- Research article
- Open Access
Distant metastasis dynamics following subsequent surgeries after primary breast cancer removal
Breast Cancer Researchvolume 21, Article number: 57 (2019)
The aim of the research was to separate the distant metastasis (DM) enhancing effect due to breast tumour removal from that due to surgical manoeuvre by itself.
DM dynamics following surgery for ipsilateral breast tumour recurrence (IBTR), contralateral breast cancer (CBC) and delayed reconstruction (REC), which was performed after the original breast cancer surgical removal, was analysed. A total of 338 patients with IBTR, 239 with CBC and 312 with REC were studied.
The DM dynamics following IBTR, CBC and REC, when assessed with time origin at their surgical treatment, is similar to the analogous pattern following primary tumour removal, with a first major peak at about 18 months and a second lower one at about 5 years from surgery. The time span between primary tumour removal and the second surgery is influential on DM risk levels for IBTR and CBC patients, not for REC patients.
The role of breast tumour removal is different from the role of surgery by itself. Our findings suggest that the major effect of reconstructive surgery is microscopic metastasis acceleration, while breast tumour surgical removal (either primary or IBTR or CBC) involves both tumour homeostasis interruption and microscopic metastasis growth acceleration. The removal of a breast tumour would eliminate its homeostatic restrains on metastatic foci, thus allowing metastasis development, which, in turn, would be supported by the forwarding action of the mechanisms triggered by the surgical wounding.
In the middle of the nineteenth century, the arguments set out by Virchow, who suggested that the disease starts as a single focus within the breast, then migrates to the axillary lymph nodes and ultimately to distant organs, supported the Halsted operation that was adopted as the default therapy worldwide . However, among resected patients, 30% of node-negative and 75% of node-positive women still developed distant metastases and succumbed . The failure of mastectomy and other more aggressive operations to cure patients and, moreover, novel biology-based assumptions on the disease course  suggesting that the extent of local treatment does not affect survival supported a reduction of the extent of surgery. Additionally, clinical investigations and mathematical modelling advocated that surgical resection might not always be beneficial [4, 5] providing evidence that, while it favourably modifies the natural history of breast cancer for the majority of patients, it may also hasten the metastatic development for a number of them, by triggering growth of occult tumour deposits. The concepts underlying this new model extended to the clinical level the results of a protracted history of investigations lasting more than a century .
Helpful hints about the new model were achieved from analyses of post-resection recurrence dynamics in early breast cancer patients undergoing potentially curative removal of the primary tumour [7, 8]. A model assuming post-surgery acceleration of disease progression by a burst of growth in previously dormant micrometastases appeared to best fit the clinical data. Similar findings were observed in non-small cell lung cancer . While this acceleration apparently occurs at the time of local treatment, it is still not deciphered whether this effect can be ascribed to primary tumour removal (e.g. to removal of inhibitory factors) or to the surgical manoeuvre per se (e.g. CTC release, immune suppression and pro-angiogenic stimulus of wounding) or to both. This differentiation is important as it may open a window to new therapeutic approaches.
Clues about this subject may be detected by the analysis of the recurrence dynamics in patients who undergo subsequent breast surgical manoeuvres during the follow-up of the disease in addition to primary tumour surgical removal. Patients undergoing conservative surgery for their primary tumour may experience ipsilateral breast tumour recurrence (IBTR), and others may be diagnosed contralateral breast cancer (CBC) whatever the surgical approach for the primary tumour has been. Moreover, some patients undergoing mastectomy as the first surgical treatment call for breast reconstruction (REC) and undergo aesthetical surgery. We hypothesized different metastatic recurrence dynamics associated with the different surgical procedures due to the clinical presence (IBTR and CBC) or absence (REC) of a tumour reservoir in the breast. Therefore, we report here findings from the analysis of distant metastasis (DM) dynamics following IBTR, CBC and REC, which was carried out with the aim of unravelling the different roles, if any, of the two possible factors, i.e. breast tumour removal and surgical manoeuvre by itself.
