Amatuximab and novel agents targeting mesothelin for solid tumors.

Mesothelin (MSLN) is considered a promising target for cancer therapy. Originally extracted in 1992 after the immunization of mice with a human ovarian cancer (OC) cell line and cloned in 1996, MSLN seems to be involved in cell adhesion and metastasis. MSLN is prevalent in mesothelia tissues but is expressed in several human cancers, such as OC, pancreatic cancer, mesothelioma, and lung cancer. Amatuximab (MORAb-009) is a mouse-human chimeric monoclonal antibody with a selective affinity for MSLN. The principal mechanism of action comprises inhibition of binding of MSLN with the antigen CA125/MUC16. The highest phase of development is actually a Phase II trial (MORAb-009-201, Europe). In this review, we describe the mechanism of action of amatuximab and other MSLN-targeting novel drugs, along with a discussion about the expected efficacy, safety, and toxicity of this promising group of agents and implications for future research and clinical practice.

Plain language summary

Mesothelin (MSLN) is a glycoprotein, detectable on the surface of mesothelial cells. Although its biological function in normal cells is completely clarified, it is overexpressed in many types of cancer, and in cancerous cells, it may be involved in the promotion of cell proliferation, adhesion and migration, chemotherapy resistance, and inhibition of apoptosis. MSLN seems to be an interesting target in diagnosing and treating several solid tumors, in particular mesothelioma, which, for the aggressive nature of the disease, still represents one of the concrete challenges for modern oncology. In this review, we comprehensively describe MSLN as a potential target for cancer therapy, along with a presentation of profiles of the new agents under investigation for mesothelioma and other solid tumors. A list of ongoing clinical trials is provided.

Introduction

Mesothelin (MSLN) is considered an interesting and promising target for cancer research and therapy. It was initially identified as the cell surface antigen CAK1 by Chang et al in 1992;1 then, it was characterized and cloned as a 40-kDa glycoprotein detected on the surface of normal mesothelial cells.2 It is overexpressed by cancer cells in mesothelioma, ovarian cancer (OC), pancreatic cancer (PC), and other solid tumors. Relatively recent research detected high MSLN expression in acute myeloid leukemia3 and in cholangiocarcinoma.4 The name “mesothelin” was assigned to highlight the presence of the protein in normal mesothelial cells, including pleura, pericardium, fallopian tubes, trachea, and cornea.

The precursor, which is a 71-kDa protein that is encoded by a 2,138-bp-long cDNA and contains 628 amino acids, is then cleaved into two products, a ~31-kDa N-terminal region, called megakaryocyte potentiating factor (MPF), and the ~40-kDa mesothelin protein, which is the main form represented on the cell surface. MSLN is commonly a membrane-bound, glycosylphosphatidylinositol (GPI)-linked protein, but it is also detectable in a soluble form (soluble MSLN protein [SMP]), which is shed from cancer cells.5 Patterns of MSLN expression in some types of cancer cells are characterized by using immunohistochemistry,6 exploiting the SAGE database,7 and using the antibody mAb5B2.8 Detection of MSLN in serum is a useful marker in cancer diagnostic procedures.9

The biological function of MSLN in normal cells is not completely clarified. It is likely to be involved in cell adhesion, differentiation, and signal transduction,10 and in cancerous cells, it may be involved in the promotion of proliferation, cell migration and spread, chemotherapy resistance, and inhibition of apoptosis. The capability of MSLN to bind to the cancer antigen CA-125, also called mucin 16 (or MUC16), suggests that MSLN is involved in cell adhesion and is an important target for innovative anticancer agent.11–13 The overexpression of MSLN activates multiple intracellular pathways, including nuclear factor-kappaB (NFκB), MAPK, and PI3K pathways, with the consequent promotion of cell proliferation, migration, and metastasis to distal sites and the inhibition of apoptosis.14,15 Importantly, in recent years, the activation and stimulation of immune reactions using engineered T-cells with chimeric antigen receptors (CARs) allowed the characterization of antigens, including MSLN, overexpressed in solid tumors and in several B-cell malignancies, including acute lymphoblastic leukemia, chronic lymphocytic leukemia, and non-Hodgkin lymphoma.16,17

After the cleavage, MPF acts as a cytokine that stimulates colony formation in bone marrow megakaryocytes. MSLN is a GPI-anchored cell-surface protein that performs cell adhesion modulating activities.

MSLN as a therapeutic target in mesothelioma

Mesothelioma is a rare cancer deriving from the mesothelium, which lines the pleura and other serous cavities (such as the peritoneum, pericardium, and tunica vaginalis testis), is the main form of cancer in these structures, and is often characterized by a poor prognosis. Mesothelioma is described in the benign or malign subtypes. Surgery is the choice option for the benign form, but in case of malign transformation, the overall estimated survival is 24–36 months.18 The malignant form (malignant mesothelioma [MM]) has an epithelial morphology, or a fibrous one, also called sarcomatoid, or a combination of the two. MSLN is overexpressed in up to 95% of patients with the epithelioid form. In contrast, in the sarcomatoid form (10%–15% of all mesotheliomas), there is no overexpression of MSLN.19,20

The crude annual incidence of MM in Europe is 2 new cases per 100,000, while the prevalence is 3.5 cases per 100,000.21 According to data from the American Cancer Society, in the United States, the annual incidence is estimated to be ~3,000 new cases per year.22,23 The global incidence trend indicates 36,925 incident cases in 2015 versus 26,376 in 2005, with an overall change of 40% due to different factors (such as population growth, age trends, and change in incidence).24

The most important risk factor for the development of MM is inhalation of asbestos, which induces oncogenesis via the activation of the NF-κB-dependent pathway.25 Asbestos, whose principal components are two types of fibers, serpentine and amphibole, was largely used until 1980s–1990s, for its excellent acoustic and thermal insulation properties and its mechanical strength. A very long latency period – up to 25–40 years26 – can elapse before the development of this tumor. Moreover, developed countries are gradually promoting laws to restrict the use of asbestos, which means that some countries expect that the peak incidence has already been reached. Other known risk factors include therapeutic radiation27 and genetic factors.28

Diagnostic procedures include imaging, cytology, and immunohistochemistry, but, to date, no technique is considered individually certain for the purposes of early diagnosis.29 Surgery is applied with a prognostic/palliative intent, while standard chemotherapy is based on a treatment with cisplatin combined with an antifolate (pemetrexed or raltitrexed). New therapeutic approaches under evaluation include angiogenesis inhibitors,30 mTOR inhibitors,31 and histone deacetylase inhibitors.32 Given the overexpression of MSLN in >80% of total MM cases, new agents targeting MSLN under evaluation in clinical trials are considered a very promising field for research and therapy.

