Advancement on Clinical Application of mTOR Inhibitors in Gastrointestinal Cancers

Gastrointestinal cancers, including esophageal cancer, gastric cancer, liver cancer, pancreatic cancer, colorectal cancer, are serious threats to people's health, and traditional therapeutic drugs have limited effect on them. Signaling pathway related to mammalian target of rapamycin (mTOR) plays a very important role either in the germination or development of multiple gastrointestinal cancers. Inhibiting mTOR can effectively impede the development of tumor and improve the sensitivity of tumor to radiotherapy or chemotherapy. The research on the application of mTOR inhibitors in gastrointestinal cancers increases with years. A lot of operational schemes independent or combined with others are being explored, some of which are worthy of attention. This paper summarizes the data of all published clinical trials and reviews the clinical application of mTOR inhibitors in the treatment of gastrointestinal cancers in recent years.

and c-Met inhibitors are the representative drugs [3]. mTOR inhibitors are potential targeted antitumor agents with high activity and low toxicity, and their applications in the treatment of gastrointestinal cancer are of particular concern [4] [5]. This paper summarized the clinical application of mTOR inhibitors in gastrointestinal cancer, and provided reference for the related researchers.

mTOR and mTOR Inhibitors
mTOR is the mammalian target of rapamycin composed of 2549 amino acids with a molecular weight of 289 kDa, belonging to serine/threonine protein kinase. It widely exists in various mammalian cells and participates in many cell processes, such as cell growth, proliferation, protein synthesis, transcription and metabolism [6]. From the C-terminal to the N-terminal, mTOR is successively distributed with focal adhesion targeting domain of C-terminal, negative regulatory domain, kinase domain, FKBP12 rapamycin binding and focal adhesion targeting domain, and it belongs to phosphoinositide 3-kinase-related protein kinases (PIKKs) [7]. mTOR can form two different complexes, mTORC1 and mTORC2 by combining with different proteins. The upstream activators and downstream effectors of mTORC1 and mTORC2 are different [8], and they coordinate each other to regulate the cell cycle process [6].
In the PI3K/Akt/mTOR signaling pathway (Figure 1), the transformation from phosphorylinositol (4,5) bisphosphonate (PIP2) into phosphorylinositol (3,4,5) trisphosphonate (PIP3) will be promoted after activating phosphorylinositol-3 kinase (PI3K), and then the phosphorylinoside-dependent kinase-1 (PDK-1) is activated. PDK-1 and PDK-2 work together to phosphorylate threonine at 308 site as well as serine at 473 site of protein kinase B (Akt), thus activating Akt and regulating mTORC1. The abnormal signal of this pathway can directly lead to cell proliferation or even cancer. For example, PTEN can inhibit the transformation from PIP2 to PIP3, thus regulating the activation of Akt. Therefore, when PTEN function is lost, Akt and mTOR in downstream will be activated abnormally. A number of studies have shown that mutations in PTEN or PI3K are directly related to endometrial cancer, cervical cancer or ovarian cancer [9].
The phosphorylation of eukaryotic translation initiation factor 4E-binding protein 1 (4EBP1) in tumor cells can be inhibited by mTOR inhibitors, thus the expression of growth protein is reduced and tumor cells will be stopped in G1 phase, or even finally die off. In addition, it has been found in recent years that mTOR inhibitors can also enhance the sensitivity of tumor cells to radiotherapy [10] [11] or chemotherapy [12]. These mechanisms make mTOR inhibitors becoming antitumor targeted drugs with highly effective and low toxic.
The reported mTOR inhibitors can be divided into two categories, the one is rapamycin derivatives acting on FRB domain, and the other one is ATP competitive mTOR inhibitors acting on protein kinase domain. Rapamycin (sirolimus), everolimus, ridaforolimus, temsirolimus (CCI-779) [13] belong to rapamycin derivatives, which have been approved for marketing. Rapamycin is the first mTOR inhibitor and the first one used in clinic. It can inhibit the growth of breast cancer, ovarian cancer, prostate cancer, renal cancer, cervical cancer and other tumor cells in a concentration dependent manner. Rapamycin opens a new way for cancer treatment, but the poor water solubility and low bioavailability (<15%) limit its application. In order to overcome the shortcomings of rapamycin in physical and chemical properties, its derivatives, everolimus, ridaforolimus, CCI-779, were developed one after another. ATP competitive mTOR inhi-bitors are a new class of compounds developed in recent years, which act on the ATP binding cavity of mTOR and have excellent activity. However, due to toxicity and the shortcomings of pharmacokinetics, all of them are sluggish in stage of clinical research. For instance, there are 20 clinical trials about mTOR inhibitor BEZ235 registered in www.clinicaltrials.gov, but all of them are terminated in phase I/II. The representative compounds of ATP competitive mTOR inhibitors are BEZ-235 [14], Wye-125132 [15], Torin2 [16], PF-04691502 [17], etc.

