 50% risk carriers (82% vs 18%, P < .001), whereas the affected group consisted of an equal number of mutation carriers and 50% risk carriers (91 mutation carriers versus 90 50% risk carriers, P = .94). This difference in distribution was highly significant (P < .001).
TABLE 1.

Characteristics of the study population

HISTORY OF BC

No (Unaffected, n = 177)

Yes (Affected, n = 181)

P valued

BRCA

HB(O)C

BRCA

HB(O)C

n

(%)a

n

(%)a

n

(%)a

n

(%)a

No. of women (N)

145

(82)b

32

(18)b

91

(50)c

90

(50)c

<.001e

  Death due to cancer

0

(0)

1

(3)

9

(10)

7

(8)

 

Age at PM (years)

  Median

36.0

 

38.5

 

42.0

 

47.0

 

<.001

  Range

22–65

 

28–55

 

25–65

 

26–68

  

  <30 years

18

(12)

3

(9)

6

(7)

2

(2)

<.001

  30–39 years

74

(51)

14

(44)

26

(29)

22

(24)

 

  40–49 years

36

(25)

10

(31)

38

(42)

31

(34)

 

  ≥50 years

17

(12)

5

(16)

21

(23)

35

(39)

 

Duration of follow-up (years)

4.4

 

4.7

 

3.9

 

4.5

  

Mutation status

  BRCA1

115

(79)

 

76

(84)

  

  BRCA2

30

(21)

 

15

(16)

  

PBSO

  Yes

83

(57)

3

(9)

61

(67)

12

(13)

.13

  No

62

(43)

29

(91)

30

(33)

78

(87)

 

Age at PBSO (years)

  Median

40.0

 

45.0

 

43.0

 

49.0

 

<.01

  Range

29–57

 

35–45

 

32–65

 

37–58

  

Timing of PBSO

  Before PM

18

(22)

2

(67)

14

(23)

6

(50)

.11

  At PM

35

(42)

1

(33)

16

(26)

5

(42)

 

  After PM

30

(36)

0

(0)

31

(51)

1

(8)

 

Ovarian cancer before PM

4

(3)

0

(0)

2

(2)

1

(1)

 

Unexpected (p)MF at PM

3

(2)

2

(6)

4

(4)

1

(1)

 

Cancer after PM

  Breast cancer

1

(1)

0

(0)

0

(0)

0

(0)

 

  Ovarian cancer

2

(1)

0

(0)

1

(1)

0

(0)

 

BC, breast cancer; HB(O)C, hereditary breast(/ovarian) cancer; PM, prophylactic mastectomy; PBSO, prophylactic bilateral salpingo-oophorectomy; (p)MF, (pre)malignant findings.

a Percentage of the number of women in column in question, unless stated otherwise.

b Percentage of unaffected women.

c Percentage of affected women.

d Difference between unaffected and affected BRCA1/2 mutation carriers, unless stated otherwise.

e Difference in distribution between unaffected and affected women.

The median age at PM in the unaffected and affected group was significantly different, being 37 and 44 years, respectively (Table 2, P < .001). In the affected group, mutation carriers were significantly younger at PM than 50% risk women (42 vs 47 years, respectively; P = .045). In the unaffected group, we found no significant difference in this respect (36 vs 38.5 years, respectively; P = .102). A history of ovarian cancer was present in four mutation carriers from the unaffected group (2.3%), and in three women (1.7%) in the affected group.
TABLE 2.

Comparison between unaffected and affected women

 

Unaffected

Affected

P value

No. of women (N)

177 (%)

181 (%)

 

Age at PM (years)

  Median

37

44

<.001

  Range

22–65

25–68

 

  <30 years

21 (12)

8 (4)

<.001

  30–39 years

88 (50)

48 (27)

 

  40–49 years

46 (26)

69 (38)

 

  ≥50 years

22 (12)

56 (31)

 

PBSO

  Yes

86 (49)

73 (40)

.12

  No

91 (51)

108 (60)

 

Age at PBSO (years)

  Median

40

44

<.001

  Range

29–57

32–65

 

PM, prophylactic mastectomy; PBSO, prophylactic bilateral salpingo-oophorectomy.

