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Immunotherapeutic approach to nasopharyngeal cancer

Timothy Allen

Global Allied Pharmaceutical, Center for Excellence in Research & Development, USA

E-mail : timothy.allen@gapsos.com>

Abdullateef Al-Hadeethi

Associate editor, Global Allied Pharmaceuticals, Jordan

Ghazaleh Shoja E Razavi

Director, Clinical Development- Oncology and Respiratory, Global Allied Pharmaceutical, USA

DOI: 10.15761/GVI.1000111

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Abstract

Nasopharyngeal cancer (NPC) is a rare cancer in most populations like the Caucasians in North America; it is a leading form of cancer in a few well-defined populations, including natives of southern China, Southeast Asia, the Arctic, and the Middle East/North Africa. The distinctive racial/ethnic and geographic distribution of NPC worldwide suggests that both environmental factors and genetic traits contribute to its development. In this review we aim to discuss the pathophysiology of NPC and the active molecules involved in immunotherapy.

Key words

  EBV, NPC, immunotherapy, epidermal growth factor receptor, kinase inhibitor, monoclonal antibody, cytokine, vaccine, T cell

Abbreviations

NPC: Nasopharyngeal Cancer; EBV: Ebstein-Barr Virus; HNSCC: Head and Neck Squamous Cell Carcinoma;  HPV: Human Papilloma Virus;    Rb: Retinoblastoma;  EGFR: Epidermal Growth Factor Receptor;  DBD: DNA Binding Domain;  RTK: Receptor Tyrosine Kinase;  CTL: Cytotoxic T Lymphocyte;  TA: Trojan Antigen;  APC: Antigen Presenting Cells ;  TGN: Trans-Golgi Network.

Introduction/epidemiology

Nasopharyngeal carcinoma (NPC) is a squamous cell carcinoma with remarkable geographic and racial distribution worldwide. It is a rare malignancy with an incidence below 1/100,000 populations per year in Caucasians from North America and other Western countries. In contrast, the highest incidence is noted in the Southern Chinese population of Guangdong, Inuits of Alaska, and native Greenlanders and particularly, among the Cantonese who inhabit the central region of Guangdong Province in Southern China where the incidence is 15-25 cases per 100,000 [1].

Swelling of the lymph nodes in the neck is the initial presentation in many people, and the diagnosis of NPC is often made by lymph node biopsy. Signs and symptoms related to the primary tumor include trismus, pain, otitis media, nasal regurgitation due to paresis (loss of or impaired movement) of the soft palate, hearing loss and cranial nerve palsy. Larger growths may produce nasal obstruction or bleeding and a "nasal twang". Metastatic spread may result in bone pain or organ dysfunction. Rarely, a paraneoplastic syndrome of osteoarthropathy may occur with widespread disease [2].

Etiology and pathogenesis

In endemic regions, NPC presents as a complex disease believed to be caused by an interaction between an oncogenic EBV-induced chronic infection, environmental, and genetic factors, in a multistep carcinogenic process [2]. The highest incidence of NPC in Southern Chinese strongly indicates that both genetic susceptibility and environmental factors contribute to the tumorigenesis of NPC related to its development and progression. Viral etiologies as well as other environmental and life-style factors have been proposed as causative components of NPC.

Epstein-Barr virus (EBV)

The EBV infects and persists latently in over 90% of the world population [3]. Although primary EBV infection is typically subclinical, the virus is associated later with the development of several malignancies, including NPC [4]. Transmission, mainly through saliva, occurs earlier in life in developing countries, where living conditions are crowded and less hygienic. B lymphocytes are the primary target of EBV infection, although the route of EBV entry into epithelial cells is unclear; nevertheless, EBV replication can occur in oropharyngeal epithelial cells, as well as in B lymphocytes in both normal and malignant nasopharyngeal tissue [5].

The involvement of EBV in NPC has been postulated since 1966, when NPC patients were found to express antibodies against an antigen later identified as belonging to EBV [6]. This finding was confirmed in 1970, when anti-EBV antibodies were observed to be higher in NPC patients than in controls [7]. Subsequent studies showed that NPC patients had elevated titers of IgG and IgA antibodies to the EBV viral capsid antigen lgA and early antigen, as well as increased IgG titers against the latent viral nuclear antigens 1 and 2 (EBNA-1, EBNA-2) and neutralizing antibodies against EBV-specific DNase [8,9]. Moreover, these antibody titers, especially of IgA, preceded tumor development by several years and were correlated with tumor burden, remission, and recurrence. Based on these patterns, antibody against viral capsid antigen is now established as the basis of a screening test for NPC in high-risk populations, particularly in combination with anti-EBV DNase antibodies. More recently, circulating cell-free EBV DNA has been detected in a higher proportion of NPC patients than controls, and these levels were positively correlated with disease stage and prognosis, although prospective studies of pre-disease levels have yet to be performed [10-15].

