- Open Access
- Open Peer Review
Circulating tumor cells in breast cancer: A tool whose time has come of age
© Swaby and Cristofanilli; licensee BioMed Central Ltd. 2011
- Received: 28 October 2010
- Accepted: 21 April 2011
- Published: 21 April 2011
Circulating tumor cells (CTCs) are isolated tumor cells disseminated from the site of disease in metastatic and/or primary cancers, including breast cancer, that can be identified and measured in the peripheral blood of patients. As recent technical advances have rendered it easier to reproducibly and repeatedly sample this population of cells with a high degree of accuracy, these cells represent an attractive surrogate marker of the site of disease.
Currently, CTCs are being integrated into clinical trial design as a surrogate for phenotypic and genotypic markers in correlation with development of molecularly targeted therapies. As CTCs play a crucial role in tumor dissemination, translational research is implicating CTCs in several biological processes, including epithelial to mesenchymal transition. In this mini-review, we review CTCs in metastatic breast cancer, and discuss their clinical utility for assessing prognosis and monitoring response to therapy. We will also introduce their utility in pharmacodynamic monitoring for rational selection of molecularly targeted therapies and briefly address how they can help elucidate the biology of cancer metastasis.
- Overall Survival
- Metastatic Breast Cancer
- Median Overall Survival
- Circulate Tumor Cell
- Metastatic Breast Cancer Patient
Affecting approximately 200,000 women in the United States alone, breast cancer is now recognized to be a heterogeneous disease comprised of several common different phenotypes . Due to increased screening, awareness and consequent early detection, only approximately 5% of all breast cancer patients are initially diagnosed with incurable disease . However, despite optimal local and systemic adjuvant treatment, 30-40% of patients diagnosed with curable breast cancer eventually die of recurrent disease [3, 4]. Therefore, improved techniques to both detect and treat metastatic breast cancer are needed.
As early as the 1800's when Recaimer first coined the term "metastasis", circulating tumor cells (CTCs) have been postulated to be critical to the process [5, 6]. The development of disseminated disease has been traditionally viewed as a sequential rather than concurrent process, i.e.- the disease initially occurs at the primary site, followed by local growth with eventual dissemination to distant sites. However, emerging data is challenging this theory [7, 8]. In fact, the initiation of metastasis may be a relatively early event in tumor biology, underscoring the need to understand the significance of CTCs.
Additionally, more recent data comparing CTCs to both standard imaging for metastatic breast cancer and the newer [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) will be reviewed as well as new data correlating CTC burden as a surrogate for disease burden with the risk of developing thromboembolic disease.
Predictive and Prognostic Capability
The first large, multi-institution, double-blind, prospective clinical trial evaluated the prognostic capability of CTCs in patients with metastatic breast cancer (MBC). One hundred and seventy-seven patients with measurable disease had CTCs tested prior to beginning a new palliative treatment regimen for progressive disease, followed by repeat assessment at first follow-up visit approximately 4 weeks later. This landmark trial prospectively identified a CTC cut-off level of ≥5 cells per 7.5 ml of blood to be a reliable identifier of patients at higher risk for disease progression and decreased survival from metastatic breast cancer. Regardless of histology, hormone receptor and HER2/neu status, or whether the patient had recurrent or de novo metastatic disease, those with <5 CTCs at baseline, and more importantly, at first follow-up after beginning a new treatment regimen, had superior progression free (PFS) and overall survival (OS) (7 vs 2.1 months [p < 0.001] and 10.1 vs >18 months, [p < 0.001], respectively). Additional CTCs assessment in this same patient cohort at essentially monthly intervals following first follow-up also confirmed improved PFS and OS for patients with <5 CTCs at any subsequent time point. PFS and OS for patients with <5 CTCs ranged from 5.6 to 7 months and 18.6 to >25.0 months, respectively, compared to those with ≥5 CTCs of 1.3 to 3.6 months PFS and 6.3 to 10.9 months OS (p = 0.001) .
Subsequent analysis of the eighty-three newly diagnosed patients undergoing first-line treatment for MBC in the above study confirmed the ability of CTCs to predict response to therapy and global outcome. At first follow-up assessment, median PFS for patients with <5 CTCs was 9.5 months, vs 2.1 months for those with ≥5 CTCs (p = 0.0057). Similarly, those with <5 CTCs had a median OS of 18 months, compared to just 11 months for those with ≥5 CTCs .
