Abstract
Background:
The metastatic propensity of invasive ductal carcinoma (IDC) of the breast correlates with axillary node involvement and with expression of the proliferation antigen Ki-67, whereas ductal carcinoma in situ (DCIS) is non-metastasising. To clarify whether concomitant DCIS affects IDC prognosis, we compared Ki-67 expression and node status of size-matched IDC subgroups either with DCIS (IDC-DCIS) or without DCIS (pure IDC).
Methods:
We analysed data from 1355 breast cancer patients. End points were defined by the association of IDC (with or without DCIS) with grade, nodal status, Ki-67, and ER/HER2.
Results:
Size-matched IDC-DCIS was more likely than pure IDC to be screen detected (P=0.03), to occur in pre-menopausal women (P=0.002), and to be either ER-positive (P=0.002) or HER2-positive (P<0.0005), but less likely to be treated with breast-conserving surgery (P=0.004). Grade and Ki-67 were lower in IDC-DCIS than in pure IDC (P=0.02), and declined as the DCIS enlarged (P<0.01). Node involvement and lymphovascular invasion in IDC-DCIS increased with the size ratio of IDC to DCIS (P<0.01). A 60-month cancer-specific survival favoured IDC-DCIS over size-matched pure IDC (97.4 vs 96.0%).
Conclusion:
IDC co-existing with DCIS is characterised by lower proliferation and metastatic potential than size-matched pure IDC, especially if the ratio of DCIS to IDC size is high. We submit that IDC-DCIS is biologically distinct from pure IDC, and propose an incremental molecular pathogenesis of IDC-DCIS evolution involving an intermediate DCIS precursor that remains dependent for replication on upstream mitogens.
Keywords: breast neoplasms, pre-invasive, intraductal, Ki-67, carcinogenesis, tumour progression
Widespread use of breast cancer screening with mammography has led to a steep rise in the incidence of ductal carcinoma in situ (DCIS; van Steenbergen et al, 2009), whereas the overall incidence of invasive ductal carcinoma (IDC) is decreasing (Jemal et al, 2009). Although DCIS is pre-malignant (Pinder and Ellis, 2003), the modest improvement in breast cancer mortality attributable to such screening (Mandelblatt et al, 2009; Nelson et al, 2009) has suggested that many DCIS cases never progress to invasive disease, raising questions about the contribution of DCIS to the natural history of sporadic IDC (Allred et al, 2001; Burstein et al, 2004). In tumours containing both IDC and DCIS (IDC-DCIS), it is unclear whether the IDC component arises directly from DCIS; in tumours lacking DCIS, however, it is assumed that IDC arises de novo. One recent study implicated DCIS as the precursor of IDC-DCIS based on concordant expression of immunohistochemical markers (Steinman et al, 2007), a conclusion that has since been supported by genomic data (Aubele et al, 2000; Alexe et al, 2007; Iakovlev et al, 2008), in turn creating a quest for biomarkers that predict invasive transformation of DCIS (Schuetz et al, 2006; Castro et al, 2008). Other studies have reported differences between DCIS and IDC-DCIS, suggesting that DCIS may not have been a precursor of the invasive component (Farabegoli et al, 2002); however, some of these studies have been limited either by failure to use pure IDC as a comparator (Patla et al, 2002) or else by small cohort sizes (Mylonas et al, 2005). Yet another study concluded that the presence of DCIS was associated with a trend towards superior disease-free survival (DFS) and overall survival, but that it was not an independent predictor of outcome (Chagpar et al, 2009).
Proliferation antigen Ki-67 (Gerdes et al, 1991) is a biomarker of tumour activity, and an adverse prognostic factor in patients with IDC (Fitzgibbons et al, 2000; Jung et al, 2009). Elevated Ki-67 expression may predict progression to cancer in some precursor lesions (Shaaban et al, 2002); in DCIS, high Ki-67 expression levels may predict in situ or invasive recurrence (Simpson et al, 2007). Indeed, together with lymph node status, Ki-67 has been implicated as one of only two factors with an independent prognostic value for survival (Jung et al, 2009); in tumours not stratified for DCIS status, Ki-67 expression appears prognostically independent of tumour size and nodal status (Barnard et al, 1987; Bouzubar et al, 1989; Locker et al, 1992). Because presence of DCIS may bias the detectability of an associated IDC lesion, we chose in this study to focus on the biological characteristics – Ki-67, nodal status, and receptor expression – of similarly sized IDC with or without DCIS.
