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Journal articles on the topic 'Cancer colorectal – Cytologie'

Author: Grafiati

Published: 26 October 2024

Last updated: 31 July 2025

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1

Lucha, Paul A., Romeo Ignacio, Dennis Rowley, and Michael Francis. "The Incidence of Positive Peritoneal Cytology in Colon Cancer: A Prospective Randomized Blinded Trial." American Surgeon 68, no. 11 (2002): 1018–21. http://dx.doi.org/10.1177/000313480206801117.

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Many investigators have attempted to explain the suspected increased incidence of port site metastasis in patients undergoing laparoscopic colorectal resections for cancer with animal models in which cancer is simulated by injection of a tumor slurry into the peritoneal cavity. This approach makes the basic assumption that all patients with colorectal malignancies have viable cancer cells freely circulating within the peritoneal cavity. Recent reports in open colorectal resections have conflicting results. Some suggest that the true incidence is negligible and related to advanced-stage cancers

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2

Kobayashi, Hirotoshi, Kenjiro Kotake, Kenichi Sugihara, and Yoichi Ajioka. "Peritoneal lavage cytology in patients with curative resection for stage II and III colorectal cancer: A multi-institutional prospective study." Journal of Clinical Oncology 42, no. 3_suppl (2024): 11. http://dx.doi.org/10.1200/jco.2024.42.3_suppl.11.

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11 Background: Although various prognostic factors in patients with colorectal cancer has been reported, the usefulness of intraoperative lavage cytology in patients with colorectal cancer is controversial. The aim of this study was to clarify the usefulness of intraoperative lavage cytology in patients with curative resection for pSage II-III colorectal cancer in a prospective multicenter study. Methods: The 20 member hospitals of the Japanese Society for the Cancer of the Colon and Rectum prospectively registered the patients diagnosed as stage II or III colorectal cancer preoperatively betw

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3

Potjo, Lehlohonolo, Mahlomola Kutoane, and Isabel Nyangu. "Assessment of the Knowledge and Utilization of Cervical Cancer Screening Services Amongst Women in Maseru District Lesotho." American Journal of Nursing and Health Sciences 6, no. 2 (2025): 19–25. https://doi.org/10.11648/j.ajnhs.20250602.11.

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Cancer of the cervix can be prevented and cured, can be circumvented using vaccines and screening and can be cured when recognised earlier before progress. It is imperceptibly becoming a rare disease in many developed countries; while countries in sub-Saharan Africa remain negatively impacted. Universally, cervical cancer is the third most generic cancer ranking after breast and colorectal cancer and the fourth most pervasive cause of cancer death ranking below breast, lung, and colorectal cancer. Cervical cancer incidence in Africa is high though it varies considerably by region. The predomin

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Tatomirovic, Zeljka, Vesna Skuletic, Ivana Tufegdzic, Ljiljana Tomic, Jelena Dzambas, and Dino Tarabar. "The value of brush cytology and biopsy for the diagnosis of colorectal cancer." Vojnosanitetski pregled 74, no. 7 (2017): 659–65. http://dx.doi.org/10.2298/vsp160112115t.

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Background/Aim. Although it is well-known the high sensitivity of brush cytology for the diagnosis of colorectal adenocarcinoma, this kind of diagnostics is not routinely used, and for the past years it has even been declining. The purpose of this study was to evaluate the value of brush cytology for the diagnosis of colorectal carcinoma, by comparison the results of brush cytology and biopsy, and then the results of both diagnostic methods with the final patohistological diagnosis of colorectal resection. Methods. This retrospective study included 173 patients with brush cytology of colorecta

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Bhasin, DeepakK, Arvind Rajwanshi, Rakesh Kochhar, and SatishK Mehta. "BRUSH CYTOLOGY FOR COLORECTAL CANCER." Lancet 333, no. 8647 (1989): 1133–34. http://dx.doi.org/10.1016/s0140-6736(89)92404-5.

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6

Banerjee, Anjan, and Matt Seymour. "Peritoneal cytology in colorectal cancer." Diseases of the Colon & Rectum 42, no. 5 (1999): 686–87. http://dx.doi.org/10.1007/bf02234153.