A similar analysis of the prognostic value of CTCs among newly diagnosed MBC patients prior to beginning first-line salvage therapy was performed in a large, retrospective single-institution study . This study analyzed CTCs of 185 newly diagnosed MBC patients diagnosed between 2001 and 2007. As previously seen, patients with ≥5 CTCs at baseline had a greater than three-and-a-half fold increased risk of death, (HR = 3.64 [95% CI, 2.11-6.30, p < 0.0001]) compared to those patients with < 5 CTCs. The prognostic significance of CTCs was independent of choice of therapy (i.e. - chemotherapy with anthracyclines, taxanes, or both anthracyclines/taxanes, hormone therapy), and was also independent of hormone receptor status and HER-2/neu status. Interestingly, in this cohort, although the patient demographics were representative of the phenotypic characteristics of MBC patients in general, i.e. - approximately two-thirds of patients hormone receptor positive and approximately 20% HER-2/neu positive, greater than half of the patients had bone as their first site of metastatic disease. Upon multivariate analysis, patients with bone metastasis, compared to other sites of disease with ≥5 CTCs had an additional risk of death. (HR = 1.61; 95% CI 0.52-5.04 [p = 0.410]).
Additional analysis of CTCs and histologic breast cancer classification and phenotypes in a cohort of 517 MBC patients with either measurable or evaluable disease prior to commencement of new palliative treatment regimens has yielded interesting observations and hypothesis-generating information. Lobular histology and bony (but not visceral) disease burden were associated with higher numbers of CTCs . In this study, a closer evaluation of the chemo-naïve HER-2/neu MBC patients treated with targeted HER-2/neu therapies, showed that almost all (13 of 14) demonstrated a decline in CTCs to <5, including patients with documented clinical and radiologic disease progression. At time of the report, the median OS in these 13 patients with CTCs decline had still not been reached, indicating that CTCs of less than five, as previously shown, correlated closely with superior prognosis, despite interval, episodic progression.
Summary of clinical trials reviewed that served to validate the predictive and prognostic capability of CTCs
Line of therapy
Median PFS (months)
Median OS (months)
1. Multi-institution, double-blind, clinical trial of patients with MBC with measurable disease beginning a new therapy. CTCs assessed at baseline and at 1st follow-up clinical visit, approximately 3-4 weeks after starting therapy.14
7.0 vs 2.7; p < 0.001 baseline assessment 7.0 vs 2.1; p < 0.001 1st follow-up
>18 vs 10.1; p < 0.001 baseline assessment >18 vs 8.2; p < 0.001 1st follow-up
2. Multi-institution, double-blind, clinical trial of patients with MBC with measurable disease on treatment. CTCs assessed at 2nd follow-up and subsequent follow-up clinical visits up to 9 months of follow-up. Sub-study of #1 above.15
5.6 - 7 vs 1.3 - 6; p = n/a
18.6- >25 vs 6.3 - 10.9; p = 0.001
3. Multi-institution, double-blind, clinical trial of patients with MBC with measurable disease beginning a new therapy. CTCs assessed at baseline and 1st follow-up clinical visit, approximately 3-4 weeks after starting therapy for the 47% of patients who were being treated with 1st line palliative therapy. Sub-study of #1 above. 16
9.5 vs 4.9, p = 0.0014 baseline assessment 9.5 vs 2.1, p = 0.0057 1st follow-up
>18 vs 14.2, p = 0.0048 baseline assessment >18 vs 11.1, p = 0.0012 1st follow-up
4. Single institution, retrospective analysis of a cohort of newly diagnosed MBC patients (either with de novo MBC or newly diagnosed recurrent MBC) who had CTCs assessed at the time of initial diagnosis of MBC between 2001 and 2007. CTCs assessed at baseline, prior to starting salvage therapy.17
28.3 vs 15, p < 0.001
5. Single institution assessment of a cohort of MBC patients prior to starting a new treatment regimen. CTCs assessment correlated with histology and phenotypic subtypes of breast cancer.18
CTCs and Imaging
In the prospective, longitudinal, multi-institutional trial described above, that demonstrated the ability of CTCs to predict PFS and OS, a nested retrospective study of 138 of the 177 enrolled patients was performed with the goal of comparing the predictive ability of CTCs assessment to standard imaging . While there was no correlation between radiologic tumor burden and overall CTC levels, radiographic response was concordant with the established CTC cut-offs. Specifically, the almost two-thirds of patients who had evidence of radiographic response also had <5 CTCs at assessment, and an additional 16% had PD by both radiographic and CTCs (≥5) criteria. However, CTC responders, whether radiographic responders or non-responders, had similar significantly improved median OS. CTC non-responders, whether radiographic responders or not had worse outcome. Additionally, greater intrareader and interreader variability of interpretation of radiographic results compared to CTC enumeration was found (15.2% vs 0.7%). A separate retrospective study comparing the predictive capability of [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) imaging to CTCs enumeration in a cohort of 115 patients with MBC, again demonstrated CTCs superiority. As FDG-PET/CT is considered to be a promising new imaging modality in assessment of response for MBC patients [20–23], this radiographic assessment was performed at the same intervals as CTCs assessment, approximately 3 months after commencement of a new treatment regimen for progression of disease. In 102 evaluable patients, CTCs response correlated with FDG-PET/CT response 67% of the time, and in multivariate analysis was the most significant predictor of OS (p = 0.04). CTCs response, therefore, is most likely an accurate surrogate for radiographic response as well as those with stable disease and this is reflected in the superior clinical outcome associated with low number of CTCs. On the other hand, elevated CTCs, at anytime during the course of palliative treatment signals impending treatment resistance and progression of disease.
