Is invasion a necessary step for metastases in breast cancer?
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To review the empirical evidence to support the conventional (sequential) model of breast cancer progression, which is based on the paradigm that cancer passes through several stages, including an in situ stage prior to an invasive stage, and thereafter (in some cases) disseminates to the lymph nodes and distant organs.
We review the cancer literature of the last 50 years which relates to the prevention of invasive breast cancer (through radiotherapy or surgery) and reductions in the mortality for breast cancer.
For both invasive cancers and DCIS, the literature indicates that prevention of in-breast invasive recurrences does not prevent death from breast cancer. Moreover, the presence of residual cancer cells in the breast after breast-conserving surgery does not compromise the cure rate.
We propose an alternate (parallel) model of breast cancer wherein there is a small pool of cancer stem cells which have metastatic potential from their inception and which disseminate synchronously through several routes—to the breast stroma, to the lymph nodes and to distant organs. Cancer cells which disseminate to the breast give rise to cells which make up the bulk of the tumour mass but these are not the source of the distant metastases.
KeywordsBreast cancer DCIS Invasion Metastasis Death
Part 1: The systemic nature of breast cancer
Among the milestones reached in the 20th century regarding the treatment of women with early stage breast cancer was the discovery that mortality was comparable for patients treated with mastectomy and with breast-conserving surgery (lumpectomy). Fisher  and Veronesi  challenged the iconic view put forward by Halsted nearly a century before  that breast cancer arose at a single location and spread locally within the breast and then to the regional lymph nodes before it became more widely disseminated. The new ‘systemic’ model meant that, in some cases, the breast cancer will have spread beyond the breast before diagnosis, and in these cases, it was necessary to provide systemic treatment if all cancer cells were to be eliminated. The finding of equivalence of the two surgical approaches for treating women with small cancers was lauded as a breakthrough by patient advocacy groups and their support hastened the acceptance of breast-conserving surgery in the 80s and 90s [4, 5, 6]. By changing their practice accordingly, most surgeons tacitly endorsed Fisher’s new ‘systemic’ model of breast cancer progression—but few explored the theoretical implications of the salient observations. It has been known for some time, that about one-third of women with breast cancer, following lumpectomy, experience an invasive recurrence in the same breast [1, 2]. As expected, the risk of ipsilateral invasive recurrence is much lower for women treated with mastectomy than for women treated with lumpectomy [1, 2]. Furthermore, women who experience an in-breast invasive recurrence following lumpectomy are at much greater risk for death from breast cancer than are women who do not experience a recurrence . However, neither in the American trial nor in the Italian trial was it found that the prevention of a local invasive recurrence through mastectomy was associated with a decline in breast cancer mortality [8, 9]. Elsewhere, trials of radiotherapy post-lumpectomy showed similar results, namely that radiotherapy was highly effective in preventing local recurrence, but the preventive effect of radiotherapy on breast cancer mortality was smaller than the preventive effect on local invasive recurrence [10, 11]. These observations, which continue to puzzle us today, have profound implications, which we explore here.
Part 2: The SEER study: mortality after DCIS
It has been inferred from the observation that small clusters of cancer cells often lie entirely within a duct (terminal duct-lobular units) and from studies of molecular markers of cell lineage, that most invasive ductal-type breast cancers originate within the epithelial lining of the breast duct [15, 16]. Areas of DCIS are often found in contiguity with areas of invasive cancer . It has been proposed that breast cancer resembles colon cancer and other carcinomas in that the first-born cancer cells are adjacent to the basement membrane (and associated myoepithelial cell layer in the case of breast cancer) and later, after invasion through the basement membrane, the cancer enters a higher stage wherein malignant cells are contiguous with the stroma and connective tissues of the breast .