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7

Jacobi, Elizabeth M., Gene Landon, Russell R. Broaddus, and Sinchita Roy-Chowdhuri. "Evaluating Mismatch Repair/Microsatellite Instability Status Using Cytology Effusion Specimens to Determine Eligibility for Immunotherapy." Archives of Pathology & Laboratory Medicine 145, no. 1 (2020): 46–54. http://dx.doi.org/10.5858/arpa.2019-0398-oa.

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Context.— The approval of pembrolizumab for treatment of patients with microsatellite instability-high (MSI-H) or mismatch repair–deficient (dMMR) advanced cancers has led to increased requests for MSI and/or MMR immunoperoxidase (IPOX) testing. Diagnoses for patients with advanced-stage cancer are frequently made from cytology specimens. Objective.— To investigate the feasibility of using cell block (CB) preparations of effusions for MMR IPOX evaluation. Design.— Surgical pathology cases of colorectal and endometrial carcinomas with known MMR/MSI status and matched effusions with available CB

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8

Vilella, Angels, Magdalena Garcia-Bonafe, Carlos Dolz, Hernan Andreu, Alvaro Brotons, and Javier Ibarra. "Cytologic Study for Endoscopic Diagnosis of Colorectal Cancer." Gastrointestinal Endoscopy 61, no. 5 (2005): AB266. http://dx.doi.org/10.1016/s0016-5107(05)01395-7.

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9

Zhang, Min, Lin Li, Ping Liu, and C. D’Arcy J. Holman. "Green tea for the prevention of cancer: evidence of field epidemiology." Functional Foods in Health and Disease 2, no. 10 (2012): 339. http://dx.doi.org/10.31989/ffhd.v2i10.79.

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Background: Tea is derived from the leaf of Camellia sinensis, a natural beverage widely consumed around the world. Geological and botanical evidence suggests that the tea plant originated from China. Varying methods of processing tea leaves lead to green tea, black tea, or Oolong tea, which differ in their concentrations of polyphenols. Green tea polyphenols appear to have anti-tumorigenic properties, and form 30-40% of the dry weight of green tea compared with only 3-10% of black tea. Numerous studies in multiple animal models and different cancer cell lines have demonstrated the anti-tumori

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10

Alyautdina, O. S., and O. V. Sinicina. "Intraepithelial colorectal lesions in women with cervical infection with human papillomavirus." Clinical Medicine (Russian Journal) 96, no. 5 (2018): 459–62. http://dx.doi.org/10.18821/0023-2149-2018-96-5-459-462.

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Human papillomavirus (HPV)-induced cervical cancer and colorectal cancer are closely related. Women with cervical HPV infection have more than 3 times the high risk of anal infection. Some studies indicate a persistent relationship between colorectal cancer caused by HPV infection and a similar genotype of cervical cancer. In our research, using the method of liquid cytology, a comparison of colorectal HPV lesion in patients with dysplasia of the cervix in history and a control group without pathology of the cervix was carried out. The cytological study was performed using the method of liquid

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11

FURUYAMA, Nobuaki. "Direct vision brushing cytology of colorectal cancer." Journal of the Japanese Society of Clinical Cytology 24, no. 2 (1985): 157–64. http://dx.doi.org/10.5795/jjscc.24.157.

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12

Turner, Roderick R., Dean T. Nora, Steven D. Trocha, and Anton J. Bilchik. "Colorectal Carcinoma Nodal Staging." Archives of Pathology & Laboratory Medicine 127, no. 6 (2003): 673–79. http://dx.doi.org/10.5858/2003-127-673-ccns.

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Abstract Context.—Nodal staging accuracy is important for prognosis and selection of patients for chemotherapy. Sentinel lymph node (SLN) mapping improves staging accuracy in breast cancer and melanoma and is being investigated for colorectal carcinoma. Objective.—To assess pathologic aspects of SLN staging for colon cancer. Design.—Sentinel lymph nodes were identified with a dual surgeon-pathologist technique in 51 colorectal carcinomas and 12 adenomas. The frequency of cytokeratin (CK)–positive cells in mesenteric lymph nodes, both SLN and non-SLN, was determined along with their immunohisto

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13

Cortes-Guiral, Delia, and Olivier Glehen. "Expanding Uses of HIPEC for Locally Advanced Colorectal Cancer: A European Perspective." Clinics in Colon and Rectal Surgery 33, no. 05 (2020): 253–57. http://dx.doi.org/10.1055/s-0040-1713742.