MSLN as a therapeutic target in other solid tumors

MSLN seems to be overexpressed iñ30% of all cancers.33 MSLN expression in different types of solid tumors is described comprehensively by Hassan et al34 (see also The Human Protein Atlas).35

Pancreatic cancer

PC was investigated for the expression of MSLN by Argani et al,36 Hassan et al,37 and Zervos et al,38 showing a high expression of MSLN for most of the pancreatic adenocarcinomas but not in normal pancreatic cells. At the same time, their studies revealed the presence of MSLN in other adenocarcinomas of the biliary tract. Recent data confirm the hypothesis that new immunotoxins actually investigated in clinical trials, such as LMB-100 (previously named RG7787), might have synergistic anticancer effects when used in combination with taxanes or other standard chemotherapy.39

Ovarian cancer

OC expresses, especially in the non-mucinous variant of cancer cells, high levels of MSLN. Hanaoka et al40 showed that 68.8% of OCs and 24.2% of borderline-type tumors express high MSLN levels, with implications for a shorter progression-free survival (PFS) and overall survival (OS). An analysis of MSLN expression is currently being performed by using immunohistochemistry and imaging techniques (immunoPET) with positron-emitting isotopes (89Zr-labeled mAbs and 64Cu-labeled mAbs) to evaluate the tumor uptake of innovative antibody-drug conjugate (ADC) immunotherapeutic agents.41,42 The resulting data will be helpful to predict the potential utility and efficacy of new immunoconjugates in the therapy of these types of cancer.43

Breast cancer

Currently, there is a plethora (451) of studies regarding targeted therapies for breast cancer (BC) (as reported in ClinicalTrials.gov trials register).44 However, only 5 studies correlated with MSLN as the main biomarker (for reference see Table 1). In treating BC, MSLN, as a target, may be particularly promising for triple-negative breast cancers (TNBC), one of the most aggressive forms of BC. Li et al investigated MSLN as a prognostic BC biomarker, whose expression is highly enriched especially in African–American women.45 These results are consistent with data published by Bayoglu et al46 and Parinyanitikul et al,47 who, respectively, reported a prevalence of 42.3% and 34% of patients expressing MSLN in TNBC. However, they suggested that MSLN overexpression may not have a prognostic value and does not correlate with the survival outcomes in patients with TNBC. Future work is needed to evaluate the potential of MSLN-targeted therapy in the treatment of BC.

Table 1

Summary of clinical trials investigating new agents targeting mesothelin expressing tumors