In Fig. 1, the number of PMs per year, separately for unaffected/affected BRCA mutation carriers, as well as for unaffected/affected 50% risk carriers is shown. In the unaffected group, the annual number of women undergoing PM was always larger in mutation carriers compared with 50% risk carriers, except for the first 2 years (1994/1995). Further, the number of unaffected BRCA mutation carriers undergoing PM widely differed over the years, with two peaks in 1998 and 2001, respectively. In contrast, the number of unaffected 50% risk carriers undergoing PM was quite stable over the years.
https://static-content.springer.com/image/art%3A10.1245%2Fs10434-007-9449-x/MediaObjects/10434_2007_9449_Fig1_HTML.gif
FIG. 1.

Annual number of PM in unaffected/affected BRCAa/2 mutation carriers and 0% risk carriers from HB(O)C families.

In the affected group, however, the pattern was different, whereby a shift has taken place through the years. In the early years of the study period (1994–1997), mainly women without a proven mutation underwent PM in this group. Between 1997 and 2001, approximately as many mutation carriers as 50% risk carriers underwent a PM. As of 2002, more mutation carriers have undergone a PM, although the number of PMs in 2004 again was not different between mutation and 50% risk carriers.

Prophylactic Bilateral Salpingo-oophorectomy

A considerable part of the BRCA mutation carriers undergoing PM also opted for PBSO, being 57% in the unaffected versus 67% in the affected group, respectively (Table 1, P = .13). In the HB(O)C group, however, only a minority of the women underwent a PBSO, being 15 of 122 50% risk carriers (12%). The median age at PBSO was younger in BRCA mutation carriers compared with the 50% risk carriers, both in the affected and the unaffected group. This difference, however, was not significant (P = .13 and P = .40, respectively). Further, the median age at PBSO was lower in the unaffected compared with the affected group, being 40 versus 44 years, respectively (Table 2, P < .001). In addition, unaffected BRCA mutation carriers underwent PBSO at a younger age compared with mutation carriers with a history of BC (40 vs 43 years, respectively, P < .01, Table 1).

(Pre)malignant Findings at PM

In 10 of the 358 women (2.8%), abnormal findings were unexpectedly found in the mastectomy specimens (table 1). Prior to intended PM there was no suspicion to justify an axillary nodal dissection in combination with the PM procedure. This occurred in five “unaffected” (2.8 %) as well as in five previously affected women (2.8%), and in both mutation carriers (3%) and 50% risk carriers (2.5%).

The characteristics of the unexpected (pre)malignant findings as well as the preoperative screening results are chronologically described in detail in Table 3. In 1995, in one woman both preoperative clinical breast examination (CBE) and mammography were suspicious for a malignancy. However, additional investigation, consisting of ultrasound and cytology, did not reveal a malignancy. Nevertheless, histological examination of the mastectomy specimens revealed an invasive ductal carcinoma (IDC), eventually staged as a pTxN1Mo. The patient died of metastatic breast cancer 4 years after the PM. In another two women, undergoing PM in 1996 and 1997, a lesion was found preoperatively (CBE and mammography, respectively) and classified as probably benign. No malignant abnormalities were seen at subsequent ultrasound examination, which is the reason a FNAC was not performed. However, histological examination of the mastectomy specimens revealed a small ductal carcinoma in situ (DCIS) in both women. In 2002, in one woman preoperative MRI revealed a lesion classified as probably benign. Indeed, no malignant abnormalities were found at additional ultrasound examination. Histological examination of the mastectomy specimens, however, revealed an IDC in the right, and an invasive medullar carcinoma (IMC) in the left breast. Preoperative screening in the remaining six women, performed 1–6 months preceding PM, did not show suspicious abnormalities. Still, another invasive carcinoma, three cases of DCIS, and two cases of lobular carcinoma in situ (LCIS) were found in the mastectomy specimens. All unexpected (pre)malignant findings in the affected women were found in the contralateral breast.
TABLE 3.

