Vedolizumab-associated diffuse interstitial lung disease in patients with ulcerative colitis:A case report

lNTRODUCTlON

Vedolizumab is a fully humanized monoclonal antibody.It is currently the only intestinal selective biological agent in the field of inflammatory bowel disease(IBD)that targets α4β7 gastrointestinal integrin receptors and blocks the receptor’s interaction with mucosal addressin cell adhesion molecule-1,thereby inhibiting the migration of T lymphocytes into the intestinal parenchymal tissue in order to reduce inflammation[1].In March 2020,vedolizumab produced by Takeda Pharmaceutical Company was approved for marketing in China for the first time.Although the clinical effectiveness of this brand has been continuously verified and recognized[2],safety and adverse events have also attracted negative attention.Here,we describe one fatal case of vedolizumab-associated severe interstitial lung disease in a patient with ulcerative colitis(UC).We also reviewed the existing literature in English and found only seven case reports of vedolizumab-associated lung diseases,mainly in patients with IBD.

Now it was plain that the lady must be a real Princess, since she had been able to feel the three little peas through the twenty mattresses and twenty feather beds. None but a real Princess could have had such a delicate sense of feeling.10

CASE PRESENTATlON

Chief complaints

A 61-year-old Chinese male was initially admitted to the gastroenterology department of our hospital with chief complaints of recurrent abdominal pain,diarrhea,mucopurulent hematochezia and weight loss.

It was taken to the palace and tied at the foot of the Lady Jamila s raised seat, but she ordered a longer cord to be brought so that it might be able to jump up beside her

History of present illness

The patient was diagnosed with UC 12 years prior to admission,and he had been treated with multiple conventional therapies,including,oral and topical aminosalicylates,dexamethasone enema,oral corticosteroids,selective leukocyte absorption treatment and intestinal flora adjustment treatment.In spite of these treatments,he experienced frequent flare-ups and was admitted to the hospital 3 times over the past 9 mo.Due to these failed conventional therapies,the patient was administered adalimumab 160 mg by subcutaneous injection.However,the symptoms continued with 10 to 20 bowel movements daily,and the modified Truelove and Witts severity index suggested moderately to severely active UC.As a result,the patient was started on vedolizumab.After the first dose of vedolizumab(300 mg intravenous infusion),fever at 39 °C and fatigue occurred the next day.He was treated with intravenous mezlocillin,foscarnet sodium,and ornidazole,but the fever persisted.The second dose of vedolizumab was administered 2 wk later,and the patient responded well regarding his intestinal symptoms;however,he presented with new-onset dyspnea at rest and nonproductive cough 2 d after the second vedolizumab treatment.Half a month later,the patient was admitted to the Department of Respiratory and Intensive Care Unit(RICU)due to severe dyspnea.

History of past illness

There is no secret to why our marriage has lasted while so many others have failed. There is no formula for success that I can offer, other than to express at the most important feature of our relationship is that it has never lost the sense of romance3 that bloomed when we first met. Too often marriage kills the romance that was born in the courtship of a relationship. To me, I have always felt that I am still courting Patricia, and therefore the romance has never died.

Physical examination

Vedolizumab was discontinued,and the patient was started on methylprednisolone 80 mg/day.Three days later,intubation and mechanical ventilation was initiated due to refractory hypoxia.The anti-infective treatment was adjusted to linezolid,meropenem,caspofungin,compound sulfamethoxazole tablets and foscarnet sodium without any response.