Study ID (ClinTrial.gov)	Phase	Start date/recruitment status	Sponsor or principal investigating research institute	Agent or pharmacological mechanism	Condition	Intervention	Main outcome measures
NCT01445392*	I	November 13, 2007/completed	NCI; CC	SS1P	Mesothelioma	Multicycle or single cycle SS1PPemetrexedCisplatin	Safety and MTDBest ORR
NCT01362790*	III	May 11, 2011/active, not recruiting	NCI; CC	SS1P	MesothelionmaLung adenocarcinomaPancreatic neoplasms	SS1(dsFv)PE38PentostatinCyclophosphamide	ORRSSP1 antibody formationGrade of ADEsOS; PFS; DoR
NCT01051934*	I	December 29, 2009/completed	NCI; CC	SS1P	NSCLCAdenocarcinoma	SS1(dsFv)PE38PaclitaxelCarboplatinBevacizumab	Safe and tolerable dosesPharmacokineticsDoR; ORR
NCT00066651*	I	July 2003/completed	NCI; (NCI)	SS1P	MesotheliomaSolid tumors	SS1(dsFv)PE38 immunotoxin	NA
NCT00006981*	I	December 2000/completed	NCI; (NCI)	SS1P	MesotheliomaSolid tumors	SS1(dsFv)PE38 immunotoxin	NA
NCT02810418*	III	June 10, 2016/recruiting	NCI; CC	LBM-100	NeoplasmsPancreatic neoplasms	LBM-100Nab-paclitaxel	ORR, MTD, safety and tolerability of LBM-100+ Nab-paclitaxel
NCT02798536*	I	June 7, 2016/recruiting	NCI; CC	LBM-100	Mesothelioma	LBM-100Nab-paclitaxel	MTD; average time from treatment initiation to disease progression or death; proportion of patients at MTD at RECIST; listing and frequency of treatment-related ADEs
NCT03006302*	II	June 2017/not yet recruiting	Sidney KimmelComprehensive Cancer Center	CRS-207	Metastatic pancreatic adenocarcinoma	CRS-207EpacadostatPembrolizumabGVAX	6 months survival; recommended dose of Epacadostat; 6 months survival; OS; PFS; ORR; immune-related duration of response
NCT02575807*	III	January 2016/recruiting	Aduro Biotech Inc.; Incyte Corporation	CRS-207	Platinum resistant: Ovarian cancerFallopian cancerPeritoneal cancer	CRS-207EpacadostatPembrolizumab	Number of patients reporting hematologic and non-hematologic DLTs; Adverse events by CTCAE grades; ORR; PFS
NCT02243371*	II	December 2014/active, not recruiting	Sidney KimmelComprehensive Cancer Center; Bristol MS; Aduro Botech; American Association for Cancer Research	CRS-207		CRS-207NivolumabCY	OS; number of patients experiencing treatment-related ADEs; TTP; tumor marker kinetics
NCT02004262*	II	January 2014/completed	Aduro Biotech Inc.	CRS-207	2nd line, 3rd line and greater metastatic pancreatic cancer	CRS-207GVAXGemcitabineCapecitabineErlotinibIrinotecanCyclophosphamide	OS; treatment-related ADEs
NCT03102320*	I	May 26, 2017/recruiting	Bayer	Anetumab-R	Neoplasms	Anetumab-RGemcitabineCisplatin	MTD; ORR; ADEs; DoR; DRR; PFS
NCT03023722*	II	May 11, 2017/recruiting	Howard Hochster; Bayer; Yale University	Anetumab-R	Pancreatic cancer	Anetumab-R	Response rate as measured per RECIST criteria; TTP; toxicity
NCT02839681*	II	June 2017/recruiting	NCI; CC	Anetumab-R	Lung neoplasms	Anetumab-R	Recommended Phase II dose; ORR; PFS; DoR; OS
NCT02824042*	I	September 7, 2016/recruiting	Bayer	Anetumab-R	Medical oncology	Anetumab-RItraconazole	QRS Interval duration; QT interval duration; cycle 1+2 AUC; incidence of serious and non-serious ADEs
NCT02751918*	I	June 8, 2016/recruiting	Bayer	Anetumab-R	Ovarian neoplasms	Anetumab-RPEGylated liposomal doxorubicin	MTD; incidence of serious and non-serious ADEs; AUC; incidence of positive anti-drug antibody interaction; incidence of positive neutralizing antibody iter
NCT02696642*	I	August 14, 2016/recruiting	Bayer	Anetumab-R	Neoplasms	Anetumab-R	Incidence of treatment-related ADEs, cycle 1 AUC; pharmacokinetics; immunogenicity as defined by the titer of anti-anetumab-R antibodies; immunogenicity as defined by incidence of neutralizing antibodies
NCT02639091*	I	February 3, 2016/recruiting	Bayer	Anetumab-R	Medical oncology	Anetumab-RPemetrexedCisplatin	MTD; plasma concentration of anetumab-R; tumor response evaluation following mRECIST criteria; number of patients with a positive titer of anti-drug antibodies
NCT02610140*	II	December 3, 2015/active, not recruiting	Bayer; ImmunoGen and MorphoSys	Anetumab-R	Mesothelioma	Anetumab-RVinorelbine	OS; PFS; ORR; DoR; number of patients with serious ADEs as a measure of safety and tolerability
NCT02485119*	I	August 14, 2015	Bayer	Anetumab-R	NeoplasmsBreast cancer	Anetumab-R	Number of treatment-related AEs as a measure of safety and tolerability; pharmacokinetic parameters for Bay 94-9343 (Cmax, AUC, tmax); tumor response based on RECIST; level of MSLN expression using immunohistochemistry
NCT01469793*	I	November 2011/completed	Genentech, Inc.	DMOT4039A	Metastatic pancreatic adenocarcinomaPlatinum-resistant ovarian cancer	DMOT4039A	MTD; Number of patients with DLTs; recommended Phase II dose
NCT02341625*	I	January 2015/active, not recruiting	Bristol-Myers Squibb	BMS-986148	MesotheliomaNSCLCOvarian cancerPancreatic cancerGastric cancer	BMS-986148Nivolumab	Number and grade of AEs
NCT02884726*	I–II	August 2016/active, not recruiting	Bristol-Myers Squibb	BMS-986148	Advanced and/or metastatic solid tumors	BMS-986148	Incidence and grade of AEs and SAEs;
NCT02792114*	I	June 2016/recruiting	Memorial Sloan Kettering Cancer Center	Mesothelin-targeted T-cells	Breast cancerMetastatic HER2-negative breast cancer	Cyclophosphamide, mesothelin-targeted T-cells	MTDs
NCT02930993*	I	August 2016/recruiting	China Meitan General Hospital Marino Biotechnology Ltd.	CAR-T-cells	Mesothelin-positive tumors	AntimesothelinCAR-T-cells	Safety of infusion of autologous anti-mesothelin CAR-T-cells; treatment response rate of anti-mesothelinCAR-T-cells; PFS; OS; proliferation of antimesothelinCAR-T-cells in patients; activation of anti-mesothelinCAR-T-cells in patients; •persistence of antimesothelinCAR-T-cells in patients
NCT03030001*	I–II	February 15, 2017/recruiting	Ningbo Cancer Hospital	CAR-T-cells	Solid tumorAdult advanced cancer	PD-1 antibody expressing mesothelin-specificCAR-T-cells	Safety of infusion of autologous mesothelin-specific CAR-T-cells; response evaluation criteria of solid tumor; PFS; OS
NCT02706782*	I	March 2016/recruiting	Shanghai GeneChem Co., Ltd.	CAR-T-cells	Pancreatic cancer	TAI-mesoCAR-T-cells	Number of patients with ADEs; number of patients with tumor response; detection of transferredT-cells in the circulation using quantitative methods (PCR)
NCT01583686*	I	March 30, 2012/recruiting	NCI; CC	CAR-T-cells	Cervical cancerPancreatic cancerOvarian cancerMesotheliomaLung cancer	Anti-mesothelinCARFludarabineCyclophosphamideAldesleukin	Determine a safe dose and determine if this approach will result in an objective tumor regression; determine the in vivo survival of CAR gene-engineered cells
NCT02580747*	I	October 2015/recruiting	Chinese PLA General Hospital	CAR-T-cells	Malignant mesoteliomasPancreatic cancerOvarian tumorTriple-negative breast cancerOther mesothelin-positive tumors	Anti-meso-CAR vector transducedT-cells	Occurrence of study-related adverse events; anti-tumor responses to CAR-T-meso cells infusions
NCT01355965*	I	May 2011/active, not recruiting	University of Pennsylvania	CAR-T-cells	Malignant pleural mesothelioma	Autologous T-cells	AEs; ORR
NCT02414269*	I	May 2015/recruiting	Memorial Sloan Kettering Cancer Center	CAR-T-cells	Malignant pleural diseaseMesotheliomasMetastasesLung cancerBreast cancer	iCasp9M28z T-cellinfusionsCyclophosphamide	Composite measure of severity and number of AEs; changes in serum levels of the biomarker soluble mesothelin-related peptide
NCT03054298*	I	March 1, 2017/recruiting	University of Pennsylvania	CAR-T-cells	Lung adenocarcinomaOvarian cancerPeritoneal carcinomaFallopian tube cancerMesotheliomas	Hu-CAR-T-meso cells	Number of participants with treatment-related ADEs; clinical anti-tumor effect by RECIST criteria (modified for mesothelioma); PFS; OS
NCT02159716*	I	June 2014/completed	University of Pennsylvania	CAR-T-cells	Metastatic pancreatic adenocarcinomaEpithelial ovarian cancerMalignant epithelial pleural mesothelioma	CAR-T-meso	Number of ADEs

Note:

All trial information is available at https://ClinicalTrials.gov/ct2/show/[NCTidentifier].

