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1.
Eur J Cancer ; 51(8): 925-34, 2015 May.
Article in English | MEDLINE | ID: mdl-25864037

ABSTRACT

BACKGROUND: A microsatellite instability (MSI) phenotype is found in about 12% of colorectal cancers (CRCs) and is associated with a low recurrence rate after curative surgery. Several studies have identified clinical and pathological factors predictive of recurrence in resected CRC, but not in the MSI subgroup. PATIENTS AND METHODS: This multicentre retrospective study included patients with stage I, II or III MSI CRCs. Disease-free survival (DFS) was calculated with the Kaplan-Meier method. Factors associated with DFS were identified in univariate and multivariate Cox analyses. RESULTS: We studied 521 patients with MSI CRC. Respectively 11%, 51% and 38% of patients were at stage I, II and III. Mean age was 68.7years and 36% of the patients received adjuvant chemotherapy. Median follow-up was 32.8months. The disease recurrence rates were 6% and 21% in stage II and III patients, respectively. The 3-year DFS rate was 77%. In univariate analysis, age, bowel obstruction, lymph node invasion, stage T4, vascular emboli, lymphatic invasion and perinervous invasion were associated with poorer DFS (P<0.05). Three relevant independent predictors of poor DFS were identified in multivariate analysis, namely bowel obstruction (HR=2.46; 95%CI 1.31-4.62, P=0.005), vascular emboli (HR=2.79; 95%CI 1.74-4.47, P<0.001) and stage T4 (HR=2.16; 95%CI 1.31-3.56, P=0.002). CONCLUSIONS: Bowel obstruction, vascular emboli and stage T4 are independently associated with MSI CRC recurrence, suggesting that screening for vascular emboli in routine clinical practice may assist with adjuvant chemotherapy decision-making.


Subject(s)
Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/genetics , Microsatellite Instability , Aged , Aged, 80 and over , Biomarkers, Tumor/genetics , Chemotherapy, Adjuvant , Colorectal Neoplasms/therapy , Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/therapy , Digestive System Surgical Procedures , Disease-Free Survival , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies
2.
Anticancer Res ; 30(10): 4297-301, 2010 Oct.
Article in English | MEDLINE | ID: mdl-21036755

ABSTRACT

BACKGROUND: Colorectal cancer (CRC) patients whose tumours have microsatellite instability (MSI) do not benefit from adjuvant 5-fluorouracil. However, the predictive value of MSI is not known for FOLFOX, now recommended in adjuvant setting. PATIENTS AND METHODS: MSI phenotype was assessed by the pentaplex method. Three-year relapse and disease-free survival (DFS) of patients treated for CRC with FOLFOX 4 in an adjuvant setting were compared according to MSI phenotype. RESULTS: A total of 105 patients (19 MSI, 86 microsatellite stable, MSS) were included. Stage II patients more frequently exhibited MSI (58%) than MSS (21%); (p=0.002). Patients with MSI relapsed significantly less than those with MSS (10.5% vs. 35.0%; p=0.04). DFS was similar for MSI and MSS (p=0.1). In univariate analysis, stage (p=0.0006) and MSI status (p=0.017) were significant predictors of DFS. CONCLUSION: MSI status was associated with significantly fewer relapses and a better prognosis. FOLFOX4 did not alter survival of patients with MSI and can be administered to them.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/genetics , Microsatellite Instability , Adult , Age Factors , Aged , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Chemotherapy, Adjuvant , Colorectal Neoplasms/surgery , Disease-Free Survival , Female , Fluorouracil/administration & dosage , Humans , Leucovorin/administration & dosage , Male , Middle Aged , Multivariate Analysis , Neoplasm Staging , Organoplatinum Compounds/administration & dosage
3.
Gastroenterol Clin Biol ; 34(4-5): 325-8, 2010.
Article in English | MEDLINE | ID: mdl-20627638

ABSTRACT

Small bowel adenocarcinoma is a rare condition with poor prognosis. Like colorectal cancer, small bowel carcinoma may be a part of genetic syndromes with carcinogenetic pathways different from sporadic forms. We report a case of 41-year-old man with small bowel carcinoma revealing hereditary non polyposis colorectal cancer (HNPCC) syndrome. This report supports the systematic study of the MSI status in every patient with a small bowel carcinoma below 60-year-old of age in order to screen for HNPCC syndrome even in the absence of a family history of related cancers.