Patients and methods
Patients
Tumour data obtained from 2271 consecutive patients undergoing surgery for primary invasive breast cancer between October 2000 and September 2008 in a single centre were analysed retrospectively. Male patients (n=2), patients with histopathological diagnoses other than ductal carcinoma, such as lobular carcinoma (n=75), those who had received neoadjuvant chemotherapy (n=56), those with metastatic disease (n=71) and samples with incomplete pathological examination or data (n=712) were excluded.
Tumour morphology
The remaining evaluable samples numbered 1355. They were divided into three subgroups based on the association of IDC with DCIS or otherwise, into pure IDC, IDC associated with co-existing DCIS (IDC-DCIS), and pure DCIS. Within the group of IDC-DCIS, the samples were further classified into (1) small IDC–large DCIS, (2) large IDC–small DCIS, and (3) IDC-DCIS with comparable sizes, based on respective median sizes of IDC (1.8 cm) and DCIS (1.5 cm) as the cut-off values. The three subgroups were thus defined to be (1) small IDC (<1.8 cm) large DCIS (⩾1.5 cm), (2) large IDC (⩾1.8 cm) small DCIS (<1.5 cm), and (3) all remaining IDC-DCIS samples. The IDC to DCIS size ratio for each tumour sample was also determined. Sizes of DCIS within IDC-DCIS tumours were initially reported either in terms of largest diameter (cm/mm) or else as a percentage of IDC size; in the latter group, DCIS diameters were calculated from the IDC diameters and rounded to the nearest decimal place. Tumours with DCIS reported to be <1% IDC size were defined for this study as pure IDC.
Immunohistochemistry
Immunohistochemistry was performed on formalin-fixed paraffin-embedded specimens in a reference laboratory by a dedicated pathologist followed a standard protocol. Immunohistochemistry for ER and PR was performed using 6F11 and 1A6 antibodies respectively, and detected by the polymer EnVision system (Dako, Glostrup, Denmark). ER/PR results were reported with a semi-quantitative H-score ranging from 0 to 300; a score above 10 was considered positive. The immunohistochemistry assay used for HER2 was A0485 (polyclonal antibody; Dako). HER2 was considered positive with either 3+ immunoreactivity or amplification by fluorescent in situ hybridisation (FISH) with a ratio of HER2 to chromosome 17 centromeric region >2.2, using PathVysion Vysis FISH (Abbott, Chicago, IL, USA). Expression of Ki-67 was assessed by immunostaining with antibody SP6, and was reported as the percentage of positive tumour cells. In cases of IDC-DCIS, Ki-67 values of the invasive cancer component alone were used for comparative analyses.
Statistical analysis
The median test was used to calculate statistical differences in the Ki-67 index between subgroups; if a difference was found, Spearman's correlation statistics were used to define the relationship between these co-variables. When comparing IDC-DCIS and pure IDC, partial correlations were calculated by controlling for sizes of the invasive cancer component.
Nodal status, lymphovascular invasion, and outcomes
The number of involved nodes, and the presence or absence of lymphovascular invasion, was determined by routine haematoxylin–eosin staining. Patient DFS were ascertained using Kaplan–Meier methodology.
Results
Patients, demographics, histology, and mode of primary tumour detection
The median age of the 1355 subjects was 48 years (range 24–91 years). All were women; most (64.3%) were pre-menopausal, consistent with local epidemiology. Of all tumour samples, 616 (45.5%) were IDC-DCIS; 543 (40.1%) were pure IDC; and the remaining 196 (14.4%) were pure DCIS. Screening mammography detected breast lesions in 169 cases (12.5%), whereas 1036 (76.5%) were self-discovered; 5.7 and 11.5% of patients with IDC and IDC-DCIS, respectively, were diagnosed by screening mammography, whereas 34.2% of patients with pure DCIS were diagnosed by this mode (data not shown). After correcting for IDC size, a partial correlation coefficient of −0.091 (P=0.003) favoured pure IDC self-detection and IDC-DCIS screen detection; these data may be pertinent to future cost-efficacy analyses related to screening. Breast-conserving surgery was more common in pure IDC than in IDC-DCIS (47.3 vs 39.0%, P=0.004), however, implying that more extensive DCIS lesions tended to favour mastectomy despite the higher frequency of screen detection in this group (Table 1).
