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Mammary metaplastic carcinoma encompasses epithelial‐only carcinoma (high‐grade adenosquamous carcinoma or pure squamous cell carcinoma), biphasic epithelial and sarcomatoid carcinoma and monophasic spindle cell carcinoma.
To evaluate the clinicopathological features of a large series of 34 metaplastic carcinomas.
10 epithelial‐only, 14 biphasic and 10 monophasic metaplastic carcinomas were assessed for nuclear grade, hormone receptor status, HER2/neu (cerbB2) oncogene expression, Ki‐67 and p53, lymph node status and recurrence on follow‐up.
Intermediate to high nuclear grade were assessed in most (33/34) tumours. Oestrogen and progesterone receptors were negative in 8 of 10 epithelial‐only, all 14 biphasic, and 9 of 10 monophasic tumours, cerbB2 was negative in 7 of 10 epithelial‐only, all 14 biphasic and 8 of 10 monophasic tumours. Ki‐67 was found to be positive in 6 of 10 epithelial‐only, 6 of 14 biphasic, and 7 of 10 monophasic tumours, whereas p53 was positive in 6 of 10 epithelial‐only, 7 of 14 biphasic, and 8 of 10 monophasic tumours. Lymph node metastases were seen in 7 of 7 epithelial‐only, 7 of 11 biphasic, and 3 of 7 monophasic tumours. Recurrences were seen in 4 of 7 epithelial‐only, 8 of 9 biphasic, and 4 of 9 monophasic tumours.
All three subtypes of metaplastic carcinoma are known to behave aggressively, and should be differentiated from the low‐grade fibromatosis‐like metaplastic carcinoma, which does not metastasise. Oncological treatment options may be limited by the frequently negative status of hormonal receptor and cerbB2.
Metaplastic carcinoma of the breast denotes a heterogeneous group of uncommon malignant entities. This term is used by many to denote tumours with mixed epithelial and sarcomatoid components, as well as primary squamous or mixed adenocarcinoma and squamous cell carcinoma (SCC; fig 11).
In those cases with a sarcomatoid component the tumour cells can be classified into monophasic, composed of spindle cells only, or biphasic, being admixed with a carcinomatous (either ductal carcinoma or SCC) component.1 Other authors have systematically grouped the tumours into various diagnostic labels based on the presence of heterologous elements or osteoclastic giant cells, or on whether the tumour cells are monophasic, biphasic or squamoid.2,3,4,5,6 More recent literature presents cases with sarcomatoid components, with or without accompanying carcinomas. Several large series have evaluated as many as 24 cases, with particular emphasis on the clinical outcome7,8,9 and the role of immunohistochemistry in the differentiation of this lesion from other disease entities, including phyllodes tumours and primary mammary sarcomas.10,11 Metaplastic carcinoma is generally considered to be high grade, with clinical features similar to those of infiltrating duct carcinoma (IDC), although it may rarely present as inflammatory carcinoma.12 Recently, a low‐grade variant, the fibromatosis‐like group, has been reported, with a better outcome and mostly local recurrences but not distant metastases.13,14,15 SCC, and mixed adenocarcinoma and SCC have scarcely been dealt with in the literature in terms of outcome. In this study, a series of metaplastic carcinomas, including tumours from all three categories, are assessed and the clinical and pathological parameters reported.
The histopathology files from five institutions were searched for metaplastic carcinoma of the breast. All the cases were formalin‐fixed and routinely processed. All the histological slides were retrieved and reviewed, and the diagnosis was confirmed. Each tumour was assessed for three components:
The sarcomatoid or solid component, when present alone, had to coexpress cytokeratin (AE1/AE3 or CAM5.2 or both) and vimentin, as shown by immunohistochemistry (AE1/AE3 (Dako, Glostrup, Denmark; 1:300), CAM5.2 (Becton Dickenson, San Jose, California, USA; 1:70) and vimentin (Dako; 1:2000)).
All the mammary metaplastic carcinomas were divided into three groups:
For each component, the tumour was assessed for the nuclear grade as 1–3, indicating mildly, moderately or highly pleomorphic nuclear morphology. Immunohistochemistry was carried out on a representative section on all cases for the following antibodies by using the avidin–biotin method with microwave antigen retrieval. The following parameters were assessed by immunohistochemistry:
For oestrogen and progesterone receptors, moderate to strong nuclear staining of 10% or more of the tumour cells was considered to be positive and for cerbB2, moderate to strong complete membrane staining of 10% or more of the tumour cells was considered to be positive. MIB1 and p53 staining was expressed as a percentage of cells showing moderate to strong nuclear staining, and was considered to be positive if the expression was >10%.
