22 results on '"Ozdemir, N. Y."'
Search Results
2. Evaluation of prognostic factors and treatment in advanced small bowel adenocarcinoma: report of a multi-institutional experience of Anatolian Society of Medical Oncology (ASMO)
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Aydin, D., Mehmet Sendur, Kefeli, U., Unal, O. U., Tastekin, D., Akyol, M., Tanrikulu, E., Ciltas, A., Ustaalioglu, B. B., Dede, D. S., Esbag, O., Inal, A., Bilir, C., Bilici, A., Harputlu, H., Berk, V., Sevinc, A., Ozdemir, N. Y., Yildirim, E., Sonkaya, A., Ustaoglu, M. A., Gumus, M., Aydin, D., Department of Medical Oncology, Dr. Lutfi Kirdar Kartal Education and Research Hospital, Semsi Denizer Street, Istanbul, 34890, Turkey, Sendur, M.A., Department of Medical Oncology, Numune Education and Research Hospital, Ankara, Turkey, Kefeli, U., Department of Medical Oncology, School of Medicine, Kocaeli University, Kocaeli, Turkey, Unal, O.U., Department of Medical Oncology, Faculty of Medicine, Dokuz EylulUniversity, Izmir, Turkey, Tastekin, D., Department of Medical Oncology, Faculty of Medicine, Selcuk University Meram, Konya, Turkey, Akyol, M., Department of Medical Oncology, Faculty of Medicine, Katip Celebi University, Izmir, Turkey, Tanrikulu, E., Department of Medical Oncology, Faculty of Medicine, Marmara University, Istanbul, Turkey, Ciltas, A., Department of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey, Ustaalioglu, B.B., Department of Medical Oncology, Haydar- Pasa Education and Research Hospital, Istanbul, Turkey, Dede, D.S., Department of Medical Oncology, Faculty of Medicine, Yildirim Beyazit University, Ankara, Turkey, Esbag, O., Ankara Oncology Education and Research Hospital, Department of Medical Oncology, Ankara, Turkey, Inal, A., Department of Medical Oncology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey, Bilir, C., Department of Medical Oncology, Faculty of Medicine, Karaelmas University, Zonguldak, Turkey, Bilici, A., Department of Medical Oncology, Faculty of Medicine, Medipol University, Istanbul, Turkey, Harputlu, H., Department of Medical Oncology, Faculty of Medicine, Inonu University, Malatya, Turkey, Berk, V., Department of Medical Oncology, Faculty of Medicine, Erciyes University, Kayseri, Turkey, Sevinc, A., Department of Medical Oncology, Faculty of Medicine Gaziantep University, Gaziantep, Turkey, Ozdemir, N.Y., Department of Medical Oncology, Numune Education and Research Hospital, Ankara, Turkey, Yildirim, E., Department of Medical Oncology, Dr. Lutfi Kirdar Kartal Education and Research Hospital, Semsi Denizer Street, Istanbul, 34890, Turkey, Sonkaya, A., Department of Medical Oncology, School of Medicine, Kocaeli University, Kocaeli, Turkey, Ustaoglu, M.A., Department of Medical Oncology, Dr. Lutfi Kirdar Kartal Education and Research Hospital, Semsi Denizer Street, Istanbul, 34890, Turkey, and Gumus, M., Department of Medical Oncology, Faculty of Medicine, Bezmialem University, Istanbul, Turkey
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Male ,Chi-Square Distribution ,Time Factors ,Turkey ,Prognostic Factors ,Palliative Care ,Kaplan-Meier Estimate ,Adenocarcinoma ,Middle Aged ,Disease-Free Survival ,Treatment Outcome ,Risk Factors ,Small Bowel Adenocarcinoma ,Antineoplastic Combined Chemotherapy Protocols ,Intestinal Neoplasms ,Intestine, Small ,Multivariate Analysis ,Chemotherapy ,Humans ,Advanced ,Female ,Retrospective Studies - Abstract