Abbreviations: ADEs, adverse drug events; AEs, adverse events; AUC, area under the curve; CAR, chimeric antigen receptor; CC, National Institutes of Health Clinical Center; CTCAE, common terminology criteria for adverse events; CY, cyclophosphamide; DLT, dose-limiting toxicity; DoR, duration of response; DRR, durable response rate; MSLN, mesothelin.; MTD, maximum tolerated dose; NA, not available; NCI, National Cancer Institute; NSLC, non-small-cell lung cancer; ORR, objective response rate; OS, overall survival; PCR, polymerase chain reaction; PFS, progression-free survival; RECIST, Response Evaluation Criteria in Solid Tumors; SAEs, serious adverse drug events; TTP, time to progression.

Lung cancer

Ordonez, Miettinen and Sarlomo-Rikala performed immunohistochemistry studies using the MSLN-specific antibody 5B2 and showed that 38%–40% of lung adenocarcinomas stain positively for MSLN.48,49 In another study, the presence of the MSLN precursor was detected in 82% of lung adenocarcinoma, and its mature form was detected in 55% of patients.50

Head and neck cancers

The expression of MSLN in the human leptomeninges and meningiomas is not completely studied and understood. There are similarities in the structure and functions of the pleura and leptomeninges, and this suggests that MSLN might play a role in the meningeal function and could be expressed in meningiomas.51 Future research is necessary to better understand the possible role of MSLN as a target for therapy of gliomas, meningiomas, and/or other head and neck cancers. The overexpression of MSLN was also determined by immunohistochemistry in thymic carcinomas, suggesting that MSLN is a potential important target for this type of cancer.52,53

Gastric cancer

Tomoaki et al investigated the expression and extracellular secretion of MSLN in human gastric cancer cell lines and found lower expression levels in the human gastric cancer compared to those noted in human mesothelioma cells,54 and the levels were not specific to gastric cancer. Recently, Han et al55 found that 25.6% of a cohort of 117 patients with gastric carcinoma showed high levels of MSLN expression, which was associated with a poor prognosis. They concluded that MSLN-targeted therapies merit further research in patients with gastric carcinomas.

MSLN targeting: amatuximab (MORAb-009)

Amatuximab (alternative names: MORAb-009, anti-MSLN monoclonal antibody [MAb]) is a chimeric, humanized IgG1/k MAb that targets the cell surface MSLN. The precursor of MORAb-009 was isolated by Chowdhury et al in 199856 from a mouse splenic mRNA and was then optimized by fusing the gene encoding MSLN Fv (SS1 scFv) with human IgG1 and kappa regions.57 Amatuximab consists in 83% of human and 17% of murine sequences, and it is comprised of 2 identical heavy and 2 identical light chains connected by disulfide bonds. The substance can potentially reduce tumor growth by inhibiting MSLN binding to the extracellular substrate and also by antibody-dependent cellular cytotoxicity (ADCC). Amatuximab is not yet commercially available, and the highest development phase is Phase II. It is actually investigated in trials for the treatment of pleural mesothelioma and PC in the USA, Europe, Canada, and South America. Today, the primary focus is to evaluate its efficacy against mesotheliomas.

Pharmacology

Pharmacodynamics

After the characterization of amatuximab, Hassan et al57 performed preclinical studies to investigate the ability of amatuximab to target the MSLN protein expressed in some human cancer cells, to internalize in cancer cells after binding MSLN and to exert ADCC.

Results from the preclinical studies indicate a potential relevant interaction between amatuximab and tumorigenic cells/tissues overexpressing MSLN, and specifically:

In immunohistochemistry studies, MSLN-positive tumor cells show strong cell surface staining, as reported by investigational medicinal product (IMP) dossier and by independent studies;1,58

In antibody-dependent cytotoxicity studies, amatuximab enhances ADCC in MSLN-positive cancer cell lines, but not at comparable levels in MSLN-negative cell lines;59,60

In standard in vivo murine xenograft studies, Hassan et al57 and Morphotek Inc. investigated the potential effects of amatuximab as a single agent or in combination with gemcitabine and rituximab. Amatuximab alone resulted in a significant reduction of tumor dimension in the intervention group (amatuximab-treated) compared to the control group (29.9% difference). Rituximab had no measurable effects, while some synergy with gemcitabine was detected, as an additive effect;

In adhesion blocking assays, amatuximab inhibited the interaction of MSLN-expressing cells with MUC16-expressing cells, a factor considered of great importance for reducing cell adhesion, migration patterns, and finally metastasis.61

Pharmacokinetics (PK)

Amatuximab, in actual clinical trials, is administered intravenously at the identified maximum tolerated dose (MTD) of 200 mg/m2. The main available data about MORAb-009 PK are described by Hassan et al,62 Gupta et al,63 and Fujisaka et al.64 The population PK analysis of the data collected from previous Phase I and Phase II studies in PC or malignant pleural mesothelioma (MPM) describes a two-compartment model, incorporating parallel linear and nonlinear (Michaelis–Menten) pathways for elimination from the central compartment. The nonlinear elimination is related to the interaction with the variable cell internalization of the antigen-antibody complex Ab-MSLN. In summary, PK studies estimate that a dose of 5 mg/kg, administered weekly, achieves a steady-state Cmin of 83.1 mg/mL and is considered a balanced reference dose for efficacy and safety in ~80% of subjects. The serum concentration–time profile of amatuximab suggests that after 5 weeks of weekly dosing, 89% of the steady-state concentration level is reached. Factors, including weight, age, gender, and race, seem not to influence the pharmacological effects of amatuximab. Combination schedules with other chemotherapy drugs, for example, cisplatin and pemetrexed therapies, show synergic potentiation and reach a higher steady state Cmin. Other models to investigate the distribution of amatuximab in the body and the patterns of penetration in cancer formations are based on imaging techniques using SPECT.65