Of note, while CTC level does not correlate with radiographic measurable disease burden, CTC burden does correlate with extent of bony disease involvement. Relative to those without bone involvement, patients with multiple sites of disease including bony disease with ≥5 CTC had significantly worse outcome (p = 0.0008). This is in contrast to patients with minimal or no bone involvement, suggesting a potential biologic link between bone metastases and CTCs .
CTCs and Thromboembolic Disease
In a single institution, retrospective review, Mego and colleagues assessed CTCs level in 290 MBC patients prior to starting a new palliative treatment regimen. The presence of ≥1 CTCs, - the cut-off commonly employed in the adjuvant setting [14, 26], was associated with a four-fold increase in thrombosis compared to patients who had no CTCs . Although not statistically significant, patients with ≥5 CTCs were almost twice as likely to experience a thrombotic event (6.6 vs 11.6%, p = 0.076). When lines of therapy and extent of tumor burden were controlled for by multi-variate analysis, evidence of at least one CTC was still associated with greater than five-fold increase in the risk of thrombosis compared with those without any detectable CTC, thus confirming that CTCs, while not directly correlated with volume of disease burden, are a marker of increased morbidity that ultimately impacts mortality.
This observation indicates a potential role of clotting factors in the peripheral blood in some steps of the metastatic process. In fact, the environment in the bloodstream is highly unfavorable to tumor cells due to physical forces, presence of immune cells and death upon detachment (anoikis), which contributes to metastatic insufficiency . Coagulation factors play an important role in metastasis and enhance breast cancer progression in animal models [29, 30]. The binding of tumor cells to coagulation factors, including tissue factor, fibrinogen, fibrin and thrombin, creates an embolus and facilitates arrest in capillary beds followed by the establishment of metastasis . This concept is further supported by a meta-analysis that showed anticoagulation therapy has beneficial effects on cancer patient survival . However, the anti-metastatic effect of heparin is not a result of its anticoagulant activity but rather its ability to inhibit the interactions between some oligosaccharides present on tumor cells and P-selectin on platelets [33, 34].
Elevated CTCs, whether at baseline or at any time throughout the course of MBC are an ominous prognostic indicator. Whether by standard imaging studies and/or PET/CT imaging, elevated CTCs while on treatment, regardless of radiographic assessment, ultimately are predictive of an ineffective therapy. Similarly, low CTCs, especially while on treatment, predict for favorable survival as well as response to therapy. CTCs also reflect tumor biology as well as aspects of the host microenvironment as patients with elevated CTCs have an increased risk of developing thromboembolic disease. Taken as a whole, CTCs, while not directly correlated with volume of disease burden, are a marker of increased morbidity that ultimately impacts mortality.
Despite major advances in our understanding of cancer biology, we still lack detailed insight into the mechanisms of tumor establishment and dissemination. CTCs play a crucial role in tumor dissemination in relation to several biological processes, including epithelial to mesenchymal transition (EMT,) the process whereby epithelial cells lose cell-to-cell adhesion mediated by down-regulation of epithelial associated E-cadherin, and up-regulation of mesenchymal N-cadherin, allowing them to invade the extracellular matrix and migrate to a distant site . The c-DNA of various genes such as Twist1, Akt2 and PI3Kα, associated with EMT and the stem cell marker, ALDH1, can be detected in CTCs. In patients with MBC not responding to the prescribed therapeutic regimen, the identification of EMT markers in the CTCs was considerably higher than in normal healthy individuals without a cancer diagnosis as well as patients with MBC who were responding to therapy .