Subject(s)
Adenocarcinoma/pathology , Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis , Duodenal Neoplasms/pathology , Adaptor Proteins, Signal Transducing/genetics , Adenocarcinoma/therapy , Adult , Duodenal Neoplasms/therapy , Exons , Humans , Male , MutL Protein Homolog 1 , Mutation , Nuclear Proteins/genetics
4.
Rev Med Suisse ; 6(250): 1081-2, 1084-5, 2010 May 26.
Article in French | MEDLINE | ID: mdl-20564868

ABSTRACT

Incidence of colorectal cancers (CRCs) increases with age. The surgical and medical management of elderly patients needs to be improved. Until recently, these patients were not included into controlled clinical trials. Between 2004 and 2007, 88 patients (median age 79) had surgery for CRC in our hospital. In half the cases, patients had an emergency surgery (40/88). Twenty patients had dementia, with no relationships between dementia and emergency surgery (50% vs. 45% for patients without dementia), nor between dementia and median length of hospital stay (16 days vs. 22 days). In metastatic setting (20 patients), chemotherapy was omitted in 10 cases, usually patients with dementia (5 patients; p = 0.002) Standard therapy was hardly applicable because many patients were frail. In the future, usefulness of participation to the staffs of a geriatrist will be assessed prospectively.


Subject(s)
Colorectal Neoplasms/mortality , Colorectal Neoplasms/surgery , Aged , Aged, 80 and over , Chemotherapy, Adjuvant , Cohort Studies , Colorectal Neoplasms/drug therapy , Female , Humans , Male , Postoperative Complications , Retrospective Studies
5.
Ann Endocrinol (Paris) ; 70(6): 468-72, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19744643

ABSTRACT

OBJECTIVE: We report a case of a medullary thyroid carcinoma discovered by F-18 fluorodeoxyglucose-positron emission tomography (F-18 FDG PET). PATIENT AND METHODS: A 73-year-old man with a history of surgical removal of sigmoid colon cancer underwent F-18 FDG PET to search for distant metastases and / or local recurrence because of elevated CEA level and new episode of occlusion. F-18 FDG PET images showed increased focal FDG uptake in the right lobe of the thyroid. Thyroid ultrasound showed one thyroid nodule in each lobe. RESULTS: The fine needle aspiration result was suspicious and calcitonin level was elevated. The subject underwent thyroidectomy without lymph node dissection. The pathology showed a 14 mm medullary thyroid carcinoma. There was no germline mutation of RET. CONCLUSIONS: F-18 FDG PET can detect primitive or secondary malignant thyroid tumors. Thus, thyroid incidentaloma revealed by 18 FDG PET uptake always necessitates careful evaluation.


Subject(s)
Carcinoma, Medullary/diagnostic imaging , Colonic Neoplasms/pathology , Fluorodeoxyglucose F18 , Positron-Emission Tomography , Thyroid Neoplasms/diagnostic imaging , Aged , Biopsy, Fine-Needle , Calcitonin/analysis , Carcinoembryonic Antigen/analysis , Carcinoma, Medullary/pathology , Carcinoma, Medullary/secondary , Colonic Neoplasms/therapy , Diagnosis, Differential , Humans , Male , Neoplasm Metastasis/diagnostic imaging , Neoplasm Recurrence, Local/diagnostic imaging , Thyroid Neoplasms/pathology , Thyroid Neoplasms/secondary , Thyroidectomy , Ultrasonography
6.
Rev Med Suisse ; 5(204): 1116-8, 1120, 1122-3, 2009 May 20.
Article in French | MEDLINE | ID: mdl-19580209

ABSTRACT

Colorectal cancer (CRC) is predominantly a disease of the elderly. The increase of life expectancy will no doubt lead to an increase of these cancers. Few studies have been specially designed for older patients treated for CRC. In general, publications consisted of small phase II studies or retrospective analyses of the subpopulation of elderly patients (from large phase III) -- patients over the age of 65 as compared with younger patients. Therefore we now need to offer specific treatment combining oncologist and geriatric physicians to better codify and adapt treatments to the physiological age of the patient. This is a review of the different stages of care for elderly patients with colorectal cancer in the light of recent publications.