Table 1. Demographic, detection, and surgical data of patients with pure IDC, IDC-DCIS, and pure DCIS.
|
IDC-DCIS
|
|||||
|---|---|---|---|---|---|
| Characteristics | All cases | Pure IDC | All IDC-DCIS | Small IDC–large DCIS | Large IDC–small DCIS |
| Age at diagnosis | |||||
| Median (range) | 48 (24–91) | 49 (24–91) | 47 (26–86) | 47 (26–83) | 47 (29–86) |
| ⩽35 | 7.5 (101) | 8.1 (44) | 6.7 (41) | 7.4 (14) | 6.8 (15) |
| 36–50 | 53.5 (726) | 47.5 (258) | 58.1 (358) | 60.3 (114) | 54.5 (121) |
| ⩾51 | 38.5 (521) | 43.3 (235) | 35.2 (217) | 32.3 (61) | 38.7 (86) |
| Unknown | 0.5 (7) | 1.1 (6) | 0.0 (0) | 0.0 (0) | 0.0 (0) |
| Menopausal status | |||||
| Pre-menopausal | 64.3 (871) | 58.6 (318) | 67.2 (414) | 70.4 (133) | 62.6 (139) |
| Post-menopausal | 35.7 (484) | 41.4 (225) | 32.8 (202) | 29.6 (56) | 37.4 (83) |
| Mode of discovery | |||||
| Mammographic screening | 12.5 (169) | 5.7 (31) | 11.5 (71) | 18.5 (35) | 4.5 (10) |
| Self-detected | 76.5 (1036) | 82.7 (449) | 77.4 (477) | 68.8 (130) | 86.9 (193) |
| Others | 11.1 (150) | 11.6 (63) | 11.0 (68) | 12.7 (24) | 8.6 (19) |
| Primary surgery | |||||
| Mastectomy and axillary dissection | 15.1 (205) | 16.0 (87) | 18.8 (116) | 16.9 (32) | 19.4 (43) |
| Lumpectomy and axillary surgery (including sentinel lymph node biopsy) | 40.3 (546) | 47.3 (257) | 39.0 (240) | 22.8 (43) | 47.7 (106) |
| Lumpectomy alone | 1.8 (24) | 1.5 (8) | 0.5 (3) | 0.5 (1) | 0.0 (0) |
| Others | 42.8 (580) | 35.2 (191) | 41.7 (257) | 59.8 (113) | 32.9 (73) |
| Total number | 1355 | 543 | 616 | 189 | 222 |
Abbreviations: IDC=invasive ductal carcinoma; DCIS=ductal carcinoma in situ. Data are presented as percentages, with numerical results following in parentheses.
Tumour size and proliferation rate
As shown in Table 2, median sizes of IDC and DCIS were 1.8 and 1.5 cm (range 0.01–10.0 and 0.1–10.0 cm) respectively. Median Ki-67 levels were higher in pure IDC, compared with IDC-DCIS of comparable invasive size, as determined by the one-tailed median test (P=0.03). There was also an overall difference between IDC±DCIS and increasing Ki-67 levels, such that pure IDC was associated with higher Ki-67 than was IDC-DCIS (Spearman's correlation coefficient 0.07, P=0.02). After controlling for the sizes of the invasive component, the partial correlation coefficient was still significant at 0.08 (P=0.01). In addition, more patients with pure IDC had a higher Ki-67 expression (Figure 1). Analyses on other subgroups were concordant: IDC-DCIS comprised large IDC (⩾1.8 cm) with small DCIS (<1.5 cm) correlated with higher Ki-67 levels than IDC-DCIS with small IDC (<1.8 cm) and large DCIS (⩾1.5 cm), which in turn had higher Ki-67 levels than pure DCIS (correlation coefficient, −0.2; P<0.005). Furthermore, higher IDC to DCIS size ratio was associated with higher Ki-67 (Pearson's correlation coefficient, 0.125; P=0.002).
