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All Studies   All Outcomes    Recent:   

Oral antivirals for COVID-19 among patients with cancer

Guermazi et al., Research Square, doi:10.21203/rs.3.rs-3876022/v1
Jan 2024  
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Retrospective 67 cancer outpatients treated with nirmatrelvir/ritonavir or molnupiravir, compared to 56 untreated concurrent controls, reporting lower mortality with treatment. However, Figure 3 shows the opposite results for invasive mechanical ventilation, ~2 times higher for the treatment groups versus the control group. The discrepancy suggests that the groups are not comparable in some key aspect such as treatment availability or decisions, baseline conditions, and/or prevalence of non-COVID-19 related death. ECOG ≥2 was much more common for controls vs. treated patients. One possibility is that controls had more advanced existing disease and were more likely to choose not to receive life-sustaining treatments. The higher use of remdesivir for controls may also indicate greater severity and/or more delayed treatment based on prescribing guidelines, and may also contribute to increased mortality due to side effects within a more vulnerable population. Remdesivir shows increased mortality with longer followup1.
Confounding by contraindication. Hoertel et al. find that over 50% of patients that died had a contraindication for the use of Paxlovid2. Retrospective studies that do not exclude contraindicated patients may significantly overestimate efficacy.
Black box warning. The FDA notes that "severe, life-threatening, and/or fatal adverse reactions due to drug interactions have been reported in patients treated with paxlovid"3.
Use may promote the emergence of variants that weaken host immunity and potentially contribute to long COVID4.
Kamo et al. show significantly increased risk of acute kidney injury. Resistant variants are likely6,7.
Study covers molnupiravir and paxlovid.
Guermazi et al., 24 Jan 2024, retrospective, preprint, 5 authors, study period 1 April, 2020 - 1 August, 2023. Contact: dorra_guermazi@brown.edu.
This PaperPaxlovidAll
Oral antivirals for COVID-19 among patients with cancer
Dorra Guermazi, Panos Arvanitis, Kendra Vieira, Jeremy L Warner, Dimitrios Farmakiotis
doi:10.21203/rs.3.rs-3876022/v1
Purpose: Immunocompromised individuals, such as those diagnosed with cancer, are at a signi cantly higher risk for severe illness and mortality when infected with SARS-CoV-2 (COVID-19) than the general population. Two oral antiviral treatments are approved for COVID-19: Paxlovid® (nirmatrelvir/ritonavir) and Lagevrio® (molnupiravir). There is a paucity of data regarding the bene t from these antivirals among immunocompromised patients with cancer, and recent studies have questioned their e cacy among vaccinated patients, even those with risk factors for severe COVID-19. Methods: We evaluated the e cacy and safety of nirmatrelvir/ritonavir and molnupiravir in preventing severe illness and death using our database of 457 patients with cancer and COVID-19 from Brown University-a liated hospitals. 67 patients received nirmatrelvir/ritonavir or molnupiravir and were compared to 56 concurrent controls who received no antiviral treatment despite being eligible to receive it. Results: Administration of nirmatrelvir/ritonavir or molnupiravir was associated with improved survival and lower 90-day all-cause and COVID-19-attributed mortality (p<0.05) and with lower peak O2 requirements (ordinal odds ratio [OR] 1.52, 95% con dence interval [CI] 0.92-2.56). Conclusion: Acknowledging the small size of our sample as a limitation, we concluded that early antiviral treatment might be bene cial to immunocompromised individuals, particularly those with cancer, when infected with SARS-CoV-2. Larger-scale, well-strati ed studies are needed in this patient population.