Laboratory examinations

The efficacy and safety of vedolizumab in patients with moderate to severe IBD have been confirmed in several pivotal clinical trials[5,6].An integrated study analyzed 2830 IBD patients who used vedolizumab from 2009 to 2013 and showed that vedolizumab did not increase their risk of infection or malignancy,and the most common adverse events were nasopharyngitis,abdominal pain,headache and joint pain[7].However,in the past 4 years,7 cases of noninfectious lung injury related to vedolizumab have been reported,including 4 cases of UC and 3 cases of CD.In 2017,Sudheer[8]first reported a 58-year-old white man with UC who developed acute respiratory distress syndrome requiring intubation and mechanical ventilation after receiving 3 doses of vedolizumab.By withholding vedolizumab and applying the steroid,the patient was successfully discharged home.Another case was described by Eva[9]of a 52-year-old female with UC who suffered from new onset dyspnea and dry cough with chest CT showing diffuse ground-glass opacities.She was being treated with intravenous vedolizumab every 8 weeks for 2 years.Laboratory work did not identify infection,and the pathology of TBLB showed small bronchiole injury with debris and accumulation of mononuclear cells,macrophages and histiocytes.The fact that a complete resolution of symptoms and radiographic abnormalities was achieved by discontinuation of vedolizumab without any other treatments highly suggested vedolizumab-induced lung toxicity.Another recently published case has a similar clinical course as ours.A 39-year-old male diagnosed with UC presented with acute severe interstitial lung injury while receiving vedolizumab treatment[10].While vedolizumab cessation and systemic steroid administration helped this patient,our patient was refractory to his therapy and finally passed away.Cucinotta[11]reported the off-label use of vedolizumab in a 13-year-old child with UC,and after three doses of vedolizumab,the child developed a persistent cough that resolved after vedolizumab discontinuation.

Imaging examinations

A diagnosis of vedolizumab-associated interstitial lung disease was made.The Naranjo adverse drug reaction scale[4]was calculated to be 6(causality:probable).

Pathology

On histopathology,irregular glandular structures in the hyperplastic fibrous tissue were noted with scattered lymphocytes infiltrated in the interstitium.Intranuclear vacuoles,nuclear fragmentation,binuclear cells were seen(Figure 2).No tumor cells were noted and immunohistochemistry showed that adenoid structures were positive for cytokeratin AE1/AE3;epithelial cells were positive for the epidermal growth factor receptor(EGFR),p53 and negative for vimentin;positive immunostaining for Ki67 in some larger epithelial cells accounted approximately 15%;negative immunostaining for desmin was detected.

There was no significant medical history.

FlNAL DlAGNOSlS

On high-resolution computed tomography(HRCT),new-onset diffuse infiltrates,interlobular thickening and fibrosis were noted compared to a HRCT from one month prior(Figure 1).

TREATMENT

Upon arrival to the RICU,a body temperature of 36.8 degrees Celsius,a blood pressure of 128/90 mmHg,a heart rate of 97 beats/min,and a respiratory rate of 28 times/min were noted.The remaining physical examination was unremarkable except for diffuse inspiratory crackles in both lungs.

OUTCOME AND FOLLOW-UP

Unfortunately,after nine days of hospitalization,the patient died due to respiratory failure.

DlSCUSSlON

Lab data revealed the following:white blood cells 11.10 × 10/L,neutrophils 68.6%,lymphocytes 23.2%,hemoglobin 130 g/L and platelets 328 × 10/L.Serum C-reactive protein was increased at 111 mg/L(normal range ≤ 8 mg/L),erythrocyte sedimentation rate at 64 mm/h(normal range ≤ 15 mm/h),fecal calprotectin at 250.9 ug/g(normal range 0-50 ug/g)and procalcitonin was normal at 0.07 ng/mL(normal range ≤ 0.5 ng/mL).A fecal occult blood test showed positive occult blood with 0-1 white blood cells per high-power field.Stool cultures forwere all negative.Arterial blood gas analysis showed that pOwas 41 mmHg breathing ambient air.Extensive microbiology assays(blood and sputum culture,1,3-beta-D-glucan,galactomannan testing,aspergillus antibody,cryptococcal capsular polysaccharide antigen,mycoplasma antibody,human immunodeficiency virus antibody,cytomegalovirus,Epstein-Barr virus,A and B influenza virus PCR assays,and,antibodies of Toxoplasma gondii,rubella,herpes simplex virus and legionella)identified no infectious causes.Serologic examination included rheumatoid factor,antinuclear antibody panel,ds-DNA antibodies,anti-extractable nuclear antigen antibodies,myositis antibody panel,antineutrophil cytoplasmic antibody panel,and immunoglobulin,which were not elevated to pathologic levels.Cardiogenic pulmonary edema was excluded due to normal myocardial enzymes,Btype natriuretic peptide,echocardiogram and echocardiography.Some tumor markers,including,carcinoma embryonic antigen,cytokeratin 19 fragment and neuron-specific enolase,were increased at 7.68 ng/mL(normal range 0-5 ng/mL),12.37 ng/mL(normal range 0-5 ng/mL)and 26.61 ng/mL(normal range 0-24 ng/mL),respectively,while alpha-fetoprotein and carcinoma antigen 125 and 199 were in the normal range.Bronchoalveolar lavage(BAL)and transbronchial lung biopsy(TBLB)were also performed.Cultures from the BAL were negative for bacteria,mycobacteria and fungi.Samples from the BAL and the peripheral blood were sent together for metagenomic next-generation sequencing(mNGS).This sequencing uses an untargeted DNA/RNA sequencing method to detect all potential pathogens,including,bacteria,fungi,viruses,and parasites[3].In brief,the negative results of both mNGS and multiple microbiological cultures together effectively excluded infection.

