Editorial Volume 1 Issue 1
Department of Surgery, Aristotle University of Thessaloniki, Greece
Correspondence: Georgios Tsoulfas, Aristotle University of Thessaloniki, 66 Tsimiski Street, Thessaloniki, Greece, Tel 30- 6971895190, Fax 30-2310332022
Received: May 13, 2014 | Published: May 14, 2014
Citation: Tsoulfas G (2014) Management of Colorectal Hepatic Metastases: Time for Targeted Patient Care. Gastroenterol Hepatol Open Access 1(2): 00004. DOI: 10.15406/ghoa.2014.01.00004
From the slightly less than 150,000 new cases of colorectal cancer (CRC) in the US every year, approximately 15% will have hepatic metastatic disease at the time of diagnosis, whereas another 50% will develop them during the course of their disease.1 Although recent advances in neoadjuvant and adjuvant therapy after colon resection have decreased the number of cases with metastatic disease and newer chemotherapeutic agents, such as irinocetan, cetuximab and bevacizumab have improved the response rates, the two-year survival with only chemotherapy remains at 40% at best for patients with metastatic disease. The result is that surgical treatments remain the main therapeutic approach as resection of the hepatic metastases with a curative intent has been shown to lead to 5-year survivals of 30-40%.2 Adding to that, a combination of improved surgical techniques and better pre- and intra-operative patient assessment have led to a significant increase in the number and type of patients whose hepatic metastatic disease is now considered resectable, as opposed to few years ago, when these same patients would not have enjoyed the possibility of a curative treatment. The critical factors have been-
Despite this progress, one of the things that remains apparent when we see different patients with similar disease load responding to the same treatment in different manners is that patient and tumor biology still dictate the ultimate result (as evidenced by survival and recurrence).
Components of the stroma include angiogenic cells, fibroblasts and cells of the immune system. These cells of the microenvironment through processes such as growth suppressor evasion, proliferative signaling and resistance to apoptosis and cell death are directly involved in the carcinogenic process, including the aspects of metastatic potential and chemo resistance. The balance of the relation between the tumor microenvironment and the tumor itself can lead to tumor progression through an active network of nontumoral cells and molecules that create a permissive environment for the establishment and progression of hepatic metastatic disease.3 The other way that the hepatic microenvironment can play a role is through the existence of liver disease, such as hepatitis B or C viral infections, which activate the immune system and through the eventual establishment of cirrhosis lead to oncogenic transformation of the virally infected hepatocytes.
In addition to the liver and tumor microenvironment, there is the element of genetic involvement. Through powerful genome-wide mapping technologies and translational bioinformatics, it has been possible to elucidate a number of genes and molecules that have the potential to act as biomarkers for the development of hepatic metastases as well as their response to the different therapeutic regiments. The emerging possibilities appear endless; however, there are several issues that remain. These include the high cost of this technology as well as the ethical and legal issues that can present significant challenges. Moreover, the original enthusiasm has to be tempered by the fact that from the hundreds of biomarkers that have been proposed, only very few, such as KRAS have actually been integrated to clinical practice as of yet.4
In order for the progress seen with the use of new surgical techniques and improved chemotherapeutic regiments in the management of hepatic metastases from CRC to continue, it is vital to understand and recognize the role of the organ and tumor microenvironment as well as the contribution of the patient’s genomic identity. Once this happens, it will be possible to identify and implement therapeutic strategies that are patient targeted as they will be tailored to the patient’s genomic signature. The results will be more focused. All of this underscores the need for proper and rigorous validation of data, so that it can be moved to the clinical stage. To achieve that it is essential that emphasis is given on the creation of data and tissue banks, so that the proper research can be conducted. If this recipe is followed, then the best is yet to come.
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The author declares that there is no conflicts of interest.
©2014 Tsoulfas. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.