Declarations Competing Interests DF has received research support from Viracor, Astellas and Merck, and consultant fee from Viracor. All other authors have nothing to disclose. Ethics approval: The study was approved by the Lifespan Institutional Review Board (IRB). The study was conducted in accordance with the declaration of Helsinki. Consent to publish: All authors agreed to the publication of the manuscript. Consent to participate: The study was approved by the Lifespan Institutional Review Board (IRB) with a waiver of informed consent given its retrospective design and de-identi ed data. Supplementary Files This is a list of supplementary les associated with this preprint. Click to download. SupplementaryMaterial.pdf
References
Anwar, Nguyen, Nagasaka, Ou, Chan, Overview of Drug-Drug Interactions Between Ritonavir-Boosted Nirmatrelvir (Paxlovid) and Targeted Therapy and Supportive Care for Lung Cancer, JTO Clin Res Rep, doi:10.1016/j.jtocrr.2022.100452
Arayici, Effects of SARS-CoV-2 infections in patients with cancer on mortality, ICU admission and incidence: a systematic review with meta-analysis involving 709,908 participants and 31,732 cancer patients, J Cancer Res Clin Oncol, doi:10.1007/s00432-022-04191-y
Arvanitis, Lerner, Vieira, Almaghlouth, Farmakiotis, Outpatient anti-spike monoclonal antibody administration is associated with decreased morbidity and mortality among patients with cancer and COVID-19, Clin Exp Med, doi:10.1007/s10238-023-01019-y
Bernal, Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized Patients, N Engl J Med, doi:10.1056/NEJMoa2116044
Butler, Molnupiravir plus usual care versus usual care alone as early treatment for adults with COVID-19 at increased risk of adverse outcomes (PANORAMIC): an open-label, platformadaptive randomised controlled trial, Lancet, doi:10.1016/S0140-6736(22)02597-1
Choueiri, Breakthrough SARS-CoV-2 infections among patients with cancer following two and three doses of COVID-19 mRNA vaccines: a retrospective observational study from the COVID-19 and Cancer Consortium, Lancet Reg Health Am, doi:10.1016/j.lana.2023.100445
Dodd, Freidlin, Korn, Platform Trials -Beware the Noncomparable Control Group, N Engl J Med, doi:10.1056/NEJMc2102446
Dormuth, Kim, Fisher, Piszczek, Kuo, Nirmatrelvir-Ritonavir and COVID-19 Mortality and Hospitalization Among Patients With Vulnerability to COVID-19 Complications, JAMA Netw Open, doi:10.1001/jamanetworkopen.2023.36678
Dryden-Peterson, Nirmatrelvir Plus Ritonavir for Early COVID-19 in a Large U.S. Health System: A Population-Based Cohort Study, Ann Intern Med, doi:10.7326/m22-2141
Elkrief, Learning through a Pandemic: The Current State of Knowledge on COVID-19 and Cancer, Cancer Discov, doi:10.1158/2159-8290.Cd-21-1368
Eng, Disposition of Nirmatrelvir, an Orally Bioavailable Inhibitor of SARS-CoV-2 3C-Like Protease, across Animals and Humans, Drug Metab Dispos, doi:10.1124/dmd.121.000801
Farley, New Drug Application (NDA) 217188: PAXLOVID (nirmatrelvir tablets; ritonavir tablets), copackaged, FDA
Farmakiotis, COVID-19 Treatments for Nonhospitalized Patients, JAMA, doi:10.1001/jama.2022.6167