Table 2. Tumour size, grade, and Ki-67 expression in patients with pure IDC vs IDC-DCIS.
|
IDC-DCIS
|
|||||
|---|---|---|---|---|---|
| Characteristics | All cases | Pure IDC | All IDC–DCIS | Small IDC–large DCIS | Large IDC–small DCIS |
| IDC size (cm) | |||||
| Median (range) | 1.8 (0.01–10.0) | 1.8 (0.12–10.0) | 1.8 (0.01–8.00) | 0.7 (0.01–1.7) | 2.5 (1.8–8.0) |
| ⩽2 | 50.0 (678) | 58.0 ((315) | 58.9 (363) | 100 (189) | 15.8 (35) |
| >2–5 | 32.6 (442) | 37.9 (206) | 38.3 (236) | 0.0 (0) | 79.3 (176) |
| >5 | 2.9 (39) | 4.1 (22) | 2.8 (17) | 0.0 (0) | 5.0 (11) |
| DCIS size (cm) | |||||
| Median (range) | 1.5 (0.1–10.0) | NA | 1.0 (0.1–10.0) | 3.4 (1.5–10.0) | 0.3 (0.1–1.4) |
| Grade | |||||
| 1 | 9.4 (128) | 8.3 (45) | 13.3 (82) | 15.3 (29) | 12.2 (27) |
| 2 | 30.9 (419) | 35.5 (193) | 36.7 (226) | 41.6 (77) | 32.0 (71) |
| 3 | 44.1 (598) | 54.7 (297) | 48.9 (301) | 41.8 (79) | 55.9 (124) |
| Unknown | 15.5 (210) | 1.5 (8) | 1.1 (7) | 2.1 (4) | 0.0 (0) |
| Ki-67 index (%) | |||||
| Mean, median | 21.3, 13.0 | 25.3, 15.0 | 21.0, 14.0 | 19.1, 12.0 | 23.5, 15.5 |
| ⩽10 | 45.7 (619) | 40.1 (218) | 44.0 (271) | 47.6 (90) | 36.0 (80) |
| >10–20 | 21.2 (287) | 19.7 (107) | 22.7 (140) | 22.8 (43) | 23.9 (53) |
| >20 | 33.1 (449) | 40.1 (218) | 33.3 (205) | 29.6 (56) | 40.1 (89) |
| Total number | 1355 | 543 | 616 | 189 | 222 |
Abbreviations: IDC=invasive ductal carcinoma; DCIS=ductal carcinoma in situ. Results are presented as percentages, with raw data following in parentheses.
Figure 1.
Percentage of invasive ductal carcinoma (IDC) with and without ductal carcinoma in situ (DCIS) with different Ki-67 levels. The higher the Ki-67 level, the larger the proportion of pure IDC, and vice versa for IDC-DCIS. Black bars, pure IDC; white bars, IDC-DCIS.
Receptor expression profile
Compared with pure IDC, IDC-DCIS tumours were more often ER positive (81.5 vs 74.0%, P=0.002), PR positive (74.7 vs 70.5%, P=0.114), and/or HER2 positive (25.5 vs 16.2%, P<0.0005). These IDC-DCIS trends were similar in pure DCIS (Table 3), supporting the view that the IDC-DCIS phenotype reflects that of the associated (presumably precursor) DCIS. Moreover, as HER2 expression and ER expression tend to be inversely related, this dual finding suggests a broader dependence of IDC-DCIS on mitogenic signalling.