The medical records of the patients were reviewed, with emphasis on lymph node status at the time of surgery, if performed, and the follow‐up duration and outcome—whether the patient was alive or dead, and if deceased, whether the death was related to the breast tumour.
A total of 34 metaplastic carcinomas were included in this report. These included 10 cases showing epithelial phenotype only, with 2 cases of mixed adenocarcinoma and SCC; and 8 cases of pure SCC. Of the 14 cases with biphasic phenotype showing mixed epithelial and sarcomatoid or spindle cell phenotypes, 10 cases had adenocarcinoma (all IDCs) and the remaining four cases had SCC as the epithelial component. The remaining 10 cases showed a monophasic pattern composed entirely of sarcomatoid or spindle cells with a phenotypic coexpression of epithelial and mesenchymal markers by immunohistochemistry.
Table 11 shows the patients' age, tumour size and histomorphological characteristics, and the immunohistochemistry results for each of these groups. Table 22 lists the axillary lymph node status and the clinical outcome. Of the patients who were alive but had recurrent disease, two were from the epithelial‐only group, with one having brain metastasis (1 year) and the other having contralateral high‐grade ductal carcinoma (1 year). Of the three patients from the biphasic group, who were alive with disease, two had recurrences (1 and 3 years, respectively) and one had brain metastasis (1 year). Of the two patients from the monophasic group, who were alive with disease, one had recurrence (1 year) and one had lymph node metastasis (3 years).
Metaplastic carcinoma is a rare malignancy of the breast, characterised by its high‐grade nature. In this report, a large series of 34 cases was assembled, and we evaluated the biological parameters and clinical outcome between the squamoid carcinomas and the sarcomatoid or spindle cell carcinomas (fig 22)) for similarity.
Most metaplastic carcinomas are sporadic, but there may be a slight propensity for metaplastic spindle cell carcinoma to arise from pre‐existing lesions, including papillomas, complex sclerosing lesions and nipple adenomas.16,17 Metaplastic or spindle cell carcinomas arising from such lesions can show a varying degree of malignancy, ranging from low to high grade. This type of lesion should also be differentiated from the so‐called reactive spindle cell nodule, which is believed to be benign and may also complicate pre‐existing lesions such as papillomas or complex sclerosing lesions.18
In this series of 34 sporadic metaplastic carcinomas, we identified 24 cases of metaplastic carcinoma with a sarcomatoid or spindle cell component, with 14 (58%) of the 24 cases being biphasic and 10 (42%) of the 14 cases being monophasic. This is essentially in agreement with the rates of 11–33% reported in the literature.3,10,13,19
In all the cases, levels of hormone receptors (oestrogen and progesterone receptors) and expression of the cerbB2 oncogene were low, with oestrogen and progesterone receptors being positive in only 4 (12%) and 3 (9%) of the 34 cases, respectively. Expression of the cerbB2 oncogene was also low, being only positive in 5 (15%) of the 34 cases. The generally low percentage of expression of the hormone receptors is in agreement with the 0–25% reported in the literature.9,12 Expression of cerbB2 warrants further discussion, as a low cerbB2 expression had been reported in metaplastic carcinoma. In our series of biphasic and monophasic tumours, only 2 (8%) of the 24 cases were positive for cerbB2; an even lower figure of 0% had been reported9 in the literature. This is in contrast with the general impression that in high‐grade (grade 3) breast carcinomas, the cerbB2 positivity rate is about 35%,20,21 thus suggesting that metaplastic carcinoma may be biologically different from high‐grade IDC.
The expression of Ki‐67 and p53 among the three groups of metaplastic carcinomas in our series, with a 10% positivity as the cut‐off, was high, with 6 (60%) of 10 cases, 6 (43%) of 14 cases and 7 (70%) of 10 cases, respectively, showing > 10% positivity for epithelial‐only, biphasic and monophasic metaplastic carcinomas. For p53, >10% staining was seen in 4 (40%) of 10 cases of epithelial‐only carcinomas, 6 (43%) of 14 cases of biphasic carcinomas and 8 (80%) of 10 cases of monophasic metaplastic carcinomas. Although the expression of p53 and Ki‐67 has not been extensively reported for metaplastic carcinoma of the breast, one sporadic case report noted the expression of these markers.22 Another report on a series of 24 low‐grade spindle cell carcinoma of the breast showed that all the cases were <5% positive for Ki‐67,14 in stark contrast to the observation in this case series. This provides strong evidence for the high grade and aggressive nature of metaplastic carcinoma in general, irrespective of the histological subtypes—whether epithelial‐only, biphasic or monophasic. The biological behaviour of the low‐grade spindle cell carcinoma is probably distinct, and it would be prudent to consider this as a separate entity.