Patients and methods
At the National Cancer Institute of Milan, three randomized clinical trials have been carried out in the past, investigating the role of different surgical approaches for primary tumour removal. Moreover, since preliminary results of the first trial on the breast-conserving treatment for early breast cancer, which provided evidence that conservative surgery plus chest wall radiotherapy was comparable to more aggressive resections , patients received breast-conserving treatment as routine practice outside randomized clinical trials (out-trial patients). All axillary node-positive (N+) patients were offered systemic adjuvant treatment with cyclophosphamide + methotrexate + fluorouracil (CMF) or CMF plus doxorubicin, while no further post-surgical systemic treatment was recommended to axillary node-negative (N−) patients. Adjuvant hormone therapy was not utilized within the randomized clinical trials and seldom employed for out-trial patients, as it was not considered mandatory at that time. Two other randomized clinical trials were accomplished on patients who, following mastectomy or breast-conserving treatment, were found to be axillary node positive (N+). Patients with one to three positive axillary lymph nodes were randomly allocated to receive either 12 courses of CMF or 8 courses of the same regimen followed by 4 courses of doxorubicin, while patients with > 3 positive axillary nodes were randomized to receive either four courses of doxorubicin followed by 8 courses of CMF or 2 courses of CMF and 1 course of doxorubicin for a total of 12 courses. All clinical data from patients enrolled into the reported clinical trials or treated outside of trials were systematically recorded and stored in standard format. Detailed descriptions of patients, treatments and follow-up modalities have been reported elsewhere [10,11,12,13,14]. In particular, data for patients suffering IBTR are reported in ref. .
A further database was analysed, including all breast cancer patients undergoing mastectomy who underwent delayed reconstructive surgery at Haukeland University Hospital, Bergen, Norway. The reconstructive procedures were implant surgery, implants combined with flaps, deep inferior epigastric perforator flaps and transverse rectus abdominis myo-cutaneous flaps. A paired control was randomly selected from patients with identical T and N stages, age ± 2 years, and follow-up without recurrence equal to or longer than the time to reconstruction of the respective matched reconstructed patient (defined as “reference time”, i.e. the time origin for the analysis of DM dynamics for controls). Patient characteristics and details of the study have been reported in ref. . All studies supplying the analysed databases were approved by the institutional ethics committees and review boards in accordance with the Declaration of Helsinki.
The analysis of recurrence dynamics was focused on DM as the first event after the second surgery (the studied timing periods are outlined in Fig. 1): DM-free survival times were calculated as time elapsed since the second surgery (for IBTR, CBC or REC) to DM occurrence or to the last documented follow-up with no evidence of disease. Second primary tumours, including contralateral breast cancers, were considered as competing events, and the corresponding event-free survival times were censored at the time of their occurrence. The DM dynamics was studied by estimating with the life-table method the hazard rate for DM, i.e. the conditional probability of manifesting DM during a certain time span, given that the patient is clinically DM free at the beginning of the interval . A discretization of the time axis in 6-month units was applied, and a Kernel-like smoothing procedure  was adopted.
A CONSORT diagram for IBTR, CBC and REC patients and matched controls is reported in Fig. 2.
Among patients undergoing conservative surgery, 92% received chest wall radiation therapy, mostly at the total dose of 50 Gy (daily dose 2 Gy) with high energy plus 10 Gy (daily dose 2 Gy) as a boost with orthovoltage to the ipsilateral breast. Following the diagnosis of IBTR or CBC, the treatment was decided on an individual basis. Median follow-up times after IBTR and after CBC were 151 months and 144 months, respectively. The number of patients suffering DM diagnosis within 10 years from IBTR and CBC was 138 and 84, respectively.
In the Norwegian study, the matched control group included patients who were extracted from a total of 868 (see the “Patients and Methods” section in ref. ). Median follow-up after reconstruction or reference time for controls was 137 months. The number of patients suffering DM within 10 years for REC and controls was 44 and 45, respectively.