WOS: 000388782200027 PubMed ID: 27837629 Purpose: Small bowel adenocarcinoma (SBA) is a rare tumor of the gastrointestinal system with poor prognosis. Since these are rarely encountered tumors, there are limited numbers of studies investigating systemic treatment in advanced SBA. The purpose of this study was to evaluate the prognostic factors and systemic treatments in patients with advance SBA. Methods: Seventy-one patients from 18 Centers with advanced SBA were included in the study. Fifty-six patients received one of the four different chemotherapy regimens as first-line therapy and 15 patients were treated with best supportive care (BSC). Results: Of the 71 patients, 42 (59%) were male and 29 (41%) female with a median age of 56 years. Median follow-up duration was 14.3 months. The median progression free survival (PFS) and overall survival (OS) were 7 and 13 months, respectively (N=71). In patients treated with FOLFOX (N=18), FOLFIRI (N=11), cisplatin-5-fluoroura-cil/5-FU (N=17) and gemcitabine alone (N=10), median PFS was 7, 8, 8 and 5 months, respectively, while median OS was 15, 16, 15 and 11 months, respectively. No significant differences between chemotherapy groups were noticed in terms of PFS and OS. Univariate analysis revealed that chemotherapy administration, de novo metastatic disease, ECOG PS 0 and 1, and overall response to therapy were significantly related to improved outcome. Only overall response to treatment was found to be significantly prognostic in multivariate analysis (p = 0.001). Conclusions: In this study, overall response to chemotherapy emerged as the single significant prognostic factor for advanced SBAs. Platin and irinotecan based regimens achieved similar survival outcomes in advanced SBA patients.
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- 2016
3. Outcome of 561 non-metastatic triple negative breast cancer patients: Multi-center experience from Turkey
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Budakoglu, B., Altundag, K., SERCAN AKSOY, Kaplan, M. A., Ozdemir, N. Y., Berk, V., Ozkan, M., Algin, E., Kandemir, N., Dogu, G. G., Harputluoglu, H., Arslan, U. Y., Coskun, U., Isikdogan, A., and Oksuzoglu, B.
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cancer patient ,Turkey ,retrospective study ,cisplatin ,Triple Negative Breast Neoplasms ,progesterone receptor ,Turkey (republic) ,systemic therapy ,Breast cancer ,distant metastasis ,cancer diagnosis ,middle aged ,breast carcinoma ,skin and connective tissue diseases ,cancer survival ,multimodality cancer therapy ,disease free survival ,bone metastasis ,combination chemotherapy ,lymph node metastasis ,breast tumor ,capecitabine ,adult ,lung metastasis ,mastectomy ,clinical trial ,Prognosis ,adjuvant chemotherapy ,Survival Rate ,aged ,female ,Receptors, Estrogen ,Lymphatic Metastasis ,cancer grading ,soft tissue metastasis ,Receptors, Progesterone ,estrogen receptor ,overall survival ,premenopause ,prevalence ,Breast Neoplasms ,anthracycline ,medical record ,cancer prognosis ,Article ,Disease-Free Survival ,cancer radiotherapy ,follow up ,Humans ,navelbine ,human ,outcome assessment ,lymph vessel metastasis ,Neoplasm Staging ,Retrospective Studies ,cancer staging ,major clinical study ,tumor recurrence ,axillary lymph node ,clinical feature ,Treatment ,cancer recurrence ,multicenter study ,triple negative breast cancer ,prostaglandin receptor ,epidermal growth factor receptor 2 ,pathology ,Neoplasm Recurrence, Local ,Triple negative ,Follow-Up Studies - Abstract
Purpose: Triple-negative breast cancers account for 15% of breast carcinomas and, when present as early-stage disease, they are associated with higher rates of recurrence and early distant metastasis risk when compared to hormone receptor positive and human epidermal growth factor receptor (HER-2) positive breast cancers. In this study we aimed to explore the basic clinicopathological characteristics, prognostic factors and recurrence patterns of non-metastatic triple negative breast cancer patients. Methods: In this study 561 non-metastatic triple-negative breast cancer female patients admitted to 8 different cancer centers in Turkey between 2000 and 2010 were retrospectively evaluated through their medical records, to identify the basic clinico-pathological characteristics, prognostic factors and recurrence patterns. Results: The ratio of triple-negative breast cancer was 12%. The median age of patients was 48 years, of whom 311 (55.4%) were premenopausal. The majority had early-stage