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AbstractLocally advanced colorectal cancer is a challenge for surgeons and medical oncologist; 10 to 20% colorectal cancer debut as locally advanced disease, with tumors extending through the colon wall with perforation and/or invasion of adjacent organs or structures. Those locally advanced tumors have a worse prognostic at any stage due not only to systemic dissemination but also in a high percentage of patients, to locoregional recurrence, in fact, peritoneal carcinomatosis of colorectal origin is so predictable that we can assess the risk for each patient according to some histopathologica

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14

Fitzgerald, N., C. Gauvreau, S. Memon, et al. "The OncoSim Cancer Simulation Platform: A Tool to Project the Population Effects of Cancer Control Interventions in Canada." Journal of Global Oncology 4, Supplement 2 (2018): 77s. http://dx.doi.org/10.1200/jgo.18.20300.

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Background: Cancer control interventions exert their effects over multiple decades. To evaluate diverse and competing opportunities to reduce future cancer burden it is desirable to understand long-term effects prior to any new program implementation or significant change. Internationally, modeling is becoming an accepted source of planning information for decision-makers. Aim: We will describe the construction and use of the OncoSim microsimulation model, which was developed to evaluate cancer control strategies in Canada. Methods: OncoSim is a suite of models (cancers of the lung, colorectum

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15

Woo, Pauline P. S., Jane J. Kim, and Gabriel M. Leung. "What Is the Most Cost-Effective Population-Based Cancer Screening Program for Chinese Women?" Journal of Clinical Oncology 25, no. 6 (2007): 617–24. http://dx.doi.org/10.1200/jco.2006.06.0210.

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Purpose To develop a policy-relevant generalized cost-effectiveness (CE) model of population-based cancer screening for Chinese women. Methods Disability-adjusted life-years (DALYs) averted and associated screening and treatment costs under population-based screening using cervical cytology (cervical cancer), mammography (breast cancer), and fecal occult blood testing (FOBT), sigmoidoscopy, FOBT plus sigmoidoscopy, or colonoscopy (colorectal cancer) were estimated, from which average and incremental CE ratios were generated. Probabilistic sensitivity analysis was undertaken to assess stochasti

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16

Brouwer, Richard, Alistair MacDonald, Ronnie Matthews, James Gunn, John R. Monson, and John E. Hartley. "Brush Cytology for the Diagnosis of Colorectal Cancer." Diseases of the Colon & Rectum 52, no. 4 (2009): 598–601. http://dx.doi.org/10.1007/dcr.0b013e3181a0ad44.

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17

Barsouk, Adam, Kalyan Saginala, John Sukumar Aluru, Prashanth Rawla, and Alexander Barsouk. "US Cancer Screening Recommendations: Developments and the Impact of COVID-19." Medical Sciences 10, no. 1 (2022): 16. http://dx.doi.org/10.3390/medsci10010016.

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The USPSTF and ACS recommend screening for breast, cervical, colorectal, and lung cancers. Rates of cancer screening, diagnosis, and treatment decreased significantly in the US and other developed nations during the height of the COVID-19 pandemic and lockdown (April 2020) and have since recovered, although not to baseline levels in many cases. For breast cancer, the USPSTF recommends biennial screening with mammography for women aged 50–74, while the ACS recommends annual screening for women aged 45–54, who may transition to biennial after 55. Minority and rural populations have lower rates o

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18

Diaz-Mercedes, Sherley, Ivan Archilla, Sara Lahoz, et al. "Cytology Smears: An Enhanced Alternative Method for Colorectal Cancer pN Stage—A Multicentre Study." Cancers 14, no. 24 (2022): 6072. http://dx.doi.org/10.3390/cancers14246072.

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Stage II colorectal cancer (CRC) recurrence remains a clinical problem. Some of these patients are true stage III CRC with a pN0 pathology stage. This large prospective multicentre cohort study aimed at evaluating the diagnostic ability of lymph node (LN) cytology smears to perform the pN stage and compare it with the conventional haematoxylin and eosin (H&E) pathology pN stage. Additionally, we used the One-Step Nucleic Acid Amplification (OSNA), a high-sensitive molecular method of LN staging. A total of 3936 fresh LNs from 217 CRC surgical specimens were examined by three methods, H&amp

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19

Kim, Hyung Kyung, Eunkyung Han, Jeonghyo Lee, et al. "Artificial-Intelligence-Assisted Detection of Metastatic Colorectal Cancer Cells in Ascitic Fluid." Cancers 16, no. 5 (2024): 1064. http://dx.doi.org/10.3390/cancers16051064.