Fendler, Functional immune responses against SARS-CoV-2 variants of concern after fourth COVID-19 vaccine dose or infection in patients with blood cancer, Cell Rep Med, doi:10.1016/j.xcrm.2022.100781
Gentry, Nguyen, Thind, Kurdgelashvili, Williams, Characteristics and outcomes of US Veterans with immunocompromised conditions at high risk of severe SARS-CoV-2 infection with or without receipt of oral antiviral agents, Clin Infect Dis, doi:10.1093/cid/ciad504
Gleeson, Kidney Transplant Recipients and Omicron: Outcomes, effect of vaccines and the e cacy and safety of novel treatments, medRxiv, doi:10.1101/2022.05.03.22274524
Grivas, Association of clinical factors and recent anticancer therapy with COVID-19 severity among patients with cancer: a report from the COVID-19 and Cancer Consortium, Ann Oncol, doi:10.1016/j.annonc.2021.02.024
Guermazi, Arvanitis, Farmakiotis, Molnupiravir e cacy among immunocompromised patients with COVID-19: no proof of concept, Infection, doi:10.1007/s15010-023-02027-6
Hammond, Oral Nirmatrelvir for High-Risk, Nonhospitalized Adults with Covid-19, New England Journal of Medicine, doi:10.1056/NEJMoa2118542
Johnson, Molnupiravir for the treatment of COVID-19 in immunocompromised participants: e cacy, safety, and virology results from the phase 3 randomized, placebo-controlled MOVe-OUT trial, Infection, doi:10.1007/s15010-022-01959-9
Kneidinger, Outcome of lung transplant recipients infected with SARS-CoV-2/Omicron/B.1.1.529: a Nationwide German study, Infection, doi:10.1007/s15010-022-01914-8
Lin, Chemotherapy Treatment Modi cations During the COVID-19 Outbreak at a Community Cancer Center in New York City, JCO Glob Oncol, doi:10.1200/go.20.00309
Liu, E cacy and safety of Paxlovid in severe adult patients with SARS-Cov-2 infection: a multicenter randomized controlled study, Lancet Reg Health West Pac, doi:10.1016/j.lanwpc.2023.100694
Malin, Weibel, Gruell, Kreuzberger, Stegemann et al., E cacy and safety of molnupiravir for the treatment of SARS-CoV-2 infection: a systematic review and meta-analysis, J Antimicrob Chemother, doi:10.1093/jac/dkad132
Paraskevis, Real-world effectiveness of molnupiravir and nirmatrelvir/ritonavir as treatments for COVID-19 in high-risk patients, J Infect Dis, doi:10.1093/infdis/jiad324
Radcliffe, Palacios, Azar, Cohen, Malinis, Real-world experience with available, outpatient COVID-19 therapies in solid organ transplant recipients during the omicron surge, Am J Transplant, doi:10.1111/ajt.17098
Rusnak, PAXLOVID (nirmatrelvir / ritonavir): Main Protease Inhibitor of SARS-CoV-2 Corona Virus
Schmidt, COVID-19 vaccination and breakthrough infections in patients with cancer, Ann Oncol, doi:10.1016/j.annonc.2021.12.006
Sun, Lin, Wang, Gao, Ye, Paxlovid in patients who are immunocompromised and hospitalised with SARS-CoV-2 infection, Lancet Infect Dis, doi:10.1016/s1473-3099(22)00430-3
Vaishampayan, Parchment, Jasti, Hussain, Taxanes: an overview of the pharmacokinetics and pharmacodynamics, Urology, doi:10.1016/s0090-4295(99)00451-3
Yao, Ding, Burchell, Wolf, Friedberg, Detoxication of vinca alkaloids by human P450 CYP3A4-mediated metabolism: implications for the development of drug resistance, J Pharmacol Exp Ther
