CDK9 Expression Shows Role as a Potential Prognostic Biomarker in Breast Cancer Patients Who Fail to Achieve Pathologic Complete Response after Neoadjuvant Chemotherapy.
Patients with breast cancer with high-risk features, such as triple-negative breast cancers (TNBC), are often treated with neoadjuvant chemotherapy (NACT) prior to surgical resection . NACT can reduce the size of the breast tumor, subsequently allowing for breast-conservation surgery in patients who otherwise might require a complete mastectomy due to large tumor size . In addition, survival outcomes are significantly impacted by response to NACT. Patients with residual invasive breast cancer following NACT are reported to have a high risk of relapse , yet, some of these patients achieve long-term survival without recurrence. Thus, there is a need to identify biomarkers for patients with residual disease following NACT that can provide both prognostic information regarding outcomes and predictive information to identify patients with more aggressive disease who could benefit from additional therapies.
Cyclin-dependent kinase 9 (CDK9) is a component of the positive transcription elongation factor (P-TEFb) complex, which phosphorylates the carboxyl-terminal domain (CTD) of RNA polymerase II to promote transcription elongation . We and others have also reported that CDK9 has a transcription-independent function in promoting genome integrity [5-11]. CDK9 facilitates recovery from replication stress and interacts with ATR and several cell cycle checkpoint proteins. Furthermore, its loss results in spontaneous replication stress and genetic instability . CDK9 also promotes DNA double-strand break (DSB) repair by homologous recombination (HR) by facilitating recruitment of the BRCA1 breast tumor suppressor protein to DNA damage sites  and associates with Ku70, which is involved in DSB repair by non-homologous end joining (NHEJ) . CDK9's role in promoting genome integrity is regulated at least in part through deacetylation by the SIRT2 sirtuin deacetylase and breast tumor suppressor protein, which promotes its kinase activity  and in turn phosphorylates UBE2A and directs H2Bub1 and PCNA ubiquitinylation .
CDK9 is a protein of potential clinical significance in oncology because of its role in promoting genomic integrity in response to agents that induce replication stress and DNA damage. It has been shown to be dysregulated in a number of malignancies, including breast cancer [13, 14]. CDK9 inhibitors have also been shown to inhibit growth of breast cancer cells and tumors [15-18]. In this study, we evaluated CDK9 expression in post-NACT breast tumors.
2. Materials and Methods
2.1. Patient Selection. The patient cohort was selected from a prospectively maintained, IRB approved database of patients who underwent surgical resection for breast cancer between 2001 and 2011 at Emory University's Winship Cancer Institute. A total of 84 patients who received NACT prior to surgical resection without achieving complete pathological response had tissue from their surgical resections available for analysis. These patients were selected for inclusion in the study. Patient demographics, pathologic information, and treatment outcomes were obtained from electronic medical records. Staging was based on the AJCC 7th edition. Complete pathological response was defined as no invasive cancer in the breast or axilla. Permission for patient information used in this study was obtained from Emory's Institutional Review Board and patient confidentiality was maintained in accordance with the Health Insurance Portability and Accountability Act of 1996.
2.2. Tissue Microarray (TMA) Development. TMAs were used for this study in order to analyze tissues from multiple patients on a single slide and thus reduce the time and cost for analysis. In order to construct the TMAs, formalin-fixed paraffin embedded (FFPE) tissue blocks for each patient were acquired. These blocks contained tumor specimens from each patient's primary surgical resection. A board-certified pathologist reviewed hematoxylin and eosin (H&E) sections from each FFPE tissue block to identify representative areas of invasive ductal or lobular carcinoma. The identified area on the H&E slide was then used to guide the removal of the corresponding core from the FFPE tissue block. The removed core from each block was then placed into the TMA block in a specific row and column. Row and column location for each core was carefully recorded to ensure staining data and clinical data would be appropriately linked. Two cores of normal tissue were used as controls in every TMA constructed. These cores of normal tissue were used to assess efficacy of staining as well as to allow for comparison between cores on the same or separate TMAs for quality assurance. For more detailed information on TMA construction, please refer to the article by Rimm et al. .