On a cellular level, DCIS cells look like invasive cancer cells . Despite this, the majority of scholars are of the opinion that, because of its position vis a vis the basement membrane, DCIS is a precursor of invasive cancer, i.e. DCIS is not frankly malignant in its own right (and is not life-threatening), but some cases of DCIS can ‘progress’ to invasive breast cancer . In this scenario, the invasive in-breast recurrence post-DCIS is considered a primary invasive cancer. Some suggest that the name ‘DCIS’ should be changed to reflect the benign nature of the condition . A minority of investigators consider DCIS to be a bonafide cancer in its own right, with the potential to metastasize in the absence of invasion through the basement membrane and which, on its own, poses a small but significant threat to life .
In our SEER-based study, among patients with DCIS, the risk of invasive local recurrence 10 years after treatment was 1.3% for women with mastectomy, was 2.5% for women with lumpectomy and radiation, and was 4.9% for women with lumpectomy without radiation . The risk of death from breast cancer after treatment was 1.3% for women with mastectomy, was 0.8% for women with lumpectomy and radiation, and was 0.9% for women with lumpectomy without radiation. That is, among DCIS patients, mastectomy reduced the risk of local recurrence by 75%, but did not reduce the risk of dying of breast cancer. Likewise, radiotherapy after DCIS reduces the risk of local recurrence by 50% but did not reduce the risk of dying of breast cancer. In the largest study of its kind prior to our study (EBCTG 2010) , 3729 women with DCIS were treated with breast-conserving surgery and then were randomized to radiotherapy or to no radiotherapy. Radiotherapy reduced the risk of ipsilateral invasive cancer by more than one-half (204 cases versus 92 cases) but was associated with a small but non-significant increase in breast cancer mortality (44 deaths versus 52 deaths; HR 1.22). The authors do not conclude that preventing local invasive recurrence does not reduce mortality; rather, they dismiss this incongruity somewhat cryptically: “the differences are not significant, chance seems to be a likely explanation for them”. In the SEER study , approximately one-half of the DCIS patients who died of breast cancer did not have an invasive cancer recorded prior to their death from breast cancer. This observation supports our position that DCIS is a cancer in its own right. Similar findings were also seen in a recent study of 9799 DCIS cases from The Netherlands . In that study, the probability of developing an ipsilateral invasive breast cancer was much higher for women treated with lumpectomy (308 of 2558; 12.0%) than for women treated with mastectomy (68 of 4667; 1.5%). However, the absolute risks of breast cancer mortality at 10 years for women with lumpectomy (2.7%; 95% CI 2.1–3.4) and mastectomy (2.6%; 95% CI 2.1–3.1) were similar. Furthermore, of the 284 women who died of breast cancer, only 43% experienced a prior invasive breast cancer (ipsilateral or contralateral).
A large case–control study from Sweden also came to similar conclusions . In that study, 96 women diagnosed with primary DCIS between 1992 and 2012 who later died of breast cancer were identified and compared with a group of 318 controls (women diagnosed with primary DCIS who were alive at the time of death of the corresponding case). Treatment by mastectomy or the addition of radiotherapy after lumpectomy was not associated with a lower risk of subsequent death from breast cancer. The odds ratio for death from breast cancer for patients treated with lumpectomy plus radiotherapy (versus with lumpectomy alone) was 1.46 (95% CI 0.81–5.63) and that for patients treated with mastectomy (versus with lumpectomy alone) was 2.26 (95% CI 1.29–4.06). Furthermore, of the 96 cases, 15 developed distant metastases without a preceding ipsilateral or contralateral invasive breast cancer. The authors report that all medical records for cases and controls were retrieved and that the follow-up of subsequent breast events and causes of death was complete. The authors suggest that these results may indicate that some DCIS has an inherent potential for metastatic spread .