Zhang, Yang, Zhou, Wei, Ma, Network Pharmacology and Bioinformatics Analysis Identi es Potential Therapeutic Targets of Paxlovid Against LUAD/COVID-19, Front Endocrinol, doi:10.3389/fendo.2022.935906
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Two oral antiviral treatments are approved for COVID-19: Paxlovid® ' '(nirmatrelvir/ritonavir) and Lagevrio® (molnupiravir). 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Hammond et al., "Oral Nirmatrelvir for High-Risk, Nonhospitalized ' 'Adults with Covid-19," New England Journal of Medicine, vol. 386, no. ' '15, pp. 1397–1408, 2022, doi: 10.1056/NEJMoa2118542.', 'journal-title': 'New England Journal of Medicine'}, { 'key': 'ref5', 'doi-asserted-by': 'publisher', 'first-page': '509', 'DOI': '10.1056/NEJMoa2116044', 'article-title': '"Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized ' 'Patients," (in eng)', 'volume': '386', 'author': 'Jayk Bernal A', 'year': '2022', 'unstructured': 'A. Jayk Bernal et al., "Molnupiravir for Oral Treatment of Covid-19 in ' 'Nonhospitalized Patients," (in eng), N Engl J Med, vol. 386, no. 6, pp. ' '509–520, Feb 10 2022, doi: 10.1056/NEJMoa2116044.', 'journal-title': 'N Engl J Med'}, { 'key': 'ref6', 'doi-asserted-by': 'publisher', 'author': 'Dryden-Peterson S', 'year': '2023', 'unstructured': 'S. Dryden-Peterson et al., "Nirmatrelvir Plus Ritonavir for Early ' 'COVID-19 in a Large U.S. Health System: A Population-Based Cohort ' 'Study," (in eng), Ann Intern Med, vol. 176, no. 1, pp. 77–84, Jan 2023, ' 'doi: 10.7326/m22-2141.', 'DOI': '10.7326/m22-2141'}, { 'key': 'ref7', 'doi-asserted-by': 'publisher', 'DOI': '10.1093/infdis/jiad324', 'article-title': '"Real-world effectiveness of molnupiravir and nirmatrelvir/ritonavir as ' 'treatments for COVID-19 in high-risk patients," (in eng)', 'volume': '11', 'author': 'Paraskevis D', 'year': '2023', 'unstructured': 'D. Paraskevis et al., "Real-world effectiveness of molnupiravir and ' 'nirmatrelvir/ritonavir as treatments for COVID-19 in high-risk ' 'patients," (in eng), J Infect Dis, Aug 11 2023, doi: ' '10.1093/infdis/jiad324.', 'journal-title': 'J Infect Dis, Aug'}, { 'key': 'ref8', 'doi-asserted-by': 'publisher', 'author': 'Johnson MG', 'year': '2023', 'unstructured': 'M. G. 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Ma, "Network Pharmacology and ' 'Bioinformatics Analysis Identifies Potential Therapeutic Targets of ' 'Paxlovid Against LUAD/COVID-19," (in eng), Front Endocrinol (Lausanne), ' 'vol. 13, p. 935906, 2022, doi: 10.3389/fendo.2022.935906.', 'journal-title': 'Front Endocrinol (Lausanne)'}, { 'issue': '2', 'key': 'ref13', 'doi-asserted-by': 'publisher', 'first-page': '100452', 'DOI': '10.1016/j.jtocrr.2022.100452', 'article-title': 'Overview of Drug-Drug Interactions Between Ritonavir-Boosted ' 'Nirmatrelvir (Paxlovid) and Targeted Therapy and Supportive Care for ' 'Lung Cancer," (in eng)', 'volume': '4', 'author': 'Anwar K', 'year': '2023', 'unstructured': 'K. Anwar, L. Nguyen, M. Nagasaka, S. I. Ou, and A. Chan, "Overview of ' 'Drug-Drug Interactions Between Ritonavir-Boosted Nirmatrelvir (Paxlovid) ' 'and Targeted Therapy and Supportive Care for Lung Cancer," (in eng), JTO ' 'Clin Res Rep, vol. 4, no. 2, p. 100452, Feb 2023, doi: ' '10.1016/j.jtocrr.2022.100452.', 'journal-title': 