Considerable research has been directed toward determining whether at least part of the international pattern in the incidence of NPC can be explained by the distribution of different EBV strains. Compared with the prototype B95.8 EBV strain, consistent nucleotide variation in the amino terminus of the oncogenic viral latent membrane protein 1 (LMP1), including the loss of a XhoI restriction site, has been detected in EBV in NPC tumors from southern and northern Chinese, Malaysians, Alaska natives, and some U.S. Caucasians, but not North Africans. Other types of sequence variations in the LMP1 carboxyl terminus-including the number of copies of a 33-bp repeat element, a 15-bp insertion in the third repeat element, and a 30-bp deletion in the carboxyl terminus-have repeatedly been detected in Chinese NPC tumors [16-21]. The 30-bp deletion, also detected in a proportion of native Alaskans, Caucasian, Malaysian, and North African NPC, seems to enhance the transforming potential of LMP1 in vitro, and may be present in more aggressive disease forms. However, there is no strong evidence that the deleted variant is associated with increased risk of NPC, and there is a lack of large, well-designed epidemiologic studies of risk associations with EBV variants. Furthermore, the detection of specific LMP1 mutations in NPC tumors from diverse regions suggests that EBV strain variation is not geographically correlated with NPC incidence. Alternatively, the predominance of specific LMP1 variants in NPC could be influenced by immune selection, as certain key LMP1 mutations may produce a reduced cytotoxic T lymphocyte (CTL) response [22].

Salt-preserved fish and other foods

The non-viral exposure most consistently and strongly associated with the risk of developing NPC is consumption of salt-preserved fish, a traditional staple food in several NPC-endemic areas. In studies of Chinese populations, the relative risk of NPC associated with weekly consumption of salt-preserved fish, compared with no or rare consumption, generally ranged from 1.4 to 3.2, whereas that for daily consumption of salt-preserved fish ranged from 1.8 to 7.5 [23].

Tobacco and other smoke

The majority of case-control studies examining cigarette smoking and risk of NPC in a variety of populations reported an increased risk of 2- to 6-fold. In two studies from China, NPC cases were up to 5-fold more likely to have been exposed to domestic wood fire than controls [24], but other studies found no such association [25,26].

Human leukocyte antigen genes

Searching for genes conferring susceptibility to NPC has focused on the human leukocyte antigen (HLA) genes. These genes encode proteins required for the presentation of foreign antigens, including the presentation of viral peptides to the immune system for targeted tumor cell death. For example, because virtually all NPC tumors contain EBV, individuals who inherit HLA alleles with a reduced ability to present EBV antigens may have an increased risk of developing NPC, whereas individuals with HLA alleles that present EBV efficiently may have a lower risk.

Some HLA alleles have been consistently associated with NPC risk. Thus, in southern Chinese and other Asian populations, HLA-A2-B46 and B17 were generally associated with a 2- to 3-fold increase in NPC risk [27-29]. In contrast, a 30%-50% lower risk of NPC was found in association with HLA-A11 in both Chinese and Caucasians, B13 in Chinese, and A2 in Caucasians. In a meta-analysis of studies performed in southern Chinese populations, the combined evidence suggested a positive association of NPC risk with HLA-A2, B14, and B46, and an inverse association with HLA-A11, B13, and B22. In a linkage study, a gene closely linked to the HLA locus conferred a 21-fold excess risk for developing NPC; a separate study mapped an NPC susceptibility locus to a region near HLA-A. However, the reported associations between NPC risk and other HLA genes, including class II alleles, must be interpreted with caution due to the probability of chance findings based on multiple comparisons [30-32].

Immunotherapy for nasopharyngeal cancer

Kinase inhibitor drugs

There are no kinase inhibitors which are currently approved by FDA for NPC. However, a few drugs are in phase I-III clinical trials as shown in

Erlotinib: Erlotinib is an aquinazoline derivative with antineoplastic properties. Erlotinib, acting as an adenosine triphosphate competitor reversibly binds to the intracellular catalytic domain of epidermal growth factor receptor (EGFR) tyrosine kinase, thereby reversibly inhibiting EGFR phosphorylation and blocking the signal transduction events and tumorigenic effects associated with EGFR activation.