The appearance of a local invasive recurrence after DCIS is predictive of a large increase in the risk of dying of breast cancer; some will argue that this supports the notion that the invasive recurrence is the bona fide malignancy. For example, Wapnir et al. reported that after local invasive recurrence in a patient with DCIS, the mortality rate increases 7.1 times . In our SEER study, invasive recurrence increased subsequent breast cancer mortality 18.1 times . However, this does not necessarily imply that that the recurrence has metastatic potential—it could be a marker of aggressivity.1
Another criticism raised against our paper and the message that DCIS could be fatal in its own right was that pathology is an inexact science and that the 3% of women who succumbed to breast cancer probably had cancers with missed foci of micro-invasion, and hence, many invasive breast cancers were misclassified as DCIS . In the SEER data set, there were 13,489 cases of DCIS with micro-invasion that we excluded from our original analysis. In SEER, the 10-year mortality rate from breast cancer was 2.8% for patients with DCIS with micro-invasion and was 1.4% for women with DCIS without micro-invasion . If the mortality of DCIS patients was confined to the subgroup of patients with micro-invasion, then 50% of DCIS patients would have to have occult micro-invasion to generate these observed rates and the concept of DCIS being a discrete category would be challenged.
Others expressed the opinion that DCIS is highly heterogeneous and we cannot assume that all women with DCIS form a single category . Perhaps, 3% of cases of DCIS are, in fact, cancer, but these few cases are outliers and the vast majority of cases of DCIS (97%) are not cancer. By the same logic, one could claim that more than 90% of stage I breast cancers are not cancer.
Support for the notion that breast cancer dissemination can occur in pre-invasive stages of tumour progression comes from the consistent finding of circulating tumour cells in the peripheral blood (or in the bone marrow) of patients with DCIS. In six studies (range 19–404 patients), between 13 and 25% of DCIS patients were found to have circulating tumour cells [29, 30, 31, 32, 33, 34]. It has been proposed that such cells derive from an occult (micro)-invasive lesion within DCIS. However, there is no difference in the frequency of circulating tumour cells in patients with DCIS, compared to those with frank invasive breast cancer [29, 30, 31]. In one study, disseminated tumour cells were detected in the bone marrow of 25% of 24 patients with pure DCIS and in 20% of 56 patients with (non-metastatic) invasive cancer (p = 0.57) . In another study, circulating tumour cells were detected in the peripheral blood of 18.7% of 48 patients with pure DCIS and in 18.8% of 404 patients with non-metastatic invasive breast cancer . The clinical significance of detecting circulating tumour cells in patients with DCIS is still unclear, but raises the important point that cells may enter circulation prior to passing the basement membrane.
Several pathology studies have reported that a significant proportion of patients with a final diagnosis of pure DCIS have positive lymph nodes (about 3%) . Nodal disease is postulated to indicate that occult invasion must be present in the primary tumour. Based on this assumption, the SEER classification automatically assigns cases of DCIS with lymph node metastasis to stage II (or stage III). However, this prejudges the importance of the observations—there is now consistent evidence that some women with confirmed DCIS will have positive lymph nodes, even when comprehensive tissue sectioning reveals no occult invasion [36, 37]; this observation is important and reflects a need to re-examine the association between non-invasive tumours and lymph node involvement.
A possible mechanism by which DCIS cells may enter circulation without breaching the basement membrane has been described for mucinous DCIS. In a study of 36 patients with mucinous DCIS, small vessels were identified within the lumen duct in 26 cases (72%) . The authors propose an alternative pathway for invasion whereby intra-ductal mucin production promotes neovascularization , but this is a rare subtype of DCIS.
A further possibility for the induction of metastases in patients with DCIS may be the iatrogenic dissemination of tumour cells at the time of pre-operative biopsy. Incisional biopsy including the diagnostic core needle biopsy has been associated with seeding of tumour cells into the circulation and has been hypothesized to increase the risk of metastatic disease . Seeding of the needle tract and mechanical displacement of cells into the lymphatic or vascular system has been documented in DCIS [40, 41], but the clinical implications are not known. Liebens et al. reviewed the clinical significance of malignant epithelial cell displacement after core needle biopsy in breast cancer patients . Tumour cell displacement on surgical specimens occurred in 22% of the patients overall, with similar rates seen for DCIS and invasive breast cancer [40, 41, 42]. However, tumour cell displacement was seen less frequently as the interval between biopsy and surgical excision lengthened, suggesting that seeded cells do not survive displacement [41, 42]. No studies to date have documented a survival disadvantage with pre-operative biopsy .