In conclusion, CTC assessment has been shown to be a repeatedly, strong and reliable predictor of outcome in metastatic breast cancer. It performs as reliably as imaging studies for assessment of response to therapy, and possibly more so. Although the mechanism is not fully elucidated, CTCs are a unique and heterogeneous cell population with established prognostic and predictive value in MBC particularly in defined subtypes of breast disease, and may related to bone biology in particular. In the era of biologically targeted therapies, molecular characterization of CTCs may hold the key to future pharmacodynamic assessment in drug development of MBC. Currently, most molecularly targeted biologic therapies are developed using the same toxicity assessment as traditional cytotoxic therapies - identifying the maximum tolerated dose. However, in the case of these newer molecularly targeted therapies, the maximum tolerated dose may not necessarily correlate with the most effective dose - i.e. receptor downregulation, protein phosphorylation, etc. The ability to repeatedly sample an accessible tumor population such as CTCs may allow selection of optimal therapies based on confirmed target delivery. Considerable effort is currently being directed at developing additional technologies to be able to reliably characterize the genomic and proteomic information contained within these cells. The full extent of CTCs utility has yet to be explored.
- American Cancer Society: Cancer Fact & Figures 2009. 2009, [http://www.cancer.gov]Google Scholar
- National Cancer Institute Surveillance Epidemiology and End Results (SEER): Cancer survival statistics. [http://seer.cancer.gov/statistics]
- Weigelt B, Peterse JL, van't Veer LJ: Breast cancer metastasis: markers and models. Nat Rev Cancer. 2005, 5: 591-602. 10.1038/nrc1670.View ArticlePubMedGoogle Scholar
- Honig SF: Treatment of metastatic disease. Disease of the Breast. Edited by: Harris JR, Lippman ME, Morrow M, et al. 1996, Philadelphia, PA: Lippincott-Raven, 669-734.Google Scholar
- Recamier JCA: L'histoire de le Meme Maladie. Gabor. 1829, 110.Google Scholar
- Ashworth TR: A case of cancer in which cells similar to those in the tumors were seen in the blood after death. Australian Med J. 1869, 14: 146.Google Scholar
- Mego M, Mani SA, Cristofanilli M: Molecular mechanisms of metastasis - clinical applications. 2010, 7 (12): 693-701. Epub 2010 Oct 19Google Scholar
- Kim MY, Oskarsson T, Acharyya S, Nguyen DX, Zhang XH-F, Norton L, Massague J: Tumor self-seeding by circulating cancer cells. Cell. 2009, 139: 1315-1326. 10.1016/j.cell.2009.11.025.View ArticlePubMedPubMed CentralGoogle Scholar
- Kagan M, Howard D, Bendele T, et al: A sample preparation and analysis system for identification of circulating tumor cells. J Clin Ligand Assay. 2002, 25: 104-110.Google Scholar
- Kagan M, Diamandis EP, Fritsche HA, et al: Tumor markers: physiology, pathobiology, technology and clinical applications. 2002, Washington, D.C.: AACC Press, 405-409.Google Scholar
- Van der Auwera I, Peeters D, Benoy IH, Elst HJ, Van Laere SJ, Prove A, Maes H, Huget P, van Dam P, Vermeulen PB, Dirix LY: Circulating tumour cell detection: a direct comparison between the CellSearch System, the AdnaTest and CK-19/mammaglobin RT-PCR in patients with metastatic breast cancer. British J of Cancer. 2010, 102: 276-284. 10.1038/sj.bjc.6605472.View ArticleGoogle Scholar
- Dotan E, Cohen SJ, Alpaugh KR, Merepol NJ: Circulating tumor cells: evolving evidence and future challenges. The Oncologist. 2009, 14: 1070-1082. 10.1634/theoncologist.2009-0094.View ArticlePubMedGoogle Scholar