Safety and expected toxicity

Amatuximab is actually under investigation in several international trials. For this reason, the safety profile is implemented day after day following the adverse events (AEs) clinical reporting and applying pharmacovigilance signal detection. Phase I and Phase II studies investigated the safety and tolerability of amatuximab; although indicating a discrete tolerability, they showed that 54.2%62 to 76.5%64 of patients experienced AEs that were considered to be associated with the amatuximab treatment. Among a total of 41 patients in two studies (24+17, respectively), 10%–29.4% experienced AEs (including cytokine release syndrome, hot flushes, pyrexia, arthralgia, and nausea) that were potentially related to immune-mediated mechanism, which is relevant to the fact that amatuximab is a MAb. Other common AEs include fatigue (the most frequent), liver function elevation (AST, ALT, ALKP, and serum bilirubin), vomiting, decrease in appetite and weight, headache, hypotension, dizziness, and allergic reactions. It is reported that only one patient died of interstitial lung disease (ILD), and the cause was related to an AE to the amatuximab treatment.

Genotoxicity/teratogenity/pregnancy: available data

To date, no genotoxicity or teratogenicity or pregnancy studies have been planned and conducted for amatuximab. Amatuximab belongs to the pharmacological class of mono-clonal antibodies and is expected not to be genotoxic.

Amatuximab in clinical studies

Amatuximab is investigated in trials for the treatment of pleural mesothelioma and PC in USA, Europe, Canada, and South America. The primary intention of researchers is the evaluation of its efficacy against mesotheliomas. An “investigational new drug application” was launched by Morphotek for amatuximab in 2006.

In this paper, we refer to amatuximab and other anti-MSLN agent studies citing the Clinical Trials Identifier (NCT number) in Medline (www.ClinicalTrials.gov).44 A summary of the clinical trials of amatuximab for MSLN-expressing tumors currently listed on ClinicalTrials.gov is presented in Table 2.

Table 2

Summary of clinical trials investigating MORb-009 for mesothelin expressing tumors

Study ID-NLM identifier (other acronyms)	Phase/number of patients enrolled	Start date/recruitment status	Sponsor or principal investigating research institute	Agent or pharmacological mechanism	Condition	Main outcome measures	Posted/published data (OS/PFS/other)
NCT0032549455,60 (MORAb-009-001)	Phase I/24	May 2006/completed	Morpohtek	MORAb-009	Pancreatic cancer Mesothelioma Ovarian cancer NSCLC	Safety and tolerability as a measure of ADE; safety and tolerability as a measure of clinical laboratory parameters; pharmacokinetics of MORAb-009; OTR; percentage of patients with antibodies against infliximab	NA
NCT0101878457,61 (MORAb-009-J081-102)	Phase I/17	November 2009/completed	Eisai CO. Ltd; Eisai Inc.	MORAb-009	Cancer mesothelin-positive	DLT; complete response and partial response; best overall response rate in the RECIST evaluation	NA
NCT0073858262,63 (Amatuximab/MORAb-009-003)	Phase II/89	December 2008/completed	Morphotek	MORAb-009PemetrexedCisplatin	Malignant pleural mesothelioma	OS; PFS; best overall response rate	PFS (months): 6.1 (in 51% treated pts) (95% CI: 5.8, 6.4) OS (months): 14.8 (95% CI: 12.4, 18.5)
NCT0057071364 (MORAb-009-002)	Phase II/155	December 2007/completed	Morphotek	MORAb-009PlaceboGemcitabine	Pancreatic cancer	OS; PFS; best overall response rate	PFS (months): 3.4 (95% CI: 1.9, 4.7) vs 3.5 (95% CI: 2.8, 4.9) OS (months): 6.5 (95% CI: 4.5, 8.1) vs 6.9 (95% CI: 5.4, 8.8)
NCT0235714765 (ARTEMIS)	Phase II/108	November 2015/active, not recruiting	Morphotek	PlaceboMORAb-009PemetrexedCisplatin	Mesothelioma, malignant	OS; PFS; ORR; DoR; health-relatedQOL; evaluate ADEs and AEs	NA
NCT0152132558,66 (MORAb-009-201)	Phase I/6	September 2011/completed	Morphotek	MORAB-009	Pancreatic cancer Mesothelioma Ovarian cancer NSCLC	Determine biodistribution of radiolabeled amatuximab in tumor and non-tumor tissue; safety of a single IV of indium-CHX-A amatuximab; pharmacokinetics and serum level; uptake of indium-CHX-A amatuximab; correlate shed serum mesothelin to imaging	NA
NCT0141345167	Phase I/7	July 2011/terminated	National Cancer Institute; National Institute of Health Cancer Center	MORAb-009	Carcinoma, pancreatic ductal Mesothelioma Ovarian neoplasms NSCLC	Biodistribution of radiolabeled amatuximab in tumor and non-tumor tissue; background ratio and maximum counts; CTCAE ADEs; pharmacokinetics; antibody uptake versus IHC mesothelin expression	NA

Abbreviations: ADEs, adverse drug events; AEs, adverse events; CHX-A, (isothiocyanatobenzyl)-cyclohexyl-; CI, confidence interval; CTCAE, common terminology criteria for adverse events; DLT, dose-limiting toxicity; DoR, duration of response; IHC, immunohistochemistry; IV, intravenous; MORb-009, amatuximab); NA, not available or not appropriate; NSCLC, non-small-cell lung cancer; ORR, objective response rate; OS, overall survival; OTR, objective tumor response; PFS, progression-free survival; QOL, quality of life; RECIST, Response Evaluation Criteria in Solid Tumors.

