key: cord-0863193-9yx3v2xa
authors: Londres, Henrry Diaz; Armada, Jorge Jiménez; Martínez, Aray Hernández; Abdo Cuza, Anselmo A; Sánchez, Yamilka Hernández; Rodríguez, Aylin Granado; Figueroa, Sarahy Sepúlveda; Llanez Gregorich, Egda M; Torres Lahera, Mery L; Peire, Francisco Gómez; González, Teresita Montero; González, Yaneth Zamora; Añé Kouri, Ana L; Palomo, Addys González; Concepción, Mayelin Troche; Pérez, Loipa Medel; Luaces-Alvarez, Patricia Lorenzo; Iglesias, Daymys Estévez; Hernández, Danay Saavedra; Suzarte, Mayra Ramos; Ramos, Tania Crombet
title: Blocking EGFR with nimotuzumab: a novel strategy for COVID-19 treatment
date: 2022-03-21
journal: Immunotherapy
DOI: 10.2217/imt-2022-0027
sha: c054406d2ca067bf7e812c1df39604b6f5f7b01f
doc_id: 863193
cord_uid: 9yx3v2xa

Background: Lung injury and STAT1 deficit induce EGFR overexpression in SARS-CoV-2 infection. Patients & methods: A phase I/II trial was done to evaluate the safety and preliminary effect of nimotuzumab, an anti-EGFR antibody, in COVID-19 patients. Patients received from one to three infusions together with other drugs included in the national guideline. Results: 41 patients (31 severe and 10 moderate) received nimotuzumab. The median age was 62 years and the main comorbidities were hypertension, diabetes and cardiovascular disease. The antibody was very safe and the 14-day recovery rate was 82.9%. Inflammatory markers decreased over time. Patients did not show signs of fibrosis. Conclusion: Nimotuzumab is a safe antibody that might reduce inflammation and prevent fibrosis in severe and moderate COVID-19 patients. Clinical Trial Registration: RPCEC00000369 (rpcec.sld.cu).

circle is established between STAT3 and PAI-1 [3] . Upregulation of PAI-1 leads to a coagulopathy characterized by intravascular thrombi [3] .

EGFR is a membrane glycoprotein with tyrosine kinase activity whose physiological role is to regulate epithelial tissue development and homeostasis [4] . There is significant evidence of EGFR's role in fibrosis. According to Venkataran et al., EGFR signaling remains active after the clearance of SARS-CoV and leads to fibrosis [5] . EGFR is also upregulated during the pathological remodeling of the lung in patients with advanced cystic fibrosis [6] , while Ishii et al. found that gefitinib, an EGFR tyrosine kinase inhibitor, had a protective effect on the lung fibrosis induced by bleomycin [7] .

EGFR is also overexpressed in squamous carcinomas or adenocarcinomas of different localization [4] . Knowledge of the role of the EGFR in malignant tumors has advanced enormously over the last 20 years, and several therapeutic drugs such as tyrosine kinase inhibitors and anti-EGFR monoclonal antibodies have been registered for epithelialderived tumors [8] [9] [10] . Nimotuzumab is a humanized antibody that targets EGFR [11] . The antibody prevents receptor dimerization, thus inhibiting tyrosine kinase activity and interfering with the cell signaling pathways involved in proliferation, inflammation, angiogenesis and survival [12, 13] . Nimotuzumab decreases IL-6 in mice xenografted with pancreatic tumor cells [13] . Blocking EGFR signaling is not the only mechanism of action underlying the efficacy of nimotuzumab. In vitro studies demonstrated that nimotuzumab exerts its effects partially through antibody-dependent cell-mediated cytotoxicity and by activating dendritic cells and specific CD8 + T cells [14, 15] .

Nimotuzumab efficacy results have been reported in more than 40 clinical trials, conducted primarily in patients with advanced cancer, including glioblastoma, squamous cell carcinoma of the head and neck, and esophageal, nasopharyngeal, pancreatic and non-small-cell lung cancers [14, [16] [17] [18] [19] [20] [21] .