Main patient characteristics at primary tumour treatment are reported in Table 1. In spite of the wide time span of patient accrual, the homogeneity of main prognostic factors across the databases, with the exception of tumour size in REC patients, is noteworthy. Axillary node involvement is near identical, as well as the frequency of ER-positive and ER-negative tumours among assessed ones, despite the fact that ER content was measured at different frequencies in the three series. Anyway, the DM dynamics of ER+ and ER− cancer have similar timing pattern  and, therefore, no modification of surgery effects on the time patterns was expected by oestrogen receptor levels. Moreover, as analysed patients suffering IBTR and CBC did not receive adjuvant endocrine therapy just like 42% of ER+ reconstructed patients, the question of whether endocrine therapy may alter DM patterns in a modern cohort remains open. HER2 status was not available and, accordingly, no specific treatment was administered.
The distribution of surgical treatments for IBTR, CBC or REC during the follow-up subsequent to primary tumour removal is reported in Fig. 3. Reconstructions were performed mainly during the first 5 years (median time 2.5 years) while IBTR removal had a more protracted distribution (median time 4.3 years) and a structured pattern . CBC treatments have a steadier pattern consistent with the notion that the occurrence of a CBC may be considered a random event not time-related with primary tumour [21, 22].
The DM dynamics was analysed for the four groups in a timeframe with t = 0 at second surgery (Figs. 4 and 5 solid lines). Moreover, the influence of the time elapsed from primary tumour removal to the second surgical manoeuvre [time to second surgery] on the hazard rate for DM pattern was investigated as well (Figs. 4 and 5 dashed lines). The hazard rate pattern is similar for the three surgical groups with a first major peak at about 18 months and a second lower one at about 5 years from the second surgery, although the three levels of recurrence risk are different. Time to second surgery is apparently not influential for reconstructed patients, whereas it changes the first peak height for the other sets, showing that the influence is maximal for early re-operations, decreases afterwards and apparently disappears for time to second surgery values larger than 2 to 3 years. To ascertain whether factors known to be influent on the risk level may drive the described phenomenon, we analysed the DM dynamics by time to second surgery in IBTR patients pooled by axillary node status (node positive vs node negative) and by second surgery extent (mastectomy vs conservative surgery). In all analysed subsets, the time to second surgery aroused the same hazard rate pattern, as Fig. 5 exemplifies for the axillary nodal involvement. A comparison between REC patients and controls for DM hazard rate pattern is reported in Fig. 6, where the accelerating effect of surgery on the DM dynamics is quite evident.
Our analysis on breast cancer patients undergoing breast surgery for IBTR, CBC and REC provides two main results: (1) the DM dynamics following a new breast surgical manoeuvre performed after primary tumour removal is similar to the analogous dynamics following primary tumour removal and (2) the time span between the two operations is not associated with changes in peak timing; yet, for IBTR and CBC patients, it is related to progressive reduction of DM risk levels, while REC patients display similar DM risk levels for all time spans.
It should be emphasized that the three surgeries are performed in different clinical situations. Surgery for IBTR is strictly related to the specific multimodal dynamics of IBTR appearance  while CBC diagnosis and subsequent removal is an independent event with steady hazard rate [21, 22] and, finally, REC surgery is related to the patient’s desire and only indirectly to clinical conditions. Therefore, when comparative analyses among patients with such different tumour-host settings at the time of surgery display similar behaviours, they are reasonably attributable to the act of treatment per se. Our findings suggest that there is a metastasis-enhancing effect in all surgical interventions, which displays, however, different traits related to whether a macroscopic breast tumour is removed or not.
