Methotrexate lung disease

Changed by Henry Knipe, 15 Jun 2023
Disclosures - updated 16 Jan 2023:
  • Integral Diagnostics, Shareholder (ongoing)
  • Micro-X Ltd, Shareholder (ongoing)

Updates to Article Attributes

Body was changed:

Methotrexate lung disease is theads specific aetiological type of drug-induced lung disease. It can occur due to the administration of methotrexate, which is an antimetabolite, which is given for various reasons but commonlycommonly prescribed to treat rheumatoid arthritis. It is also given alone or in combination with other chemotherapeutic agents to treat a wide variety of malignancies including lung, breast, and head and neck epidermoid cancers, non-metastatic osteosarcoma, and advanced-stage non-Hodgkin lymphoma.

Epidemiology

It is thought to occur in ~5% (range 0.3-10%) of patients treated with methotrexate 1-2.

Clinical presentation

The typical clinical symptoms include progressive shortness of breath and cough, often associated with fever 6. Hypoxaemia and tachypnoea are always present and crackles are frequently audible. Symptoms typically manifest within months of starting therapy). There appears to be no correlation between the development of drug toxicity and the duration of therapy or total cumulative dose) 1.

Pathology

There can be several manifestations of methotrexate-related lung changes:

Previously, methotrexate was thought to cause pulmonary fibrosis, however, more recent evidence (c. 2021) has not established a causative effect 10-12.

Radiographic features

CT

CT features can be variable and included diffuse parenchymal opacification, reticular opacities, and centrilobular nodules 2. An NSIP pattern is considered the most common manifestation of methotrexate-induced lung disease 1.

Treatment and prognosis

Overall prognosis would depend on the exact form of the disease. In general, the prognosis is considered good, with most patients improving despite the continuation of therapy. Patients with lung fibrosis at presentation may have worse prognosis 2.

