Literature DB >> 27620742

Survival variability of controls and definition of imaging endpoints for longitudinal follow-up of pancreatic ductal adenocarcinoma in rats.

Cherif Akladios1, Mihaela Ignat2, Didier Mutter2, Marc Aprahamian3.   

Abstract

BACKGROUND: The 3Rs guideline is the gold standard for ethics in animal experimentation. Two of those rules, namely refinement and reduction, require further improvement. The objective of this study was to define pathways to better compliance with these prerequisites. Two methods which move us in this direction are: (1) using small animal imaging techniques for pancreatic ductal adenocarcinoma (PDAC) follow-up and (2) reduction of the number of control animals included in a study of PDAC progression under treatment.
MATERIALS AND METHODS: Firstly, we used MicroCT scan to diagnose events showing PDAC progression prior to any clinical symptoms to thereby define more humane endpoints identifiable before any painful phenomenon is observed. Secondly, in order to test the hypothesis of using a reference control group in all preclinical studies of a new treatment of PDAC, we investigated the stability of the results obtained with the control groups in three successive identical studies comparing placebo and gemcitabine in tumor-bearing Lewis rats.
RESULTS: Two imaging endpoints were found. The first was the observation of a liver metastasis assessing PDAC diffusion and, earlier than liver metastasis, the presence of bands of fluid along the flanks, with more or less a medial displacement of bowel and solid viscera, reflecting a peritoneal ascites. Results of the longitudinal follow-up of rats in the gemcitabine study revealed heterogeneity in the survival rate in the three control groups, as opposed to the survival rate in the three treated groups which did not differ statistically. As a result, the significance of improved survival with chemotherapy varied greatly according to the control group used for the comparison, ranging from no impact to a highly significant effect.
CONCLUSION: The early detection by the means of animal imaging of one or more signs indicating the onset of a critical step in the development of the disease (e.g., ascites or/and metastasis) allows the researcher to prevent the occurrence of animal pain, thereby ensuring better animal welfare. However, using a single standard control group in an effort to use fewer animals for a given model runs such a significant risk of false results that it mars the entire study. Although reducing the number of animals in a study remains the gold standard of our experimental practice, in this case it would come at the price of a loss of validity of the results.

Entities:  

Keywords:  3Rs; Ductal adenocarcinoma; Humane endpoints; MicroCT scan; Pancreas; Rat

Mesh:

Substances:

Year:  2016        PMID: 27620742     DOI: 10.1007/s00432-016-2265-6

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  5 in total

Review 1.  Humane endpoints and cancer research.

Authors:  J Wallace
Journal:  ILAR J       Date:  2000

Review 2.  Defining the moribund condition as an experimental endpoint for animal research.

Authors:  L A Toth
Journal:  ILAR J       Date:  2000

3.  Increased tumor growth and spread after laparoscopy vs laparotomy: influence of tumor manipulation in a rat model.

Authors:  D Mutter; A Hajri; V Tassetti; C Solis-Caxaj; M Aprahamian; J Marescaux
Journal:  Surg Endosc       Date:  1999-04       Impact factor: 4.584

4.  Improvement of gemcitabine-based therapy of pancreatic carcinoma by means of oncolytic parvovirus H-1PV.

Authors:  Assia L Angelova; Marc Aprahamian; Svitlana P Grekova; Amor Hajri; Barbara Leuchs; Nathalia A Giese; Christiane Dinsart; Alexia Herrmann; Ginette Balboni; Jean Rommelaere; Zahari Raykov
Journal:  Clin Cancer Res       Date:  2009-01-15       Impact factor: 12.531

Review 5.  In vivo micro-CT imaging of liver lesions in small animal models.

Authors:  Lucia Martiniova; Daniel Schimel; Edwin W Lai; Andrea Limpuangthip; Richard Kvetnansky; Karel Pacak
Journal:  Methods       Date:  2009-06-09       Impact factor: 3.608

  5 in total

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