Checkpoint inhibitor drugs

A few of this class of drugs are under clinical trials in phases I, II, and III as in below.

Nivolumab: Nivolumab is a fully human monoclonal antibody directed against the negative immunoregulatory human cell surface receptor PD-1 (programmed death-1 or programmed cell death-1/PCD-1) with immunopotentiation activity. Nivolumab binds to and blocks the activation of PD-1, an Ig superfamily transmembrane protein, through its ligands PD-L1 and PD-L2, resulting in the activation of T-cells and cell-mediated immune responses against tumor cells or pathogens. Activated PD-1 negatively regulates T-cell activation and effector functions through the suppression of P13K/Akt pathway activation [34].

Vaccine therapy

Although there are no vaccines which are currently approved by FDA for NPC, few vaccine formulations are in phase I clinical trials as shown in .

Mutant p53 peptide, pulsed dendritic cell vaccine: This is an anti-cancer vaccine, consisting of autologous dendritic cells, which have been pulsed with a mutant p53 peptide. The premise is that many tumor cells overexpress mutant p53 proteins, resulting in the loss of apoptosis regulation and abnormal cell proliferation. Therefore, vaccination with mutant p53 peptide pulsed dendritic cells may stimulate the host immune system to mount a CTL response against tumor cells expressing mutant p53, resulting in tumor cell lysis.

MAGE-A3 HPV-16 vaccine: This is a multi-epitope "Trojan Antigen"- ("TA") construct vaccine with immunostimulatory and anti-tumor activities. It consists of human melanoma antigen A3 (MAGE-A3) and human papillomavirus (HPV) 16 peptide epitopes, which are linked by the furin-sensitive linker peptide, RVKR (arginine-serine-lysine-arginine). The TA-construct enters the cytoplasm of antigen-presenting cells (APCs) where it is processed in the endoplasmic reticulum (ER) and the trans-Golgi network (TGN), by the endopeptidase, furin. This process releases the epitopes from the RVKR linker peptide and, together with various exopeptidases, generates MHC class I-binding peptides. Expressed on the cell surfaces of APCs, these MHC class I-binding peptides stimulate a cytotoxic T lymphocyte (CTL) response against tumor cells that display the same peptide epitopes on their cell surfaces.

Conclusions and future perspectives

Ongoing research activities have increased our understanding of the tumor microenvironment, various immunotherapeutic modalities and combination therapies (i.e., combining chemotherapy with immunotherapy). However, the effects of such modalities in combination with chemotherapy in cancer patients are still in the exploratory phase.  Moreover, the complete perspective of immunotherapy treatment has not been realized and/or utilized. Proper pre-clinical and clinical designs are the important pillars for understanding the future of immunotherapy in treating cancer patients.

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Editorial Information

Editor-in-Chief

Charles J. Malemud
Case Western Reserve University

Article Type

Review Article

Publication history

Received: April 20, 2016
Accepted: May 24, 2016
Published: May 27, 2016

Copyright

©2016 Allen T. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Allen T, Al-Hadeethi A, Razavi GSE (2016) Immunotherapeutic approach to nasopharyngeal cancer. Glob Vaccines Immunol 1: DOI: 10.15761/GVI.1000111

Corresponding author

Timothy Allen

Global Allied Pharmaceutical, Center for Excellence in Research and Development, 160 Vista Oak Dr. Longwood, FL 32779, USA, Tel: 1-321-945-4283.

E-mail : timothy.allen@gapsos.com

Drug

Clinical trial identifier number

Phase

Study design

Target

Erlotinib

NCT01316757

Phase II

Open label, Efficacy Study

EGFR

Table 1. Non-FDA approved kinase inhibitor drugs [33]

Drug

Clinical trial identifier number

Phase

Study design

Target

Nivolumab

NCT02339558

Phase II

Efficacy Study, Open Label

PD-1

Table 2. Non-FDA approved check point inhibitor drugs [34]

Drug

Clinical trial identifier number

Phase

Study design

Target

Mutant p53 peptide pulsed dendritic cell vaccine

NCT00404339

Phase I

Randomized

CTL

MAGE-A3 HPV-16 vaccine

NCT00704041

Phase I

Randomized, Open Label, Safety/Efficacy Study,

Cancer cells

Table 3. Non-FDA approved vaccines [35]