Given that acute lung injury and functional loss of STAT1 can lead to EGFR overexpression, we hypothesized that EGFR blockade with nimotuzumab would be an effective strategy to control inflammation and to prevent an excessive fibrosis after SARS-CoV-2 infection.

Patients & methods EGFR expression was evaluated by immunohistochemistry in lung samples from COVID-19 deceased patients. 20 lung fragments were obtained from the Department of Pathology of the hospitals Luis Díaz Soto and Salvador Allende (Havana, Cuba). Fragments were fixed in formaldehyde and embedded in paraffin blocks. Slides with lung tissue sections were deparaffinized and washed in phosphate buffer solution and distilled water. The endogenous peroxidase activity (Dako, CA, USA) was blocked and EGFR antigenic resuscitation was done using proteinase K (Dako). Samples were incubated with a murine anti-human EGFR monoclonal antibody for EGFR3 for 1 h. Subsequently, the sections were incubated with horseradish peroxidase (Dako) and the enzymatic reaction was developed with diaminobenzidine tetrahydrochloride (Dako). Tissue sections were also contrasted with Mayer's hematoxylin (Dako). Positive expression was defined by the presence of a brown color located in the plasma membrane of the different cell subtypes. The percentage of positive cells per histological field was quantified on five images digitized with a DP20 digital camera coupled to an optical microscope (Olympus CX31, Tokyo, Japan), at 40 × and 100 × magnification.

A prospective, noncontrolled, multicenter phase I/II trial was done to assess the effect and tolerability of nimotuzumab in individuals with COVID-19. Diagnosis was confirmed by PCR. Nimotuzumab was administered together with the standard of care (SOC): low-molecular-weight heparin, steroids and antibiotics, according to the national COVID-19 guideline [22] . Patients could also receive CIGB-258, a peptide with immunoregulatory properties which obtained Emergency Use Authorization from the Cuban regulatory agency [23] . Inclusion criteria were the following: express willingness of the patient, any gender, any ethnicity and age ≥18 years. In addition, patients should have severe disease according to one of the following conditions: oxygen saturation (SpO 2 ) <94% on room air at sea level or need for oxygen therapy to maintain SpO 2 >93%, a pressure of arterial oxygen to fractional inspired oxygen (PaO 2 /FiO 2 ) <300 mm Hg, a respiratory rate >30 breaths/min or lung infiltrates >50%. Patients with moderate symptoms at high risk of worsening were also included. Subjects with moderate illness were those with evidence of lower respiratory disease according to the clinical assessment or imaging, who had an SpO 2 ≥94% on room air at sea level. High-risk patients were those aged ≥65 years or with comorbidities such as diabetes mellitus, hypertension, chronic kidney disease, cardiovascular disease, immunodeficiency, obesity or cancer. The protocol was approved by the ethics committees of the participating hospitals and by the National Regulatory Agency, CECMED. All patients signed the informed consent. The protocol was listed in the public registry of clinical trials (https://rpcec.sld.cu/ensayos/RPCEC00000369-En). Treatment consisted of nimotuzumab intravenous infusions up to a maximum of three doses, administered every 72 h. The recommended number of doses was two for moderate patients and three for individuals with severe disease. The main criterion for discontinuation was the occurrence of serious adverse events related to the investigational product. The loading dose was 200 mg, while subsequent doses of the antibody consisted of 100 mg. Nimotuzumab was diluted in 250 ml of saline solution (0.9%) and administered over 2 h.

The objectives of the study were to evaluate the preliminary safety and effect of nimotuzumab in the treatment of severe or moderate COVID-19. Adverse events were classified according to frequency, intensity, causal relationship and consequences for the subject. Intensity was graded according to the Common Terminology Criteria for Adverse Events, version 5 [24] .