Characteristics of unexpected (pre)malignant findings in the PM specimens

 

Preoperative

 

Year of PM

Genetic risk group

History of BC before PM

Histology

Grade

Tumor size (mm)

ER/PR status

CBE

Mx

MRI

1995

HB(O)C

No

IDC

NA

NA

NA

SC

SC

 

a, b

1996

HB(O)C

No

DCIS

II

<2

NA

PB

nl

 

a

1996

BRCA1

No

LCIS

NA

NA

NA

nl

nl

  

1997

HB(O)C

Yes

DCIS

I

NA

NA

nl

  

c

1997

BRCA1

Yes

DCIS

II

<2

NA

nl

PB

 

a

1997

BRCA1

Yes

IDC

II

3

Negative

nl

  

c

1998

BRCA1

Yes

DCIS

NA

<2

NA

nl

nl

  

2000

BRCA1

Yes

LCIS

NA

NA

NA

nl

nl

  

2002

BRCA1

No

IDC

III

5

Negative

nl

nl

PB

a

   

IMC

III

6

Positive

    

2003

BRCA2

No

DCIS

II

<2

NA

nl

nl

  

PM, prophylactic mastectomy; BC, breast cancer; DCIS, ductal carcinoma in situ; LCIS, lobular carcinoma in situ; IDC, invasive ductal carcinoma; IMC, invasive medullar carcinoma; CBE, clinical breast examination; Mx, mammography; MRI, magnetic resonance imaging; SC, suspicion of cancer; PB, probably benign; nl, normal; NA, not applicable.

a Additional investigation normal.

b Macroscopic palpable tumor; microscopic no clear border, therefore tumor size and grade not determinable.

c Treated previously for BC at another hospital. No information about preoperative imaging available.

Cancer During Follow-up After PM

After PM, no incident breast cancer cases were observed in 50% risk carriers.

In BRCA mutation carriers, ovarian cancer was detected in two women in the unaffected group, and in one woman in the affected group (Table 1).

One BRCA1 mutation carrier from the unaffected group presented in 2001, 3.5 years after PM (no malignant findings at histological examination), with metastatic adenocarcinoma in an axillary lymph node, morphologically and immunohistochemically consistent with breast cancer. Additional dissemination examinations also revealed metastases in bone and liver. Review of the preoperative data (physical examination and mammography) at the presentation of metastatic disease did not show malignant alterations, while meticulous reexamination of all pathology slides and additional investigation of frozen tissue material did not detect a primary breast cancer.

Reconstructive Breast Surgery

In Table 4, the numbers and types of reconstructive breast surgery, as well as the numbers and types of complications after breast reconstruction (BR) are shown. Of the total population (n = 358), 276 women underwent BR in combination with PM, being 60% unaffected and 40% affected women. The presence or absence of a BRCA1/2 mutation did not influence the BR rate (P = .23 for unaffected, and P = .10 for affected women), or the type of BR (P = .25 for unaffected, and P = .68 for affected women). Unaffected women mainly opted for BR (94%), consisting of 163 immediate and three delayed reconstructions, while a considerable part of the affected women did not opt for BR (37%) (P < .001). Further, unaffected women mainly opted for BR by means of (silicon) prosthesis (96%). In contrast, affected women opting for BR (102 immediate, and 8 delayed) more often had a reconstruction by means of autologeous tissue compared with unaffected women, being 13% versus 3%, respectively (P = .004).
TABLE 4.

Breast reconstruction (BR) in women undergoing PM

History of BC

No (Unaffected)

Yes (Affected)

P value

Number of women

177

(%)

181

(%)

Breast reconstruction (BR)

  No

9

(5)

68

(37)

<.001

  Yes

166

(94)

110

(61)

 

  Unknown a

2

(1)

3

(2)

 

Type of BR

  Silicon prosthesis

159

(96)

95

(86)

.004

  Autologeous tissue

6

(3)

14

(13)

 

  Unknown a

1

(1)

1

(1)

 

Therapy first BC b

  BCT

7

(6)

 

  BCT/RT

33

(30)

 

  MAST

67

(67)

 

  MAST/RT

3

(3)

 

Women with complications after BR

  No

84

(51)

55

(50)

.92

  Yes

82

(49)

55

(50)

 

Total number of complications after BR c

127

 

88

  

  Early (<6 weeks after BR)

42

(33)

31

(35)

.74

  Late (>6 weeks after BR)

85

(67)

57

(65)

 

Surgery due to late complication

  No

38

(30)

24

(27)

.67

  Yes

89

(70)

64

(73)

 

Early complications

Surgery due to early complication

  No

27

(64)

17

(55)

.42

  Yes

15

(36)

14

(45)

 

Type of early complication

Infection

8

(19)

14

(45)

.09

Necrosis

11

(26)

4

(13)

 

Bleeding

20

(48)

12

(39)

 

Prosthesis luxation

2

(5)

0

(0)

 

Poor arterial inflow

0

(0)

1

(3)

