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Spots Global Cancer Trial Database for Neoadjuvant Treatment for Advanced Rectal Carcinoma

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Trial Identification

Brief Title: Neoadjuvant Treatment for Advanced Rectal Carcinoma

Official Title: A Phase III Study Evaluating Two Neoadjuvant Treatments Radiochemotherapy (5 Weeks - 50Gy+Capecitabine) and Radiotherapy (1week - 25Gy) in Patient Over 75 With Locally Advanced Rectal Carcinoma

Study ID: NCT02551237

Study Description

Brief Summary: The purpose of the study is to compare pre-operative radio-chemotherapy (RT + capecitabine) to a short course RT associated with a delayed surgery, with two primary objectives: the efficacy evaluation (rate of R0 resection) and the preservation of autonomy (score IADL).

Detailed Description: Colorectal cancer is one of the most frequent cancers diagnosed in France. The average age of diagnosis in 2012 was 70 years old for men and 73 years for women, confirming that colorectal cancer is a disease of the elderly population. The literature concerning combined treatments of colorectal cancer in the elderly is extremely limited. The application of combined treatments in the geriatric population is associated with an increase in the therapeutic complications. These post-operative complications together with the comorbidities and age are unfavorable prognostic factors for survival in patients with cancer of the rectum; this explains why the improved results obtained during the last decades are perceptible in younger patients and not in the elderly. In the general population, pre-operative radio-chemotherapy has imposed itself as a standard treatment for the cancer of the rectum locally advanced. The utilization of fluoropyrimidines associated with radiotherapy (RT) delivered in fractions \[long course RT (50 Gy in 5 weeks), surgery planned 6 to 8 weeks later\] increases the complete histological response rate and decreases significantly the rate of local relapse. The short-course RT \[short course RT using the Swedish model (5x5 Gy in 5 days), with the surgery programmed the following week\] is the standard neoadjuvant protocol in an important number of countries and/or academic groups. The studies that have compared the fractioned RT scheme to the short-course RT protocols have not shown any evidence of a change in efficacy of the short course RT concerning the following criteria: rate of R0 resection, rate of sphincter conservation, rate of relapse at 3 years, the disease free survival or the overall survival. Similarly, there appears to be no difference in severe toxicities in the long term. It should however be noted that short-course RT followed by immediate surgery may be less efficient than combined treatment in patients with a distal T3 cancer, even though these conclusions published by Ngan have been criticized by certain. On the other hand, the fractioned combined treatments results in more tumor and stage reduction and thus more sterilization. Nevertheless a retrospective analysis, performed in the Stockholm region, in patients irradiated with short-course protocol but operated with a delay of at least 4 weeks resulted in a sterilization rate of 8%. This result is even more interesting since in this cohort, 46% of the patients had a tumor classified T4 and that 38% of the patients had a primitive tumor considered inoperable. In the elderly population, the neoadjuvant treatment has rarely been studied. An exploratory analysis of the PRODIGE 2 study, based on age as the criteria, has shown that pre-operative radio-chemotherapy is significantly more toxic in the elderly population, from 70 years of age. Globally the lower tolerance for the pre-operative radio-chemotherapy results in more frequent early termination of RT and a statistically significant decrease in the number of patients operated. Furthermore, if the type of surgery was not significantly different between patients \<70 years and those ≥70 years, we observe a non-significant increase in the rate of prolonged stoma (patients amputated without closure of the stoma). These differences in the surgical procedures is also observed in other publications, placing the emphasis on the fact that in the absence of any difference in the clinical presentation or the characteristic of the tumor, the risk of real or supposed decompensation modifies the surgical care. These data, as well as those in the literature, provides evidence that the pre-operative radio-chemotherapy strategy followed by surgery, the standard strategy in younger patients, is associated with more side effects in the elderly, resulting in the benefit-risk balance, in this population, to be more questionable. It is therefore necessary to conduct a specific studies in the elderly population, with cancer of the rectum with the objective to maintain the carcinological results obtained with classical radio-chemotherapy with at the same time better controlling the secondary effects of the treatment and the risk of decompensation of the patients: the short course radiotherapy associated with a delayed surgery may be a therapeutic scheme well adapted to this population. The investigators therefore propose a study comparing pre-operative radio-chemotherapy (RT + capecitabine) to a short course RT associated with a delayed surgery, with two primary objectives: the efficacy evaluation (rate of R0 resection) and the preservation of autonomy (score IADL).

Eligibility

Minimum Age: 75 Years

Eligible Ages: OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Centre Hospitalier d'Abbeville, Abbeville, , France

Clinique Claude Bernard, Albi, , France

CHU Amiens Picardie, Amiens, , France

Polyclinique Maymard, Bastia, , France

Centre Hospitalier de Beauvais, Beauvais, , France

CHU de Besançon, Besancon, , France

Cebtre Hospitalier de Blois, Blois, , France

Hôpital Avicenne, Bobigny, , France

Institut Bergonié, Bordeaux, , France

Centre François Baclesse, Caen, , France

CHU Henri Mondor, Créteil, , France

Centre Hospitalier de Dax, Dax, , France

Centre Georges François Leclerc, Dijon, , France

CHU DIJON (Hôpital du Bocage), Dijon, , France

CHIC des Alpes du Sud- site de Gap, GAP, , France

CHU de Grenoble Hôpital A Michallon, Grenoble, , France

Hôpital Privé Sainte Marguerite, Hyeres, , France

CHD de Vendée, La Roche-sur-yon, , France

Institut Hospitalier Franco-Britannique, Levallois-perret, , France

Centre Hospitalier Universitaire de Limoges, Limoges, , France

Centre Léon Bérard, Lyon, , France

Hôpital privé Jean Mermoz, Lyon, , France

CHU Timone, Marseille, , France

Institut Paoli Calmettes, Marseille, , France

Centre azuréen de cancérologie, Mougins, , France

Hôpital Américain de Paris, Neuilly-sur-seine, , France

Centre Antoine Lacassagne, Nice, , France

Chu Caremeau, Nimes, , France

Centre Médical Oncogard Institut de cancérologie du Gard, Nîmes, , France

Hôpital TENON, Paris, , France

CHU de Bordeaux, Pessac, , France

Centre Hospitalier Annecy Genevois, Pringy, , France

Centre Henri Becquerel, Rouen, , France

Hôpital d'instruction des Armées, Saint Mande, , France

Clinique Pasteur, Toulouse, , France

Institut de Cancérologie de Lorraine, Vandoeuvre Les Nancy, , France

Gustave Roussy Cancer Campus Grand Paris, Villejuif, , France

Contact Details

Name: Eric Francois

Affiliation: Centre Antoine Lacassagne

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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