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Ascites cytology is a cost-effective test for metastatic colorectal cancer (CRC) in the abdominal cavity. However, metastatic carcinoma of the peritoneum is difficult to diagnose based on biopsy findings, and ascitic aspiration cytology has a low sensitivity and specificity and a high inter-observer variability. The aim of the present study was to apply artificial intelligence (AI) to classify benign and malignant cells in ascites cytology patch images of metastatic CRC using a deep convolutional neural network. Datasets were collected from The OPEN AI Dataset Project, a nationwide cytology da

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20

Yokomizo, H., and Y. Takii. "Significance of Intraoperative Periotoneal Lavage Cytology in Colorectal Cancer." Nippon Daicho Komonbyo Gakkai Zasshi 60, no. 1 (2007): 8–12. http://dx.doi.org/10.3862/jcoloproctology.60.8.

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21

Gozalan, Ugur, Ahmet Cinar Yasti, Yunus Nadi Yuksek, Erhan Reis, and Nuri Aydin Kama. "Peritoneal cytology in colorectal cancer: incidence and prognostic value." American Journal of Surgery 193, no. 6 (2007): 672–75. http://dx.doi.org/10.1016/j.amjsurg.2006.10.020.

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22

Fujii, Shoichi, Hiroshi Shimada, Shigeru Yamagishi, et al. "Evaluation of intraperitoneal lavage cytology before colorectal cancer resection." International Journal of Colorectal Disease 24, no. 8 (2009): 907–14. http://dx.doi.org/10.1007/s00384-009-0733-z.

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23

Rekhraj, Sushil, Omer Aziz, Emmanouil Zacharakis, and Paul Ziprin. "Peritoneal cytology in colorectal cancer: incidence and prognostic value." American Journal of Surgery 196, no. 4 (2008): 617–18. http://dx.doi.org/10.1016/j.amjsurg.2007.10.011.

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24

Gordon, Ian L., Eric B. Rypins, Raymond B. Wuerker, and James J. Jakowatz. "Cytologic detection of colorectal cancer after administration of oral lavage solution." Cancer 68, no. 1 (1991): 106–10. http://dx.doi.org/10.1002/1097-0142(19910701)68:1<106::aid-cncr2820680121>3.0.co;2-3.

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25

Wang, Xin, Xiaoxia Qin, Jian Zhang, Yankai Zhao, and Yingchao Gao. "Screening for colorectal cancer: Study on the shedding cells of feces." Cytojournal 21 (April 25, 2024): 16. http://dx.doi.org/10.25259/cytojournal_107_2023.

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Objective: The objective of this study was to explore the enrichment efficiency of an improved fecal exfoliated cell enrichment method and its application in colorectal cancer screening. Material and Methods: Samples were collected from a cohort of 100 colorectal cancer patients being treated at the First Hospital of Hebei Medical University from January 2021 to June 2022. Patient samples were equally divided between control and experimental groups corresponding to the enrichment method being applied to the fecal exfoliated cells. Samples consisted of natural stool and bowel cleansing enema so

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26

Marmarelis, Melina, Lawrence N. Shulman, Joseph O. Jacobson, and Andrew David Norden. "Molecular testing for colorectal and lung cancer at an academic cancer center satellite site: Opportunities for improvement." Journal of Clinical Oncology 34, no. 7_suppl (2016): 229. http://dx.doi.org/10.1200/jco.2016.34.7_suppl.229.

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229 Background: Given their prevalence, colorectal and lung cancer are treated in both academic and community settings. Appropriate use of targeted therapies in these diseases is challenging given the need for biomarker testing prior to use. Rapidly changing practice standards, limited resources, and barriers to tissue processing make this particularly challenging in the community. We examined the use of biomarker testing and targeted therapies in colorectal and lung cancer at one of the Dana-Farber Cancer Institute satellite sites. Methods: Patients who had their first visit for colorectal ca

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27

Moon, Chulso, Maxie Gordon, David Moon, and Thomas Reynolds. "Microsatellite Instability Analysis (MSA) for Bladder Cancer: Past History and Future Directions." International Journal of Molecular Sciences 22, no. 23 (2021): 12864. http://dx.doi.org/10.3390/ijms222312864.