 

Pneumothorax

1

(2)

0

(0)

 

Late complications

Surgery due to late complication

  No

11

(13)

7

(12)

.91

  Yes

74

(87)

50

(88)

 

Type of late complication

  Infection

4

(4)

0

(0)

.33

  Necrosis

1

(1)

3

(5)

 

  Capsular formation

31

(37)

20

(35)

 

  Prosthesis luxation

2

(2)

3

(5)

 

  Poor cosmetic appearance d

31

(37)

19

(34)

 

  Dog ear

16

(19)

12

(21)

 

PM, prophylactic mastectomy; BC, breast cancer; BR, breast reconstruction; BCT, breast conserving therapy; BCT/RT, BCT in combination with radiotherapy; MAST, therapeutic mastectomy; MAST/RT, MAST in combination with radiotherapy.

a Surgery performed at another hospital, not included in P value calculation.

b Data shown for women with a BR after PM.

c One woman can have ≥1 complication.

dIncluding asymmetry.

In 137 of 276 women opting for BR (49.6%) one or more complications were registered, totaling 215 complications. Surgical reinterventions were performed in 153 cases (124 for late complications).

Concerning the number of complications, this was not different between unaffected and affected women, neither for the moment of the complication (i.e., early or late) (P = .74), the necessity of reintervention due to the complication (P = .67), nor for the type of complication (P = .09 for early complications and P = .33 for late complications).

DISCUSSION

In this study we updated and extended the long-term experiences at the Rotterdam Family Cancer Clinic with prophylactic mastectomy (PM) in proven BRCA1/2 mutation carriers and in 50% risk carriers from a HB(O)C family. We compared the data of PM and breast reconstruction (if performed) in women with (affected) and without a personal history of BC (unaffected women) and further distinguished between women with a BRCA 1 or 2 mutation, and women without a proven mutation. While within the unaffected group, especially BRCA1/2 mutation carriers opted for PM, we observed that within the affected group an equal number of mutation carriers and 50% risk carriers from a HB(O)C family opted for PM. Women carrying a BRCA 1 or 2 mutation are known to have an increased risk of developing contralateral primary BC,20,21 which is even more apparent among women who are younger when diagnosed with a primary breast carcinoma (age <50 years).22,23 For high-risk women without a proven mutation inconsistent results on the risk of developing a contralateral breast cancer (CBC) were reported. Shahedi et al.24 as well as Kirova et al.25 reported an increased risk of developing CBC in non-BRCA1/2 women, while Tilanus et al.26 concluded that the rate of CBC was only slightly and insignificantly increased in non-BRCA1/2 compared with sporadic breast cancer patients. In view of these results, one expects that after a first diagnosis of breast cancer, especially mutation carriers will opt for prophylactic removal of the remaining breast tissue. In our study sample, however, also a considerable part of the women without a proven BRCA1/2 mutation opts for prophylactic mastectomy, especially after a history of breast cancer. It has to be mentioned that, since information on the BRCA1/2 mutation status is not always known in the latter group and genetic testing is missing a number of mutations, it is likely that some of these patients are in fact mutation carriers. Further, the group of women with a history of breast cancer, with and without a gene mutation, may partly consist of women who initially chose for surveillance, and eventually opted for PM after the diagnosis of breast cancer. This is in accordance with an earlier report indicating that women may be more likely to undergo PM after a previous diagnosis of BC.27 This might also partly explain the higher age at the time of PM in the group with a history of BC.

We found that the age at PM was younger in unaffected women, both for mutation carriers as for 50% risk carriers. Further, we found a significant difference between unaffected and affected mutation carriers in the distribution of the numbers of PM over the various age categories, with the highest numbers of PM in the age group of 30–40 for unaffected and 40–50 for affected carriers, respectively. Moreover, the distribution of PM over the various age categories remained completely identical to the age distribution reported in a previous study on PM from our institute,5 indicating consistency over time.