Table 3. Comparative receptor expression profile – ER/PR and HER2 protein immunohistochemical status – of pure IDC, IDC-DCIS, and pure DCIS.
| Receptor phenotype | Pure IDC | IDC-DCIS | Pure DCIS |
|---|---|---|---|
| ER-negative | 26.0 (141) | 18.5 (114) | 22.4 (44) |
| ER-positive | 74.0 (402) | 81.5 (502) | 77.6 (152) |
| PR-negative | 29.5 (160) | 25.3 (156) | 25.0 (49) |
| PR-positive | 70.5 (383) | 74.7 (460) | 75.0 (147) |
| HER2-negative | 82.9 (450) | 73.2 (451) | 65.3 (128) |
| HER2-positive | 16.2 (88) | 25.5 (157) | 34.7 (68) |
Abbreviations: ER=oestrogen receptor; PR=progesterone receptor; IDC=invasive ductal carcinoma; DCIS=ductal carcinoma in situ.
Results are presented as percentages, with numerical case data following in parentheses.
Metastasis and survival
Table 4 shows that most patients (66.4%) were free of nodal involvement; 301 (22.2%) had 1–3 involved lymph nodes, whereas 137 (10.1%) had 4 or more involved nodes. Within the 616 IDC-DCIS samples, the mean value of IDC to DCIS size ratio was 5 (range 0.025–50). There was a trend towards higher number of involved lymph nodes in pure IDC compared with IDC-DCIS (Pearson's correlation coefficient, 0.052; P=0.078). Within the IDC-DCIS group, higher IDC to DCIS size ratio correlated with more involved lymph nodes (Pearson's correlation coefficient, 0.112; P=0.006). Similarly, IDC-DCIS cases with large IDC–small DCIS were more often associated with lymphovascular invasion (57.7%) than were small IDC–large DCIS (27.0% P<0.0005); this finding was confirmed by the correlation between higher IDC-DCIS size ratio with lymphovascular invasion (Spearman's correlation coefficient, 0.163, P<0.0005). With a median follow-up of 29.3 months, the 5-year DFS rates of the IDC-DCIS and pure IDC subgroups were 97.40 and 96.00% respectively (not significant; P=0.38).
Table 4. Nodal status and lymphovascular invasion in pure IDC vs IDC-DCIS.
|
IDC-DCIS
|
|||||
|---|---|---|---|---|---|
| Characteristics | All cases | Pure IDC | All IDC–DCIS | Small IDC–large DCIS | Large IDC–small DCIS |
| Lymph node status | |||||
| Negative | 66.4 (900) | 58.9 (320) | 62.3 (384) | 72.0 (136) | 55.4 (123) |
| 1–3 lymph nodes | 22.2 (301) | 26.7 (145) | 25.3 (156) | 17.5 (33) | 29.7 (66) |
| 4–9 lymph nodes | 6.9 (94) | 8.7 (47) | 7.6 (47) | 6.3 (12) | 10.8 (24) |
| >9 lymph nodes | 3.2 (43) | 5.0 (27) | 2.6 (16) | 1.1 (2) | 3.6 (8) |
| Unknown | 1.3 (17) | 0.7 (4) | 2.1 (13) | 3.2 (6) | 0.5 (1) |
| Lymphovascular invasion | |||||
| Negative | 65.2 (884) | 60.8 (330) | 58.3 (359) | 73.0 (138) | 42.3 (94) |
| Positive | 34.8 (471) | 39.2 (213) | 41.7 (257) | 27.0 (51) | 57.7 (128) |
| Total number | 1355 | 543 | 616 | 189 | 222 |
Abbreviations: IDC=invasive ductal carcinoma; DCIS=ductal carcinoma in situ. Data are presented as percentages, with total case numbers following in parentheses.
Discussion
Breast cancer is a heterogenous disease, and much research has been directed towards identifying subtypes to aid risk stratification. The paradigm of early breast cancer management is thus shifting towards ‘personalising’ therapy as a function of morphological, biological, and molecular disease variables (Epstein, 2009). In situ cancer – especially DCIS – has attracted much interest because of its rising incidence in the mammography era, but there are few studies scrutinising the significance of IDC co-existing with DCIS (Chagpar et al, 2009). Currently, the association of DCIS in IDC has no bearing on systemic treatment, which depends entirely on the pathological and molecular characteristics of IDC. It therefore remains unclear whether IDC-DCIS behaves identically to pure IDC or otherwise, notwithstanding that this distinction could have significant implications for adjuvant treatment in early breast cancer.
