Abstract
We analyzed the subgross distribution of the invasive component in 875 consecutive cases of breast carcinomas using large-format histology sections and compared the immunophenotype (estrogen and progesterone receptor expression, HER2 overexpression and expression of basal-like markers, CK5/6, CK14, and epidermal growth factor receptor) in unifocal, multifocal, and diffuse tumors. Histology grade and lymph node status were also analyzed. Unifocal invasive carcinomas comprised 58.6% (513/875), multifocal invasive carcinomas 36.5% (319/875), and diffuse invasive carcinomas 4.9% (43/875) of the cases. The proportion of lymph node-positive cases was significantly higher in multifocal and diffuse carcinomas compared to unifocal cancers, but no other statistically significant differences could be verified between these tumor categories. Histological multifocality and diffuse distribution of the invasive tumor component seem to be negative morphologic prognostic parameters in breast carcinomas, independent of the molecular phenotype.
1. Introduction
Breast carcinoma is a heterogeneous group of diseases; individual cases deviate from each other in morphology, phenotype, and prognosis. Using DNA microarray technique and cluster analysis, five distinct genetic types of the disease were delineated: luminal A, luminal B, HER2 positive, basal-like, and normal breast like tumors [1, 2]. These tumor subtypes can also be identified with sufficient accuracy during routine diagnosis, using a simple panel of immunohistochemical markers, including antibodies tracing estrogen receptors (ER), progesterone receptors (PR), c-erbB-2 oncoprotein overexpression (HER2), and some myoepithelial markers [3, 4]. The recommended myoepithelial markers for delineating the basal-like tumors vary in different studies, cytokeratin (CK)5/6, CK14, CK17, and/or epidermal growth factor receptor (EGFR) being used most often [3, 5–8]. Significant differences in survival of patients with different molecular subtypes of breast carcinoma have been recently evidenced; Luminal A tumors have a significantly better 5- and 10-year survival compared to luminal B, HER2 positive, basal-like, and unclassified tumors [9].
Using large-format histologic sections in diagnostic routine, we have repeatedly evidenced that breast carcinoma has a complex subgross morphology with a considerable proportion of the tumors being either multifocal or diffuse [10–13]. The most recent studies on breast cancer multifocality indicate that multifocality and diffuse distribution of the invasive tumor component represent survival-related negative prognostic parameters [14–17]. As we have not found corresponding data in the literature, we designed the present study with the aim to analyze the relation of subgross appearance of the lesions (unifocal, multifocal, or diffuse distribution of the invasive component) and some phenotypic tumor features, such as ER, PR, and HER2 expression, basal-like phenotype, and histology grade. We focused on the invasive component of the tumor and did not analyze the distribution of the in situ ductal or lobular components in this study. We also tested the relation of the subgross histologic distribution of the lesions to presence of lymph node metastasis (LNM).
2. Materials and Methods
2.1. Study Population
This study is a retrospective analysis of 875 consecutive breast carcinoma cases diagnosed at the Department of Pathology and Clinical Cytology of the Central Hospital in Falun, Sweden, during the period January 2005−December 2009. Patients with recurrent breast carcinomas that were diagnosed before the study period were excluded. We also excluded purely in situ carcinomas (132 cases), microinvasive (<1 mm) carcinomas, and carcinomas which were not routinely stained for the immunohistochemical markers listed below. The subgross parameters, histology grade, LNM, ER, PR, and HER2 status were analyzed during the entire study period. The basal-like phenotype was routinely assessed from September 2006 to the end of the study period. The study was approved by the Regional Ethical Committee in Uppsala-Örebro region.