- Riethdorf S, Fritsche H, Muller V, Rau T, Schindlbeck C, Rack B, Janni W, Coith C, Beck K, Janicke F, Jackson Sm, Gornet T, Cristofanilli M, Pantel K: Clin Cancer Res. 2007, 13: 920-928. 10.1158/1078-0432.CCR-06-1695.View ArticlePubMedGoogle Scholar
- Cristofanilli M, Budd GT, Ellis MJ, Stopeck A, Matera J, Miller MC, Reuben JM, Doyle GV, Allard WJ, Terstappen LWMM, Hayes DF: Circulating tumor cells, disease progression, and survival in metastatic breast cancer. N Engl J Med. 2004, 351: 781-789. 10.1056/NEJMoa040766.View ArticlePubMedGoogle Scholar
- Hayes DF, Cristofanilli M, Budd GT, Ellis MJ, Stopeck A, Miller MC, Allard WJ, Doyle GV, Terstappen LWMM: Circulating tumor cells at each follow-up time point during therapy of metastatic breast cancer patients predict progression-free and overall survival. Clin Cancer Res. 2006, 12: 4218-4224. 10.1158/1078-0432.CCR-05-2821.View ArticlePubMedGoogle Scholar
- Cristofanilli M, Hayes DF, Budd GT, Ellis MJ, Stopeck A, Reuben JM, Doyle GV, Matera J, Allard WJ, Miller MC, Fritsche HA, Hortobagyi GN, Terstappen LWMM: J Clin Oncol. 2005, 23: 1420-1430. 10.1200/JCO.2005.08.140.View ArticlePubMedGoogle Scholar
- Dawood S, Broglio K, Valero V, Reuben J, Handy B, Islam R, Jackson S, Hortobagyi GN, Fritsche H, Cristofanilli M: Cancer. 2008, 113: 2422-2430. 10.1002/cncr.23852.View ArticlePubMedGoogle Scholar
- Giordano A, Giuliano M, Jackson S, Reuben JM, De Laurentiis M, Handy BC, Ueno NT, Andreopoulou E, Alvarez RH, Valero V, De Placido S, Horotobagyi GN, Cristofanilli M: Circulating tumor cells (CTCs) in metastatic breast cancer: Prognosis, molecular subtypes and metastatic sites. 2011.Google Scholar
- Budd GT, Cristofanilli M, Ellis MJ, Stopeck A, Borden E, Miller MC, Matera J, Repollet M, Doyle GV, Terstappen LWMM, Hayes DF: Circulating tumor cells versus imaging - predicting overall survival in metastatic breast cancer. Clin Cancer Res. 2006, 12: 6403-6409. 10.1158/1078-0432.CCR-05-1769.View ArticlePubMedGoogle Scholar
- Hodgson NC, Gulenchyn KY: Is there a role for positron emission tomography in breast cancer staging?. J Clin Oncol. 2008, 26: 712-720. 10.1200/JCO.2007.13.8412.View ArticlePubMedGoogle Scholar
- Gennari A, Donati S, Salvadori B, Giorgetti A, Salvadori PA, Sorace O, Puccini G, Pisani P, Poli M, Dani D, Landucci E, Mariani G, Conte PF: Role of 2-[18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) in the early assessment of response to chemotherapy in metastatic breast cancer patients. Clin Breast Cancer. 2000, 1: 156-161. 10.3816/CBC.2000.n.014. discussion 162-163View ArticlePubMedGoogle Scholar
- Dose Schwarz J, Bader M, Jenicke L, Hemminger G, Janicke F, Avril N: Early prediction of response to chemotherapy in metastatic breast cancer using sequential 18F-FDG PET. J Nucl Med. 2005, 46: 1144-1150.PubMedGoogle Scholar
- Couturier O, Jerusalem G, N'Guyen JM, Hustinx R: Sequential positron emission tomography using [18F]fluorodeoxyglucose for monitoring response to chemotherapy in metastatic breast cancer. Clin Cancer Res. 2006, 12: 6437-6443. 10.1158/1078-0432.CCR-06-0383.View ArticlePubMedGoogle Scholar
- De Giorgi U, Valero V, Rohren E, Dawood S, Ueno NT, Miller MC, Doyle GV, Jackson S, Andreopoulou E, Handy BC, Reuben JM, Fritsche HA, Macapinlac HA, Hortobagyi GN, Cristofanilli M: Circulating tumor cells and [18F]-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography for outcome prediction in metastatic breast cancer. J Clin Oncol. 2009, 27: 3303-3311. 10.1200/JCO.2008.19.4423.View ArticlePubMedGoogle Scholar
- De Giorgi U, Valero V, Rohren E, Mego M, Doyle GV, Miller MC, Ueno NT, Handy BC, Reuben JM, Macapinlac HA, Hortobagyi GN, Cristofanilli M: Circulating tumor cells and bone metastases as detected by FDG-PET/CT in patients with metastatic breast cancer. Annals of Oncol. 2010, 21: 33-39. 10.1093/annonc/mdp262.View ArticleGoogle Scholar