2.3. TMA Staining. After the TMAs were constructed, they were cut into sections for staining. A rabbit polyclonal CDK9 antibody from Abcam at 1:1600 dilution was used in the immunohistochemistry (IHC) staining process. The TMA sections underwent antigen retrieval using either the Target Retrieval Solution (TRS) or Trilogy system. Tissue was blocked with 3% hydrogen peroxide for 5 minutes and then incubated with the primary antibody for 40 minutes. Dako's EnVision+ Dual Link System-horseradish peroxidase (HRP) was used to detect antibody-antigen interaction.
2.4. IHC Scoring. The TMA sections were analyzed by a board-certified pathologist who was blinded to patient outcomes. The TMA slides contained samples from each of the 84 patients in our study. Each core sample was analyzed for intensity and extent of staining. A previously validated scoring system was used to combine staining intensity (scored from 1 to 3) and extent (1-100%) into an IHC score . The staining extent was then converted into a number between 1 and 3, with 1=0-50%, 2=51-80%, and 3=81-100%. IHC was then calculated according to the following formula: IHC= [(1+intensity)/3] x extent. High expression of CDK9 was defined as IHC score greater than 3, while low expression was defined as IHC score less than or equal to 3.
2.5. Statistics. The primary aim of this study was to determine if there was any difference in overall survival (OS) between high tumor CDK9 expression and low tumor CDK9 expression in residual tumor following NACT. Secondary outcomes analyzed included locoregional recurrence-free survival (LRFS), distant failure-free survival (DFFS), recurrence-free survival (RFS), and event-free survival (EFS). OS was calculated from date of surgery to patient death. Locoregional recurrence was defined as a biopsy proven recurrence of the primary breast cancer within the ipsilateral breast or chest wall, or in the axillary, internal mammary or supraclavicular lymph nodes. Distant failure was defined as a biopsy proven recurrence in any other location. RFS was calculated as time from date of surgery to first recurrence. Events were defined as any type of recurrence or patient death. EFS was calculated as time from date of surgery to earliest event. Survival was estimated using the Kaplan-Meier method, and log-rank p-values were reported for survival curves. Univariate cox proportional hazards models were fit for OS, LRFS, DFFS, RFS, and EFS. Additionally, time-dependent coefficient models were explored in cases where the hazards were not proportional over time. Chi-squared or Fisher's Exact tests were used to compare pathologic response across expression groups, as well as CDK9 expression across subtype and receptor groups. Complete pathologic response was defined as no residual tumor in the breast and nodes following neoadjuvant chemotherapy.
A total of 84 patients were analyzed for tumor expression levels of CDK9 using the TMA staining protocol. In this cohort, 6 patients (7.1%) demonstrated a local recurrence while 23 patients (27.4%) demonstrated a distant recurrence (Table 1). Additional descriptive information including patient survival is available in Table 1. Of the 84 patients in the cohort, 67 patients' samples were analyzed for CDK9 expression. The excluded samples were not analyzed because they did not remain intact during the staining process and therefore were not able to be interpreted by the pathologist. CDK9 staining revealed that 36 patients (53.7%) had high expressing tumors and were thus classified as CDK9 positive while 31 patients (46.3%) had low expressing tumors and were classified as CDK9 negative. The median follow-up time was 8.2 years, and the range was 0.6-12.4 years.
High CDK9 expression was associated with increased OS starting from the third year after the patient's initial surgery. A time-dependent covariate was fit to a Cox proportional hazards model in order to evaluate the risk of death between groups beyond 3 years, which yielded a statistically significant hazard ratio (HR): 0.26, 95% CI: 0.07-0.98, p=0.046 shown in Table 2. However, Kaplan-Meier analysis for OS did not demonstrate significant improvement with high CDK9 levels (Figure 1, p=0.127).
CDK9 expression was not shown to have a significant impact on DFFS, LRR, RFS, and EFS (Figure 2, p=0.2854, Figure 3 p=0.8518, Figure 4 p=0.5369, and Figure 5 p=0.4566, respectively). CDK9 expression was not significantly associated with age, stage, receptor status, or breast cancer subtype (Table 3).