Subject(s)
Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/therapy , Aged , Antineoplastic Agents/therapeutic use , Humans , Postoperative Complications
7.
Rev Med Suisse ; 5(204): 1126, 1128, 1130 passim, 2009 May 20.
Article in French | MEDLINE | ID: mdl-19580210

ABSTRACT

Every year in Europe and in USA, more than 60% of new cases of cancer are diagnosed at the patient's of more than 65 years with a mortality of more than 70%. Pain, is a major symptom which often accompanies cancer. It is always painful and intolerable, notably when pain is linked to bone metastases to elderly patients often poly pathological. In 1/3 of cases pain is present at the time of diagnosis of cancer and in 2/3 of cases at the advanced diseases. The bone metastases occupy the third place after the pulmonary and liver metastases. They are in order of frequency linked in breast cancer, the kidney and the prostate cancer. Bone metastases are at the origin of the loss of the elderly autonomy, with for consequence an impairment of quality of life. Validated tools are at now available to assess this pain. The different treatments offered in bone metastases pain are: the chemotherapy, the surgery, radiotherapy, bisphosphonates and analgesic treatment.


Subject(s)
Bone Neoplasms/complications , Bone Neoplasms/secondary , Pain/etiology , Adrenal Cortex Hormones/therapeutic use , Aged , Analgesics, Opioid/therapeutic use , Bone Neoplasms/therapy , Humans , Pain/drug therapy , Pain Measurement
9.
Cancer Biomark ; 4(2): 83-91, 2008.
Article in English | MEDLINE | ID: mdl-18503159

ABSTRACT

AIMS: The Epidermal Growth Factor-Receptor (EGF-R) is frequently overexpressed in colorectal carcinoma (CRC) and patients can benefit from anti-EGF-R therapy. Yet, the relationship, within tumours, between EGF-R and the activity of downstream effectors such as the non-receptor tyrosine kinase p60c-src and the signal transducer and activator of transcription 3 (STAT3) has not been extensively analyzed. METHODS AND RESULTS: We evaluated EGF-R, tyrosine 416-phosphorylated p60c-src (P-p60c-src), STAT3 and tyrosine 705-phosphorylated STAT3 (P-STAT3) on Tissue Micro Array (TMA) from 126 patients with CRC. Composite immunohistochemistry scores based on the intensity of labelling and the percentage of positive cells were determined on TMA for EGF-R, P-p60c-src, STAT3 and P- STAT3. A high score was found in 56%, 61%, 62% and 27% of the cases for EGF-R, P-p60c-src, STAT3 and P-STAT3 respectively. There was a significant correlation between EGF-R and P-p60c-src (p=0.006) and between P-p60c-src and P-STAT3 (p=0.0009). STAT3 was significantly correlated with vascular emboli (p=0.03) and perineural invasion (p=0.02). CONCLUSIONS: The correlations between EGF-R, P-p60-src and P-STAT3 and some stage-related pathological features point to a critical role for a EGF-R-connected p60c-src-kinase-mediated pathway involving STAT3 and contributing to cell survival and proliferation within CRC tumours.


Subject(s)
Colorectal Neoplasms/metabolism , ErbB Receptors/metabolism , Proto-Oncogene Proteins pp60(c-src)/metabolism , STAT3 Transcription Factor/metabolism , Signal Transduction/physiology , Aged , Colorectal Neoplasms/mortality , Colorectal Neoplasms/pathology , Humans , Immunohistochemistry , Neoplasm Staging , Phosphorylation , Prognosis , Tissue Array Analysis , Tyrosine/metabolism
10.
Ann Oncol ; 19(5): 927-34, 2008 May.
Article in English | MEDLINE | ID: mdl-18056916