Our data show that, despite preoperative (imaging) examination, the presence of unexpected microscopic (pre)malignant findings in this group of high-risk women is real (3%). Other studies reporting on high-risk and/or pathologic findings in prophylactically removed breast tissues, described percentages varying from 0.1–57%.8,2729 However, the comparison of frequencies of unexpected (pre)malignant findings between studies is hampered by differences in population selection, preoperative screening methods, pathological examination of the specimens, and definition of what is considered (pre)malignant [e.g., lobular carcinoma in situ (LCIS)]. The percentage of unexpected invasive carcinomas in these studies ranged from 0.1–7.7% (0.8% in our study). Most of these studies, however, did not provide information about the outcome of preoperative physical breast or imaging examination, which at the moment is a standard procedure at our institution. It might be that since the implementation of institutional guidelines concerning preoperative breast examination in 2000, and the introduction of magnetic resonance imaging (MRI), being more sensitive in detecting carcinomas in high-risk women,30,31 as detection tool, the number of unexpected malignant findings in the PM specimens is decreasing.

With a 3% incidence of unexpected microscopic (pre)malignant findings, the potential role of sentinel node biopsy (SN) for all patients undergoing PM has been discussed. However, the majority of the (pre)malignant findings we found in this series, represents DCIS/LCIS; settings for which a sentinel node biopsy is not standardly indicated. Invasive cancer was found in only 0.8% of the patients in this series. Therefore, in our opinion, routine use of SN in all patients undergoing PM is not warranted, which is also supported in the paper by Boughey et al.32

A previous study from our institution, investigating the efficacy of PM in unaffected women with a proven BRCA1/2 mutation, observed no cases of breast cancer after PM.5 The mean follow-up in that study was 3 years. In the current cohort, one BRCA1 mutation carrier presented with metastatic disease 3.5 years after PM (no primary BC found), suggesting the presence of an occult primary tumor that was never found, despite a thorough reexamination of the specimen at the presentation of the metastatic disease. This finding emphasizes the fact that despite thorough examination of the mastectomy specimens, the presence of an occult breast cancer cannot be ruled out completely and indicates that a form of surveillance after PM might be relevant.

The number of reconstructions after risk-reducing mastectomy was lower in the affected group. This may be due to the fact that BR after previous radiotherapy and/or therapeutic mastectomy not always leads to satisfactory cosmetic results.15,33 Some patients abandon, in consultation with and/or at the advice of their (oncological/plastic) surgeon, from BR for this reason. Other women have accepted the mutilation/alteration of body image caused by mastectomy, are reluctant to undergo renewed surgery, and prefer the use of external prosthesis.

During the follow-up period of this study, 49.6% of the women with immediate or delayed BR after PM showed complications. In total 215 complications were registered, leading to surgical reintervention in 153 cases. These findings are consistent with several other reports,34,35 though there are also studies reporting lower,11,15,33 or even higher36 complication rates after (immediate) BR. However, the literature in this area is difficult to compare, in part because not all previous series compare bilateral prophylactic mastectomy in unaffected women with risk-reducing mastectomies in women after a previous therapy for breast cancer. Furthermore, data may not be comparable because of different definitions of complications. Moreover, some studies describe the complication rate as a percentage of the total number of reconstructions,11,15,33 while others, like our study, present the percentage of women with complications.3436

We found no differences in the numbers of complications after (immediate) breast reconstruction in unaffected women compared with previously affected women in this study. This finding appears to be in contrast with earlier reports (also from our institution) describing the occurrence of more complications after mastectomy followed by (immediate) breast reconstruction in affected women. These studies report negative effects of preoperative radiotherapy on the cosmetic outcome of the reconstruction, in particular the risk of capsular formation would be increased, having negative consequences on the symmetry of the breasts. Further, asymmetry can be expected to occur more often after previous therapeutic mastectomy. Although we have no explanation for our findings, it is possible that the experience of the surgeons at our institution is important. Indeed, where previously BR by means of silicon prosthesis after breast conserving therapy was performed, this is not done anymore.

In summary, we confirmed our previous findings that prophylactic mastectomy strongly reduces the risk of developing breast cancer in both BRCA1/2 mutation carriers and 50% risk carriers. As the frequency of unexpected cancers in this high-risk group remains real, preoperative imaging and careful histological examination is warranted. Further, we found a substantial complication rate after breast reconstruction, which mainly concerned late cosmetic issues, almost always leading to additional surgery. In this respect, patients should be informed preoperatively that an optimal cosmetic effect cannot unconditionally be achieved in just one single operation. Concerning the complication rate after BR, we did not find a significant difference between affected and unaffected women. In our opinion, our data are providing additional data on this issue and may help to inform women considering prophylactic mastectomy and their physicians, in the complex process of decision-making.

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© Society of Surgical Oncology 2007