The main effect variables were the following: rate of patients recovered 14 days after the first infusion, length of stay in the intensive care unit (ICU), rate of patients whose PO 2 /FiO 2 ratio improved and rate of patients requiring mechanical ventilation after nimotuzumab. Hematology including neutrophil, lymphocyte and platelet counts was evaluated before nimotuzumab and every 48 h. Other biochemical parameters including creatinine, aspartate aminotransferase, alanine aminotransferase, C-reactive protein, ferritin, lactate dehydrogenase (LDH) and D-dimer were measured over time. In addition, IL-6 and PAI-1 were measured using an IL-6 Quantikine R ELISA Kit (Cat# S6050; R&D Systems, MN, USA) and a quantitative PAI-1 ELISA set (BE59351; BL International GmbH, Hamburg, Germany). PAI-1 was measured in plasma. The evolution of the lung lesions was measured by serial x-ray or CT scan.

Demographics, comorbidities and previous and concurrent therapies were reported in the two disease severity groups. Descriptive statistics were used to display qualitative variables, while mean and standard deviation or median and interquartile range were used for quantitative variables with normal or non-normal distribution, respectively. Receiver operating characteristic curves were built for all baseline laboratory variables to predict COVID-19 mortality. The odds ratios (ORs) for the variables associated with the highest lethality risk were determined. Data processing was done with the R package (www.r-project.org/) and SPSS-25 software (IBM Corp., NY, USA).

EGFR expression was detected in the lung necropsy specimens of the 20 evaluated patients who died from COVID-19. In 19 samples (95%), more than 60% of the cells showed EGFR expression, while one tissue section had 25% EGFR positivity. Positive cells morphologically resemble type I and II pneumocytes, alveolar macrophages and fibroblasts. Figure 1 shows the EGFR expression in the lung sections from two representative deceased COVID-19 patients.

After the demonstration of EGFR expression in the lung tissue from deceased COVID-19 patients, a clinical trial using the anti-EGFR monoclonal antibody nimotuzumab was performed. From 19 May to 19 June 2021, [23] . All patients who entered the trial with a severe condition were treated at the ICU, while moderate patients received nimotuzumab at the hospital conventional ward. The time lag between the onset of symptoms and nimotuzumab treatment was 8.5 days, while for the severe patients the time interval between ICU admission and nimotuzumab was 3 days.

Seven patients (17.07%) received a single dose of nimotuzumab, 29 (70.7%) received two infusions, and five subjects (12.19%) required three doses of the antibody. Nimotuzumab was very safe. There were only four related adverse events in two patients (4.87%). The two individuals with adverse reactions both had severe disease; one subject developed grade 1 tremors, while the second patient presented grade 2 chills, headache and tremors. The events were classified as possibly related to nimotuzumab and occurred after the first antibody infusion. No grade 3 or 4 related adverse events were detected.

Eight patients (one moderate and seven severe; 19.5%) of the 41 receiving nimotuzumab required invasive mechanical ventilation. The mean time between nimotuzumab and the use of invasive mechanical ventilation was 3.6 days. 34 patients out of 41 (82.92%) recovered 14 days after receiving the first monoclonal antibody infusion. Regarding disease severity, nine of ten moderate patients (90%) recuperated, while 25 of the 31 severe patients (80.64%) were discharged by day 14. The median time at the ICU of the severely ill subjects was 9 days.

Surprisingly, patients who received nimotuzumab concomitantly with CIGB-258 and the SOC had a worse outcome as compared with patients who received nimotuzumab plus the SOC alone. Overall, eight of 12 severe patients (66.7%) who received CIGB-258 recovered, compared with 17 of 19 individuals (89.5%) treated with nimotuzumab plus steroids, anticoagulant and antibiotics. In the moderate setting, only one subject received nimotuzumab and CIGB-258, and did not recover. The rest of the moderate patients (nine) who received nimotuzumab plus the SOC rapidly improved. The most prevalent cause of death of the individuals receiving nimotuzumab and CIGB-258 was septic shock.

On day 7 of treatment, 76.2% of the subjects with a severe condition had an improved PO 2 /FiO 2 ratio. The percentage of the affected area of both lung fields was calculated both before treatment with nimotuzumab and at the time of discharge. There was a significant reduction in the affected area of both lungs at discharge, according to the Wilcoxon matched-pairs signed rank test. CT scan images were acquired before and at discharge in 24 patients. At discharge, all patients but four (82.4%) had CT scan abnormalities including ground-glass opacities, consolidation, reticulation (crazy-paving appearance), septal thickening and decreased lung volumes. Follow-up CT scans were done in 15 patients after 30-60 days. Minor CT abnormalities, but no sign of fibrosis, persisted in one case (6%). Figure 2 shows serial images of three patients before treatment with nimotuzumab, at the time of discharge and 30-60 days after hospitalization.