- Lang JE, Mosalpuria K, Cristofanilli M, Krishnamurthy S, Reuben J, Singh B, Bedrosian I, Meric-Bernstam F, Lucci A: HER2 status predicts the presence of circulating tumor cells in patients with operable breast cancer. Breast Cancer Res Treat. 2009, 113: 501-507. 10.1007/s10549-008-9951-2.View ArticlePubMedGoogle Scholar
- Mego M, De Giorgi U, Broglio K, Dawood S, Valero V, Andreopoulou E, Handy B, Reuben JM, Cristofanilli M: Circulating tumor cells are associated with increased risk of venous thromboembolism in metastatic breast cancer patients. British J Cancer. 2009, 101: 1813-1816. 10.1038/sj.bjc.6605413.View ArticleGoogle Scholar
- Trepel M, Arap W, Pasqualini R: In vivo phage display and vascular heterogeneity: implications for targeted medicine. Curr Opin Chem Biol. 2002, 6: 399-404. 10.1016/S1367-5931(02)00336-8.View ArticlePubMedGoogle Scholar
- Palumbo JS, et al: Fibrinogen is an important determinant of the metastatic potential of circulating tumor cells. Blood. 2000, 96: 3302-3309.PubMedGoogle Scholar
- Palumbo JS, et al: Factor XIII transglutaminase supports hematogenous tumor cell metastasis through a mechanism dependent on natural killer cell function. J Thromb Haemost. 2008, 6: 812-819. 10.1111/j.1538-7836.2008.02938.x.View ArticlePubMedGoogle Scholar
- Akl EA, et al: Parenteral anticoagulation for prolonging survival in patients with cancer who have no other indication for anticoagulation. Cochrane Database Syst Rev; CD006652. 2007Google Scholar
- Zielinski CC, Hejna M: Warfarin for cancer prevention. N Engl J Med. 2000, 342: 1991-1993. 10.1056/NEJM200006293422612.View ArticlePubMedGoogle Scholar
- Fuster MM, Brown JR, Wang L, Esko JD: A disaccharide precursor of sialyl Lewis X inhibits metastatic potential of tumor cells. Cancer Res. 2003, 63: 2775-2781.PubMedGoogle Scholar
- Meng S, Tripathy D, Shete S, Ashfaq R, Saboorian H, Haley B, Frenkel E, Euhus D, Leitch M, Osborne C, Clifford E, Perkins S, Beitsch P, Khan A, Morrison L, Herlyn D, Terstappen LWMM, Lane N, Wang J, Uhr J: uPar and HER-2 gene status in individual breast cancer cells from blood and tissues. PNAS. 2006, 46: 17361-17365.View ArticleGoogle Scholar
- Atkas B, Tewes M, Fehm T, Hauch S, Kimming R, Kasmie-Bauer S: Stem cell and epithelial-mesenchymal transition markers are frequently overexpressed in circulating tumor cells of metastatic breast cancer patients. Breast Cancer Res. 2009.Google Scholar
- Wang LH, Pfister TD, Parchment RE, Kummar S, Rubinstein L, Evrad YA, Gutierrez ME, Murgo AJ, Tomaszewski JE, Doroshow JH, Kinders RJ: Monitoring drug-induced H2Ax as a pharmacodynamic biomarker in individual circulating tumor cells. Clin Cancer Res. 2010, 16: 1073-1083. 10.1158/1078-0432.CCR-09-2799.View ArticlePubMedPubMed CentralGoogle Scholar
- Riethdorf S, Muller V, Zhang L, Rau T, Loibl S, Komor M, Roller M, Huober J, Fehm T, Schrader I, Hilfrich J, Holms F, Tesch H, Eidtmann H, Untch M, von Minckwitz G, Pantel K: Detection and HER2 expression of circulating tumor cells: prospective monitoring in breast cancer patients treated in the neoadjuvant GeparQuattro trial. Clin Cancer Res. 2010, 16: 2634-2645. 10.1158/1078-0432.CCR-09-2042.View ArticlePubMedGoogle Scholar
- S0500: A Randomized Phase III Trial to Test the Strategy of Changing Therapy Versus Maintaining Therapy for Metastatic Breast Cancer Patients who Have Elevated Circulating Tumor Cell Levels at First Follow-Up Assessment. A trial of the Southwest Oncology Group. [http://www.swog.org/]
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/9/43/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.