ABSTRACT

Arterial hypertension (HT) has been reported in all studies involving bevacizumab, an antiangiogenic agent designed to target vascular endothelial growth factor (VEGF). The mechanism underlying bevacizumab-related HT is not yet clearly understood. As far as endothelial dysfunction and microvascular rarefaction are hallmarks in all forms of HT, we tested the hypothesis that anti-VEGF therapy could alter the microcirculation in nontumor tissues and, thus, result in an increase in blood pressure (BP). We used intravital video microscopy to measure dermal capillary densities in the dorsum of the fingers. Microvascular endothelial function was assessed by laser Doppler flowmetry combined with iontophoresis of pilocarpine (acetylcholine analogue). All measurements were carried out in 18 patients before and after a 6-month treatment with bevacizumab (mean cumulative dose: 3.16 +/- 0.90 g). Mean BP was increased after 6 months of therapy compared with baseline, from 129 +/- 13/75 +/- 7 mmHg to 145 +/- 17/82 +/- 7 mmHg for systolic BP and diastolic BP, respectively (P < 0.0001). Compared with the baseline, mean dermal capillary density at 6 months was significantly lower (75 +/- 12 versus 83 +/- 13/mm(2); P < 0.0001), as well as pilocarpine-induced vasodilation (P < 0.05). Thus, bevacizumab treatment resulted in endothelial dysfunction and capillary rarefaction; both changes are closely associated and could be responsible for the rise in BP observed in most patients.


Subject(s)
Angiogenesis Inhibitors/adverse effects , Antibodies, Monoclonal/adverse effects , Blood Pressure/drug effects , Hypertension/chemically induced , Microcirculation/drug effects , Neovascularization, Pathologic/drug therapy , Adenocarcinoma/blood supply , Adenocarcinoma/drug therapy , Adenocarcinoma/secondary , Aged , Angiogenesis Inhibitors/pharmacology , Angiogenesis Inhibitors/therapeutic use , Antibodies, Monoclonal/pharmacology , Antibodies, Monoclonal/therapeutic use , Antibodies, Monoclonal, Humanized , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bevacizumab , Capillaries/drug effects , Cholinergic Agents/administration & dosage , Cholinergic Agents/pharmacology , Colorectal Neoplasms/blood supply , Colorectal Neoplasms/drug therapy , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/physiopathology , Endothelium, Vascular/drug effects , Endothelium, Vascular/physiopathology , Female , Fingers/blood supply , Forearm/blood supply , Humans , Iontophoresis , Laser-Doppler Flowmetry , Male , Microscopy, Video , Middle Aged , Pilocarpine/administration & dosage , Pilocarpine/pharmacology , Vasodilation/drug effects
11.
Anticancer Res ; 27(4C): 2715-9, 2007.
Article in English | MEDLINE | ID: mdl-17695437

ABSTRACT

BACKGROUND: Microsatelite instability (MSI) is the consequence of the inactivation of a mismatch repair gene and is observed in approximately 15% of colon cancer cases. Patients with MSI colon cancer do not benefit from 5-fluorouracil (5-FU)-based chemotherapy. A current treatment of reference for colon cancer is a combination of 5-FU and oxaliplatin (FOLFOX). The aim of this study was to determine the efficiency of the FOLFOX treatment in patients with metastatic MSI colon cancer. PATIENTS AND METHODS: Tumour specimens were collected from patients with metastatic colon cancer treated with FOLFOX 4 modified or FOLFOX 6; these two regimens are based on 85 mg/m2 and 100 mg/m2 oxaliplatin, respectively. The MSI status was assessed by measuring the length of five monomorphic mononucleotide markers. The FOLFOX regimen was evaluated as a first-line treatment according to WHO criteria. RESULTS: Forty patients (22 men, 18 women), median age 63.5 years (27-83 years) were treated with FOLFOX 4 or 6. Nine patients had tumours exhibiting high MSI (MSI group) and 31 patients had tumours exhibiting microsatellite stability (MSS group). In the MSS group, 11 partial responses (36%) were observed, while there were only two in the MSI group (22%) (no significant difference). The two patients who were responders in the MSI group were treated with FOLFOX 6. The overall survival was not significantly different for MSI and MSS patients. CONCLUSION: No significant differences in the overall response rate or overall survival between the two groups of patients were observed. However, these results suggest that patients with MSI colon cancer are more sensitive to a higher dose of FOLFOX.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Colorectal Neoplasms/drug therapy , Microsatellite Instability , Adult , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Colorectal Neoplasms/genetics , Colorectal Neoplasms/pathology , Female , Fluorouracil/administration & dosage , Humans , Leucovorin/administration & dosage , Male , Middle Aged , Neoplasm Metastasis , Organoplatinum Compounds/administration & dosage , Oxaliplatin
12.
Ann Endocrinol (Paris) ; 68(5): 332-6, 2007 Oct.
Article in French | MEDLINE | ID: mdl-17707761