Inflammatory markers including C-reactive protein, ferritin, LDH, neutrophil-to-lymphocyte ratio and D-dimer decreased over time. Receiver operating characteristic curves were performed to establish the correlation between laboratory parameters at baseline and the probability of dying of patients with severe disease. Patients with Creactive protein values above 118.54 mg/l, LDH above 333 U/l, absolute leukocyte count above 8.95 × 10 9 /l and ferritin above 490.5 μg/l were more likely to die. Remarkably, the biomarkers associated with the highest lethality risk were LDH ≥333 U/l (OR: 11.25; 95% CI: 1.15-110.5) and absolute leukocyte count ≥8.95 × 10 9 /l (OR: 9.33; 95% CI: 0.96-90.9).

Serum IL-6 concentration was evaluated in 28 patients, 21 classified as severe and seven as moderate. The median IL-6 concentration at the time of inclusion in the clinical trial was 43.83 pg/ml for severe patients and 46.47 pg/ml for subjects with moderate disease. No significant differences were identified when comparing the two illness subsets (Mann-Whitney test: p > 0.05). At day 7, IL-6 increased in four patients of the 29 (13.7%), while it decreased or stabilized in the rest. Globally, the median IL-6 concentration diminished from 46.5 to 14.51 pg/ml at day 7. PAI-1 levels in plasma were evaluated only in five patients with moderate disease, on account of the limitations of the quantification system. Notably, PAI-1 was elevated in these five patients (reference values 4-43 ng/ml). The median PAI-1 level at baseline was 123 ng/ml and declined to 77.3 ng/ml at day 7 of treatment.

The symptoms of COVID-19 are extremely variable, ranging from minimal to significant hypoxia with acute respiratory distress syndrome (ARDS) and multi-organ failure, which can be fatal [1] .

This clinical trial evaluated for the first time the effect of using an anti-EGFR inhibitor in the COVID-19 scenario. The overexpression of EGFR in the lung tissue from SARS-CoV-2 deceased patients was demonstrated. This finding further validates the approach of blocking EGFR as a tool to reduce inflammation or hypofibrinolysis and to prevent or revert fibrosis. Apart from in non-small-cell lung cancer, EGFR is not expressed in normal lung tissue [25] [26] [27] [28] [29] .

According to the most recent publications, COVID-19 pathogenesis can be divided into three overlapping steps: pulmonary, proinflammatory and prothrombotic. In the pulmonary phase, the virus affects the epithelial alveolar cells, causing interstitial pneumonia. In the proinflammatory stage, infected target cells and lymphocytes further overproduce inflammatory cytokines that result in acute lung injury. The last stage is characterized by an uncontrolled coagulopathy [30] . Gautret et al. proposed a clinical spectrum including an acute virologic stage followed by a cytokine storm, a procoagulation disorder and an ARDS [31] ; Lippi and coworkers divided the disease into at least five phases (incubation, respiratory, proinflammatory, prothrombotic, death or remission) [32] . We postulate that nimotuzumab can be used when there is evidence of lower respiratory disease, corresponding to the pulmonary or respiratory stage of the disease. At this stage, EGFR is overexpressed by the respiratory cells after the STAT1 loss and the acute lung damage [3] . The antibody can also be useful in the inflammatory and prothrombotic phases of the disease, given the crucial regulatory role of EGFR in inflammation and immunothrombosis. EGFR activation has been found to trigger the proinflammatory response and PAI-1 secretion [33, 34] . Nimotuzumab was very safe, and only two patients had tremors, chills or headache. Adverse reactions commonly seen in cancer trials consist mostly of fatigue, nausea, vomiting, chills, anorexia and fever [16, 20, 35] . Other recently recommended anti-inflammatory drugs for COVID-19, like tocilizumab or baricitinib, might provoke serious adverse reactions including bacteremia and lung abscess [36] or grade 3 or 4 adverse events such as hyperglycemia, anemia, decreased lymphocyte count and acute kidney injury, respectively [37] .