The enhancing effect of surgical primary tumour removal on metastatic disease is well supported by a long history of investigations  and from a few clinical studies in humans (e.g. ). It enables to explain the multipeak pattern of the hazard rate for recurrence in patients with early breast cancer undergoing surgery or surgery plus adjuvant chemotherapy . Here, we confirm that this enhancing effect is observable even when surgical manoeuvres are performed in the breast area at a later date. The result of our analysis apparently diverges from the outcome of a previous investigation on the same subject  suggesting that traumas or intervening surgical procedures unrelated to cancer are not associated with an increased cumulative rate of breast cancer recurrence in a 2-year window. Although this discrepancy may be related to the shortness of the analysed interval, a subtler inference could be considered on the basis of the known topological specificity of cell populations [25, 26] and of the finding that, in an animal model, acceleration in tumour growth by mobilization of bone marrow-derived cells may be different after operative injuries to different organs . Indeed, one could speculate that surgery in the breast area may stimulate distant breast cancer foci, unlike surgery in other sites. Unfortunately, this hypothesis cannot be disentangled since data on non-breast interventions were not available for comparison.
Of note, the hazard rate peaks, in particular the first one, have different heights in IBTR, CBC and REC (Fig. 4). This occurrence is in keeping with the notion that the sudden acceleration of metastasis development takes action on the underlying DM dynamics, which is different in IBTR, CBC and REC patients. Indeed, patients with IBTR have an intrinsic high risk of DM (similar to N+ patients) that was unpredictable by the usual prognostic factors at the initial treatment and that is revealed when IBTR emerges in advance of the competing DM events [15, 28]. In comparison with these patients, women suffering CBC display a considerably lower first hazard rate peak (about 60% peak to peak) in keeping with the concept that CBC is a second primary, unrelated to the first one [21, 29, 30]. Accordingly, patients with CBC actually fit to a population with “average” DM risk . Finally, patients undergoing REC have better prognosis due to favourable selection criteria: they had no previous recurrence event and factors such as smoking, obesity and diabetes excluded patients from being offered complex breast reconstructive procedures. Moreover, the baseline risk in this population may be influenced by features here not accounted for, such as socioeconomic conditions, better general health and low body mass index, which is recently emerging as a prognostic factor in breast cancer .
While there is a substantial body of evidence indicating that the surgery-associated tissue trauma and wound healing can promote growth, angiogenesis and metastatic ability of cancers , data on the possible homeostatic connection between primary tumour and its metastases are lacking. Our finding that the time to second surgery is influential on the risk level only for IBTR and CBC patients and not for REC patients suggests that tumour removal, which occurs in the former groups only, plays a specific role on metastasis development. This idea is in agreement with the recalled model of breast cancer metastatic development  if one takes into account that the manifestation of IBTR or CBC, i.e. of a macroscopic breast tumour, is preceded by a number of months of subclinical disease. According to the tumour homeostasis concept , during this time span, the growing tumour exerts constraints on distant microscopic foci, somehow mimicking the homeostatic processes underlying the control of size in adult organs and organisms [34, 35]. Although the molecular characteristics of these mechanisms are largely unknown, recent reports have provided initial interesting findings [36, 37], which may have oncological important implications as well .
In patients suffering IBTR or CBC, a number of metastatic foci are related to the previous breast cancer, although a few of them may be associated with the new breast neoplastic lump. The emerging restrictive interference results into some freeze of the microscopic metastases in the conditions existing when the new homeostatic action is starting. Taking into account the hazard rate dynamics for the DM related to the primary breast cancer , such a freeze should have effects depending on time to second surgery: the shorter this time, the higher the underlying DM risk. Consequently, while the DM dynamics after the IBTR or CBC removal maintains the usual time-related pattern, the corresponding hazard rate level would depend on time to second surgery. Following 2 to 3 years, the time to second surgery loses its prognostic value, in keeping with the drop of DM risk attributable to the primary breast cancer .