breast cancer at the time of diagnosis (16.8% stage I, 48.1% stage II, 35.1 % stage III) and the most commonly identified variant was invasive ductal carcinoma (84.1%). Grade II and III tumors were 27.1 and 48.5%, respectively. Adjuvant chemotherapy was administered to 90.5% of women and adjuvant radiotherapy to 41.2%. Median patient follow up was 28 months (range 3-290). During the follow up period 134 (23.8%) patients developed metastatic disease. In most of these cases, metastatic sites were bone, soft tissue, and lung. Factors affecting disease free survival (DFS) and overall survival (OS) were age (both p
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- 2014
4. Cisplatin plus docetaxel combination in the first-line treatment of metastatic non-small cell lung cancer
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Kaya, A. O., Buyukberber, S., Dane, F., Isikdogan, A., Ustaalioglu, B. O., Coskun, U., Perran Fulden Yumuk, Dogu, G. G., Ozdemir, N. Y., Sevinc, A., Gumus, M., Ozkan, M., Yildiz, R., Ozturk, B., Yaman, E., and Benekli, M.
- Abstract
Aims. To evaluate activity and toxicity of cisplatin plus docetaxel combination in the first-line treatment of chemotherapy-naive patients with metastatic non-small cell lung cancer.
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- 2010
5. Gemcitabine and Cisplatin Combination Chemotherapy in Triple Negative Metastatic Breast Cancer Previously Treated with a Taxane/Anthracycline Chemotherapy; Multicenter Experience
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OZKAN, M., primary, BERK, V., additional, KAPLAN, M. A., additional, BENEKLI, M., additional, COSKUN, U., additional, BILICI, A., additional, GUMUS, M., additional, ALKIS, N., additional, DANE, F., additional, OZDEMIR, N. Y., additional, COLAK, D., additional, and DIKILITAS, M., additional
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- 2012
- Full Text
- View/download PDF
6. Multiple primary malignant neoplasms: Multi-center results from Turkey
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Babacan, N. A., Aksoy, S., Cetin, B., Ozdemir, N. Y., Benekli, M., Uyeturk, U., Kaplan, M. Ali, Kos, T., Karaca, H., berna oksuzoglu, Zengin, N., Buyukberber, S., [Babacan, N. A.] Cumhuriyet Univ, Fac Med, Dept Med Oncol, Sivas, Turkey -- [Aksoy, S. -- Ozdemir, N. Y. -- Kos, T. -- Zengin, N.] Ankara Numune Training & Res Hosp, Dept Med Oncol, TR-06100 Ankara, Turkey -- [Cetin, B. -- Benekli, M. -- Buyukberber, S.] Gazi Univ, Fac Med, Dept Med Oncol, Ankara, Turkey -- [Uyeturk, U. -- Oksuzoglu, B.] Dr Abdurrahman Yurtaslan Ankara Oncol Educ & Res, Dept Med Oncol, Ankara, Turkey -- [Kaplan, M. Ali] Dicle Univ, Fac Med, Dept Med Oncol, Diyarbakir, Turkey -- [Karaca, H.] Erciyes Univ, Fac Med, Dept Med Oncol, Kayseri, Turkey, Aksoy, Sercan -- 0000-0003-4984-1049, and benekli, mustafa -- 0000-0003-3184-4946
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second primary ,cancer ,chemotherapy ,multiple primary malignancies - Abstract
WOS: 000313394000024, PubMed ID: 23335539, Purpose: Multiple primary malignant neoplasms (MPMNs) are defined as a diagnosis of two or more independent primary malignancies of different histologies/origins in an individual. The frequency of MPMN is being increasing. In this study we aimed to determine the frequency and clinical features of second primary cancers (SPCs). Methods: From January 1990 to December 2010, patients with MPMNs were screened in 5 centers. Data were obtained retrospectively from hospital charts. Results: Three hundred seventy-seven patients with MPMNs were evaluated. The median age at initial cancer diagnosis was 61 years (range 18-88). The median age at second cancer was 64 years (range 20-89). The median time between two cancer diagnoses was 15 months (range 0-504). Male to female ratio was 1.44 (M/F 223/154). The most frequent initial cancer types were head and neck (54 patients, 14.3%), breast (54 patients, 14.3%), and colorectal (43 patients, 