Initially, a Phase I clinical trial (NCT00325494) was planned,66 recruiting 24 subjects with PC or mesothelioma or non-small-cell lung cancer (NSLC) or OC. The primary outcome measures included the evaluation of safety and tolerability of amatuximab, the frequency and severity of the AEs and of the serious adverse events (SAEs), laboratory parameters, and cardiovascular examinations. The dose range that was investigated was between 12.5 and 400 mg/m2. The MTD was set to 200 mg/m2. A similar Phase I clinical trial (NCT01018784)67 was performed in 17 Japanese patients. The aims of the study were to determine dose-limiting toxicity (DLT) and MTD. In this trial, Fujisaka et al64 reached similar conclusions, and the weekly dose was determined to be 200 mg/m2. Taking into account an acceptable safety profile and the potential of obtaining clinical benefit, a subsequent Phase II, multicentric, single-arm, open-label trial (NCT00738582)68 recruited 89 patients presenting unresectable MPM, naïve to chemotherapy. Amatuximab was administered in association with standard chemotherapy regimens, with the primary objective to improve PFS. The secondary outcome measures were the OS, overall response (OR), and evaluation of the safety profile of amatuximab. The PFS was not improved in the treatment group compared to the controls. However, the combined therapy of amatuximab plus pemetrexed/cisplatin gave encouraging results in terms of the median OS (14.8 months) and the objective response rate (ORR) (39%).69

The study NCT0057071370 was a Phase II, double-blind, randomized controlled trial, in which amatuximab was administered with gemcitabine in patients with unresectable PC. The patients were randomized to gemcitabine alone or gemcitabine plus amatuximab. The primary outcome was OS, and the secondary outcome measures were PFS and best ORR. The treatment arm (gemcitabine plus placebo) showed better results compared to amatuximab, for all the three main outcomes, but no statistical analysis was provided. The posted data are available at www.ClinicalTrials.gov.44

NCT0235714771 (acronym: ARTEMIS) was another Phase II clinical trial, started in 2015 with the main objective to evaluate the OS in patients with previously untreated, unresectable MPM. The standard chemotherapy regimen was administered to all the patients in combination with amatuximab or a placebo. After four or six induction cycles, the stable patients continued maintenance therapy with either amatuximab or placebo. The PFS, ORR, objective duration of response (DoR), and health-related quality of life (QoL) were the principal secondary outcome measures. In addition, the clinical development of the drug is ongoing. Two early Phase I mono-centric studies were conducted with the objective of investigating in vivo distribution and safety of 111In radio-labeled amatuximab in MSLN-expressing cancers (NCT0152132572 and NCT0141345173). Despite the small number of recruited patients (6 and 7, respectively), Lindenberg et al65 reported their findings that 111In-amatuximab showed a good tolerability, the dosimetry profile was favorable, and the physiologic uptake was detectable in the liver, kidneys, spleen, and heart. The uptake of 111In-amatuximab was higher in mesotheliomas compared to PCs. This study was realized with the objective of refining imaging techniques in patients with advanced cancers.65

MSLN targeting: novel agents

MSLN expression is rather limited in normal tissues, but it is highly elevated in some solid human tumors, such as malignant mesothelioma, PC, OC, and lung adenocarcinoma. This provides the rational basis to test different agents potentially targeting MSLN.

A summary of new agents undergoing clinical evaluation is presented in Table 1, including monoclonal antibodies, in the form of single agents or as ADCs, immunotoxins, vaccines, and chimeric T-cells, containing Fv fragments that recognize MSLN.

SS1P

SS1P is a recombinant anti-MSLN immunogenic toxin that is constructed by the fusion of a variable fragment of a murine anti-MSLN antibody with the pseudomonas exotoxin 38 (PE38) portion. SS1P was tested both as a single agent and in combination with chemotherapy.57,69,74 In one early Phase II clinical trial (NCT01362790),75 SS1P was administered in combination with pentostatin and cyclophosphamide with the aim of decreasing the immunogenicity of SS1P in patients with mesothelioma, lung cancer, or PC. The primary objectives of this study were to evaluate the tolerability and safety of a regimen of pentostatin and cyclophosphamide in combination with SS1 (dsFv)PE38 and to evaluate the ORR stratified by tumor type and the formation of antibodies SS1P. The rationale was that the administration of a conditioning regimen of pentostatin plus cyclophosphamide delays the formation of anti-SS1P antibodies, allowing patients to receive multiple cycles of SS1P and, thus, potentiating the expected efficacy.

No data are actually available about a (completed) Phase I trial (NCT01051934)76 in which SS1P is administered in association with paclitaxel, carboplatin, and bevacizumab in lung adenocarcinoma.

LMB-100

LMB-100 (previously named RG7787) is a recombinant immunogenic toxin targeting MSLN. It is based on a humanized Fab fragment with a newly engineered PE24 and is conceived to reduce the induction of immunogenicity compared to SS1P. Two initial Phase I–II studies, started in June 2016, are recruiting patients with malignant mesothelioma (NCT02798536)77 and pretreated patients with pancreatic adenocarcinoma (NCT02810418).78 Recent data published by Zhang et al79 showed that LMB-100 enhanced its activity when it was used in combination with the taxane Nab-paclitaxel in treating mesothelioma.

CRS-207

CRS-207 is a live attenuated, recombinant Listeria monocytogenes designed to express MSLN and secrete it in the cytosol of the infected antigen-presenting cells.80

It shows a synergic activity in combination with GVAX pancreas, a cell vaccine expressing human granulocyte macrophage-colony-stimulating factor and a regimen of low dose cyclophosphamide, administered to potentiate antineoplastic activity and inhibit regulatory T-cells. In a Phase II clinical trial, cyclophosphamide/GVAX and CRS-207 prolonged survival in patients with PC with a favorable toxicity.81 The same combination was investigated in pretreated patients with metastatic adenocarcinoma of the pancreas compared to chemotherapy standard regimens or to CRS-207 as a single agent (NCT02004262).82 Two other Phase II studies are active. Although they are not yet recruiting patients, they intend to combine GVAX/CRS-207 with nivolumab (NCT02243371)83 or CRS-207 with epacodostat, an inhibitor of indolamine 2,3-dioxygenase (NCT03006302),84 and this study started in June 2017, with the aim of improving survival in the same setting. CRS-207 and epacadostat are also under investigation in OC (platinum-resistant), peritoneal tumor, and fallopian tumor (NCT02575807).85

The combination of CRS-207 with cyclophosphamide and standard chemotherapy was tested in a Phase I study that was completed in June 2017, which enrolled 60 patients with MPM (NCT01675765).86 The main outcome measures are safety, the number of subjects reporting AEs, the induction of an immune response to MSLN by enzyme-linked immunosorbent spot assay, the objective tumor response and the time to progression. To date, no data have been posted about the results of this trial.