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Microsatellite instability (MSI), the spontaneous loss or gain of nucleotides from repetitive DNA tracts, is a diagnostic phenotype for gastrointestinal, endometrial, colorectal, and bladder cancers; yet a landscape of instability events across a wider variety of cancer types is beginning to be discovered. The epigenetic inactivation of the MLH1 gene is often associated with sporadic MSI cancers. Recent next-generation sequencing (NGS)-based analyses have comprehensively characterized MSI-positive (MSI+) cancers, and several approaches to the detection of the MSI phenotype of tumors using NGS

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28

Spinelli, Irene, Simona Moffa, Francesca Fianchi, et al. "Lynch Syndrome and Thyroid Nodules: A Single Center Experience." Genes 15, no. 7 (2024): 859. http://dx.doi.org/10.3390/genes15070859.

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Background: Lynch syndrome (LS) is a genetic disease with increased risk of colorectal cancer and other malignancies. There are few reported cases of thyroid cancer in LS patients. The aim of this study is to investigate the presence of thyroid nodules in LS patients and to explore their association with the genetic features of the disease. Methods: A retrospective and descriptive analysis was conducted to include all LS patients followed at the CEMAD (Centro Malattie Apparato Digerente) of Fondazione Policlinico Universitario A. Gemelli IRCCS. The characteristics of LS disease, gene mutations

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29

Halpern, Marisa, Rivka Gal, Lea Rath-Wolfson, Rumelia Koren, Ruben Weil, and Arieh Avni. "Brush Cytology and Biopsy in the Diagnosis of Colorectal Cancer." Acta Cytologica 41, no. 3 (1997): 628–32. http://dx.doi.org/10.1159/000332675.

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30

Stadler, Z. K., R. Stern, V. Devlin, et al. "Adherence to extracolonic cancer screening in Lynch syndrome kindreds." Journal of Clinical Oncology 27, no. 15_suppl (2009): 1513. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.1513.

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1513 Introduction: In addition to colorectal cancer (CRC), Lynch syndrome (LS) patients are at increased risk of extracolonic malignancies including endometrial (EC), ovarian (OC), upper gastrointestinal and urothelial tract cancers. Although the efficacy of extracolonic cancer screening in LS has not been clearly demonstrated, multi-organ screening is routinely recommended for LS patients (Lindor et al., JAMA 2006). Anecdotal evidence suggests that adherence to such screening may be inferior to CRC screening. Methods: 35 adults, identified in the context of genetic counseling and testing (GCT

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31

Bitsianis, Stefanos, Ioannis Mantzoros, Elissavet Anestiadou та ін. "Effect of Intraperitoneal Chemotherapy with Regorafenib on IL-6 and TNF-α Levels and Peritoneal Cytology: Experimental Study in Rats with Colorectal Peritoneal Carcinomatosis". Journal of Clinical Medicine 12, № 23 (2023): 7267. http://dx.doi.org/10.3390/jcm12237267.

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Cytoreductive surgery (CRS), combined with hyperthermic intraperitoneal chemotherapy, has significantly improved survival outcomes in patients with peritoneal carcinomatosis from colorectal cancer (CRC). Regorafenib is an oral agent administered in patients with refractory metastatic CRC. Our aim was to investigate the outcomes of intraperitoneal administration of regorafenib for intraperitoneal chemotherapy (IPEC) or/and CRS in a rat model of colorectal peritoneal metastases regarding immunology and peritoneal cytology. A total of 24 rats were included. Twenty-eight days after carcinogenesis

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32

Majidova, N. B., C. F. Gurbanova, and F. A. Gurbanova. "Importance of Cytological Screening in the Diagnosis of Cervical Diseases." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 7, no. 3 (2022): 159–64. http://dx.doi.org/10.26693/jmbs07.03.159.

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The purpose of the study was to compare the conventional Pap smear with liquid-based cytology in the early diagnosis of cervical diseases. Materials and methods. The study included 150 women between the ages of 18 and 73 with cervical diseases. The comparison was held on the basis of the results of histology of liquid-based and conventional Pap smears taken from cervix. Bethesda classification was used to make the diagnosis. Diagnostic performance was calculated in terms of sensitivity, specificity, positive predictive value and negative predictive value. Results and discussion. During the sen

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33

Sugarbaker, Paul H., Tom Deng, and David Chang. "Peritoneal cytology as an indicator of peritoneal metastases in colorectal cancer." Journal of Surgical Oncology 124, no. 3 (2021): 361–66. http://dx.doi.org/10.1002/jso.26520.