The clinical trial provided initial evidence that nimotuzumab, in combination with other drugs including steroids, decreases inflammatory markers, including IL-6. IL-6 is a pleiotropic cytokine that has a central role in the immune response as well as inflammation [38] . Remarkably, in our series, no differences were found between moderate and severe patients regarding IL-6 concentration. IL-6 levels did not further increase in 86% of the patients after blocking EGFR and treatment with steroids. Other molecules targeting the IL-6 receptor pathway, including tocilizumab or baricitinib, had significant clinical effect when combined with steroids [36, 39] .

Preliminary information on PAI-1 levels was also obtained. PAI-1 was elevated in the five evaluated patients. Previously, PAI-1 has been shown to be augmented in ARDS and particularly in COVID-19 [40] , but notably, Cugno 10 .2217/imt-2022-0027

Immunotherapy (Epub ahead of print) future science group et al. did not find differences in PAI-1 concentration among patients with mild, moderate or severe disease [41] . As well as endothelial cells, senescent alveolar type II cells secrete PAI-1, which promotes a profibrotic phenotype [42] . According to Alberti et al., EGFR activation triggers coexpression of IL-6 and PAI-1, via transcriptional activation of NF-κB [33] . The activation of the IL-6 pathway might also be the driver of the PAI-1 secretion during the cytokine storm [43] . Our initial findings on the reduction of PAI-1 could be attributed either to the direct inhibition of EGFR or to the IL-6 decrease. In our dataset, 19.5% of the 41 patients needed mechanical ventilation after nimotuzumab. The recovery rates were 80.6 and 90% for severe and high-risk moderate patients, respectively. Even though a direct comparison is not possible, these figures compare favorably with other anti-inflammatory drugs that obtained emergency use authorization for COVID-19. The RECOVERY study evaluating the anti-IL-6R monoclonal antibody tocilizumab versus usual care, enrolled 4116 patients, mostly receiving noninvasive respiratory support or oxygen. Almost all patients received corticosteroids; recovery rates were 62 versus 58% in patients requiring noninvasive ventilation and 81 versus 77% in patients requiring solely oxygen [36] . No significant effect on subsequent ventilation was seen, and globally, 31% of the tocilizumab patients progressed to respiratory support [36] . In another double-blind study in 438 subjects with bilateral pulmonary infiltrates and hypoxemia (COVACTA), the mortality rate was 19.7 versus 19.4% for tocilizumab or placebo [44] . The incidence of mechanical ventilation among patients not ventilated at baseline was 27.9% (tocilizumab) versus 36.7% (placebo) [44] . Recently, a JAK inhibitor, baricitinib, showed clinical benefit in hospitalized patients. A randomized study of 1033 patients (67% moderate and 33% severe) compared remdesivir plus baricitinib versus remdesivir plus placebo [37] . The incidence of death or ventilation was lower in the experimental than in the control group (22.5 vs 28%) [37] . The second trial, by Marconi et al., compared baricitinib plus SOC versus SOC in 1525 patients. Overall, 75% of the patients did not require ventilation or high-flow oxygen at baseline. The percentage of individuals who died or required ventilation or high-flow oxygen was 27.5% in the baricitinib cohort versus 30.5% in the control group [39] .

After this phase I/II study was concluded, nimotuzumab was included in the national guideline to treat COVID-19 patients. In order to assess the impact of using nimotuzumab in the real-world scenario, the recovery rate was compared with a paired retrospective cohort. Control patients received standard treatment according to the national protocol, but not nimotuzumab. Overall, 1151 severe or critical patients receiving nimotuzumab and 969 matching controls were compared. The 14-day recovery rate of the nimotuzumab cohort was 79.8%, compared with 45.3% in the control group.