2.2. Large-Section Histopathology
All specimens were prepared by the method of large-section histopathology, which has been a routine procedure in our laboratory since 1982. The method has been described in detail elsewhere [18]. Briefly, all cases were discussed by a preoperative tumor board, and the radiological (mammography, ultrasound, and magnetic resonance imaging) appearance was registered, including the extent and distribution. This information, together with the whole-specimen radiograph received with the surgical specimen, guided the pathologist during the workup. The sector-resection specimens were sliced into 3-4 mm-thick tissue slices parallel to the pectoralis fascia. The slices were also radiographed. One to five of the most representative slices (measuring up to 9 × 8 cm) were selected for embedding into large paraffin blocks. Larger slices were bisected and embedded into separate blocks. Mastectomy specimens were sliced perpendicular to the pectoralis fascia to visualize the surgical margin in one histological plane. All cases were discussed again on postoperative tumor board to check the concordance of the radiological and histological findings. Most cases which were discrepant in favour of radiology findings were solved with additional sampling of the specimen for histological analysis.
2.3. Immunohistochemistry
The largest invasive tumor focus was sampled for routine immunostaining. The following antibodies were used: ER (Ventana Medical Systems, clone : SP1, 1 : 200), PR (Dako, clone : PgR 636, 1 : 50), CK5/6 (Dako, clone : D5/16 B4, 1 : 100), CK14 (Novocastra, clone : LL002, 1 : 20), EGFR (Dako, clone : E 30, 1 : 25), and HER2 (Dako, code A 0485, 1 : 250). Additional foci were only stained in selected cases. Nuclear staining >10% of the tumor cells were the criterion of ER and PR positivity, cytoplasmic staining in >10% for CK5/6 and CK14 positivity, and membranous and cytoplasmic staining in >10% of the tumor cells for EGFR positivity. HER2 positivity was assessed in accordance with the criteria of the manufacturer; all 2+ equivocal cases underwent fluorescence in situ hybridisation test.
2.4. Diagnostic Criteria
The distributions of the invasive component and of the in situ component of the same lesion were determined separately. For the purpose of the present study, the tumors were classified based on the distribution of the invasive lesions. They were considered to be “unifocal” if only one invasive focus could be observed in the large sections, with the tumor focus containing or not containing an in situ component. “Multifocal” invasive lesions were characterized by the presence of multiple well-delineated invasive tumor foci separated from each other by uninvolved breast tissue, regardless of the distance between the foci. Tumors that were dispersed over a large area in the section, much like a spider's web, with no distinct tumor mass were classified as “diffuse.” The size of the diffuse tumors was equal to the extent of the disease in many cases and was rather comparable to the extent of the disease in multifocal cases than to the size of the individual foci. When the distribution of the lesions was assessed, in each case, an attempt was made to summarize the findings in different levels of the large sections to reconstruct the in vivo situation before operation. Detailed correlation between radiological and pathological findings was essential. If a secondary surgical intervention was performed in addition to the primary sector resection, an attempt was made to summarize the findings in the entire excised tissue. However, sector resection specimens (average size of 9 × 6 cm) were sufficient for categorizing the findings in most cases. Typical cases of unifocal, multifocal, and diffuse invasive breast carcinomas are illustrated in Figure 1.
Figure 1.
Typical cases of unifocal (left), multifocal (central), and diffuse (right) invasive breast carcinomas documented in large-format histology sections. The lesions are marked in the lower images.
LNM was defined as presence of metastatic deposit(s) in at least one of the lymph nodes of the case, irrespective on the size of the deposit(s). Both sentinel and nonsentinel nodes were assessed on routinely stained sections. The sentinel lymph nodes were additionally stained on CK8/18 (BD Biosciences, clone Cam 5.2, 1 : 50). Tumors expressing at least one of the basal (myoepithelial) markers (CK5/6, CK14, EGFR) in at least one of the invasive tumor foci were categorized as basal-like tumors. Triple-negative tumors were defined as negative for all of the following markers: ER, PR, and HER2. The tumors were graded according to the Notthingham (Bloom-Richardson-Elston-Ellis) grading system [19]. Tumor size was defined as the largest dimension of the largest invasive focus.