11.4%). The most frequent second cancer types were lung (76 patients, 20.2%), colorectal (39 patients, 10.3%) and breast (33 patients, 8.8%). The most common cancer pairs in females were breast-gynecologic cancers (15 patients, 9.7%), colorectal-breast cancers (9 patients, 5.8%) and breast-colorectal cancers (7 patients, 4.5%). The most common cancer pairs in males were head and neck-lung cancers (29 patients, 13%), bladder-lung cancers (9 patients, 4%), and bladder-prostate cancers (7 patients, 3%). The median follow up was 36 months (range 1-595). Conclusion: Physicians should be aware of SPCs probabilities. Newly developed suspicious lesions should be evaluated rigorously. Histopathologic evaluations of suspicious lesions for second tumors should be used extensively if needed. In our series, the most common pairs were breast-gynecologic cancers in females and head and neck-lung cancers in males.
7. Variations in tumor marker levels in metastatic breast cancer patients according to tumor subtypes
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Kos, T., Aksoy, S., Mehmet Sendur, Arik, Z., Civelek, B., Kandemir, N., Ozdemir, N. Y., Zengin, N., and Altundag, K.
8. New treatment trends in small cell carcinoma of the urinary bladder
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Sendur, M. A. N., SERCAN AKSOY, Yazici, O., Akinci, M. B., Ozdemir, N. Y., and Zengin, N.
9. Evaluation of erectile dysfunction risk factors in young male survivors of colorectal cancer
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Sendur, M. A. N., Aksoy, S., Ozdemir, N. Y., Yaman, S., Yazici, O., Muhammed Bulent Akinci, Uncu, D., Zengin, N., and Altundag, K.
10. Can bevacizumab be a new treatment approach in metastatic melanoma?
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Nahit Sendur, M. A., Ozdemir, N. Y., SERCAN AKSOY, Akinci, M. B., and Zengin, N.
11. Tyrosine kinase inhibitors may change the metastatic pattern
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Sendur, M. A. N., SERCAN AKSOY, Ozdemir, N. Y., and Zengin, N.
12. Effect of body mass index on the efficacy of adjuvant tamoxifen in premenopausal patients with hormone receptor positive breast cancer
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Mehmet Sendur, Aksoy, S., Ozdemir, N. Y., Zengin, N., Yazici, O., Sever, A. R., and Altundag, K.
13. Whole body 18F-FDG PET/CT imaging in the detection of primary tumours in patients with a metastatic carcinoma of unknown origin
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Kaya, A. O., Coskun, U., Unlu, M., Akdemir, U. O., Ozdemir, N. Y., Zengin, N., mustafa benekli, Yildiz, R., Yaman, E., Ozturk, B., Gumus, M., Uner, A., Yamac, D., Ucgul, E., and Buyukberber, S.
- Abstract
Purpose: The aim of this study was to evaluate the role of whole body 18F-FDG PET/CT imaging in the detection of primary tumors in patients with a metastatic cancer from an unknown primary site. Methods: The study population consisted of 43 patients with a biopsy proven metastatic disease, negative conventional diagnostic procedures (including CT/MRI/endoscopic procedures) and a whole body 18F-FDG PET/CT examination. Patients' records were retrospectively analyzed. According to the final pathologic diagnoses, rate of detection of the primary tumor site was determined. Additionally, overall patient survival was calculated to evaluate the prognostic value of 18F-FDG PET/CT findings. Results: A primary tumor site was shown by 18F-FDG PET/CT in 24 patients (24/43; 55.8%). In 18 patients 18F-FDG PET/CT scans were negative (18/43; 41.8%). In a patient with an adenocarcinoma metastasis 18F-FDG PET/CT was falsely positive for an inflammatory lesion in the lung. Among the 18F-FDG PET/CT positive and negative groups median overall survival was not significantly different (log-rank p=0.573). Conclusion: Whole body 18F-FDG PET/CT imaging has a high rate of detection of a primary tumor in patients with a carcinoma of unknown origin.