From these observations, we conclude that the patterns of local recurrence and of mortality after DCIS and after primary invasive breast cancer are qualitatively similar and differ only by degree. Fisher and Veronesi pointed out that after primary invasive cancer, preventing local recurrence (by mastectomy versus lumpectomy) does not reduce mortality (if it did then we would recommend mastectomy) [7, 8]. The same holds true for DCIS. By extension, an in-breast invasive event following a diagnosis of DCIS might better be described as a local invasive recurrence than as a new primary cancer. However, what has been accepted for invasive cancer has not been accepted for DCIS.
To summarize: if an in-breast invasive recurrence observed after DCIS were a primary breast cancer, then preventing it should also prevent subsequent metastases (which could potentially be fatal), and if so, preventing the recurrence should prevent (at least some) deaths. However, preventing the invasive in-breast recurrence after DCIS did not result in fewer deaths—therefore, the recurrence is not a primary invasive cancer—therefore, the DCIS has inherent malignant potential. Our position here has not been widely accepted—most commentators continue to describe DCIS as a precursor lesion with little or no inherent malignant potential .
Part 3: The stage distributions of breast cancer in the clinic and in the population
At this point in the essay, we have argued that the condition called DCIS came into prominence in the latter half of the 20th century as pathology techniques improved and as mammography screening identified increasing numbers of women with small, non-palpable asymptomatic breast cancers; that because of various issues of ascertainment, the actual number of cases of DCIS in the population at any given time is likely to exceed the number of cancers at a later stage, in contrast to the greater number of invasive versus non-invasive cancers in lesions removed by surgeons and classified by pathologists. We have shown that an invasive in-breast event following a case of DCIS that has been surgically removed is better characterized as local invasive recurrence rather than as a new primary cancer, and we propose that local recurrences following DCIS do not have the ability to metastasize. We now explore the implications of these hypotheses regarding primary invasive breast cancer.
Part 4: Are primary invasive breast cancers and local invasive recurrences following DCIS distinct?
A tale of three women: a thought experiment
Woman A is worried about getting breast cancer, and even though she has no family history or any dominant risk factor, she decides to have a bilateral prophylactic mastectomy at age 30. She is now age 60 and she is doing well with no cancer history. Unbeknownst to her, she was destined to develop DCIS at age 40, but this was pre-empted by the preventive surgery.
Woman B opts not for surgery, but goes for annual mammography. At age 40, she has an abnormal mammogram and a small focus of DCIS is discovered upon biopsy. She has breast-conserving surgery. The margins are clear. Despite this, 5 years later, she is diagnosed with an invasive recurrence in her breast, 2 cm in diameter. The nodes are clear.
Woman C does not go for mammography but instead goes to her doctor for an annual physical exam. At age 45, the physician feels a lump and the biopsy reveals a stage I invasive breast cancer, 2 cm in size. Nodes are clear.
In this light, we propose that in-breast invasive recurrences post-DCIS and primary invasive breast cancers are two facets of the same condition which differ according to the frame of reference of the observer. From the starting point of DCIS, risk factors which lead from progression of DCIS to invasive cancer include young age, high grade, and positive surgical margins . From the point of view of the invasive cancer, the most important factor which predicts a prior diagnosis of DCIS is calendar year . If we surmise correctly, breast cancers with and without a documented prior history of DCIS should carry a similar prognosis. Based on data from the Henrietta Banting Database at Women’s College Hospital in Toronto , we estimate the 15-year breast cancer-specific mortality rate after an invasive local recurrence (node-negative) following a diagnosis of DCIS to be 16% (Woman B). Based on data from the SEER registry , we estimate the 15-year breast cancer-specific mortality rate after a diagnosis of node-negative primary invasive breast cancer under 5 cm to be 15% (Woman C). The prognoses of Woman B and C are almost identical.
