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1.
Clin Transl Oncol ; 13(12): 862-8, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22126729

ABSTRACT

In Spain 22,000 new cases of colorectal cancer are diagnosed each year, with 13,075 deaths resulting from this disease. Around 70% of colorectal cancers are localised in the colon and 30% in the rectum. A group of Spanish experts established recommendations on what would be the best strategy in the treatment of locally advanced rectal cancer (LARC). Adequate assessment of local tumour extension, including high-resolution magnetic resonance imaging and endorectal ultrasound, is essential for successful treatment. The three cornerstones in the treatment of LARC are surgery, radiotherapy and chemotherapy. Most patients will need a total mesorectal excision (TME). Preoperative chemo-radiotherapy (CRT) is preferred for the majority of patients with T3/T4 disease and/or regional node involvement, and adjuvant chemotherapy is recommended after a patient-sharing decision. Capecitabine, after showing a trend in improved downstaging in neoadjuvant stratum and the convenience of its oral administration, represents an alternative to 5-FU as perioperative treatment of LARC.


Subject(s)
Expert Testimony , Neoadjuvant Therapy , Practice Guidelines as Topic , Rectal Neoplasms/therapy , Combined Modality Therapy , Digestive System Surgical Procedures , Humans
2.
Clin. transl. oncol. (Print) ; 13(12): 862-868, dic. 2011. tab
Article in English | IBECS | ID: ibc-125994

ABSTRACT

In Spain 22,000 new cases of colorectal cancer are diagnosed each year, with 13,075 deaths resulting from this disease. Around 70% of colorectal cancers are localised in the colon and 30% in the rectum. A group of Spanish experts established recommendations on what would be the best strategy in the treatment of locally advanced rectal cancer (LARC). Adequate assessment of local tumour extension, including high-resolution magnetic resonance imaging and endorectal ultrasound, is essential for successful treatment. The three cornerstones in the treatment of LARC are surgery, radiotherapy and chemotherapy. Most patients will need a total mesorectal excision (TME). Preoperative chemo-radiotherapy (CRT) is preferred for the majority of patients with T3/T4 disease and/or regional node involvement, and adjuvant chemotherapy is recommended after a patient-sharing decision. Capecitabine, after showing a trend in improved downstaging in neoadjuvant stratum and the convenience of its oral administration, represents an alternative to 5-FU as perioperative treatment of LARC (AU)


Subject(s)
Humans , Male , Female , Expert Testimony/methods , Expert Testimony , Neoadjuvant Therapy/methods , Neoadjuvant Therapy , Practice Guidelines as Topic , Rectal Neoplasms/therapy , Combined Modality Therapy , Digestive System Surgical Procedures/methods , Digestive System Surgical Procedures
3.
Clin. transl. oncol. (Print) ; 13(3): 162-178, mar. 2011. tab, ilus
Article in English | IBECS | ID: ibc-124632

ABSTRACT

Metastatic colorectal cancer (CRC) represents an important health problem in which several biological predictive and prognostic factors have been identified, including clinical features and molecular markers that might influence the response to treatment. Actually, certain prognostic factors are considered key elements, along with disease extent, for deciding the therapeutic approach. However, a distinction between resectable/potentially resectable and unresectable patients must be made in order to establish an adequate therapeutic strategy. Different drugs and chemotherapy regimens are currently available, and their administration depends on patient characteristics, disease-related factors and the treatment objective. Moreover, special situations such as peritoneal carcinomatosis and local treatment of CRC in the setting of metastatic disease should be considered when deciding the most appropriate treatment strategy. This article reviews all the previously mentioned issues involved in the management of metastatic CRC and suggests some general recommendations for its treatment (AU)


Subject(s)
Humans , Male , Female , Colorectal Neoplasms/pathology , Colorectal Neoplasms/therapy , Neoplasm Metastasis/pathology , Neoplasm Metastasis/therapy , Practice Guidelines as Topic , Neoplasm Staging/methods , Neoplasm Staging/trends , Neoplasm Staging
4.
Ann Oncol ; 21(7): 1552-1557, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20231303

ABSTRACT

BACKGROUND: To assess whether deletions involving codons 557 and/or 558 (critical deletions) of exon 11 of KIT are relevant in the prognosis of relapse-free survival (RFS) in gastrointestinal stromal tumor (GIST) patients with a long follow-up. PATIENTS AND METHODS: A univariate and multivariate analysis for RFS were carried out on 162 localized GIST patients over the entire follow-up period and over the intervals 0-4 years and >4 years. Factors assessed among others were Fletcher/National Institutes of Health and Miettinen-Lasota/Armed Forces Institute of Pathology (M-L/AFIP) risk categories, critical deletions and non-deletion-type mutation (NDTM) within exon 11 of KIT. RESULTS: Multivariate analyses revealed that M-L/AFIP [relative risk (RR) 11.45, confidence interval (CI) 4.40-29.76, for the high-risk subgroup and RR 5.97, CI 2.09-17.06, for the intermediate subgroup] and critical deletions (RR 3.05, CI 1.59-5.85) were independent prognostic factors for RFS for the first 4 years and for the entire follow-up period. Beyond 4 years, the high-risk M-L/AFIP subgroup (RR 8.12, CI 1.48-44.4) and NDTM (RR 6.42, CI 1.17-35.12) were independent prognostic factors for RFS. The median follow-up was 84 months. CONCLUSION: Critical deletions represent a time-dependent prognostic factor limited to the first 4 years after surgery, which could help identify a subset with higher and earlier risk for relapse in GIST patients.


Subject(s)
Codon/genetics , Gastrointestinal Stromal Tumors/genetics , Neoplasm Recurrence, Local/genetics , Proto-Oncogene Proteins c-kit/genetics , Sequence Deletion/genetics , Adolescent , Adult , Child , Child, Preschool , Female , Follow-Up Studies , Gastrointestinal Stromal Tumors/mortality , Gastrointestinal Stromal Tumors/pathology , Humans , Infant , Infant, Newborn , Male , Middle Aged , Neoplasm Recurrence, Local/mortality , Neoplasm Recurrence, Local/pathology , Survival Rate , Time Factors , Treatment Outcome , Young Adult
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