14. Can targeted programmed death-1 antibody be a new treatment approach in breast cancer
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Sendur, M. A. N., SERCAN AKSOY, Demirci, S., Ozdemir, N. Y., Zengin, N., and Altundag, K.
15. Gemcitabine and Cisplatin Combination Chemotherapy in Triple Negative Metastatic Breast Cancer Previously Treated with a Taxane/Anthracycline Chemotherapy; Multicenter Experience
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Nuriye Ozdemir, Coskun U, Ahmet Bilici, Mustafa Benekli, Muhammet Ali Kaplan, Dilsen Colak, Faysal Dane, Metin Ozkan, Necati Alkis, Mustafa Dikilitas, Berk, Mahmut Gumus, Ozkan, M., Berk, V., Kaplan, M. A., Benekli, M., Coskun, U., Bilici, A., Gumus, M., Alkis, N., Dane, F., Ozdemir, N. Y., Colak, D., and Dikilitas, M.
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Adult ,Oncology ,Cancer Research ,medicine.medical_specialty ,Neutropenia ,Anthracycline ,medicine.medical_treatment ,cisplatin ,Breast Neoplasms ,Kaplan-Meier Estimate ,Deoxycytidine ,Disease-Free Survival ,Internal medicine ,Antineoplastic Combined Chemotherapy Protocols ,medicine ,Humans ,Anthracyclines ,Progression-free survival ,Triple-negative breast cancer ,Aged ,Salvage Therapy ,Chemotherapy ,Taxane ,business.industry ,Carcinoma, Ductal, Breast ,gemcitabine ,Combination chemotherapy ,Middle Aged ,EFFICACY ,medicine.disease ,Thrombocytopenia ,Metastatic breast cancer ,Gemcitabine ,Receptors, Estrogen ,Drug Evaluation ,Female ,Taxoids ,metastatic breast cancer ,Receptors, Progesterone ,Triple negative ,business ,medicine.drug - Abstract
This study was aimed to establish clinical efficacy and tolerability of gemcitabine and cisplatin combination in patients with metastatic triple negative breast cancer progressing after anthracycline and taxane based chemotherapies. Thirty-three patients who were given cisplatin and gemcitabine for triple negative and metastatic breast cancer were evaluated retrospectively. A total of 141 cycles were administered with a median 4 cycles per patient. Median follow-up time was 14 months (range, 2-36 months). Objective response rate was 27.3%. Total clinical benefit of the combination was 48.4%. The estimated median progression free survival and median overall survival were 5 months and 14 months, respectively. The most common Grade 3 and 4 toxicity were neutropenia and thrombocytopenia observed in 10 (27.7%) and 9 (24.9%) patients, respectively. The combination of the gemcitabine and cisplatin after taxane/anthracycline is well tolerated and seems to be effective with acceptable toxicity profile.