Given these equivalencies, we conclude that primary invasive breast cancers and local invasive recurrences so closely resemble each other that they are likely to be two facets of the same condition—our tendency to separate them into two distinct clinical entities is based on historical grounds that should be revisited. We cannot distinguish a primary invasive cancer from a local recurrence on histologic examination, and to our knowledge, there are no molecular tests or gene signatures that allow a pathologist to do so.
Does breast cancer metastasize?
In Part 1 above, we re-iterate the (accepted) position that a local recurrence following a case of invasive breast cancer is a marker of cancer aggressiveness (similar to positive lymph nodes) and is not a conduit of cancer spread . From this, it follows logically that local recurrences do not metastasize.
In Part 2 above, we make the case that a local invasive recurrence following DCIS is similar in many respects to a local recurrence following invasive cancer and these do not have the ability to metastasize. We extend the argument that preventing local recurrence after an invasive primary cancer through mastectomy does not prevent death, and therefore, local invasive recurrences—after DCIS or after invasive cancer—do not have the ability to metastasize. Holzel et al. came to a similar conclusion about local recurrences in 2011 by examining data from the Munich Cancer Registry . Interestingly, they thought that the metastatic potential of local recurrences was different from that of primary tumours (which did have the ability to metastasize) [57, 58].
In Part 4 above, we argue that local invasive recurrences following a diagnosis of DCIS and primary de novo invasive breast cancers are variant representations of the same malignancy, and our categorical assignment depends on the frame of reference of the observer. This leads us to the surprising conclusion that what we now describe as primary invasive breast cancers do not have the ability to metastasize. In technical terms, the bulk of the cells that make up the tumour mass of a primary invasive breast cancer does not have the intrinsic ability to travel to distant organs and to re-initiate growth at a secondary site.
Here, our position deviates from the conventional view that a breast cancer, as we know it, is a fully formed malignancy, with innate abilities to grow and to metastasize, but we are able to support our position by reference to several clinical observations. These observations have, in common, the theme that some proportion of breast cancer cells can be left in situ after standard surgical treatment without adversely affecting the prognosis of the patient (Box C: Assumptions underlying parallel model in Appendix).
Fisher and Veronesi taught us that, in terms of mortality, patients treated with lumpectomy and mastectomy have similar prognoses [8, 9]. Nevertheless, a proportion of cancers removed by lumpectomy have positive margins; if the cancer has been cut through there will be residual cancer cells in the breast. Although positive margins increase the risk of local recurrence, it has not been shown that positive margins increase mortality [59, 60]. Some surgeons will argue that those cancer cells that are left behind are removed by re-excision. However, it has not been shown that in terms of mortality women who have cancers with positive margins do better in terms of death if they undergo re-excision . The rate of local recurrence drops by 50%, but mortality drops by only a few percentage points . Some medical oncologists will argue that adjuvant chemotherapy eliminates the remaining cells. However, the prognosis of women with lumpectomy versus mastectomy is similar if we exclude women who have had chemotherapy [8, 9].
Impact of radiotherapy after breast-conserving surgery on the rates of local recurrence and breast cancer mortality in the 2005 Early Breast Cancer Trialists’ Overview (EBCTG) report
10-year risk of local recurrence (%)
10-year risk of breast cancer mortality (%)
Magnetic resonance imaging (MRI) is now used as an adjunct to diagnostic staging for breast cancer patients. When MRI was added to classical staging techniques, 20% or more of women were found to have cancers that were more extensive than what was apparent using the traditional staging techniques . When the more extensive cancers (multi-focal and multi-centric) were revealed by MRI, they were removed, often with mastectomy . The proportion of women who had a mastectomy instead of a lumpectomy increased when MRI was employed; in the COMICE trial (Comparative Effectiveness of MRI in Breast Cancer), which was limited to conservation candidates, the conversion rate from lumpectomy to mastectomy was 7% for women who had an MRI versus 1% for women who did not have an MRI . In other words, in the absence of MRI, about 20% of women who are treated with lumpectomy based on the traditional staging techniques, have residual cancer cells, but are unaware . Studies to date (mostly small and with limited follow-up) have failed to show that adding MRI to the staging improves patient survival [65, 66]. That is, even though MRI is effective at detecting with accuracy the extent of a breast cancer, it is expensive and its use results in more extensive surgery, but does not reduce mortality and MRI is not endorsed in current surgical guidelines as a part of the workup of a patient with early stage breast cancer. It is possible that studies to date are too small and that the follow-up period is too short to show a benefit associated with MRI staging. It has been argued that the cancer cells that are left behind are not “clinically important”, as opposed to the ones that are surgically removed . The argument that some cancer cells are clinically important and others are not is not based on any observable or measurable difference in the two cell populations—there is no way of telling them apart. It is possible that ‘clinical importance’ is determined by a critical number of cells, that is, the cells that are left behind are too few to be relevant. If so, this would be a departure from what medical oncologists consider a fundamental principal; i.e. that if untreated, cancer cells have the ability to flourish and will proliferate continuously until they threaten life.