This study reports the largest cohort yet published relating to this issue, showing that the extent of DCIS with IDC correlates with lower Ki-67 index and fewer involved lymph nodes. Although the pre-malignant DCIS may well have permitted earlier detection of the IDC component than would otherwise occur for a pure IDC of similar size, the fact that the proliferative and metastatic differences persist after controlling for IDC size supports the impression of a biological difference between IDC-DCIS and pure IDC. This conclusion is further supported by the finding of increased ER/PR and/or HER2 expression in IDC-DCIS, suggesting in turn that the pure IDC carcinogenesis pathway could favour the therapeutically challenging basaloid phenotype, which is already known to be associated with multiple defects in tumour suppressor genes such as TP53 and the BRCA DNA repair genes.
These results imply that IDC-DCIS tends to have lower disease aggressiveness than pure IDC, particularly as DCIS-IDC size ratios increase. Such a model is reminiscent of colorectal cancer that may arise either through a polyp-dependent (adenoma carcinoma) process, or through a non-polyp-dependent (de novo) pathway associated with greater invasive and metastatic potential (Tanaka, 2009). In preclinical models of breast cancer, disruption of the TP53 pathway and/or constitutive activation of HER2, FAK or KRAS produce DCIS, but further inhibition of pRb signalling and/or activation of the phosphatidylinositol 3′-kinase pathway appear necessary to promote malignant progression (Lightfoot et al, 2004; Golubovskaya et al, 2009; Wu et al, 2009). Comparative genomic hybridisation studies have also identified genetic pathways – for example through loss of genetic material of 16q associated with well-differentiated to intermediately differentiated DCIS and grade 1 IDC, or gains of 8q, 17q, and 20q associated with poorly differentiated DCIS and grade 3 IDC (Buerger et al, 2001) – that support a linear progression model for the transition from normal to DCIS to IDC. However, the heterogeneity of genetic changes in DCIS compared to IDC suggests other breast cancer progression pathways (Gao et al, 2009). Hence, given that fast-replicating (high Ki-67) tumours might be expected to contain a higher burden of dysfunctional tumour suppressor genes, our study results raise the possibility that pure IDC tumours arise as a result of more drastic tumour suppressor gene defects, whereas IDC-DCIS tumours tend to evolve as a result of a more incremental accumulation of milder suppressor gene defects (Figure 2).
Figure 2.
Hypothetical carcinogenesis model for invasive ductal carcinoma–ductal carcinoma in situ (IDC-DCIS) vs pure IDC. In this model, IDC-DCIS – intrinsically less aggressive as reflected by lower Ki-67 expression and less nodal involvement – develops stepwise from normal breast epithelium via DCIS, through acquiring minor sequential genetic dysfunctions each time, whereas pure IDC develops de novo due to major genetic event(s).
We acknowledge that this study has several important limitations. First, it is a retrospective analysis, from which almost one-third of case records originally examined were excluded due to incomplete data. Second, there were variations in pathology reporting styles, as the tumour samples were not centrally reviewed. Third, the median follow-up time of 30 months is too short to expect major differences in disease-free survival to have emerged. Fourth, it must remain speculative for now whether concomitant DCIS will emerge as a useful independent prognostic variable, as the degree of biological overlap between size-matched IDC-DCIS and pure IDC may preclude this. Finally, we acknowledge that the postulation of molecular differences between IDC-DCIS and pure IDC, as posited in Figure 2, remains entirely speculative at this point, and that any such assumption is premature. We hope, however, that the indirect clinicopathological observations provided here might provoke more specific genetic and scientific hypothesis testing in this clinical context.
In conclusion, this study raises the possibility that the association or otherwise of IDC with a DCIS precursor, and the relative sizes of these two lesions, could be factored into future adjuvant therapeutic decision-making. If verified, this distinction would in turn suggest an as-yet-undetermined molecular basis for the divergent clinical behaviour of these breast lesion subtypes. Future work is needed to test the observations noted here, and to explore molecular explanations for the putative differences in natural history.
Footnotes
Authors' contributions
HW and RE conceived and drafted the article. SL participated in statistical analysis. All authors read and revised the article.
The authors declare no conflict of interest
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