- Published
- 2012
16. Preoperative platelet-to-lymphocyte ratio is a predictor of prognosis in patients with ampullary carcinoma.
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Demirci NS, Ozdemir NY, Erdem GU, Bozkaya Y, Yazici O, and Zengin N
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- Adult, Aged, Aged, 80 and over, Carcinoma mortality, Carcinoma pathology, Carcinoma surgery, Common Bile Duct Neoplasms mortality, Common Bile Duct Neoplasms pathology, Common Bile Duct Neoplasms surgery, Disease-Free Survival, Female, Humans, Male, Middle Aged, Multivariate Analysis, Neoplasm Invasiveness, Neoplasm Staging, Pancreaticoduodenectomy, Preoperative Period, Prognosis, Proportional Hazards Models, Retrospective Studies, Survival Rate, Ampulla of Vater, Carcinoma blood, Common Bile Duct Neoplasms blood, Lymphocyte Count, Platelet Count
- Abstract
Aim: To emphasize the significance of the platelet-to-lymphocyte ratio (PLR) in estimating the postoperative prognosis or survival measures in patients with carcinoma of the ampulla of Vater., Methods: We retrospectively reviewed 82 patients, who underwent pancreaticoduodenectomy for ampullary carcinoma between July 2001 and April 2014. We investigated the predictive significance of the preoperative PLR for disease-free survival (DFS) or overall survival (OS). The possible correlations between the PLR and clinical or pathological features were also evaluated., Results: The 5-year DFS and OS rates of the patients with carcinoma of the ampulla of Vater after pancreaticoduodenectomy were 51 % and 64 %, respectively. Multivariate analysis revealed a significantly worse OS in patients with a PLR ≥ 212 [hazard ratio (HR): 3.446; 95% confidence interval (CI): 1.4-8.43; p = 0.007], lymphovascular invasion (HR: 2.973; 95% CI: 1.25-7.03; p = 0.013), or pathological stage pT3/4 (HR: 2.761; 95% CI: 1-7.1; p = 0.035). Similarly, DFS was significantly worse in patients with lymphovascular invasion (HR: 2.24; 95% CI: 1.1-4.56; p = 0.025) or stage pT3/4 (HR: 2.243; 95% CI, 1.03-4.84; p = 0.04)., Conclusion: The preoperative PLR shows a predictive significance for the prognosis of postoperative patients with carcinoma of the ampulla of Vater. We suggest that because of its predictive value, the PLR can be used in the development of further approaches to monitor and manage patients with poor prognosis Tab. 4, Fig. 1, Ref. 45).
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- 2018
- Full Text
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17. Variations in tumor marker levels in metastatic breast cancer patients according to tumor subtypes.
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Kos T, Aksoy S, Sendur MA, Arik Z, Civelek B, Kandemir N, Ozdemir NY, Zengin N, and Altundag K
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- Adult, Aged, Aged, 80 and over, Breast Neoplasms classification, Breast Neoplasms metabolism, Carcinoma, Ductal, Breast classification, Carcinoma, Ductal, Breast metabolism, Carcinoma, Lobular classification, Carcinoma, Lobular metabolism, Female, Follow-Up Studies, Humans, Immunoenzyme Techniques, Middle Aged, Neoplasm Invasiveness, Neoplasm Metastasis, Neoplasm Recurrence, Local classification, Neoplasm Recurrence, Local metabolism, Neoplasm Staging, Prognosis, Receptor, ErbB-2 metabolism, Receptors, Estrogen metabolism, Receptors, Progesterone metabolism, Retrospective Studies, Biomarkers, Tumor metabolism, Breast Neoplasms pathology, Carcinoembryonic Antigen metabolism, Carcinoma, Ductal, Breast secondary, Carcinoma, Lobular secondary, Mucin-1 metabolism, Neoplasm Recurrence, Local pathology
- Abstract
Purpose: To investigate whether serum CA 15-3 and CEA levels show differences among subgroups of breast cancer patients at the time of diagnosis of early-stage disease and at disease relapse., Methods: Patients with metastatic breast cancer diagnosed from 2000 to 2010 were retrospectively analyzed. Data were obtained from medical charts. CA 15-3 and CEA levels of patients with metastatic disease at the time of diagnosis or who relapsed during follow-up were evaluated. Four different breast cancer subtypes were defined: estrogen receptor (ER) and/or progesterone receptor (PR) positive and HER-2 negative (luminal A), ER and/or PR positive and HER-2 positive (luminal B), ER and PR negative and HER-2 positive (HER-2 overexpressing) and triple negative (ER, PR and HER-2 negative). Fifty-eight (13.7%) of the patients were metastatic at the time of diagnosis., Results: 423 metastatic breast cancer patients were included. Of the patients, 232 (54.8%) had luminal A disease, 70 (16.5%) luminal B, 53 (12.5%) HER-2 overexpressing, and 