Treatment with CIGB-258, an immunoregulatory peptide, was not an exclusion criterion, given that this was the first trial designed to assess the impact of nimotuzumab in COVID-19-associated inflammation. Remarkably, combining two drugs like nimotuzumab or CIGB-258, which decrease IL-6 by different mechanisms, did not have an additive effect, and patients died mainly as a result of coinfections and septic shock. It is worth considering that infections are very frequent in hospitalized older patients bearing chronic diseases [45] . The use of IL-6 or IL-6Rblocking antibodies in combination with JAK inhibitors to treat COVID-19 patients is also not recommended.

Finally, our study found a significant reduction of the affected lung areas and no signs of fibrosis in those subjects evaluated 30-60 days after discharge. A recent meta-analysis in 250,351 survivors demonstrated that 65% of the patients had increased oxygen requirement while chest imaging abnormalities persisted in 62.2% of all survivors up to 6 months after recovery [46] . In our small series, CT scan anomalies persisted in only 6% of the patients evaluated up to 60 days after discharge. Long-term evaluation of the sequelae of the nimotuzumab-treated patients, including pulmonary function tests, is planned.

In summary, our preliminary results suggest that nimotuzumab is a safe antibody that might reduce IL-6 and PAI-1 and prevent fibrosis in severe and moderate COVID-19 patients at high risk of aggravation. In spite of the patients' poor prognosis, the ventilation rate was lower than 20% and the recovery rate was above 80% for the severe cases. These results should be interpreted with caution, given the small sample size and the uncontrolled nature of the trial. A larger series of patients has been evaluated, and a controlled trial in the COVID-19 or post-COVID setting is planned.

• Lung injury and STAT1 deficit can induce EGFR overexpression in SARS-CoV-2-infected cells.

• EGFR overexpression further worsens inflammation, immune thrombosis and fibrosis.

• This clinical trial evaluated for the first time the effect of using an anti-EGFR antagonist (nimotuzumab) in combination with other drugs in the COVID-19 scenario. • EGFR overexpression in the lung tissue from SARS-CoV-2 deceased patients was demonstrated.

• The antibody was very safe. There were only four related adverse events in two subjects.

• The 14-day recovery rate was 82.9%. Regarding disease severity, 90% of the moderate patients and 80.64% of the severe patients recuperated by day 14. All authors reviewed and approved the final manuscript.

The authors are very grateful to all physicians, nurses and general staff working with hospitalized COVID-19 patients.

This study was funded by the Cuban Ministry of Health and the Center of Molecular Immunology. TCR, MRS, DSH, DEI, PLLA, LMP, MTC, AGP and ALAK currently work for the Center of Molecular Immunology, the institution that generated and originally patented nimotuzumab. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized in the production of this manuscript.

The protocol was approved by the ethic committees of the participating hospitals and by the National Regulatory Agency, CECMED.

All patients signed the informed consent before trial inclusion. The protocol was listed in the public registry of clinical trials (https://rpcec.sld.cu/ensayos/RPCEC00000369-En).

The authors certify that this manuscript reports original clinical trial data on 41 patients (RPCEC00000369). Individual participant data that underlies the results reported in the article, after deidentification are available along with the study protocol. The data will be available 9 months after article publication and will end 36 months following article publication. The information will be shared with investigators whose proposed use of the data has been approved by an independent review committee identified for this purpose and for individual participant data meta-analysis. Proposals may be submitted up to 36 months following article publication. After this date the data will be available in our data warehouse but without investigator support other than deposited metadata. Information regarding submitting proposal and accessing data may be found at https://rpcec.sld.cu/ensayos/RPCEC00 000369-En.

IL-6 inhibitors in the treatment of serious COVID-19: a promising therapy?