ABSTRACT

Sunitinib inhibits numerous tyrosine kinase receptors involved in tumor growth, angiogenesis, and metastatic invasion. It is indicated in case of metastatic renal carcinomas and gastrointestinal stromal tumors (GIST) resistant to imatinib. Prospective and retrospective studies have shown association between use of sunitinib and hypothyroidism affecting more than 50% of patients in some series. More amazing, was the non-visualisation of thyroid tissue evaluated with thyroid ultrasonography in two cases. Mechanisms of this side effect are not elucidated. Some studies have suggested destructive thyroiditis but no evidence of autoimmunity has been demonstrated. Anti angiogenic effect could be another hypothesis. Recently antithyroperoxidase activity of sunitinib has been demonstrated. Because hypothyroidism is easily accessible to treatment, screening of thyroid abnormalities is mandatory every three months to improve quality of life of these patients. This unique thyroid side effect of sunitinib with the non-visualisation of thyroid suggests a possible and promising antitumor activity in thyroid cancer.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Hypothyroidism/drug therapy , Indoles/therapeutic use , Pyrroles/therapeutic use , Clinical Trials as Topic , Humans , Sunitinib
14.
Br J Cancer ; 94(12): 1823-32, 2006 Jun 19.
Article in English | MEDLINE | ID: mdl-16773076

ABSTRACT

We performed a meta-analysis of all published studies relating intratumoural microvessel density (MVD) (45 studies) or vascular endothelial growth factor (VEGF) expression (27 studies), both reflecting angiogenesis, to relapse free (RFS) and overall survival (OS) in colorectal cancer (CRC). For each study, MVD impact was measured by risk ratio between the two survival distributions with median MVD as cutoff. Eleven studies did not mention survival data or fit inclusion criteria, six were multiple publications of same series, leaving 32 independent studies for MVD (3496 patients) and 18 for VEGF (2050 patients). Microvessel density was assessed by immunohistochemistry, using antibodies against factor VIII (16 studies), CD31 (10 studies) or CD34 (seven studies). Vascular endothelial growth factor expression was mostly assessed by immunohistochemistry. Statistics were performed for MVD in 22 studies (the others lacking survival statistics) including nine studies (n = 957) for RFS and 18 for OS (n = 2383) and for VEGF in 17 studies, including nine studies for RFS (n = 1064) and 10 for OS (n = 1301). High MVD significantly predicted poor RFS (RR = 2.32 95% CI: 1.39-3.90; P < 0.001) and OS (RR = 1.44; 95% CI: 1.08-1.92; P = 0.01). Using CD31 or CD34, MVD was inversely related to survival, whereas it was not using factor VIII. Vascular endothelial growth factor expression significantly predicted poor RFS (RR = 2.84; 95% CI: 1.95-4.16) and OS (RR=1.65; 95% CI: 1.27-2.14). To strengthen our findings, future prospective studies should explore the relation between MVD or VEGF expression and survival or response to therapy (e.g. antiangiogenic therapy). Assessment of these angiogenic markers should be better standardised in future studies.


Subject(s)
Adenocarcinoma/blood supply , Adenocarcinoma/mortality , Colorectal Neoplasms/blood supply , Colorectal Neoplasms/mortality , Neovascularization, Pathologic , Vascular Endothelial Growth Factor A/biosynthesis , Adenocarcinoma/metabolism , Aged , Antigens, CD34/biosynthesis , Capillaries , Colorectal Neoplasms/metabolism , Disease-Free Survival , Factor VIII/biosynthesis , Female , Humans , Immunohistochemistry , Male , Middle Aged , Platelet Endothelial Cell Adhesion Molecule-1/biosynthesis , Prognosis , Survival Analysis , Survival Rate
15.
Rev Mal Respir ; 23(2 Pt 1): 149-51, 2006 Apr.
Article in French | MEDLINE | ID: mdl-16788439