68 (16.1%) triple negative disease. Preoperative CA 15-3 levels were raised in 48.1% of the luminal A group, in 42.8% of the luminal B group, in 26.0% of the HER-2 overexpressing group, and in 33.3% of the triple negative group. CA 15-3 levels after relapse were raised in 44.5% of the luminal A group, in 33.3% of the luminal B, in 28.9% of the HER-2 overexpressing, and in 38.8% of the triple negative group. Preoperative CEA levels were elevated in 44.3% of the luminal A group, in 28.5% of the luminal B, in 43.4% of the HER-2 overexpressing, and in 14.3% of the triple negative group. CEA levels after relapse were raised in 60.8%, 54.7%, 51.1%, and 36.0% of the patients in the 4 subgroups, respectively., Conclusion: This study showed that there are differences between the breast cancer subgroups in terms of tumor marker levels in metastatic breast cancer patients. Tumor marker elevation was lower in the triple negative group as compared to the luminal groups. Monitoring CEA levels in luminal A group may be beneficial in determining early relapses. However, this retrospective study requires further prospective confirmative cohort studies.
- Published
- 2013
18. Tyrosine kinase inhibitors may change the metastatic pattern.
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Sendur MA, Aksoy S, Ozdemir NY, and Zengin N
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- Adenocarcinoma enzymology, Adenocarcinoma of Lung, ErbB Receptors antagonists & inhibitors, ErbB Receptors metabolism, Erlotinib Hydrochloride, Female, Humans, Lung Neoplasms enzymology, Middle Aged, Treatment Outcome, Adenocarcinoma drug therapy, Adenocarcinoma secondary, Antineoplastic Agents therapeutic use, Lung Neoplasms drug therapy, Lung Neoplasms pathology, Protein Kinase Inhibitors therapeutic use, Quinazolines therapeutic use, Skin Neoplasms secondary
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- 2013
19. New treatment trends in small cell carcinoma of the urinary bladder.
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Sendur MA, Aksoy S, Yazici O, Akinci MB, Ozdemir NY, and Zengin N
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- Humans, Carcinoma, Small Cell therapy, Urinary Bladder Neoplasms therapy
- Published
- 2012
20. Multiple primary malignant neoplasms: multi-center results from Turkey.
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Babacan NA, Aksoy S, Cetin B, Ozdemir NY, Benekli M, Uyeturk U, Ali Kaplan M, Kos T, Karaca H, Oksuzoglu B, Zengin N, and Buyukberber S
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- Adolescent, Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Neoplasms, Multiple Primary pathology, Neoplasms, Multiple Primary therapy, Retrospective Studies, SEER Program, Turkey epidemiology, Neoplasms, Multiple Primary epidemiology
- Abstract
Purpose: Multiple primary malignant neoplasms (MPMNs) are defined as a diagnosis of two or more indepen-dent primary malignancies of different histologies/origins in an individual. The frequency of MPMN is being increasing. In this study we aimed to determine the frequency and clinical features of second primary cancers (SPCs)., Methods: From January 1990 to December 2010, patients with MPMNs were screened in 5 centers. Data were obtained retrospectively from hospital charts., Results: Three hundred seventy-seven patients with MPMNs were evaluated. The median age at initial cancer diagnosis was 61 years (range 18-88). The median age at second cancer was 64 years (range 20-89). The median time between two cancer diagnoses was 15 months (range 0-504). Male to female ratio was 1.44 (M/F 223/154). The most frequent initial cancer types were head and neck (54 patients, 14.3%), breast (54 patients, 14.3%), and colorectal (43 patients, 11.4%). The most frequent second cancer types were lung (76 patients, 20.2%), colorectal (39 patients, 10.3%) and breast (33 patients, 8.8%). The most common cancer pairs in females were breast-gynecologic cancers (15 patients, 9.7%), colorectal-breast cancers (9 patients, 5.8%) and breast-colorectal cancers (7 patients, 4.5%). The most common cancer pairs in males were head and neck-lung cancers (29 patients, 13%), bladder-lung cancers (9 patients, 4%), and bladder-prostate cancers (7 patients, 3%). The median follow up was 36 months (range 17horbar;595)., Conclusion: Physicians should be aware of SPCs probabilities. Newly developed suspicious lesions should be evaluated rigorously. Histopathologic evaluations of suspicious lesions for second tumors should be used extensively if needed. In our series, the most common pairs were breast-gynecologic cancers in females and head and neck-lung cancers in males.