Tumour size as a marker of metastatic potential: mammography screening
Tumour size (diameter in centimeters) is a strong and consistent predictor of breast cancer survival . That is, the size attained by the breast cancer at the time of diagnosis is a good predictor of whether or not the cancer has metastasized prior to diagnosis. From this, it has been inferred that the more cancer cells there are in the breast, the greater the probability that a cell or a small clone of cells will break off from the tumour mass and will lodge elsewhere and flourish. This conventional view (the sequential model) is based on the premise that cancer metastases originate from the in-breast cancer mass—the larger the cancer, the more cells there are and the greater the probability of a metastasis occurring. However, the size-survival association is also consistent with the alternate position that the in-breast tumour is a marker of cancer aggressiveness and not a source of metastases. In this sense, cancer within the breast is analogous to cancer within the lymph nodes; the greater the number of nodes involved, the higher the risk of recurrence.
The conventional view has also been challenged by Christoph Klein who notes that the mean time of cancer diagnosis to cancer recurrence is far too short to support a model that a metastasis is the result of a dislodging of a single cell and subsequent clonal exponential growth, and he has proposed an alternate model of parallel progression, whereby the primary (in-breast) cancer and the metastases arise simultaneously and grow synchronously . The parallel model (versus the sequential model) is supported indirectly by the results of mammography screening trials. If the size of the cancer (in terms of the number of cancer cells) is proportional to its metastatic potential (and curability), then a 2 cm cancer, which contains eight times as many cells as a 1 cm cancer, should have a much worse prognosis than a 1 cm cancer, and reduction of cancer size from 2 to 1 cm through early detection should have a dramatic effect on mortality (perhaps as much as a 7/8th reduction) and not a mere drop of 30% or so (i.e. the best case scenario).
If the size of the breast cancer is a marker of aggression rather than a source of metastases, then the null outcome from mammography is to be expected (Fig. 8). Furthermore, we should expect the size of the mass to be of limited predictive ability and that the size/survival relationship is not constant, but varies according to pathologic subtype. In triple-negative breast cancer, in BRCA1-positive breast cancer, and in small HER2-positive breast cancers, the relationship between tumour size and survival is much attenuated, and for these women, tumour size is a very poor predictor of survival . Furthermore, among breast cancers of 6 cm or greater, there is very little correlation between tumour size and node status or prognosis [75, 76]. For example, in a cross-sectional SEER-based study, the probability of lymph node metastases being present at diagnosis was 19% for 1 cm cancers, was 35% for 2 cm cancers, was 60% for 6 cm cancers, and was 65% for 10 cm cancers . Assuming that large cancers were once small cancers, this implies that a breast cancer has 16% chance of metastasizing as it grows from 1 to 2 cm, but only a 5% chance of metastasizing as it grows from 6 to 10 cm (despite the fact that a 6 cm cancer contains approximately 200 times more cells). In contrast, the relationship between lymph node status and survival is canonical and varies little across clinical subtypes [77, 78]. Furthermore, it is often argued that there is a beneficial effect of screening, independent of tumour size, which is evidence in favour of screening [79, 80]. For example, we have found that tumour palpability is strong adverse prognostic factor in the Henrietta Banting database and we interpreted this to mean that palpability per se is a marker of aggressivity, rather like tumour grade, vessel count and nodal status, and to some extent, this may explain the relatively good prognosis of mammogram-detected cancers . If the sequential model was true, we would expect screening to be highly effective. Furthermore, we would expect that the goal of screening would be realized largely by identifying cancers when they are small and node-negative. However, the negative statistical association between tumour size and survival is equally strong for node-positive breast cancer patients as it is for node-negative breast cancer patients [68, 73] and tumour size is predictive of survival even among women who present with stage IV breast cancers . We interpret this to mean that tumour size, nodal status, and the presence of distant metastases are three complementary prognostic factors, as befits a parallel model, rather than a sequential model. It is also possible that under the parallel model, that screening has a beneficial effect, e.g. perhaps, smaller cancers are more likely to have fewer distant micrometastases than larger cancer, and therefore, these are more amenable to chemotherapy than larger cancers (with more micrometastases).