Differential diagnosis

See also

  • -<p><strong>Methotrexate lung disease</strong> is the specific aetiological type of <a href="/articles/drug-induced-lung-disease-1">drug-induced lung disease</a>. It can occur due to the administration of methotrexate which is an antimetabolite, which is given for various reasons but commonly to treat <a href="/articles/rheumatoid-arthritis">rheumatoid arthritis</a>. It is also given alone or in combination with other chemotherapeutic agents to treat a wide variety of malignancies including <a href="/articles/lung-cancer-3">lung</a>, <a href="/articles/breast-cancer">breast</a>, and head and neck epidermoid cancers, non-metastatic <a href="/articles/osteosarcoma">osteosarcoma</a>, and advanced-stage <a href="/articles/non-hodgkin-lymphoma">non-Hodgkin lymphoma</a>.</p><h4>Epidemiology</h4><p>It is thought to occur in ~5% (range 0.3-10%) of patients treated with methotrexate<sup> 1-2</sup>.</p><h4>Clinical presentation</h4><p>The typical clinical symptoms include progressive shortness of breath and cough, often associated with fever <sup>6</sup>. Hypoxaemia and tachypnoea are always present and crackles are frequently audible. Symptoms typically manifest within months of starting therapy). There appears to be no correlation between the development of drug toxicity and the duration of therapy or total cumulative dose)<sup> 1</sup>.</p><h4>Pathology</h4><p>There can be several manifestations of methotrexate-related lung changes:</p><ul>
  • -<li>inflammatory: fibrotic disease<ul>
  • +<p><strong>Methotrexate lung disease</strong> is ads specific aetiological type of <a href="/articles/drug-induced-lung-disease-1">drug-induced lung disease</a>. It can occur due to the administration of methotrexate, which is an antimetabolite, commonly prescribed to treat <a href="/articles/rheumatoid-arthritis">rheumatoid arthritis</a>. It is also given alone or in combination with other chemotherapeutic agents to treat a wide variety of malignancies including <a href="/articles/lung-cancer-3">lung</a>, <a href="/articles/breast-cancer">breast</a>, and head and neck epidermoid cancers, non-metastatic <a href="/articles/osteosarcoma">osteosarcoma</a>, and advanced-stage <a href="/articles/non-hodgkin-lymphoma">non-Hodgkin lymphoma</a>.</p><h4>Epidemiology</h4><p>It is thought to occur in ~5% (range 0.3-10%) of patients treated with methotrexate<sup> 1-2</sup>.</p><h4>Clinical presentation</h4><p>The typical clinical symptoms include progressive shortness of breath and cough, often associated with fever <sup>6</sup>. Hypoxaemia and tachypnoea are always present and crackles are frequently audible. Symptoms typically manifest within months of starting therapy). There appears to be no correlation between the development of drug toxicity and the duration of therapy or total cumulative dose)<sup> 1</sup>.</p><h4>Pathology</h4><p>There can be several manifestations of methotrexate-related lung changes:</p><ul>
  • -<a title="Organising pneumonia" href="/articles/organising-pneumonia">organising pneumonia</a> (formerly called bronchiolitis obliterans with organising pneumonia or BOOP)</li>
  • -<li>
  • -<a href="/articles/acute-interstitial-pneumonitis">acute interstitial pneumonia</a> with <a href="/articles/non-cardiogenic-pulmonary-oedema-2">non-cardiogenic pulmonary oedema</a>
  • +<p>non-immunosuppresive</p>
  • +<ul>
  • +<li><p><a href="/articles/methotrexate-induced-pneumonitis" title="methotrexate-induced pneumonitis">methotrexate-induced pneumonitis</a>: 1% of rheumatoid arthritis patients starting methotrexate <sup>10</sup></p></li>
  • +<li><p><a href="/articles/pleural-effusion">pleural effusion</a> / pleuritis <sup>15</sup> but also reported in rheumatoid arthritis in general <sup>14</sup></p></li>
  • +<li><p><a href="/articles/organising-pneumonia" title="Organising pneumonia">organising pneumonia</a>: has been associated with methotrexate use but can also occur in the setting of new diagnosis rheumatoid arthritis <sup>13</sup></p></li>
  • +</ul>
  • -<li><a href="/articles/pulmonary-fibrosis">pulmonary fibrosis</a></li>
  • -<a href="/articles/pleural-effusion">pleural effusion</a> and symptomatic pleuritis occur infrequently</li>
  • +<p><a href="/articles/immunosuppression">immunosuppresive</a></p>
  • +<ul>
  • +<li><p>superimposed pulmonary infection <sup>10</sup></p></li>
  • +<li><p><a href="/articles/pulmonary-lymphoproliferative-disease" title="Pulmonary lymphoproliferative disease">pulmonary lymphoproliferative disease</a> <sup>16</sup></p></li>
  • -<li>superimposed pulmonary infection: from <a href="/articles/immunosuppression">immunosuppression</a>
  • +</ul><p>Previously, methotrexate was thought to cause pulmonary fibrosis, however, more recent evidence (c. 2021) has not established a causative effect <sup>10-12</sup>.</p><h4>Radiographic features</h4><h5>CT</h5><p>CT features can be variable and included diffuse parenchymal opacification, reticular opacities, and centrilobular nodules <sup>2</sup>. An <a href="/articles/non-specific-interstitial-pneumonia-1">NSIP</a> pattern is considered the most common manifestation of methotrexate-induced lung disease <sup>1</sup>.</p><h4>Treatment and prognosis</h4><p>Overall prognosis would depend on the exact form of the disease. In general, the prognosis is considered good, with most patients improving despite the continuation of therapy. Patients with lung fibrosis at presentation may have worse prognosis <sup>2</sup>.</p><h4>Differential diagnosis</h4><ul>
  • +<li>
  • +<p><a href="/articles/rheumatoid-arthritis-associated-interstitial-lung-disease" title="Rheumatoid arthritis associated interstitial lung disease">rheumatoid arthritis associated interstitial lung disease</a> <sup>10</sup></p>
  • +<ul>
  • +<li><p>more common</p></li>
  • +<li><p>fibrotic pattern</p></li>
  • +</ul>
  • -<li>pulmonary lymphoproliferative disease: from immunosuppression</li>
  • -</ul><h4>Radiographic features</h4><h5>CT</h5><p>CT features can be variable and included diffuse parenchymal opacification, reticular opacities, and centrilobular nodules <sup>2</sup>. An <a href="/articles/non-specific-interstitial-pneumonia-1">NSIP</a> pattern is considered the most common manifestation of methotrexate-induced lung disease <sup>1</sup>.</p><h4>Treatment and prognosis</h4><p>Overall prognosis would depend on the exact form of the disease. In general, the prognosis is considered good, with most patients improving despite the continuation of therapy. Patients with lung fibrosis at presentation may have worse prognosis <sup>2</sup>.</p><h4>See also</h4><ul><li><a href="/articles/rheumatoid-arthritis-pulmonary-manifestations-1">pulmonary manifestations of rheumatoid arthritis</a></li></ul>
  • +<li><p><a href="/articles/non-fibrotic-hypersensitivity-pneumonitis-3" title="Non-fibrotic hypersensitivity pneumonitis">non-fibrotic hypersensitivity pneumonitis</a> <sup>10</sup></p></li>
  • +</ul><h4>See also</h4><ul><li><p><a href="/articles/rheumatoid-arthritis-pulmonary-manifestations-1">pulmonary manifestations of rheumatoid arthritis</a></p></li></ul>

References changed:

