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1.
J Surg Oncol ; 73(1): 47-58, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10649280

ABSTRACT

Locally recurrent cancer of the rectum has been under-recognized as a complication, although it affects up to 40% of patients treated with surgery alone. Even in the best centers, rates average 25%. While radiotherapy may reduce recurrence, it is now apparent that total mesorectal excision is the most effective modality, with rates as low as 5%. The dramatic decrease in local recurrence can also be linked to increased survival in prospective studies, an effect more significant than any adjuvant therapy. The options, however, for patients with locally recurrent cancer are limited. Fifteen percent of patients with this complication die without systemic spread. Salvage by surgery offers potential cure. Other than anastomotic recurrences that can be locally resected, the best approach for long-term survival is an extensive surgical procedure requiring en bloc removal of adjacent organs and pelvic structures-so-called composite resection. With careful selection, 30% 5-year survival can be achieved and palliation is considerable, with 50% long-term local control. Intraoperative radiotherapy and brachytherapy, and/or preoperative chemoradiation may provide better results in future. Newer techniques of coloanal anastomosis, improved urinary diversion, and myocutaneous flaps for perineal reconstruction radically reduce the morbidity of these procedures. The approach to recurrent rectal cancer requires a sophisticated multidisciplinary team to obtain optimum results.


Subject(s)
Neoplasm Recurrence, Local/surgery , Pelvic Exenteration/methods , Rectal Neoplasms/surgery , Brachytherapy , Chemotherapy, Adjuvant , Humans , Intraoperative Care , Neoplasm Recurrence, Local/prevention & control , Palliative Care , Patient Selection , Prospective Studies , Radiotherapy, Adjuvant , Plastic Surgery Procedures , Rectal Neoplasms/prevention & control , Rectum/surgery , Risk Factors , Salvage Therapy , Survival Rate
2.
Surg Oncol Clin N Am ; 9(1): 133-42, viii, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10601529

ABSTRACT

Improved results for pancreatic resection have been attributed to the concentration of pancreatic surgery in high-volume centers. The evidence supporting a relationship between hospital case volume and operative mortality for pancreatectomy is reviewed. The surgeon's case volume does not appear to influence mortality independently, but other surgeon-related characteristics, like specialized training, have not been examined. More research is needed to elucidate the factors that have contributed to reduced mortality for this complex surgery.


Subject(s)
Pancreatectomy/methods , Pancreatic Neoplasms/surgery , Physician's Role , Clinical Competence/standards , Humans , Pancreatectomy/adverse effects , Pancreatectomy/mortality , Pancreatectomy/standards , Pancreatic Neoplasms/mortality , Prognosis , Quality Indicators, Health Care , Treatment Outcome , Workload
3.
Oncogene ; 18(37): 5187-93, 1999 Sep 16.
Article in English | MEDLINE | ID: mdl-10498868

ABSTRACT

Down regulation of the ING1 candidate tumour suppressor promotes growth in soft agar and focus formation in vitro and tumour formation in vivo. ING1 encodes a nuclear, cell cycle-regulated protein, overexpression of which efficiently blocks cell growth and is capable of inducing apoptosis in different experimental systems. Here we present the first report of ING1 mutation and expression analysis in a total of 452 cancer samples. One germline missense alteration and three germline silent alterations were detected in 377 primary breast cancers while marked (2 - 10-fold) decreases in ING1 mRNA expression were seen in 44% of primary breast cancers and in ten of ten breast cancer cell lines examined. Furthermore, the majority of breast cancers (58%) showing decreased ING1 expression had metastasized to regional lymph nodes whereas only 9% of cancers with elevated ING1 expression, compared to adjacent normal tissues, were metastatic. Thus, ING1 mutation is very rare in breast or ovarian cancers, however, repression of ING1 expression frequently accompanies tumour development of breast cancer.


Subject(s)
Breast Neoplasms/genetics , Gene Expression Regulation, Neoplastic , Genes, Tumor Suppressor , Neoplasm Proteins/biosynthesis , Ovarian Neoplasms/genetics , Protein Biosynthesis , Adult , Amino Acid Substitution , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Canada , Cell Cycle Proteins , Codon/genetics , DNA-Binding Proteins , Disease Progression , Female , Humans , In Situ Hybridization , Inhibitor of Growth Protein 1 , Intracellular Signaling Peptides and Proteins , Japan , Lymphatic Metastasis/genetics , Middle Aged , Neoplasm Proteins/genetics , Nuclear Proteins , Ovarian Neoplasms/metabolism , Ovarian Neoplasms/pathology , Point Mutation , Polymorphism, Single-Stranded Conformational , Proteins/genetics , RNA, Messenger/biosynthesis , RNA, Neoplasm/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction , Tumor Cells, Cultured , Tumor Suppressor Proteins
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