Coronavirus disease 2019 (COVID-19): the portrait of a perfect storm

An aberrant STAT pathway is central to COVID-19

Epidermal growth factor receptor targeting in cancer

Overactive epidermal growth factor receptor signaling leads to increased fibrosis after severe acute respiratory syndrome coronavirus infection

Immunolocalization of transforming growth factor alpha and epidermal growth factor receptor in lungs of patients with cystic fibrosis

Gefitinib prevents bleomycin-induced lung fibrosis in mice

Efficacy and safety of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) monotherapy for advanced EGFR-mutated non-small cell lung cancer: systematic review and meta-analysis

Mechanisms of innate and acquired resistance to anti-EGFR therapy: a review of current knowledge with a focus on rechallenge therapies

How specific molecular-targeted agents can make obsolete a 'one size fits all' approach in EGFR-mutated NSCLC treatment

Humanization of a mouse monoclonal antibody that blocks the epidermal growth factor receptor: recovery of antagonistic activity

antiangiogenic and proapoptotic activity of h-R3: a humanized anti-EGFR antibody

EGFR high expression, but not KRAS status, predicts sensitivity of pancreatic cancer cells to nimotuzumab treatment in vivo

Nimotuzumab: beyond the EGFR signaling cascade inhibition

Nimotuzumab induces NK cell activation, cytotoxicity, dendritic cell maturation and expansion of EGFR-specific T cells in head and neck cancer patients

Nimotuzumab for patients with inoperable cancer of the head and neck

Use of the humanized anti-epidermal growth factor receptor monoclonal antibody h-R3 in combination with radiotherapy in the treatment of locally advanced head and neck cancer patients

A randomised phase II study of chemoradiotherapy with or without nimotuzumab in locally advanced oesophageal cancer: NICE trial

Nimotuzumab, an anti-EGFR monoclonal antibody, in the treatment of nasopharyngeal carcinoma

EGFR-targeting therapy as an evolving concept: learning from nimotuzumab clinical development

Use of nimotuzumab combined with cisplatin in treatment of nasopharyngeal carcinoma and its effect on expressions of VEGF and MMP-2

Estructuración del Protocolo Cubano de Actuación para la Atención de Casos COVID-19

CIGB-258, a peptide derived from human heat-shock protein 60, decreases hyperinflammation in COVID-19 patients

Composite grading algorithm for the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Over-expression of EGFR is closely correlated to poor prognosis in Tunisian patients with non-small-cell lung adenocarcinoma

EGFR and COX-2 protein expression in non-small-cell lung cancer and the correlation with clinical features

MicroRNA-128-b regulates epidermal growth factor receptor expression in non-small-cell lung cancer

Differential expression of RBM5, EGFR and KRAS mRNA and protein in non-small-cell lung cancer tissues

Fang Q. miRNA-9 inhibits proliferation and migration of lung squamous cell carcinoma cells by regulating NRSF/EGFR. Technol

Overview of COVID-19 inflammatory pathogenesis from the therapeutic perspective

Natural history of COVID-19 and therapeutic options

COVID-19: unravelling the clinical progression of nature's virtually perfect biological weapon

Ligand-dependent EGFR activation induces the co-expression of IL-6 and PAI-1 via the NFkB pathway in advanced-stage epithelial ovarian cancer

EGFR inhibitors from cancer to inflammation: discovery of 4-fluoro-N-(4-(3-(trifluoromethyl)phenoxy)pyrimidin-5-yl)benzamide as a novel anti-inflammatory EGFR inhibitor

EGFR-targeting as a biological therapy: understanding nimotuzumab's clinical effects

Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

Baricitinib plus remdesivir for hospitalized adults with COVID-19

IL-6 in inflammation, autoimmunity and cancer

Efficacy and safety of baricitinib for the treatment of hospitalised adults with COVID-19 (COV-BARRIER): a randomised, double-blind, parallel-group, placebo-controlled phase 3 trial

Fibrinolytic abnormalities in acute respiratory distress syndrome (ARDS) and versatility of thrombolytic drugs to treat COVID-19

Complement activation and endothelial perturbation parallel COVID-19 severity and activity

PAI-1 regulation of TGF-beta1-induced alveolar type II cell senescence, SASP secretion, and SASP-mediated activation of alveolar macrophages

IL-6 trans-signaling induces plasminogen activator inhibitor-1 from vascular endothelial cells in cytokine release syndrome

Tocilizumab in hospitalized patients with severe COVID-19 pneumonia

Senescence and host-pathogen interactions

Short-term and long-term rates of postacute sequelae of SARS-CoV-2 infection: a systematic review