The Application of mTOR Inhibitors in Treating
Gastrointestinal Cancers mTOR inhibitors have been used in treating gastrointestinal cancers for about 10 years, the therapeutic schemes and clinical results are different according to different cancers. In this paper, the clinical trials database collected by the National Medical Library of the USA was investigated and five main types of gastrointestinal cancers were searched respectively. The published clinical trial data and results were summarized below.

Esophagus Carcinoma
The

Gastric Carcinoma
The incidence rate of gastric carcinoma (GC) ranks fifteenth among all cancers, and the five year survival rate is 31.5%. In 2019, there will be 27,510 new cases of GC in the USA, accounting for 1.6% of new cancer cases, and 11140 patients will die accounting for 1.8% of all cancer deaths [1]. Surgical operation may be effective in early treatment of GC, but inoperable for about two-thirds patients. New targeted therapies for GC have emerged based on many cancer-related molecular pathways. In human GC, PI3K/Akt and mTOR are known to be activated in approximately 30% and 60% of patients, respectively. Therefore, in the era of molecular-targeted agents, inhibition of the mTOR pathway represents a novel therapeutic strategy in the treatment of GC [19].
In 2007, Novartis Pharmaceuticals launched a single arm, multi-center phase II study (NCT00519324) [20] of everolimus in patients with advanced GC. This study was to evaluate the efficacy and safety of everolimus in the treatment of advanced GC. A total of 54 patients with median age of 63 years old were enrolled in the trial, and given 10 mg/day of everolimus orally. The results showed that the tumor volume of 45% patients was smaller than baseline. The disease control rate (DCR) was 56.0%, and the median progression-free survival (PFS) was 2.7 months. In the follow-up time of median (9.6 months), the median OS was 10.1 months. Common grade 3 or 4 adverse events include anemia, loss of appetite, and fatigue, and there is no significant difference in the security of various groups.
Compared with the best supportive care (BSC), everolimus did not significantly improve the OS of patients with AGC. The safety of everolimus in the treatment of GC is consistent with that in other cancers.
In the clinical trials of mTOR inhibitors, GC has the most records, which shows the researchers' attention in this field.

Hepatocellular Carcinoma
The incidence rate of hepatocellular carcinoma (HCC) is thirteenth among all cancers, with a five year survival rate of 18.4%. In 2019, 42,030 new cases of HCC will arise in the USA, accounting for 2.4% of new cancer cases, and 31,780 patients will be killed by this cancer, accounting for 5.2% of all cancer deaths [1].
Because the occurrence of liver cancer is relatively unconspicuous, it is often in late stage when diagnosed, and only about 30% patients can be treated by surgery [25]. Studies have shown that the mTOR/AKT pathway is frequently up-regulated in 40% -50% of hepatocellular carcinomas. Inhibition of AKT and mTOR signals not only inhibits the production of VEGF, but also regulates the expression of other angiogenic factors (such as nitric oxide and angiogenin), thereby effectively delaying the progression of HCC [26]. In terms of HCC cells, mTOR can also enhance the resistance of HCC to chemotherapy by transforming ordinary HCC cells into tumor stem cells. Overactivated mTOR can change the biological behavior and characteristics of HCC cells, so that some HCC cells have characteristics similar to those of stem cells and form cancer stem cells (CSC) [27]. After transformation into tumor stem cells, the HCC cells obtained more significant invasion and migration capacity, and showed stronger tolerance to anti-tumor drugs such as sorafenib [28].
In 2009, University of Regensburg launched an open label, randomized, and multi-center phase III study (NCT00355862) [29] in order to compare sirolimus-containing versus sirolimus-free immunosuppression in patients undergoing liver transplantation for HCC. A total of 525 patients were recruited and divided into two groups: group A (264 patients) did not receive sirolimus, group B (261 patients) received sirolimus. The primary end point was relapse free survival (RFs), and OS was the secondary end point. The results showed that the RFs rate of group A was 64.5%, and that of group B was 70.2%, which had no statistical difference. Group B showed a better RFs rate in three years after transplantation, and a better OS in five years. Interestingly, low-risk patients benefit the most from sirolimus rather than high-risk patients. The number of serious adverse events occurred in group A (860 cases) and group B (874 cases) was same. The results showed that the RFs of liver cancer patients treated with sirolimus had no significant improvement after 5 years. However, the benefits in RFs and OS were evident in the first five years, especially in low-risk patients. This trial provides the first high-level evidence for selecting immunosuppression in liver transplantation recipients with HCC.
It has been proved that mTOR inhibitors used directly in the treatment of HCC cannot work well, and may be more suitable as chemosensitizers and radiosensitizers [10] [30] for the treatment of HCC.