2.5. Study Execution
All of the large histological sections belonging to this series (average number of sections per case 6, range of 1–34) were reviewed for the purposes of postoperative tumor board. Histological data, including the distribution of lesions, were determined according to the diagnostic criteria described above and registered in a database. “Multicentricity,” which is defined as the presence of malignant structures in different quadrants of the same breast, was not analyzed because it represents a clinical and/or radiological parameter. Phenotypic parameters were obtained from the department's database. The statistical analysis (comparison of proportion using chi-square test) was carried out using commercially available software (MedCalc statistics for biomedical research, MedCalc Software, Belgium), with P-values <.01 regarded significant.
3. Results
The distribution of the invasive lesions could be accurately analyzed in 875 invasive cases. Unifocal invasive carcinomas comprised 58.6% (513/875), multifocal invasive carcinomas 36.5% (319/875), and diffuse invasive carcinomas 4.9% (43/875) of the cases.
Histology grade was determined in 870 of the invasive carcinomas of which 22.8% (198/870) were grade 3. As demonstrated in Table 1, there were 115 unifocal, 80 multifocal, and 3 diffuse grade 3 invasive carcinomas. The percentage of unifocal and multifocal grade 3 cases were very similar (22.6% versus 25.2%). The proportion of grade 3 cases among diffuse invasive carcinomas was only 7.0%, but the difference was not statistically significant as only 3 such cases were found.
Table 1.
Immunophenotypic parameters, histology grade and node status by invasive tumor distribution (unifocal, multifocal, and diffuse) in 875 consecutive breast cancer cases, Falun 2005–2009.
| Phenotype | Invasive tumor distribution | Significance level | ||||
|---|---|---|---|---|---|---|
| Unifocal | Multifocal | Diffuse | Total | Unifocal versus multifocal | Unifocal versus diffuse | |
| ER positive | 83.1% (423/509) | 81.8% (256/313) | 97.7% (42/43) | 83.4% (721/865) | P = .7852 | P = .0178 |
| PR positive | 66.3% (331/499) | 64.9% (203/313) | 53.5% (23/43) | 65.1% (557/855) | P = .8289 | P = .1565 |
| HER2 positive | 9.6% (48/501) | 15.2% (48/315) | 4.8% (2/42) | 11.4% (98/858) | P = .0419 | P = .4334 |
| Triple negative | 11.2% (56/499) | 10.5% (33/313) | 2.4% (1/42) | 10.5% (90/854) | P = .9083 | P = .1144 |
| Basal-like | 12.5% (37/296) | 11.3% (22/195) | 3.7% (1/27) | 11.6% (60/518) | P = .6020 | P = .2896 |
| Grade 3 | 22.6% (115/509) | 25.2% (80/318) | 7.0% (3/43) | 22.8% (198/870) | P = .5664 | P = .0245 |
| Node positive | 27.3% (140/513) | 54.2% (173/319) | 55.8% (24/43) | 38.5% (337/875) | P < .0001 | P = .0001 |
Tumor size could be accurately assessed in 511 unifocal (average size 16.0 mm, range 3–70 mm), 315 multifocal (average size 19.5 mm, range 2–60 mm), and in 41 diffuse (average size 45.6 mm, range 20–85 mm) invasive carcinomas. This difference was not statistically significant when unifocal and multifocal tumors were compared (P = .7375), but the differences became significant when the diffuse group was added to analysis (P = .0003).
ER status was assessed in 865 invasive breast carcinomas. There were 83.4% (721/865) ER-positive and 16.6% (144/865) ER-negative cases. There were 83.1% (423/509) unifocal, 81.8% (256/313) multifocal, and 97.7% (42/43) diffuse ER-positive invasive cancers. The differences were statistically not significant.