Our study aimed to determine if CDK9 expression in residual breast tumors following the use of NACT correlated with clinical outcomes. We found that high CDK9 expression was significantly associated with improved OS beyond 3 years, suggesting that high CDK9 expression is a favorable prognostic factor for long-term clinical outcome. We also observed a trend towards improved DFFS but not LRFS with high CDK9 expression compared with low CDK9 expression, suggesting that CDK9 expression may be more prognostic for distant failure. Interestingly, we did not observe any significant separation of the OS curve before 3 years, suggesting that CDK9 expression is not a good surrogate for short-term response to treatment. Given that low CDK9 expression leads to increased spontaneous DNA damage and genetic instability, we speculate that patients with residual breast tumors with low CDK9 expression may have more aggressive disease and thus poorer prognoses. This paradoxical observation is in contrast to another study investigating CDK9 expression in patients with de novo pancreatic adenocarcinoma tumors, which showed that high CDK9 expression has worse clinical outcome  as well as its current investigation as a therapeutic target for cancer treatment [22-25].
In addition, while high expression of CKD9 was observed in fewer TNBC then ER+/PR+/Her2neu--tumors, this was not statistically significant. Due to low event numbers, a multivariable analysis was unable to be performed. Future studies using an increased sample size could yield stronger and more statistically significant results.
One of the difficulties with the study was loss of tumor core samples during the TMA staining process. During staining, some samples either became detached from the TMA slide or folded over themselves. Those particular samples became unreadable by the pathologist and had to be excluded from analysis. This resulted in significant decrease of the study sample size. Future studies using the TMA staining process should attempt to place multiple core samples per patient. The probability of losing multiple samples is lower and would allow for more patient data to be analyzed. In addition, the number of events available for analysis was small. Although a multivariate analysis is desirable, this was not feasible given the low number of events for each time point. A longer follow-up period maybe required to obtain a proper sample of events and demonstrate significance in our data. Increasing the patient cohort number could also provide the additional data necessary to reach statistical significance. Ultimately an independent cohort, as well as a randomized clinical trial, may validate the prognostic significance of CDK9 expression following neoadjuvant chemotherapy. One potential benefit of this work is that, with further validation, patients with low CDK9 expression in residual breast tumors following NACT may benefit from more aggressive adjuvant therapies, including enrollment in clinical trials of novel therapies.
The results of this study do not show a significant relationship between CDK9 expression in residual breast tumors following NACT and improved patient LRR, RFS, and EFS. However, our findings of improved survival after 3 years suggest that, with further validation, CDK9 expression could have a future role as a prognostic biomarker for patients with breast cancer who fail to achieve a pathologic complete response after NACT.
The data used to support the findings of this study are available from the corresponding author upon request.
The content of the paper is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
Ashley J. Schlafstein, Allison E. Withers, and Soumon Rudra contributed equally to this manuscript and are co-first authors.
Multiple contributors aided in designing and completing various aspects of the study. Dr. Shahrzad Ehdaivand read sample sections from FFPE tissue blocks to identify regions of invasive tumor for TMA construction. Development of the TMA was accomplished with the help of the Ms. Dianne Alexis at the Winship Pathology Core Lab. Ms. Alexis also assisted with IHC protocol development and TMA slide staining. TMA slides for CDK9 were interpreted by Emory pathology fellow, Dr. Saul Harari. Statistical analysis was performed by Dr. Jeff Switchenko. Figures were created using statistical software R. Research reported in this publication was supported in part by the Biostatistics and Bioinformatics Shared Resource of Winship Cancer Institute of Emory University and NIH/NCI P30CA138292 to W.J.C and NIH/ NCI R01CA178999, R01CA178999S1, and WCI Brenda Nease 53237 to David S. Yu.
 S. S. Mougalian, P. R. Soulos, B. K. Killelea et al., "Use of neoadjuvant chemotherapy for patients with stage i to III breast cancer in the United States," Cancer, vol. 121, no. 15, pp. 2544-2552, 2015.
 T. A. Buchholz, K. K. Hunt, G. J. Whitman, A. A. Sahin, and G. N. Hortobagyi, "Neoadjuvant chemotherapy for breast carcinoma: Multidisciplinar^ considerations of benefits and risks," Cancer, vol. 98, no. 6, pp. 1150-1160, 2003.