BAY 94-9343

BAY 94-9343, also called anetumab ravtansine is an antibody drug, conjugate to DM4, which is a tubulin polymerase inhibitor. Anetumab is designed to target MSLN on the cell surface and release the maytansinoid tubulin inhibitor into the cytoplasm after antibody internalization.87 In vitro, anetumab is markedly and selectively cytotoxic for MSLN overexpressing cells.

Several Phase I studies are still recruiting patients presenting different malignancies. An early Phase II study (NCT02610140),88 started in December 2015, investigated anetumab at a dose of 6.5 mg/kg, administered as a monotherapy to patients with pretreated MPM compared to vinorelbine as standard therapy. The primary objective is to test the superiority of anetumab ravtansine in PFS. The secondary outcome measures include the OS, DoR, ORR, patient-reported outcomes, and number of patients reporting ADEs as a measure of safety and tolerability. The study is active but is not actually recruiting patients.

Anetumab has reached Phase II of clinical development as a single agent in PC (NCT03023722)89 and lung cancer (NCT02839681),90 and these two studies just started to recruit patients (May and June 2017, respectively). Another trial is investigating anetumab in combination with pembrolizumab for MPM (NCT03126630).91

DMOT4039A

DMOT4039A is an ADC consisting of the humanized IgG1 anti-MSLN mAb h7D9.v3 (αMSLN), combined with the antimitotic agent monomethyl auristatin E, by means of a protease-labile linker. After binding the ADC to the specific biological antigen, the complex MSLN-ADC is then internalized, and the free form is released into the cytosol, which induces G2/M-phase growth arrest, cell death, and apoptosis.92 The specific antiproliferative activity in vitro and its potent antitumor activity in xenograft cancer models93 encourage researchers to test DMOT4039A in clinical trials. A multicenter, open-label, Phase I study is planned to assess the safety, tolerability, and PK of DMOT4039A in patients with unresectable PC or platinum-resistant OC (NCT01469793).94 Cohorts of participants receive escalation doses of DMOT4039A. A total of 54 out of the 71 enrolled patients were treated every 21 days, and MTD was assessed at 2.4 mg/kg. Alternatively, in a weekly regimen, the dose was determined to be 1 mg/kg. Across both the schedules, the most common toxicities were gastrointestinal symptoms. In addition, grade 3 hyperglycemia and grade 3 hypophosphatemia, at 2.8 mg/kg, caused an interruption of dose escalation. A total of 6 patients (4 OC; 2 PC) had confirmed partial responses with DMOT4039A at 2.4–2.8 mg/kg every 21 days.95

BMS-986148

BMS-986148 is an anti-MSLN MAb-cytotoxic drug conjugate. No data are available about the detailed pharmacology of this agent, but it might be related to ADC MDX-1204, a MAb conjugated with the potent alkylating agent duocarmycin (MED2460).96 After cellular internalization, this agent prevents proliferation, leading to cell death and apoptosis. An initial first Phase I study planned to investigate the safety and tolerability of BMS-986148 in combination with nivolumab, with the principal aim of highlighting the most hazardous AEs and SAEs (NCT02341625).97 The secondary outcome measures consisted of the evaluation of PK parameters, immunogenicity, and a better understanding of pharmacodynamics. The anti-tumor activity was defined in terms of the ORR, DoR, PFS, and OS. This Phase I–II study should enroll a total of more than 400 patients with MM, NSCLC, OC, PC, and gastric cancer. A smaller parallel Phase I study (NCT02884726)98 started in October 2016 in a single center in Japan, with preliminary data planned by the end of 2017, is expected to provide important information about safety and tolerability of BMS-986148 in subjects with advanced and/or metastatic solid tumors.

CARs

CARs are cited by the journal Science as one of the “breakthroughs of 2013,”99 representing a promising concept of bio-immunotherapy. CARs are obtained by the combination of an antigen-recognition domain on the cell surface, derived from the single-chain variable fragment (scFv) and one (in first-generation CARs) or more (in third- to fourth-generation CARs) stimulatory domains inside the cell, which activate an immunologic response.100 The concept that led to CARs, together with adoptive T-cell processes, represents one of the main strategies applied to manipulate patient T-cells ex vivo, a process which involves removing the patient’s T-cells, genetically modifying them and infusing them back into the patient. However, because the CARs are capable of recognizing the target antigen via the scFv-binding domain, this results in T-cell activation in a major histocompatibility-independent manner.101 The possibility to adapt the binding moiety, while retaining the principal structure, confers CARs the opportunity to recognize any type of target and, therefore, to potentially affect any type of specific-antigen-expressing cancer. CARs demonstrate promising results against hematologic malignancies and show only minor results in the treatment of solid tumors. Few data on clinical trials are published to date. A summary of the ongoing trials involving CARs for solid tumors overexpressing MSLN was recently reported by Wang et al.102

A major concern with CARs is the potential dramatic risk of toxicity, predominantly labeled “on-target/off-tumor” toxicity and as a “cytokine stench phenomenon”;103 and probably, this is one of the reasons why clinical trials investigating CARs are proceeding at moderate speed.

Discussion and future perspectives

The only realistic weapon currently available in modern oncology is the identification of new biological targets and biomarkers, essentially specific to the single type of cancer, and an increasingly detailed understanding of their biological pathways.

Although, in recent decades, it has been possible to increase the OS or PFS in many patients, some types of cancer remain a concrete challenge for modern oncology. Important factors such as the difficulty of obtaining a precise diagnosis when the disease is still at an early stage, the aggressive nature of the disease, or a poor differentiation in the expression of biomarkers between healthy and malignant cells are critical key points that still make it difficult to manage some cancers. Mesothelioma certainly falls into this “difficult” cancer group and still requires more knowledge specifically aimed at understanding how the inflammatory processes, as in the case of asbestos, which has a very long latency period, are triggered.