Pancreatic Carcinoma
The incidence rate of pancreatic carcinoma is eleventh in all cancers, with a five year survival rate of 9.3%. In 2019, it is estimated that 56,770 new cases of pancreatic cancer will be added in the USA, accounting for 3.2% of the new cancer cases, and 45,750 patients will be killed by this cancer, accounting for 7.5% of the total cancer deaths [1]. Pancreatic carcinoma responds poorly to most chemotherapeutic drugs. As targeted therapies produce mild adverse reactions due to their specificity and targeted inhibition, they have become the preferred treatments for cancers in recent years [31].
In 2009, Novartis pharmaceuticals launched a randomized, double-blind, multi-center clinical phase II study (NCT01658436) to evaluate the efficacy and safety of everolimu in the treatment of advanced pancreatic neuroendocrine tumors (PNET). A total of 256 patients were enrolled in the clinical trial, 130 of whom were assigned to the everolimus group and 126 to the placebo group, with a median follow-up period of 43 months. The median PFS was 11 months in the everolimus group and 4.6 months in the placebo group. The most common side effects in the everolimus group were stomatitis, rash, diarrhea, tiredness, edema, abdominal pain, nausea, fever and headache. In view of the efficacy and unique mechanism, FDA approved Novartis pharmaceuticals' new drug Afinitor (everolimus) in May 2011 for treatment of PNET which cannot be surgically removed. The drug is the only one approved for PNET in the USA for nearly 30 years.
ATP competitive mTOR inhibitors have novel structures and inhibiting mechanisms, the representative one is BEZ235. In 2012, Novartis pharmaceuticals launched a multi-center, two stages, phase II study (NCT02315625) [32] to evaluate the efficacy of oral BEZ235 to patients with PNET. In the first group, 11 patients were given 400 mg BEZ235 twice a day. Due to tolerance problems, another 20 patients received 300 mg BEZ235 twice daily in the second group.
The trial ended in June 2014, wherein 8 cases (72.7%) in first group and 8 cases (40.0%) in second group of grade 3 or 4 adverse events were reported, including hyperglycemia, diarrhea, nausea and vomiting. The trial showed that PNET patients with everolimus resistant had poor tolerance to BEZ235 at doses of 400 or 300 mg. Although evidence for disease stability was observed in the trial, the study did not enter the second phase due to poor patient tolerance.

Colorectal Cancer
The incidence rate of colorectal cancer is the fourth in all cancers, with a five year survival rate of 64.4%. In 2019, it is estimated that 145,600 new cases of colorectal cancer will arise in the USA, accounting for 8.3% of new cancer cases, and 51,020 people will be killed by this cancer, accounting for 8.4% of all cancer deaths [1]. Because of the limited effect of mTOR inhibitors on colorectal cancer, all reported trials used them in combination with other drugs [33].
Up to now, the FDA has approved three kinds of anti-VEGF treatment methods for colorectal cancer: bevacizumab, ziv-aflibercept and regorafenib. Among them, bevacizumab is the most widely studied, and has shown significant efficacy in the treatment of colorectal cancer. mTOR can theoretically enhance the antitumor effect of anti-VEGF drugs. In vitro experiment, the combination of anti-VEGF and mTOR inhibitors showed better effects than using them independently. So, Novartis pharmaceuticals conducted a phase II study to test the efficacy of bevacizumab combined with everolimus in patients with refractory colorectal cancer.
In 2007, Novartis Pharmaceuticals and Genentech, Inc. launched a phase II study (NCT00597506) [34], and evaluate the efficacy of the combination of be-vacizumab and everolimus to refractory metastatic colorectal cancer (MCRC). A total of 50 patients were recruited for the trial and given bevacizumab (10 mg/kg) combined with everolimus (10 mg/day), then the biomarkers of the treatment were evaluated. The baseline biomarker profile of each patient was used as his/her reference control. A total of 41 biomarkers in every patient were analyzed. Three markers (FGFb, IL8, VEGF-C) were excluded from the statistical analysis, and more than 10% samples could not be detected. The changes of 26 markers were statistically significant (P < 0.05), of which 12 markers were highly significant (P < 0.0001). Among them, three markers including Ang2, MCP-1 and VEGF-R2 were down regulated, while MMP-2, PAI-1 activity, PAI-1 total level, PLGF, SDF-1, VCAM-1, VEGF-A, VEGF-D and vWF were up regulated.
In this study, more than 20% patients had a stable period of disease for six months or more, which indicated that some patients benefited greatly from this combination therapy. Note that most of the patients who participated in this trial were previously resistant to bevacizumab treatment, indicating the addition of everolimus delayed the bevacizumab resistance and improved clinical results.

Summary
In recent years, drug-development in treatment of gastrointestinal tumors is relatively slow. mTOR inhibitors have a good application prospect due to its high bioactivity and low toxicity. Only 30% of clinical trial results about mTOR inhibitors have been published, with about 35% of trials aborted for various reasons.
According to the published clinical data, the effect of using mTOR inhibitor alone in treatment of gastrointestinal tumor is limited. This may be because the complex feedback regulation pathways in the tumor interfere with the therapeutic effect of mTOR inhibitors. Therefore, the best application direction of mTOR inhibitors in the future should be combination drug therapy (with platinum drugs, cytotoxic drugs, antibody drugs, radiotherapy, etc.). In addition, the expression of S6K1, an important factor in mTOR pathway, is correlated with tumor development, which can be used as a diagnostic factor for tumor development.