 P. Cortazar, L. Zhang, M. Untch et al., "Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis," The Lancet, vol. 384, no. 9938, pp. 164-172, 2014.
 N. F. D. S. Paparidis, M. C. Durvale, and F. Canduri, "The emerging picture of CDK9/P-TEFb: more than 20 years of advances since PITALRE," Molecular BioSystems, vol. 13, no. 2, pp. 246-276, 2017.
 H. Liu, C. H. Herrmann, K. Chiang et al., "55K isoform of CDK9 associates with Ku70 and is involved in DNA repair," Biochemical and Biophysical Research Communications, vol. 397, no. 2, pp. 245-250, 2010.
 T. C. Nepomuceno, V. C. Fernandes, T. T. Gomes et al., "BRCA1 recruitment to damaged DNA sites is dependent on CDK9," Cell Cycle, vol. 16, no. 7, pp. 665-672, 2017.
 S. K. Radhakrishnan and A. L. Gartel, "CDK9 phosphorylates p53 on serine residues 33, 315 and 392," Cell Cycle, vol. 5, no. 5, pp. 519-521, 2006.
 K. Storch and N. Cordes, "The impact of CDK9 on radiosensitivity, DNA damage repair and cell cycling of HNSCC cancer cells," International Journal of Oncology, vol. 48, no. 1, pp. 191-198, 2016.
 D. S. Yu and D. Cortez, "A role for cdk9-cyclin k in maintaining genome integrity," Cell Cycle, vol. 10, no. 1, pp. 28-32, 2011.
 D. S. Yu, R. Zhao, E. L. Hsu et al., "Cyclin-dependent kinase 9-cyclin K functions in the replication stress response," EMBO Reports, vol. 11, no. 11, pp. 876-882, 2010.
 H. Zhang, S.-H. Park, B. G. Pantazides et al., "SIRT2 directs the replication stress response through CDK9 deacetylation," Proceedings of the National Acadamy of Sciences of the United States of America, vol. 110, no. 33, pp. 13546-13551, 2013.
 A. Shchebet, O. Karpiuk, E. Kremmer, D. Eick, and S. A. Johnsen, "Phosphorylation by cyclin-dependent kinase-9 controls ubiquitin-conjugating enzyme-2A function," Cell Cycle, vol. 11, no. 11, pp. 2122-2127, 2012.
 E. Cerami, J. Gao, U. Dogrusoz et al., "The cBio Cancer Genomics Portal: an open platform for exploring multidimensional cancer genomics data," Cancer Discovery, vol. 2, no. 5, pp. 401-404, 2012.
 J. Gao, B. A. Aksoy, and U. Dogrusoz, "Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal," Science Signaling, vol. 6, no. 269, p. l1, 2013.
 Y. Li, Q. Guo, C. Zhang et al., "Discovery of a highly potent, selective and novel CDK9 inhibitor as an anticancer drug candidate," Bioorganic & Medicinal Chemistry Letters, vol. 27, no. 15, pp. 3231-3237, 2017.
 P. Mitra, R.-M. Yang, J. Sutton, R. G. Ramsay, and T. J. Gonda, "CDK9 inhibitors selectively target estrogen receptor-positive breast cancer cells through combined inhibition of MYB and MCL-1 expression," Oncotarget, vol. 7, no. 8, pp. 9069-9083, 2016.
 S. Rajput, N. Khera, Z. Guo, J. Hoog, S. Li, and C. X. Ma, "Inhibition of cyclin dependent kinase 9 by dinaciclib suppresses cyclin B1 expression and tumor growth in triple negative breast cancer," Oncotarget, vol. 7, no. 35, pp. 56864-56875, 2016.
 S. Sengupta, M. C. Biarnes, and V. C. Jordan, "Cyclin dependent kinase-9 mediated transcriptional de-regulation of cMYC as a critical determinant of endocrine-therapy resistance in breast cancers," Breast Cancer Research and Treatment, vol. 143, no. 1, pp. 113-124, 2014.
 D. L. Rimm, R. L. Camp, L. A. Charette, D. A. Olsen, and E. Provost, "Amplification of tissue by construction of tissue microarrays," Experimental and Molecular Pathology, vol. 70, no. 3, pp. 255-264, 2001.