The finding that patients undergoing REC do not present any effect from the time to second surgery, while displaying the usual time-related pattern in the post-reconstruction DM dynamics, suggests that the reconstructive surgical manoeuvre, in the absence of any breast tumour removal, may act on metastasis development differently from IBRT and CBC surgical removal. As a working hypothesis, it may be assumed that surgical manoeuvres prominently act on the microenvironment of tumour foci turning it into conducive (e.g. by activating angiogenesis) and thus sustaining growth . This facilitating action would simply speed up the clinical appearance of some metastases that would emerge later according to their own dynamics. This hypothesis is suggested by the comparison between the hazard rate patterns for DM in REC patients and in the matched paired control group (Fig. 6). This comparison suggests that the reconstruction is associated with a decrease of the hazard rate for DM at the fourth year and a concomitant increase of the hazard rate at the second year.
The present findings are coherent with and integrate the evidence coming from separate studies on IBTR and REC, resorting to advanced time scale statistical modelling [16, 40]. The overall picture provided support to the biological hypothesis, underlying the observed distant metastasis dynamics following surgeries performed after primary breast cancer surgical removal, according to different tumour homeostasis-related and surgical wound-related effects on metastasis development.
The analysed databases did not included data on HER2, preventing investigations on triple-negative patients. Moreover, we could not analyse the possible role of anaesthetic management, which potentially influences the long-term outcome most probably in patients undergoing more extended surgery , due to missing information about this factor.
In summary, the findings of the present analysis support the concept that the impact of breast tumour surgical removal (either primary or IBTR or CBC) on microscopic metastases is twofold, inasmuch as two different factors, i.e. tumour homeostasis interruption and surgical wound effects, are involved. The removal of a breast tumour would result into the sudden elimination of the restrains on metastatic foci, thus allowing metastasis development, which, in turn, would be supported by the forwarding action of the mechanisms triggered by the surgical wounding. This surgery-related phenomenon would underlie the behaviour of DMs in the REC group, where no detectable tumour deposit is removed. While associations of such latter phenomenon with surgical-related inflammatory conditions and different anaesthesia modalities are suggested from a few clinical data [41,42,43], the biological mechanisms underlying tumour homeostasis are largely unknown. Investigations in this field are urgently warranted.
Contralateral breast cancer
Cyclophosphamide + methotrexate + fluorouracil
Ipsilateral breast tumour recurrence
Axillary node negative
Axillary node positive
Baum M, Demicheli R, Hrushesky W, Retsky M. Does surgery unfavourably perturb the “natural history” of early breast cancer by accelerating the appearance of distant metastases? Eur J Cancer. 2005;41:508.
Brinkley D, Haybittle JL. A 15 year follow up study of patients treated for carcinoma of the breast. British J Radiology. 1968;41:215.
Fisher B. Laboratory and clinical research in breast cancer: a personal adventure: the David A. Karnofsky memorial lecture. Cancer Res. 1980;40:3863.
Demicheli R, Retsky MW, Swartzendruber DE, Bonadonna G. Proposal for a new model of breast cancer metastatic development. Ann Oncol. 1997;8:1075.
Retsky MW, Demicheli R, Swartzendruber DE, Bame PD, Wardwell RH, Bonadonna G, et al. Computer simulation of a breast cancer metastasis model. Breast Cancer Res Treat. 1997;45:193.
Demicheli R, Retsky MW, Hrushesky WJM, Baum M, Gukas ID. The effects of surgery on tumor growth: a century of investigations. Ann Oncol. 2008;19:1821.
Demicheli R, Retsky MW, Hrushesky WJM, Baum M. Tumor dormancy and surgery-driven dormancy interruption in breast cancer: learning from failures. Nature Clin Pract Oncol. 2007;4:699.
Saphner T, Tormey DC, Gray R. Annual hazard rates of recurrence for breast cancer after primary therapy. J Clin Oncol. 1996;14:2738.
Demicheli R, Fornili M, Ambrogi F, Higgins K, Boyd JA, Biganzoli E, et al. Recurrence dynamics for non-small-cell lung cancer: effect of surgery on the development of metastases. J Thorac Oncol. 2012;7:723.