ABSTRACT

BACKGROUND: Carcinomatous meningitis is a major complication in Non Small Cell Lung Cancer (NSCLC). Despite treatment with radiotherapy alone or in combination with intrathecal and systemic chemotherapy, its prognosis remains poor. OBSERVATION: We report a case of a female non-smoker with adenocarcinoma with bronchoalveolar features presenting with carcinomatous meningitis three years after the diagnosis of her primary tumour. Gefitinib treatment was proposed because of the persistence of meningitic symptoms despite cranial irradiation. Clinical response was observed within 3 weeks and lasted for 9 months. CONCLUSION: Gefitinib may be effective in treating carcinomatous meningitis complicating NSCLC and should be considered in this situation given the absence of effective alternatives.


Subject(s)
Adenocarcinoma, Bronchiolo-Alveolar/drug therapy , Antineoplastic Agents/therapeutic use , Carcinoma, Non-Small-Cell Lung/drug therapy , Chemotherapy, Adjuvant , Lung Neoplasms/pathology , Meningitis/drug therapy , Protein Kinase Inhibitors/therapeutic use , Quinazolines/therapeutic use , Adenocarcinoma, Bronchiolo-Alveolar/pathology , Adenocarcinoma, Bronchiolo-Alveolar/radiotherapy , Carboplatin/administration & dosage , Carcinoma, Non-Small-Cell Lung/pathology , Carcinoma, Non-Small-Cell Lung/radiotherapy , Cisplatin/administration & dosage , Combined Modality Therapy , Cranial Irradiation , ErbB Receptors/antagonists & inhibitors , Female , Gefitinib , Humans , Lung Neoplasms/drug therapy , Lung Neoplasms/surgery , Meningitis/radiotherapy , Middle Aged , Neoplasm Proteins/antagonists & inhibitors , Paclitaxel/administration & dosage , Palliative Care , Pneumonectomy , Vinblastine/administration & dosage , Vinblastine/analogs & derivatives , Vinorelbine
16.
J Chir (Paris) ; 142(5): 291-6, 2005.
Article in French | MEDLINE | ID: mdl-16292207

ABSTRACT

Strategies for the treatment of metastatic colorectal cancer must take into account the contribution of monoclonal antibodies. A group of new efficient tools in oncology, these drugs target tumor antigens. Bevacizumab recognizes VEGF. Vascular endothelial growth factor (VEGF) is a key mediator in angiogenesis. This antibody combined with chemotherapy increases the survival of patients treated for metastatic colorectal cancer. Median survival of patients treated with antibodies and chemotherapy is 20 months, compared with only 15 months for patients treated with chemotherapy alone. Cetuximab is a monoclonal antibody that binds competitively and with high affinity to the EGF receptor. Cetuximab is currently approved for use in patients with pretreated colorectal cancer. EGF is a major cell growth factor. The side effects of these new biotherapies are different from chemotherapy: bevacizumab affects vascular elements and the most common side effect of anti-EGFR treatment is acneiform skin rash.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Antineoplastic Agents/therapeutic use , Colorectal Neoplasms/drug therapy , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal/adverse effects , Antibodies, Monoclonal, Humanized , Antimetabolites, Antineoplastic/administration & dosage , Antimetabolites, Antineoplastic/therapeutic use , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/adverse effects , Antineoplastic Agents, Phytogenic , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bevacizumab , Camptothecin/administration & dosage , Camptothecin/analogs & derivatives , Camptothecin/therapeutic use , Cetuximab , Clinical Trials, Phase II as Topic , Colorectal Neoplasms/mortality , Colorectal Neoplasms/surgery , Combined Modality Therapy , Epidermal Growth Factor/antagonists & inhibitors , Fluorouracil/administration & dosage , Fluorouracil/therapeutic use , Follow-Up Studies , Humans , Irinotecan , Leucovorin/administration & dosage , Leucovorin/therapeutic use , Organoplatinum Compounds/administration & dosage , Organoplatinum Compounds/therapeutic use , Oxaliplatin , Randomized Controlled Trials as Topic , Risk , Time Factors , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vitamin B Complex/administration & dosage , Vitamin B Complex/therapeutic use
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