In a recent study in the New England Journal of Medicine , among all invasive breast cancers diagnosed from 2001 to 2013 in the SEER database, there was a dramatic difference in the distribution of biologic category according to tumour size; tumours with favourable biologic characteristics made up 38% of the tumours that were 1 cm or less in size, and this steadily decreased to only 9% of the tumours greater than 5 cm, whereas tumours with unfavourable biologic features made up only 14% of the tumours 1 cm or less, increasing to 36% of the tumours greater than 5 cm. Furthermore, while both tumour size and biologic features had a major influence on prognosis, large tumours with favourable biologic features had a better prognosis than small tumours with unfavourable biologic features. These observations suggest that tumour size may be a marker of tumour aggressivity, as are grade and ER status, rather than an indicator of the pool of cancer cells that are the source of dissemination.
Our model suggests that positive lymph nodes, in-breast lesions, and distant metastases result from dissemination via parallel pathways which are downstream from a common (but unseen) source. The malignant potential of the underlying cancer source predicts the size of the cancer, the number of nodes involved, and the presence of metastases at the time of diagnosis and thereafter.
By extension, it is disingenuous to refer to cancer stage to distinguish between patients with different prognoses, because the term ‘stage’ infers a natural course of progression, i.e. the patient passes through various ‘stages’ of cancer. If we consider the involvement of regional nodes and distant metastases to be independent and parallel processes, then the description should be cross-sectional and should not assume natural history, e.g. the size of the cancer, the nodal status, and the metastatic status should be stated explicitly using three separate variables.
In an early study, Horak et al. correlated the density of small blood vessels within the breast cancer with the probability of concurrent lymph node metastases . In this study, microvessel density was strongly correlated with the presence of nodal metastases, such that only 2 of 50 tumours with vessel counts of 99/mm3 or less were node-positive, whereas 32 of 39 tumours with counts above 140/mm2 were node-positive. From this, the authors infer that the extent of angiogenesis within the primary cancer is an indicator of its metastatic potential. This interpretation has appeal, but the data are also consistent with the model that the breast primary and the node metastasis both derive from a common precursor. Similarly, the observation that a breast primary cancer and the distant metastases are concordant for one or more genetic markers is no guarantee that the metastasis is a subclone of the breast cancer—it might be that the two have a common ancestor. Indeed, Hosseini et al. , in a recent paper, propose that the latter scenario is, in fact, the case—a comparison of the early cancer precursor, the in-breast primary, and the metastases found that the metastatic lesion more closely resembled the (hypothetical) precursor lesion than the much larger breast tumour.