 S. K. Maithel, I. Coban, P. J. Kneuertz et al., "Differential expression of ERCC1 in pancreas adenocarcinoma: High tumor expression is associated with earlier recurrence and shortened survival after resection," Annals of Surgical Oncology, vol. 18, no. 9, pp. 2699-2705, 2011.
 A.-L. Kretz, M. Schaum, J. Richter et al., "CDK9 is a prognostic marker and therapeutic target in pancreatic cancer," Tumor Biology, vol. 39, no. 2, 2017.
 F. Morales and A. Giordano, "Overview of CDK9 as a target in cancer research," Cell Cycle, vol. 15, no. 4, pp. 519-527, 2016.
 S. Boffo, A. Damato, L. Alfano, and A. Giordano, "CDK9 inhibitors in acute myeloid leukemia," Journal of Experimental & Clinical Cancer Research, vol. 37, no. 1, 2018.
 M. H. Rahaman, M. Kumarasiri, L. B. Mekonnen et al., "Targeting CDK9: A promising therapeutic opportunity in prostate cancer," Endocrine-Related Cancer, vol. 23, no. 12, pp. T211-T226, 2016.
 Y. A. Sonawane, M. A. Taylor, J. V. Napoleon, S. Rana, J. I. Contreras, and A. Natarajan, "Cyclin Dependent Kinase 9 Inhibitors for Cancer Therapy," Journal of Medicinal Chemistry, vol. 59, no. 19, pp. 8667-8684, 2016.
Ashley J. Schlafstein [ID], (1) Allison E. Withers, (1) Soumon Rudra, (1) Diana Danelia, (1) Jeffrey M. Switchenko [ID], (2) Donna Mister, (1) Saul Harari, (3) Hui Zhang, (1) Waaqo Daddacha, (1) Shahrzad Ehdaivand, (3) Xiaoxian Li, (3) Mylin A. Torres [ID], (1) David S. Yu [ID] (1)
(1) Department of Radiation Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA (2) Department of Biostatistics and Bioinformatics, Rollins School of Public Health and Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA (3) Department of Pathology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA
Correspondence should be addressed to Mylin A. Torres; email@example.com and David S. Yu; firstname.lastname@example.org
Received 24 April 2018; Revised 10 July 2018; Accepted 1 September 2018; Published 14 October 2018
Academic Editor: Marie McIlroy
Table 1: Descriptive Statistics. This table shows clinicopathologic characteristics of the study participants including demographic information, tumor characteristics, and survival data. Variable Level N = 84 % Negative 31 46.3 CDK9 Positive 36 53.7 Missing 17 -- Negative 32 39.0 ER status Positive 50 61.0 Missing 2 -- Negative 40 48.8 PR status Positive 42 51.2 Missing 2 -- Negative 63 77.8 Her2Neu status Positive 18 22.2 Missing 3 -- Triple negative 22 27.5 Subtype ER???? 33 41.3 Other 25 31.3 Missing 4 -- Age at diagnosis (years) <50 32 38.1 50 52 61.9 2 43 52.4 Stage 3 39 47.6 Missing 2 -- Death No 53 63.1 Yes 31 36.9 Locoregional recurrence No 78 92.9 Yes 6 7.1 Distant failure No 61 72.6 Yes 23 27.4 Recurrence (LR or Distant) No 58 69.0 Yes 26 31.0 Event (Recurrence or Death) No 49 58.3 Yes 35 41.7 Table 2: Overall survival-3 years. This table shows an increase in overall survival after 3 years with tumors positive for CDK9 as compared to those negative for CDK9. Covariate Level Hazard Ratio Overall Type3 survival P-value (years) HR P-value CDK9 (Less than Positive 0.99 (0.30-3.23) 0.982 0.982 3 years) Negative -- CDK9 (Greater Positive 0.26 (0.07-0.98) 0.046 0.046 than 3 years) Negative -- Number of observations in the original data set = 84. Number of observations used = 67. Table 3: CDK9 expression and breast cancer subtype/receptor status. This tables shows no significant association of CDK9 expression with breast cancer subtype and receptor status. CDK9 Covariate Statistics Level Negative N=31 ER status N (Col %) Negative 