- Published
- 2012
21. Can bevacizumab be a new treatment approach in metastatic melanoma?
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Sendur MA, Ozdemir NY, Aksoy S, Akinci MB, and Zengin N
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- Bevacizumab, Double-Blind Method, Humans, Melanoma mortality, Melanoma secondary, Angiogenesis Inhibitors therapeutic use, Antibodies, Monoclonal, Humanized therapeutic use, Melanoma drug therapy
- Published
- 2012
22. Mitomycin-C in combination with fluoropyrimidines in the treatment of metastatic colorectal cancer after oxaliplatin and irinotecan failure.
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Alkis N, Demirci U, Benekli M, Yilmaz U, Isikdogan A, Sevinc A, Ozdemir NY, Koca D, Yetisyigit T, Kaplan MA, Uncu D, Unek T, and Gumus M
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- Adult, Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols administration & dosage, Antineoplastic Combined Chemotherapy Protocols adverse effects, Camptothecin administration & dosage, Camptothecin analogs & derivatives, Colorectal Neoplasms mortality, Colorectal Neoplasms pathology, Female, Fluorouracil administration & dosage, Humans, Irinotecan, Leucovorin administration & dosage, Male, Middle Aged, Mitomycin administration & dosage, Neoplasm Metastasis, Organoplatinum Compounds administration & dosage, Oxaliplatin, Tegafur administration & dosage, Uracil administration & dosage, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Colorectal Neoplasms drug therapy, Fluorouracil therapeutic use, Mitomycin therapeutic use, Salvage Therapy
- Abstract
Purpose: To retrospectively evaluate the efficacy and tolerability of mitomycin-C (MMC) in combination with fluoropyrimidines as salvage 3rd -or 4th-line therapy in metastatic colorectal cancer (MCRC) patients., Methods: All patients in this study had previously failed oxaliplatin and irinotecan-based chemotherapy. Patients were treated with MMC (6 mg/m(2) intravenously/i.v.) on day 1 in combination with either oral UFT (500 mg/m(2)) and oral leucovorin (LV) (30 mg) on days 1-14 every 3 weeks (group A) or infusional 5-fluorouracil (5-FU) by deGramont regimen with i.v. LV (200 mg/m(2)) on days 1 and 2, every 2 weeks (group B)., Results: Thirty-nine MCRC patients were analyzed. Twenty-two of them were in group A and 17 in group B. Thirty-three were evaluable for clinical efficacy. The clinical benefit in the intent-to-treat (ITT) population was 30.8%. Median progression free survival (PFS) was 6 months (95% confidence interval/ CI 4-8) and median overall survival (OS) 9 months (95% CI 6.5-11.5). Median PFS was 3 months (95% CI 2.4-3.6) in group A and 7 months (95% CI 5.1-8.9) in group B (p=0.009). Median OS was 7 months (95% CI 4.3-9.7) in group A and 12 months (95% CI 5.4-18.6) in group B (p=0.422). The combination of MMC and fluoropyrimidines was generally well tolerated. The most common severe toxicities were nausea and vomiting, neutropenia, hepatotoxicity and diarrhea., Conclusion: MMC in combination with fluoropyrimidines is safe and active in heavily-pretreated MCRC patients. This combination remains a viable option in these patients. However, better therapies are urgently needed.
- Published
- 2011
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