The critical events occur unseen; normal cells are transformed into small clusters of cancer cells with multi-potent metastatic potential and these give rise to early lesions in the breast as well as subclinical latent metastatic deposits. Typically, months to years will pass before the metastases become manifest, and during this time period, we may see the emergence of breast cancer in the breast and in the nodes. The relative timing of the appearance of cancer cells in the breast in the nodes and in distant organs is governed by factors which determine the dynamic growth of cancer within the various niches. It is of interest in this regard that the majority of cancer patients who develop distant metastases present with cancer stages I to III (i.e. they rarely present at stage IV) , whereas the majority of women who have positive axillary lymph nodes and breast cancer present with cancer in both sites synchronously (i.e. lymph node status rarely transitions from negative to positive after the initial diagnosis) [85, 86]. These observations suggest that the early cancer-forming cells have many properties in common with cancer stem cells and cancer progenitor cells.
Implications for prevention
The parallel model proposed here may be relevant to cancer prevention. Under the conventional (sequential) model, we expect a reduction in cancer mortality to parallel a reduction in cancer incidence and prevention trials were designed accordingly, with incidence as the primary endpoint. However, as outlined in Fig. 2, we speculate that the pathways from early cancers to in breast tumours and to metastases are distinct and separable, and that there is no pathway from in-breast cancer to metastases. Under the parallel model, a factor that prevents in-breast cancer (i.e. incidence) may not prevent cancer deaths. We have recently summarized the epidemiologic evidence that tamoxifen chemoprevention prevents cancer but does not appear to prevent death . This may be because tamoxifen interrupts one pathway (the in-breast recurrence pathway) but does not interrupt the other (the metastatic pathway). This could also be true for lifestyle interventions, such as diet and exercise, and, therefore, to evaluate the effectiveness of a prevention intervention, it is necessary to consider breast cancer mortality as the primary endpoint.
Implications for screening
The strong association between cancer size and mortality is not under dispute, but under the parallel model, we no longer support the paradigm of early detection, namely that if we can identify a cancer when it is small we can advance the date of diagnosis and this in turn will reduce the likelihood of subsequent mortality. Under the parallel model, tumour size is a marker of aggressiveness, as is lymph node status and tumour palpability, but the tumour is not a conduit of metastatic cells.
Implications for treatment
Under the sequential model, if we can identify a cancer when it is small and before it has metastasized we expect to cure it through surgery alone. If the metastases are local (regional lymph nodes), the chance of curing the patients with surgery and chemotherapy is high and a proportion of cancers with subclinical latent metastases will also be cured by a combination of chemotherapy and surgery.
In the parallel model, the potential for metastases is present from the outset—not once the cancer reaches a particular size. Chemotherapy should be introduced early in the clinical course. We should have as a research goal identifying cancers which have a high chance of metastases when small and to identify metastatic disease before it is clinically apparent by new sensitive imaging and molecular techniques, possibly including circulating tumour DNA.
The goal of preventing local invasive cancer after DCIS is a laudable one, but one that has limited clinical benefit in that this will not prevent mortality. If we wish to reduce the mortality rate for women with DCIS, it is necessary to have the means to identify women at sufficiently high risk to be candidates for systemic therapy.
Our understanding of the nature of breast cancer is formulated by knowledge collected and synthesized over several decades. Traditionally, we see each breast cancer at a moment in time and within a narrow visual frame, rather than as a dynamic process, whereby cancer cells appear (and possibly disappear) within the breast and elsewhere. The conventional model describes breast cancers as a mass of cells, malignant in appearance, and which have the ability to divide and to metastasize and typically which pass through four stages before death ensues. We have reviewed here many of the seminal clinical findings over the past century and have tried to reconcile some contradictions and explain some outliers. By close analysis of patient outcomes, we challenge the conventional view of breast cancer progression as a sequential series of events. We believe that the temporal sequence of invasion, growth, and metastasis should be reinterpreted according to a new frame of reference (summarized in Box C: Assumptions underlying parallel model in Appendix). If we accept these assumptions, then it follows that minute cancers are capable of metastasizing prior to invasion into the breast and in contrast, what we currently consider to be malignant breast cancers are not the source of metastases.
Consider for example the observation that men with nicotine-stained teeth have a much higher risk of dying of lung cancer than men with unstained teethed (perhaps 20-fold higher). This does not imply that brushing your teeth prevents lung cancer.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflicts of interest.
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