PR was assessed in 855 cases. There were 65.1% (557/855) PR-positive and 34.9% (298/855) PR-negative cases. 66.3% (331/499) of the unifocal, 64.9% (203/313) of the multifocal, and 53.5% (23/43) of the diffuse invasive carcinomas were PR positive. The differences were statistically not significant.
During the study period, 858 invasive breast carcinomas were tested for HER2 overexpression and 11.4% (98/858) were found to be HER2 positive: 9.6% (48/501) unifocal, 15.2% (48/315) multifocal, and 4.8% (2/42) diffuse tumors. The differences were statistically not significant.
The proportion of triple negative cases was 10.5% (90/854) in the present series, 11.2% (56/499) among the unifocal, 10.5% (33/313) among the multifocal, and 2.4% (1/42) among the diffuse cases. The differences were statistically not significant.
Carcinomas were routinely stained for basal markers in 518 cases. Of those, 11.6% (60/518) expressed basal-like phenotype, 12.5% (37/296) of the unifocal, 11.3% (22/195) of the multifocal, and 3.7% (1/27) of the diffuse tumors. The differences were statistically not significant.
LNM was determined in all cases of the present series of invasive breast carcinomas and 38.5% (337/875) of the cases had some form of metastatic tumor spread (including macrometastases, micrometastases, and isolated cancer cells/cellgroups). The proportion of lymph node positive cases was 27.3% (140/513) in the group of unifocal cancers, 54.2% (173/319) in the group of multifocal cancers, and 55.8% (24/43) in the group of diffuse tumors. These differences were statistically highly significant.
4. Discussion
Breast cancer is a disease with wide variation in subgross morphology. Tumor multifocality has been evidenced in a substantial proportion of the cases in early whole organ studies and is seen in >30% in the series of cases documented with large-format histology slides [10–13]. In addition, 5% of the invasive carcinomas exhibit a diffuse, spider's web-like growth pattern [14]. Modern radiology methods, especially if used in combination (multimodality approach), are able to indicate the growth pattern of the tumor in the vast majority of the cases [18]. Detailed radiological-pathological correlation and regular use of large-format histology slides enables the breast pathologist to correctly assess tumor size, disease extent, and multifocality or diffuse growth and to confirm or correct the preoperative radiological results.
The prognostic significance of tumor multifocality has recently received special attention as, in contrast to some previous publications [20], recent long-term followup studies have demonstrated significantly lower breast cancer-specific survival in multifocal than in unifocal tumors [15–17]. Multifocality seems to be a negative morphologic parameter independent of treatment modalities [16]. Diffuse invasive carcinomas have an even worse prognosis than the multifocal tumors [14, 17]. The question arises whether differences in survival between unifocal, multifocal, and diffuse breast carcinomas can be explained with differences in their molecular phenotype. The present study was carried out on a recent series of cases, thus survival of the patients could not be tested.
The greater metastatic capacity of multifocal and diffuse tumors compared to the unifocal ones has been repeatedly proven in independent studies [10–12, 20–22] and was also confirmed in the present study. In fact, this was the only statistically significant difference between unifocal versus multifocal and unifocal versus diffuse invasive carcinomas in the present series.
The relation of tumor multifocality and tumor phenotype is rarely studied in the literature. Histology grade, ER, PR, and HER2 status represent well-established, routinely assessed morphological prognostic parameters [23, 24]. According to our results, no significant differences could be demonstrated between these tumor categories with respect to histology grade, ER, PR, and HER2 status. The same finding has been reported by Litton et al., but their study was limited to women ≤35 years [25]. In the study of Oh et al., no significant differences were found between unifocal and multifocal/multicentric tumors regarding nuclear grade and ER status [26].
While multifocal breast carcinomas had a tendency to show more unfavourable phenotype, although statistically not significantly different, compared to the unifocal tumors, the diffuse invasive carcinomas exhibited an opposite tendency. They were less often ER negative, less often triple negative, less often HER2 positive, or basal-like than the unifocal cancers. Although this is a remarkable phenomenon as these tumors have the less favourable outcome, this may be explained by the high percentage of invasive lobular carcinomas in this subgroup [10, 14].