Although the global use of asbestos, considered as – albeit not unique – the main cause of mesothelioma, is banned in most advanced countries since the 1980s and 1990s, the long latency prior to diagnosis of mesothelioma (up to 40 years)26,104 suggests that the incidence peak has not yet been reached in many countries. Furthermore, a very poor prognosis after diagnosis of mesothelioma (12–24 months) makes it really urgent to implement research on how to treat mesotheliomas. Treatment options depend on the age and status of the patients and on the stage at diagnosis. Surgery is not considered sufficient without adjuvant therapy, and thus, several chemotherapy programs are applied, including cisplatin, the antimetabolites pemetrexed or raltitrexed, gemcitabine, vinorelbine and, optionally, a combination with antiangiogenic agents like bevacizumab.18,105

MSLN, along with other biomarkers, is one of the targets that researchers are currently focusing on for diagnosing and treating mesotheliomas. Although the role of MSLN in cancer progression is not yet completely understood,106 many drugs targeting MSLN are currently under investigation in international, multicentric clinical trials. Hassan et al,34 Zhao et al,96 and, recently, Mancuso and Neal107 comprehensively reviewed the main strategies for targeting MSLN in mesothelioma and other solid tumors. By reading, in parallel, the data summarized by Hassan’s review34 and the results of Inaguma’s original immunohistochemistry research53 (using anti-MSLN antibodies 5B2 and MN-1), it is easy to appreciate how MSLN overexpression in many solid tumors makes this target a formidable potential ground for oncology research.

In the present paper, we describe the pharmacological profile of the promising anti-MSLN agent amatuximab, along with a summary of respective clinical trials (Table 2). Furthermore, we propose emerging data about prognostic factors in some solid tumors and updates about new agents targeting MSLN that are currently being investigated and provide an updated summary of the ongoing clinical trials (on Table 1), including those started in 2016 and 2017 (Table 1).

Amatuximab, an unconjugated antibody against MSLN, has an acceptable safety profile, but when it is used as a single agent, it shows only modest results in terms of stabilizing the disease.57,64 Nevertheless, a combination of amatuximab with chemotherapy shows clinical activity with no overlapping toxicities, in Phase II trials. These findings encourage researchers to perform additional studies with different chemotherapy combinations.

Immunotoxins are also considered a promising therapeutic strategy. However, to date, the main problem in using anti-MSLN recombinant immunotoxins is immunogenicity. A Phase I study shows that almost all of the enrolled patients develop anti-toxin antibodies after treatment with SS1P in combination with pemetrexed and cisplatin.69 Among the cohorts of patients treated with PE38-RIT, only one anaphylactic reaction was detected, after the first infusion of immunotoxin.108 Although immune-mediated reactions are very frequent, usually they are not serious. Skin rashes, even severity grade 3, are effectively treated with steroids.109 Many efforts have been made to reduce the immunological response to increase the effectiveness of the treatment, including a combination of an immune suppression therapy with pentostatin and cyclophosphamide, which demonstrated its clinical value. Several other strategies for reducing the immune response are under investigation, and they are included in actual research programs. Zhang et al79 recently showed that LMB-100, in combination with the taxane Nab-paclitaxel, in treating mesothelioma, has a synergistic activity, which could be useful in mitigating immunogenicity.

Antibodies against MSLN have a more efficient anti-tumor activity when they are conjugated with a cytotoxic molecule compared to the unconjugated drug, as demonstrated in pre-clinical and clinical studies.96 DM4, conjugated with anetumab, performs its cytotoxic activity mainly against rapidly replicating cells, reducing systemic toxicity, and, thus, widening its therapeutic window. Like other ADCs, it shows a favorable PK profile in terms of its half-life, increasing its therapeutic exposure with a less frequent dosing and limiting immunogenicity. On the other hand, the main toxicity associated with maytansinoid is the reduction of neutrophilis, lymphocytes, reticulocytes, and platelets along with hepatotoxicity.110,111 In conclusion, MSLN is shown to be a promising target for the treatment of several types of cancer. In treating BC, for example, MSLN may be particularly promising for the TNBC form, in which it is reported that up to 42.3% of patients show overexpression of MSLN.47 In lung adenocarcinoma, MSLN, in its mature form, is detected in 55% of patients,50 and in gastric carcinomas, the detection of elevated levels of MSLN is correlated with a poor prognosis.55

Different therapeutic strategies are under investigation after obtaining promising preclinical results. The real goal will now be to enhance its efficacy, to identify patients who can achieve the best benefit, and to limit drug-related toxicities.

Recent Phase I and II clinical trials reinforced the hypothesis that MSLN is an important target for immunotherapy, and the objective is to confirm these preliminary data. At the same time, other studies should be designed to validate the utility of MSLN as a surrogate biomarker, thus making MSLN a predictor of the potential response to therapy. Serum MSLN laboratory assessment is a useful strategy for the future development of MSLN-targeted therapies, helping to select and recruit patients who can achieve the best expected benefits by this type of treatment. To date, soluble MSLN is the only tumor biomarker that has been approved by the US Food and Drug Administration for treating mesotheliomas.112 For the purpose of selecting patients with the highest chance of benefit from the treatment, another research arm is focusing on PET and SPECT evaluation before ADC treatment. MSLN-specific tracers for SPECT and PET have been developed recently.113–116 Molecular imaging of tumor antibody uptake might have value in the upcoming drug development by identifying patients who may benefit from ADC treatment. Lamberts et al performed an 89Zr-PET imaging study with MMOT0530A, a MSLN antibody, in conjunction with a Phase I study with the ADC DMOT4039A (NCT01832116).117 The aim of the study was to evaluate the antibody tumor uptake, the whole body distribution, and the relation between the uptake, response to treatment, and MSLN expression.43 The authors demonstrated that with (89)Zr-MMOT0530A-PET, PC and OC lesions were visualized, along with antibody distribution, and they concluded that this technique might potentially guide personalized antibody-based treatments.

Together with predictive and diagnostic innovative tools, it will be of paramount importance to identify effective ways to synergically combine therapeutic strategies. A combination of ADCs, recombinant immunotoxins (RITs), MAbs with immunotherapeutic molecules, target therapies, or standard chemotherapy, when indicated, will provide pharmacological perspectives and will constitute the basis for pipelines at pharmaceutical companies.

For this reason, in addition to the current ongoing trials, new extensive randomized trials based on the combination treatments and on extended number of patients should be planned.