14 (46.67) N (Col %) Positive 16 (53.33) PR status N (Col %) Negative 17 (56.67) N (Col %) Positive 13 (43.33) Her2Neu status N (Col %) Negative 23 (76.67) N (Col %) Positive 7 (23.33) Subtype N (Col %) Triple negative 10 (34.48) N (Col %) ER+/PR+/Her2Neu- 9 (31.03) N (Col %) Other 10 (34.48) Age at diagnosis N (Col %) <50 11 (35.48) (years) N (Col %) 50 20 (64.52) Stage N (Col %) 2 16 (53.33) N (Col %) 3 14 (46.67) CDK9 Covariate Positive N=36 P-value * ER status 9 (25) 0 066 27 (75) PR status 12 (33.33) 0 057 24 (66.67) Her2Neu status 30 (83.33) 0 498 6 (16.67) Subtype 7 (19.44) 21 (58.33) 0.088 8 (22.22) Age at diagnosis 14 (38.89) 0 774 (years) 22 (61.11) Stage 20 (57.14) 0.758 15 (42.86) * The p-value is calculated by chi-square test or Fisher's exact, where appropriate. Figure 1: Overall survival. Figure 1 depicts the overall survival curves for patients with CDK9 positive versus CDK9 negative tumors. This shows a statistically nonsignificant difference in survival. However, there is a trend for increased overall survival in the group of patients with positive CDK9. CDK9 No. of Event Censored Median 5 Yr Survival Subject Survival (95% CI) Negative 31 13 (42%) 18 (58%) NA (4, NA) 65.5% (45.3%, 79.8%) Positive 36 9 (25%) 27 (75%) NA (9.7, 83.2% (66.4%, NA) 92.1%) Figure 2: Distant failure-free survival. Figure 2 shows distant failure-free survival curves for patients with CDK9 positive versus CDK9 negative tumors. This shows a statistically nonsignificant difference in the two survival curves. However, there is a trend for increased distant failure free survival in the group of patients with positive CDK9. CDK9 No. of Event Censored Median 5 Yr Survival Subject Survival (95% CI) Negative 31 10 (32%) 21 (68%) NA (3.5, 68.1% (47.5%, NA) 82.1%) Positive 36 8 (22%) 28 (78%) NA (NA, 79.7% (62.0%, NA) 89.8%) Figure 3: Locoregional recurrence-free survival. Figure 3 illustrates locoregional recurrence-free survival curves for patients with CDK9 positive versus CDK9 negative tumors. There is no statistically significant or observable difference in the two survival curves. Median No. of Survival CDK9 Subject Event Censored (95% CI) 5 Yr Survival Negative 31 2 (6%) 29 (94%) NA (NA, NA) 92.7% (73.7%, 98.2%) Positive 36 2 (6%) 34 (94%) NA (NA, NA) 97.1% (80.9%, 99.6%) Figure 4: Recurrence-free survival. Figure 4 shows curves comparing recurrence-free survival in patients with CDK9 positive versus CDK9 negative tumors. There is no statistically significant or observable difference in the two survival curves. CDK9 No. of Event Censored Median 5 Yr Survival Subject Survival (95% CI) Negative 31 10 (32%) 21 (68%) NA (3.1, 68.1% (47.5%, NA) 82.1%) Positive 36 10 (28%) 26 (72%) NA (8.3, 77.0% (59.2%, NA) 87.8%) Figure 5: Event-free survival. Figure 5 shows curves comparing event-free survival in patients with CDK9 positive versus CDK9 negative tumors. There is no statistically significant or observable difference in the two survival curves. Median No. of Survival CDK9 Subject Event Censored (95% CI) 5 Yr Survival Negative 31 13 (42%) 18 (58%) NA (2.8, 59.3% (39.5%, NA) 74.6%) Positive 36 13 (36%) 23 (64%) NA (7.4, 74.7% (57.0%, NA) 86.0%)
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|Title Annotation:||Research Article; Cyclin-dependent kinase 9|
|Author:||Schlafstein, Ashley J.; Withers, Allison E.; Rudra, Soumon; Danelia, Diana; Switchenko, Jeffrey M.;|
|Publication:||International Journal of Breast Cancer|
|Date:||Jan 1, 2018|
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