Veronesi U, Banfi A, Del Vecchio M, Saccozzi R, Clemente C, Greco M, et al. Comparison of Halsted mastectomy with quadrantectomy, axillary dissection, and radiotherapy in early breast cancer: long-term results. Eur J Cancer Clin Oncol. 1986;22:1085.
Veronesi U, Luini A, Del Vecchio M, Greco M, Galimberti V, Merson M, et al. Radiotherapy after breast preserving surgery in women with localized cancer of the breast. N Engl J Med. 1993;328:1587.
Veronesi U, Volterrani F, Luini A, Saccozzi R, Del Vecchio M, Zucali R, et al. Quadrantectomy versus lumpectomy for small size breast cancer. Eur J Cancer. 1990;26:671.
Moliterni A, Bonadonna G, Valagussa P, Ferrari L, Zambetti M. Cyclophosphamide, methotrexate, and fluorouracil with and without doxorubicin in the adjuvant treatment of resectable breast cancer with one to three positive axillary nodes. J Clin Oncol. 1991;9:1124.
Buzzoni R, Bonadonna G, Valagussa P, Zambetti M. Adjuvant chemotherapy with doxorubicin plus cyclophosphamide, methotrexate, and fluorouracil in the treatment of resectable breast cancer with more than three positive axillary nodes. J Clin Oncol. 1991;9:2134.
Demicheli R, Ardoino I, Ambrogi F, Agresti R, Biganzoli E. Significance of ipsilateral breast tumour recurrence after breast conserving treatment: role of surgical removal. Chin J Cancer Res. 2013;25:22.
Dillekås H, Demicheli R, Ardoino I, Jensen SA, Biganzoli E, Straume O. The recurrence pattern following delayed breast reconstruction after mastectomy for breast cancer suggests a systemic effect of surgery on occult dormant micrometastases. Breast Cancer Res Treat. 2016;158:169.
Marubini E, Valsecchi M. Analysing survival data from clinical trials and observational studies. Chichester: Wiley; 2004.
Ramlau-Hansen. Smoothing counting process intensities by means of Kernel functions. Ann Statistics. 1983;11:453.
Demicheli R, Ardoino I, Boracchi P, Coradini D, Agresti R, Ferraris C, Gennaro M, Hrushesky WJ, Biganzoli E. Recurrence and mortality according to estrogen receptor status for breast cancer patients undergoing conservative surgery. Ipsilateral breast tumour recurrence dynamics provides clues for tumour biology within the residual breast. BMC Cancer. 2010;30(10):656.
Demicheli R, Ardoino I, Boracchi P, Lozza L, Biganzoli E. Ipsilateral breast tumour recurrence (IBTR) dynamics in breast conserving treatments with or without radiotherapy. Int J Radiat Biol. 2010;86:542.
Rasmussen CB, Kjær SK, Ejlertsen B, Andersson M, Jensen MB, Christensen J, et al. Incidence of metachronous contralateral breast cancer in Denmark 1978-2009. Int J Epidemiol. 2014;43:1855.
Demicheli R, Biganzoli E, Boracchi P, Greco M, Retsky MW. Recurrence dynamics does not depend on the recurrence site. Breast Cancer Res. 2008;10:R83.
Peeters CF, de Waal RM, Wobbes T, Westphal JR, Ruers TJ. Outgrowth of human liver metastases after resection of the primary colorectal tumor: a shift in the balance between apoptosis and proliferation. Int J Cancer. 2006;119:1249.
Allawi Z, Cuzick J, Baum M. Does trauma or an intercurrent surgical intervention lead to a short-term increase in breast cancer recurrence rates? Ann Oncol. 2012;23:866.
Rinn JL, Bondre C, Gladstone HB, Brown PO, Chang HY. Anatomic demarcation by positional variation in fibroblast gene expression programs. PLoS Genet. 2006;2:1084.
Chi JT, Chang HY, Haraldsen G, Jahnsen FL, Troyanskaya OG, Chang DS, et al. Endothelial cell diversity revealed by global expression profiling. Proc Natl Acad Sci. 2003;100:10623.