Oh! mercy, cried the mother; what is it I see? Oh! it is that wretch13 her sister who has occasioned all this;33 but she shall pay for it ; and immediately she ran to beat her.34 The poor child fled away from her, and went to hide herself in the forest,35 not far from thence.

Strictly speaking,drug-induced pulmonary toxicity is not an extraintestinal manifestation of IBD[9,12].Even so,over half of interstitial lung disease and granulomatous lung disease cases in IBD patients are drug-related;therefore,more differential diagnoses are necessary[13].On that basis,we also reviewed 3 case reports of patients with CD.They presented with dyspnea,dry cough or fever with new-onset abnormal chest CT results(including pulmonary nodules,ground-glass opacities,pulmonary infiltrates or pleural effusions)after receiving 3-4 doses of vedolizumab[14-16].On histopathology,lung biopsies from all 3 cases revealed noncaseating granulomatous inflammation.In terms of clinical outcome,2 patients were successfully treated with prednisone,1 patient failed systemic steroid treatment but was responsive to infliximab treatment,and complete resolution of pulmonary disease was achieved in all three cases.

In our case,we made a diagnosis of vedolizumab-induced lung injury for the following reasons.First,the patient had no respiratory symptoms or interstitial changes on his previous chest CT,even though his UC was actively relapsing during the past 9 months.Second,the new symptoms following the application of vedolizumab and new-onset diffuse parenchymal changes on CT highly suggested an adverse drug reaction.Third,the resolution of intestinal symptoms and the evolution of respiratory injury occurring directly after the administration of vedolizumab may be attributed to the drug mechanism of vedolizumab itself.One study suggested that vedolizumab could induce an upregulation of β1 expression on lymphocytes(which is an integrin component involved in pulmonary homing)[14],thereby facilitating the development of pulmonary inflammation and injury.Fourth,the abnormalities in the chest CT of our case were the most severe when compared to the above published cases.The reason our patient was not responsive to systemic corticosteroid treatment was due to the devastating damage of the lung tissue and the delay in time to a diagnosis.Last,in addition to conventional microbiological tests,we also utilized the advanced mNGS technique,which has a much higher sensitivity than that of conventional tests in mixed pulmonary infection diagnoses[17].It has been reported that the sensitivity of mNGS for pathogen detection was 97.1%,with a negative predictive value of 94.1%[18].Moreover,extensive anti-infective therapy aiming to cover all possible pathogens was administered without any improvement of symptoms.All the facts discussed above basically excluded the possibility of infection.To the best of our knowledge,this is the first fatal case of vedolizumab-associated interstitial lung disease reported in China.There was an additional death reported in which a 70-yearold man with a UC flare was being treated with prednisone and vedolizumab,but this patient had previously had mild chronic shortness of breath with chest CT showing bilateral interstitial fibrosis before receiving vedolizumab;therefore,we cannot confirm that it was vedolizumab-related[19].

CONCLUSlON

Vedolizumab-related interstitial lung diseases in patients with IBD can be potentially fatal(as in our case presentation).Gastroenterologists and pulmonologists should raise their awareness regarding these cases.Timely diagnosis,early discontinuation of the offending drug and systemic corticosteroid treatment could prevent irreversible fibrosis.