5. Conclusion
Although multifocal and diffuse invasive breast carcinomas exhibited a doubled frequency of LNM compared to that in unifocal tumors, no statistically significant differences could be demonstrated between these categories regarding histology grade, ER, PR, or HER2 status and regarding the proportion of tumors with basal-like phenotype. Multifocal and diffuse distribution of the invasive tumor component seems to be an independent negative morphologic prognostic parameter in breast cancer.
Conflict of Interests
The authors declare no conflict of interests.
References
- 1.Perou CM, Sørile T, Eisen MB, et al. Molecular portraits of human breast tumours. Nature. 2000;406(6797):747–752. doi: 10.1038/35021093. [DOI] [PubMed] [Google Scholar]
- 2.Sørlie T, Tibshirani R, Parker J, et al. Repeated observation of breast tumor subtypes in independent gene expression data sets. Proceedings of the National Academy of Sciences of the United States of America. 2003;100(14):8418–8423. doi: 10.1073/pnas.0932692100. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Nielsen TO, Hsu FD, Jensen K, et al. Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma. Clinical Cancer Research. 2004;10(16):5367–5374. doi: 10.1158/1078-0432.CCR-04-0220. [DOI] [PubMed] [Google Scholar]
- 4.Livasy CA, Karaca G, Nanda R, et al. Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma. Modern Pathology. 2006;19(2):264–271. doi: 10.1038/modpathol.3800528. [DOI] [PubMed] [Google Scholar]
- 5.Cheang MCU, Voduc D, Bajdik C, et al. Basal-like breast cancer defined by five biomarkers has superior prognostic value than triple-negative phenotype. Clinical Cancer Research. 2008;14(5):1368–1376. doi: 10.1158/1078-0432.CCR-07-1658. [DOI] [PubMed] [Google Scholar]
- 6.Moinfar F. Is ‘basal-like’ carcinoma of the breast a distinct clinicopathological entity? A critical review with cautionary notes. Pathobiology. 2008;75(2):119–131. doi: 10.1159/000123850. [DOI] [PubMed] [Google Scholar]
- 7.Rakha EA, El-Sayed ME, Green AR, Paish EC, Lee AHS, Ellis IO. Breast carcinoma with basal differentiation: a proposal for pathology definition based on basal cytokeratin expression. Histopathology. 2007;50(4):434–438. doi: 10.1111/j.1365-2559.2007.02638.x. [DOI] [PubMed] [Google Scholar]
- 8.Tamimi RM, Baer HJ, Marotti J, et al. Comparison of molecular phenotypes of ductal carcinoma in situ and invasive breast cancer. Breast Cancer Research. 2008;10(4):p. R67. doi: 10.1186/bcr2128. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Dawood S, Hu R, Homes MD, et al. Defining breast cancer prognosis based on molecular phenotypes: results from a large cohort study. doi: 10.1007/s10549-010-1113-7. Breast Cancer Research and Treatment PMID: 20711652. In press. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Tot T. Clinical relevance of the distribution of the lesions in 500 consecutive breast cancer cases documented in large-format histologic sections. Cancer. 2007;110(11):2551–2560. doi: 10.1002/cncr.23052. [DOI] [PubMed] [Google Scholar]
- 11.Tot T. The metastatic capacity of multifocal breast carcinomas: extensive tumors versus tumors of limited extent. Human Pathology. 2009;40(2):199–205. doi: 10.1016/j.humpath.2008.07.001. [DOI] [PubMed] [Google Scholar]