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34

Nasu, Jiro, Kenjiro Kotake, Yasuo Koyama, et al. "Evaluation of Peritoneal Lavage Cytology in Patients with Advanced Colorectal Cancer." Japanese Journal of Gastroenterological Surgery 28, no. 10 (1995): 1991–94. http://dx.doi.org/10.5833/jjgs.28.1991.

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35

Salamanca, Isabel María Gallarín, M. T. Espín Jaime, J. M. Moran Penco, and J. Salas Martínez. "Role of Peritoneal Cytology in Patients with Early Stage Colorectal Cancer." Pathology & Oncology Research 26, no. 2 (2019): 1325–29. http://dx.doi.org/10.1007/s12253-019-00706-0.

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36

Kobayashi, Hirotoshi, Kenjiro Kotake, and Kenichi Sugihara. "Prognostic significance of peritoneal lavage cytology in patients with colorectal cancer." International Journal of Clinical Oncology 18, no. 3 (2012): 411–17. http://dx.doi.org/10.1007/s10147-012-0394-8.

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37

Kanellos, I., H. Demetriades, E. Zintzaras, A. Mandrali, I. Mantzoros, and D. Betsis. "Incidence and Prognostic Value of Positive Peritoneal Cytology in Colorectal Cancer." Diseases of the Colon & Rectum 46, no. 4 (2003): 535–39. http://dx.doi.org/10.1007/s10350-004-6595-0.

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38

Niedzielska, Julia, and Tomasz Jastrzębski. "Carcinoembryonic Antigen (CEA): Origin, Role in Oncology, and Concentrations in Serum and Peritoneal Fluid." Journal of Clinical Medicine 14, no. 9 (2025): 3189. https://doi.org/10.3390/jcm14093189.

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CEA (carcinoembryonic antigen), which belongs to the acidic glycoproteins, is primarily produced during the fetal period. Following this stage, low levels of CEA are considered physiological, while elevated concentrations are associated with a range of both benign and malignant pathologies. The liver plays a key role in CEA metabolism. The most common material used to determine CEA concentrations by various techniques is blood, and measuring CEA in peritoneal fluid holds clinical value. CEA has been found to contribute to carcinogenesis, metastasis, and treatment resistance. Therefore, its ser

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39

Sant, Milena, Gemma Gatta, Fulvia Valente, et al. "The Itacare Study." Tumori Journal 83, no. 1 (1997): 17–24. http://dx.doi.org/10.1177/030089169708300106.

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ITACARE is a collaborative study on the survival of Italian cancer patients diagnosed in the period 1978–1989. The study involves 11 Italian population-based cancer registries (CRs) (Firenze, Forlì-Ravenna, Genova, Latina, Modena, Parma, Ragusa, Torino, Varese, the childhood CR of Piedmont and the colorectal CR of Modena), and its principal aim is to identify and analyze possible differences between the areas covered by the CRs. This article describes the ITACARE database. Ten percent of the Italian population is covered by the participating CRs, most of which are located in the northern part

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Lee, Chul Seung, and In Kyu Lee. "Use of ascites CEA as a predictive value for distant metastasis in high-risk stage II and III colorectal cancer." Journal of Clinical Oncology 40, no. 4_suppl (2022): 164. http://dx.doi.org/10.1200/jco.2022.40.4_suppl.164.

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164 Background: Adjuvant chemotherapy in patients with high-risk stage II and III colorectal cancer prevents recurrence by eliminating minimal residual disease. However, patients who are at high risk of recurrence after completing standard adjuvant therapy are currently unknown. Although ascites CEA level has been associated with long-term oncologic outcomes, the clinical significance of ascites CEA in high-risk stage II and stage III colorectal cancer (CRC) has not yet been described. The present study aimed to determine the long-term oncologic impacts of ascites CEA level after curative colo

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41

Sato, Kentaro, Ken Imaizumi, Hiroyuki Kasajima, et al. "Comparison of prognostic impact between positive intraoperative peritoneal and lavage cytologies in colorectal cancer." International Journal of Clinical Oncology 26, no. 7 (2021): 1272–84. http://dx.doi.org/10.1007/s10147-021-01918-8.