Further evidence of the aggressive nature of all the histological subtypes is apparent from the lymph node status and the follow‐up result of the current cohort. Of the 25 patients who had known, histologically proven axillary status at the time of surgery 14 (56%) patients showed positive axillary lymph node metastases. This is in contrast with the reported incidence of axillary metastasis of 8% in one series,8 but the figure in our study was similar to the 40% of another series.9 This again contrasts with the reported results of the low‐grade spindle cell carcinoma, with the two large series reporting the absence of axillary metastases in all cases.13,14 The morphology of the metastases in most situations recapitulates that of the original tumour. For the epithelial‐only and the monophasic carcinomas, this poses no diagnostic problem in identifying metastasis. In the current cohort, the two adenosquamous carcinomas showed adenosquamous components in the metastases, and the SCC showed squamous or poorly‐differentiated carcinoma in the metastases. Problems may, however, arise for the biphasic carcinoma. In the four cases with metastases, three showed a carcinoma component only in the metastases, and in only one case was the metastasis biphasic. Furthermore, in one case, the metastasis seemed to be more epithelial than the primary tumour which was more spindled (figs 3A,B3A,B).). Bearing this fact in mind is important, as failure to recognise the possible morphological discrepancy between the primary and metastasis may result in inappropriate treatment and investigations for a possible new primary erroneously perceived.
Follow‐up data were available for 25 patients; 11 dead (14 alive). Among those who died, 8 (73%) died of disease, and of the survivors, 7 (50%) also had evidence of disease at the end of the follow‐up period. Viewed from another perspective, of a total of 25 patients, 15 (60%) had evidence of disease (8 died, 7 were alive). On comparing the parameters between these two groups, we found no differences between hormonal receptor status and the expression of cerbB2, Ki‐67 and p53. The only difference was the percentage of positive axillary lymph node status, which was positive in 9 (75%) of 12 patients with disease compared with 4 (40%) of 10 patients from the disease‐free group.
When we look at the individual subtype of metaplastic carcinomas, the percentage of patients with disease (dead or alive) are 4 (57%) of 7 patients, 8 (89%) of 9 patients and 3 (33%) of 9 patients, respectively, from the groups of epithelial‐only, biphasic and monophasic metaplastic carcinomas. As the number of cases in these categories is small, the significance of this if any, remains unclear. Although the diagnosis of the epithelial‐only subtype (adenosquamous or pure SCC) can be based only on morphological assessment, diagnosing the biphasic and monophasic types of metaplastic carcinoma requires the use of immunohistochemistry. Cytokeratin and vimentin positivity is the defining feature.8 Some authors reported a rather low expression of cytokeratin markers (8/18 (44%) cases for AE1/AE3, and 9/18 (50%) cases for CAM5.2), but if both markers were combined, the pick‐up rate increased to 10 (55%) of 18 cases. Furthermore, the spindle cells were reported to show the highest percentage of expression for myoepithelial markers (34bE12, smooth muscle cell actin).8 Most other recent studies report a higher percentage of AE1/AE3 expression, ranging from 63% to 100%.3,6,7,11,13 Hence, AE1/AE3 remains the most widely used and most sensitive marker, with vimentin, for defining the metaplastic spindle cells, particularly for the monophasic subtype.
In summary, we report a large series of metaplastic carcinomas, by conventional usage. The diagnosis of this group of lesions is by morphology for carcinomas with a squamous component or a pure squamous carcinoma, and by immunohistochemistry for those with a sarcomatoid or spindle cell carcinoma, coexpressing vimentin and cytokeratin. The combined use of AE1/AE3 and CAM5.2 shows a higher sensitivity than each marker alone. All three subtypes may have aggressive biological behaviour, as evidenced by the high percentage of lymph node metastases at the time of diagnosis and the rather dismal outcome, as well as the high p53 and Ki‐67 index. The absence of hormonal receptors and cerbB2 oncoprotein expression may further limit oncological treatment options.
IDC - infiltrating duct carcinoma
SCC - squamous cell carcinoma
Competing interests: None declared.