- 12.Tot T, Pekár G, Hofmeyer S, Sollie T, Gere M, Tarján M. The distribution of lesions in 1–14-mm invasive breast carcinomas and its relation to metastatic potential. Virchows Archiv. 2009;455(2):109–115. doi: 10.1007/s00428-009-0808-9. [DOI] [PubMed] [Google Scholar]
- 13.Tot T. The origins of early breast carcinoma. Seminars in Diagnostic Pathology. 2010;27(1):62–68. doi: 10.1053/j.semdp.2009.12.002. [DOI] [PubMed] [Google Scholar]
- 14.Tot T. The diffuse type of invasive lobular carcinoma of the breast: morphology and prognosis. Virchows Archiv. 2003;443(6):718–724. doi: 10.1007/s00428-003-0881-4. [DOI] [PubMed] [Google Scholar]
- 15.Boyages J, Jayasinghe UW, Coombs N. Multifocal breast cancer and survival: each focus does matter particularly for larger tumours. European Journal of Cancer. 2010;46(11):1990–1996. doi: 10.1016/j.ejca.2010.03.003. [DOI] [PubMed] [Google Scholar]
- 16.Weissenbacher TM, Zschage M, Janni W, et al. Multicentric and multifocal versus unifocal breast cancer: is the tumor-node-metastasis classification justified? Breast Cancer Research and Treatment. 2010;122(1):27–34. doi: 10.1007/s10549-010-0917-9. [DOI] [PubMed] [Google Scholar]
- 17.Tot T. Towards a renaissance of subgross breast morphology. European Journal of Cancer. 2010;46(11):1946–1948. doi: 10.1016/j.ejca.2010.03.023. [DOI] [PubMed] [Google Scholar]
- 18.Tot T, Tabár L, Dean PB. Practical Breast Pathology. Stuttgart, Germany: Thieme Publisher; 2002. [Google Scholar]
- 19.Elston CW, Ellis IO. Pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: experience from a large study with long-term follow-up. Histopathology. 1991;19(5):403–410. doi: 10.1111/j.1365-2559.1991.tb00229.x. [DOI] [PubMed] [Google Scholar]
- 20.Pedersen L, Gunnarsdottir KA, Rasmussen BB, Moeller S, Lanng C. The prognostic influence of multifocality in breast cancer patients. Breast. 2004;13(3):188–193. doi: 10.1016/j.breast.2003.11.004. [DOI] [PubMed] [Google Scholar]
- 21.Chua B, Ung O, Taylor R, Boyages J. Frequency and predictors of axillary lymph node metastases in invasive breast cancer. ANZ Journal of Surgery. 2001;71(12):723–728. doi: 10.1046/j.1445-1433.2001.02266.x. [DOI] [PubMed] [Google Scholar]
- 22.Coombs NJ, Boyages J. Multifocal and multicentric breast cancer: does each focus matter? Journal of Clinical Oncology. 2005;23(30):7497–7502. doi: 10.1200/JCO.2005.02.1147. [DOI] [PubMed] [Google Scholar]
- 23.Tavassoli FA, Devilee P, editors. World Health Organization Classification of Tumours. Tumours of the Breast and Female Genital Organs. Lyon, France: IARC Press; 2003. [Google Scholar]
- 24.Tavassoli FA, Eusebi V. Tumors of the Mammary Gland. Washington, DC, USA: American Registry of Pathology; 2009. (AFIP Atlas of Tumor Pathology: Series 4). [Google Scholar]
- 25.Litton JK, Eralp Y, Gonzalez-Angulo AM, et al. Multifocal breast cancer in women ≤35 years old. Cancer. 2007;110(7):1445–1450. doi: 10.1002/cncr.22928. [DOI] [PubMed] [Google Scholar]
- 26.Oh JL, Dryden MJ, Woodward WA, et al. Locoregional control of clinically diagnosed multifocal or multicentric breast cancer after neoadjuvant chemotherapy and locoregional therapy. Journal of Clinical Oncology. 2006;24(31):4971–4975. doi: 10.1200/JCO.2006.07.6067. [DOI] [PubMed] [Google Scholar]