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42

Chen, Y. L. "The diagnosis of colorectal cancer with cytologic brushings under direct vision at fiberoptic colonoscopy." Diseases of the Colon & Rectum 30, no. 5 (1987): 342–44. http://dx.doi.org/10.1007/bf02555451.

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43

Myrhøj, T., M. B. Andersen, and I. Bernstein. "Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer." Familial Cancer 7, no. 4 (2008): 303–7. http://dx.doi.org/10.1007/s10689-008-9193-9.

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44

Nishikawa, Takeshi, Toshiaki Watanabe, Eiji Sunami, Nelson H. Tsuno, Joji Kitayama, and Hirokazu Nagawa. "Prognostic Value of Peritoneal Cytology and the Combination of Peritoneal Cytology and Peritoneal Dissemination in Colorectal Cancer." Diseases of the Colon & Rectum 52, no. 12 (2009): 2016–21. http://dx.doi.org/10.1007/dcr.0b013e3181b4c46e.

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45

Knudsen, Amy B., Amy Trentham-Dietz, Jane J. Kim, et al. "Estimated US Cancer Deaths Prevented With Increased Use of Lung, Colorectal, Breast, and Cervical Cancer Screening." JAMA Network Open 6, no. 11 (2023): e2344698. http://dx.doi.org/10.1001/jamanetworkopen.2023.44698.

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ImportanceIncreased use of recommended screening could help achieve the Cancer Moonshot goal of reducing US cancer deaths.ObjectiveTo estimate the number of cancer deaths that could be prevented with a 10–percentage point increase in the use of US Preventive Services Task Force (USPSTF)-recommended screening.Design, Setting, and ParticipantsThis decision analytical model study is an extension of previous studies conducted for the USPSTF from 2018 to 2023. This study simulated contemporary cohorts of US adults eligible for lung, colorectal, breast, and cervical cancer screening.ExposuresAnnual

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46

Sakata, Kazuya, Masaki Okuyama, and Ken Konishi. "Clinical Value of Peritoneal Cytology of Ascites in Patients with Curative Colorectal Cancer." Nippon Daicho Komonbyo Gakkai Zasshi 67, no. 7 (2014): 437–41. http://dx.doi.org/10.3862/jcoloproctology.67.437.

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Mikhail, Hany M. S., Abdrabou N. Mashhour, Sameh G. AbdElghany, Ahmed F. A. Farag, and Amal A. M. Hareedy. "Correlation between peritoneal lavage cytology and tumour stage in patients with colorectal cancer." Arab Journal of Gastroenterology 16, no. 1 (2015): 14–19. http://dx.doi.org/10.1016/j.ajg.2015.02.002.

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Coget, Julien, France Blanchard, Aude Lamy, et al. "Cytologic and molecular characterizations of CTC detected in patients with metastatic colorectal carcinomas." Journal of Clinical Oncology 30, no. 4_suppl (2012): 485. http://dx.doi.org/10.1200/jco.2012.30.4_suppl.485.

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Abstract:

485 Background: Circulating tumor cells (CTC) appear to be associated with poor prognosis in patients with metastatic colorectal cancer (mCRC). ScreenCell technology, which is based on the separation of CTCs from other circulating cells by blood filtration, could allow clinical use of this new biomarker. The aim of our study was to demonstrate the feasibility of CTC filtration in a clinical situation and to compare CTC cytological/molecular characterizations. Methods: Sampling of venous blood was performed in 39 patients with mCRC before starting chemotherapy regimen. For cytology, blood were

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Barwick, Kenneth, Yeouda Edoute, Ehud Malberger, Jesse Lachter, and Osnat Toledano. "Fine-Needle Aspiration Cytology of Abdominal Wall Scar Lesions for Diagnosing Recurrent Colorectal Cancer." Journal of Clinical Gastroenterology 13, no. 4 (1991): 463–64. http://dx.doi.org/10.1097/00004836-199108000-00021.

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Jeevanandam, Valluvan, Michael R. Treat, and Kenneth A. Forde. "A comparison of direct brush cytology and biopsy in the diagnosis of colorectal cancer." Gastrointestinal Endoscopy 33, no. 5 (1987): 370–71. http://dx.doi.org/10.1016/s0016-5107(87)71641-1.

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