Takemoto Y, Li TS, Kubo M, Ohshima M, Ueda K, Harada E, et al. Operative injury accelerates tumour growth by inducing mobilization and recruitment of bone marrow-derived stem cells. Surgery. 2011;149:792.
Fisher B, Anderson D, Fisher ER, Redmond C, Wickerham DL, Wolmark N, et al. Significance of ipsilateral breast tumour recurrence after lumpectomy. Lancet. 1991;338:327.
Broet P, de la Rochefordiere a, Scholl SM, Fourquet A, Mosseri M, Durand JC, et al. Contralateral breast cancer: annual incidence and risk parameters. J Clin Oncol. 1995;13:1578.
Janschek E, Kandioler-Eckersberger D, Ludwig C, Kappel S, Wolf B, Taucher S, et al. Contralateral breast cancer: molecular differentiation between metastasis and second primary cancer. Breast Cancer Res Treat. 2001;67:1.
Verkooijen HM, Chatelain V, Fioretta G, Vlastos G, Rapiti E, Sappino AP, Bouchardy C, Chappuis PO. Survival after bilateral breast cancer: results from a population-based study. Breast Cancer Res Treat. 2007;105:347.
Chan DS, Norat NT. Obesity and breast cancer: not only a risk factor of the disease. Curr Treat Options in Oncol. 2015;16:22.
Ceelen W, Pattyn P, Mareel M. Surgery, wound healing, and metastasis: recent insights and clinical implications. Crit Rev Oncol Hematol. 2014;89:16.
Potter CJ, Xu T. Mechanisms of size control. Curr Opin Genet Dev. 2001;11:279.
Stanger BZ. The biology of organ size determination. Diabetes Obes Metab. 2008;10 Suppl 4:16.
Fu V, Plouffe SW, Guan KL. The Hippo pathway in organ development, homeostasis and regeneration. Curr Opin Cell Biol. 2018;49:99.
Wang Y, Yu A, Yu FX. The hippo pathway in tissue homeostasis and regeneration. Protein Cell. 2017;8:349.
Hong L, Cai Y, Jiang M, Zhou D, Chen L. The Hippo signaling pathway in liver regeneration and tumorigenesis. Acta Biochim Biophys Sin. 2015;47:46.
Retsky MW, Demicheli R, Hrushesky WJM, Forget P, DeKock M, Gukas I, et al. Reduction of breast cancer relapses with perioperative non-steroidal anti-inflammatory drugs: new findings and a review. Curr Med Chem. 2013;20:4163.
Gennaro M, Di Cosimo S, Ardoino I, Veneroni S, Mariani L, Daidone MG, de Braud F, Apolone G, Biganzoli E, Demicheli R. Dynamics of the hazard for distant metastases after ipsilateral breast tumor recurrence according to estrogen receptor status: an analysis of 2851 patients. Breast. 2018;40:131.
Sessler DI, Riedel B. Anesthesia and cancer recurrence: context for divergent study outcomes. Anesthesiology. 2019;130:3.
Pérez-González O, Cuéllar-Guzmán LF, Soliz J, Cata JP. Impact of regional anesthesia on recurrence, metastasis, and immune response in breast cancer surgery: a systematic review of the literature. Reg Anesth Pain Med. 2017;42:751.
Love RR, Love SM. Peri-operative biology in primary breast cancer: a credible therapeutic target. Breast Cancer Res Treat. 2016;156(3):411.
This work was partly supported by the Associazione Italiana per la Ricerca sul Cancro AIRC. The authors thank anonymous reviewers for their very useful comments.
Availability of data and materials
The datasets analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All studies supplying the analysed databases were approved by the institutional ethics committees and review boards in accordance with the Declaration of Helsinki.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
- Breast cancer
- Recurrence dynamics
- Metastasis development
- Second surgery
- Tumour homeostasis
- Surgery-related metastasis acceleration