Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
1.
J BUON ; 22(5): 1287-1295, 2017.
Article in English | MEDLINE | ID: mdl-29135115

ABSTRACT

PURPOSE: The Romanian Patient Access Program (Ro-PAP, CA 184-427), part of the European Expanded Access Program (EAP), was developed to evaluate the effectiveness and safety profile ipilimumab in previously treated patients with advanced melanoma (unresectable or metastatic melanoma). The objective of our retrospective observational study of patients included in this program was to provide data recorded in real-life settings. METHODS: We analysed 89 patients enrolled in Ro-PAP, CA 184-427 (54 men and 35 women) aged between 29 and 89 years. The patients received ipilimumab 3mg/kg, administered with short 30-min i.v. infusion every 3 weeks, having a total of 4 doses. Patients were assessed for tumor response, overall survival (OS) and progression-free survival (PFS), and were monitored for adverse events (AE). RESULTS: At 12 weeks after the completion of therapy, the complete and partial response rates were 6.74% each, stable disease 15.73%, with the best overall response rate 13.48% and disease control rate 29.21%. Median OS was 189.00 days (95% CI 69.50-308.49) and median PFS 124.00 days (95% CI 85.05-162.94). The level of patient functionality at the beginning of ipilimumab treatment showed to be an important predictor of outcome, as patients with ECOG performance status (PS) (0) before therapy with ipilimumab had a higher OS compared with those with impaired functionality. CONCLUSIONS: The use of ipilimumab in daily clinical practice demonstrated to be effective and safe, consistent with data coming from randomized clinical trials or other observational studies.


Subject(s)
Ipilimumab/therapeutic use , Melanoma/drug therapy , Skin Neoplasms/drug therapy , Female , Humans , Ipilimumab/pharmacology , Male , Melanoma/pathology , Romania , Skin Neoplasms/pathology , Treatment Outcome
2.
Eur J Public Health ; 24(5): 761-7, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24029456

ABSTRACT

BACKGROUND: Reducing treatment delay improves outcomes in breast cancer. The aim of this study was to determine factors influencing patient- and system-related delays in commencing breast cancer treatment in different countries. METHODS: A total of 6588 female breast cancer patients from 12 countries were surveyed. Total delay time was determined as the sum of the patient-related delay time (time between onset of the first symptoms and the first medical visit) and system-related delay time (time between the first medical visit and the start of therapy). RESULTS: The average patient-related delay time and total delay time were 4.7 (range: 3.4-6.2) weeks and 14.4 (range: 11.5-29.4) weeks, respectively. Longer patient-related delay times were associated with distrust and disregard, and shorter patient-related delay times were associated with fear of breast cancer, practicing self-examination, higher education level, being employed, having support from friends and family and living in big cities. The average system-related delay time was 11.1 (range: 8.3-24.7) weeks. Cancer diagnosis made by an oncologist versus another physician, higher education level, older age, family history of female cancers and having a breast lump as the first cancer sign were associated with shorter system-related delay times. Longer patient-related delay times and higher levels of distrust and disregard were predictors of longer system-related delay times. CONCLUSIONS: The delay in diagnosis and treatment of breast cancer remains a serious problem. Several psychological and behavioural patient attributes strongly determine both patient-related delay time and system-related delay time, but their strength is different in particular countries.


Subject(s)
Attitude to Health , Breast Neoplasms/diagnosis , Breast Neoplasms/psychology , Health Behavior , Patient Acceptance of Health Care/psychology , Patient Acceptance of Health Care/statistics & numerical data , Adult , Age Factors , Aged , Asia , Europe , Fear/psychology , Female , Humans , Middle Aged , Self-Examination/psychology , Self-Examination/statistics & numerical data , Socioeconomic Factors , Surveys and Questionnaires , Time Factors , Trust/psychology
3.
Hepatogastroenterology ; 59(118): 1874-8, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22819908

ABSTRACT

Somatostatinoma is a rare neuroendocrine tumor which especially develops in the pancreas. There are few communicated cases about extra-pancreatic localization, having as a particularity the absence of somatostatin hypersecretion syndrome and frequent association with von Recklinghausen neurofibromatosis. We present the case of a 42-year old patient with Von Recklinghausen neurofibromatosis admitted in our clinic with a chronic upper digestive obstruction syndrome. The presence of a first jejunal loop somatostatinoma was an intraoperative surprising diagnosis that imposed jejunal resection and association of complementary specific treatment. Despite the therapeutic correct management, the status of the patient deteriorated very fast, confirming the aggressiveness of this neoplasia.


Subject(s)
Adrenal Gland Neoplasms/complications , Jejunal Neoplasms/complications , Neoplasms, Multiple Primary , Neurofibromatosis 1/complications , Pheochromocytoma/complications , Somatostatinoma/complications , Adrenal Gland Neoplasms/diagnosis , Adrenal Gland Neoplasms/therapy , Adult , Barium Sulfate , Biopsy , Contrast Media , Digestive System Surgical Procedures , Disease Progression , Endoscopy, Gastrointestinal , Fatal Outcome , Gastric Dilatation/etiology , Humans , Intestinal Obstruction/etiology , Jejunal Neoplasms/diagnosis , Jejunal Neoplasms/therapy , Neurofibromatosis 1/diagnosis , Neurofibromatosis 1/therapy , Pheochromocytoma/diagnosis , Pheochromocytoma/therapy , Predictive Value of Tests , Somatostatinoma/diagnosis , Somatostatinoma/therapy , Tomography, X-Ray Computed , Treatment Outcome
4.
Wien Klin Wochenschr ; 122(11-12): 368-79, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20549373

ABSTRACT

In breast cancer, early detection as well as new developments in therapeutic options has resulted in less patients presenting with metastatic disease. However, about one-third of women with early stage breast cancer will eventually develop metastatic disease. Furthermore, approximately 20-30% of patients with breast cancer have tumors that overexpress human epidermal growth factor receptor (HER-2), which is associated with an aggressive tumor phenotype and poor prognosis. The identification of the HER-2 protein led to the development of highly effective therapeutics directed at this receptor. Trastuzumab, a recombinant, humanized, monoclonal antibody that binds to the extracellular domain of the HER-2 protein, has shown significant clinical benefit in metastatic and early-stage HER-2-positive breast cancer. Since the cancer recurs after adjuvant therapy in some women, and metastatic breast cancer eventually develops resistance to trastuzumab, there is a need for alternative treatment modalities to block HER-2 signaling. One of these treatment options is lapatinib, an orally active small molecule that inhibits the tyrosine kinases of HER-2 and the epidermal growth factor receptor type 1 (EGFR). In this consensus statement current treatment options in metastatic and locally advanced disease are discussed with a special focus on lapatinib.


Subject(s)
Antineoplastic Agents/therapeutic use , Breast Neoplasms/drug therapy , Evidence-Based Medicine/standards , Quinazolines/therapeutic use , Algorithms , Antineoplastic Agents/adverse effects , Breast Neoplasms/mortality , Breast Neoplasms/pathology , Disease Progression , Disease-Free Survival , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Delivery Systems , Drug Therapy, Combination , ErbB Receptors/antagonists & inhibitors , Europe , Female , Humans , Lapatinib , Neoplasm Staging , Neoplasms, Hormone-Dependent/drug therapy , Neoplasms, Hormone-Dependent/pathology , Quinazolines/adverse effects , Randomized Controlled Trials as Topic , Receptor, ErbB-2/antagonists & inhibitors , Receptors, Estrogen/analysis , Receptors, Progesterone/analysis
SELECTION OF CITATIONS
SEARCH DETAIL