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  • 4. Camus P, Kudoh S, Ebina M. Interstitial Lung Disease Associated with Drug Therapy. Br J Cancer. 2004;91 Suppl 2(Suppl 2):S18-23. <a href="https://doi.org/10.1038/sj.bjc.6602063">doi:10.1038/sj.bjc.6602063</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/15340374">Pubmed</a>
  • 5. Cannon G. Methotrexate Pulmonary Toxicity. Rheum Dis Clin North Am. 1997;23(4):917-37. <a href="https://doi.org/10.1016/s0889-857x(05)70366-5">doi:10.1016/s0889-857x(05)70366-5</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/9361161">Pubmed</a>
  • 6. Imokawa S, Colby T, Leslie K, Helmers R. Methotrexate Pneumonitis: Review of the Literature and Histopathological Findings in Nine Patients. Eur Respir J. 2000;15(2):373-81. <a href="https://doi.org/10.1034/j.1399-3003.2000.15b25.x">doi:10.1034/j.1399-3003.2000.15b25.x</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/10706507">Pubmed</a>
  • 7. Chhabra P, Law A, Suri V, Malhotra P, Varma S. Methotrexate Induced Lung Injury in a Patient with Primary CNS Lymphoma: A Case Report. Mediterr J Hematol Infect Dis. 2012;4(1):e2012020. <a href="https://doi.org/10.4084/MJHID.2012.020">doi:10.4084/MJHID.2012.020</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/22550565">Pubmed</a>
  • 8. Hargreaves M, Mowat A, Benson M. Acute Pneumonitis Associated with Low Dose Methotrexate Treatment for Rheumatoid Arthritis: Report of Five Cases and Review of Published Reports. Thorax. 1992;47(8):628-33. <a href="https://doi.org/10.1136/thx.47.8.628">doi:10.1136/thx.47.8.628</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/1412121">Pubmed</a>
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  • 15. Methotrexate-Induced Pleurisy. J Am Acad Dermatol. 2013;68(4):AB140. <a href="https://doi.org/10.1016/j.jaad.2012.12.579">doi:10.1016/j.jaad.2012.12.579</a>
  • 16. Iwami E, Ito F, Sasahara K et al. Pulmonary Intravascular Large B-Cell Lymphoma in a Patient Administered Methotrexate for Rheumatoid Arthritis. Intern Med. 2020;59(3):429-33. <a href="https://doi.org/10.2169/internalmedicine.3216-19">doi:10.2169/internalmedicine.3216-19</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/31619597">Pubmed</a>
  • 1. Rossi SE, Erasmus JJ, Mcadams HP et-al. Pulmonary drug toxicity: radiologic and pathologic manifestations. Radiographics. 20 (5): 1245-59. <a href="http://radiographics.rsna.org/content/20/5/1245.full">Radiographics (full text)</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/10992015">Pubmed citation</a><div class="ref_v2"></div>
  • 2. Arakawa H, Yamasaki M, Kurihara Y et-al. Methotrexate-induced pulmonary injury: serial CT findings. J Thorac Imaging. 2003;18 (4): 231-6. <a href="http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0883-5993&volume=18&issue=4&spage=231">J Thorac Imaging (link)</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/14561908">Pubmed citation</a><div class="ref_v2"></div>
  • 3. Ellis SJ, Cleverley JR, Müller NL. Drug-induced lung disease: high-resolution CT findings. AJR Am J Roentgenol. 2000;175 (4): 1019-24. <a href="http://www.ajronline.org/content/175/4/1019.full">AJR Am J Roentgenol (full text)</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/11000156">Pubmed citation</a><div class="ref_v2"></div>
  • 4. Camus P, Kudoh S, Ebina M. Interstitial lung disease associated with drug therapy. Br. J. Cancer. 2004;91 Suppl 2 : S18-23. <a href="http://dx.doi.org/10.1038/sj.bjc.6602063">doi:10.1038/sj.bjc.6602063</a> - <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750811">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/15340374">Pubmed citation</a><div class="ref_v2"></div>
  • 5. Cannon GW. Methotrexate pulmonary toxicity. Rheum. Dis. Clin. North Am. 1997;23 (4): 917-37. - <a href="http://www.ncbi.nlm.nih.gov/pubmed/9361161">Pubmed citation</a><div class="ref_v2"></div>
  • 6. Imokawa S, Colby TV, Leslie KO et-al. Methotrexate pneumonitis: review of the literature and histopathological findings in nine patients. Eur. Respir. J. 2000;15 (2): 373-81. <a href="http://erj.ersjournals.com/cgi/pmidlookup?view=long&pmid=10706507">Eur. Respir. J. (link)</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/10706507">Pubmed citation</a><div class="ref_v2"></div>
  • 7. Chhabra P, Law AD, Suri V et-al. Methotrexate induced lung injury in a patient with primary CNS lymphoma: a case report. Mediterr J Hematol Infect Dis. 02;4 (1): e2012020. <a href="http://www.mjhid.org/article/view/9884/html">Mediterr J Hematol Infect Dis (full text)</a> - <a href="http://dx.doi.org/10.4084/MJHID.2012.020">doi:10.4084/MJHID.2012.020</a> - <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340991">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/22550565">Pubmed citation</a><span class="ref_v3"></span>
  • 8. Hargreaves MR, Mowat AG, Benson MK. Acute pneumonitis associated with low dose methotrexate treatment for rheumatoid arthritis: report of five cases and review of published reports. Thorax. 1992;47 (8): 628-33. <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC463926">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/1412121">Pubmed citation</a><span class="ref_v3"></span>

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