'JTO Clin Res Rep'}, { 'key': 'ref14', 'doi-asserted-by': 'publisher', 'author': 'Farmakiotis D', 'year': '2022', 'unstructured': 'D. Farmakiotis, "COVID-19 Treatments for Nonhospitalized Patients," ' 'JAMA, vol. 327, no. 22, pp. 2247–2247, 2022, doi: ' '10.1001/jama.2022.6167.', 'DOI': '10.1001/jama.2022.6167'}, { 'key': 'ref15', 'doi-asserted-by': 'publisher', 'author': 'Liu J', 'year': '2023', 'unstructured': 'J. Liu et al., "Efficacy and safety of Paxlovid in severe adult patients ' 'with SARS-Cov-2 infection: a multicenter randomized controlled study," ' '(in eng), Lancet Reg Health West Pac, vol. 33, p. 100694, Apr 2023, doi: ' '10.1016/j.lanwpc.2023.100694.', 'DOI': '10.1016/j.lanwpc.2023.100694'}, { 'issue': '7', 'key': 'ref16', 'doi-asserted-by': 'publisher', 'first-page': '1586', 'DOI': '10.1093/jac/dkad132', 'article-title': 'Efficacy and safety of molnupiravir for the treatment of SARS-CoV-2 ' 'infection: a systematic review and meta-analysis," (in eng)', 'volume': '78', 'author': 'Malin JJ', 'year': '2023', 'unstructured': 'J. J. Malin, S. Weibel, H. Gruell, N. Kreuzberger, M. Stegemann, and N. ' 'Skoetz, "Efficacy and safety of molnupiravir for the treatment of ' 'SARS-CoV-2 infection: a systematic review and meta-analysis," (in eng), ' 'J Antimicrob Chemother, vol. 78, no. 7, pp. 1586–1598, Jul 5 2023, doi: ' '10.1093/jac/dkad132.', 'journal-title': 'J Antimicrob Chemother'}, { 'key': 'ref17', 'author': 'Rusnak J', 'year': '2023', 'unstructured': 'J. Rusnak, "PAXLOVID (nirmatrelvir / ritonavir): Main Protease Inhibitor ' 'of SARS-CoV-2 Corona Virus," A. D. A. Committee, Ed., ed, March 16, ' '2023, p. https://www.fda.gov/media/166238/download.'}, { 'key': 'ref18', 'author': 'Farley J', 'unstructured': 'J. Farley, "New Drug Application (NDA) 217188: PAXLOVID (nirmatrelvir ' 'tablets; ritonavir tablets), co-packaged ", ed. FDA, March 16, 2023, p. ' 'https://www.fda.gov/media/166237/download.'}, { 'issue': '6', 'key': 'ref19', 'doi-asserted-by': 'publisher', 'first-page': '2739', 'DOI': '10.1007/s10238-023-01019-y', 'article-title': 'Outpatient anti-spike monoclonal antibody administration is associated ' 'with decreased morbidity and mortality among patients with cancer and ' 'COVID-19," (in eng)', 'volume': '23', 'author': 'Arvanitis P', 'year': '2023', 'unstructured': 'P. Arvanitis, A. H. Lerner, K. Vieira, N. Almaghlouth, and D. ' 'Farmakiotis, "Outpatient anti-spike monoclonal antibody administration ' 'is associated with decreased morbidity and mortality among patients with ' 'cancer and COVID-19," (in eng), Clin Exp Med, vol. 23, no. 6, pp. ' '2739–2748, Oct 2023, doi: 10.1007/s10238-023-01019-y.', 'journal-title': 'Clin Exp Med'}, { 'key': 'ref20', 'doi-asserted-by': 'publisher', 'author': 'Sun F', 'year': '2022', 'unstructured': 'F. Sun, Y. Lin, X. Wang, Y. Gao, and S. Ye, "Paxlovid in patients who ' 'are immunocompromised and hospitalised with SARS-CoV-2 infection," (in ' 'eng), Lancet Infect Dis, vol. 22, no. 9, p. 1279, Sep 2022, doi: ' '10.1016/s1473-3099(22)00430-3.', 'DOI': '10.1016/s1473-3099(22)00430-3'}, { 'issue': '10', 'key': 'ref21', 'doi-asserted-by': 'publisher', 'first-page': 'e2336678', 'DOI': '10.1001/jamanetworkopen.2023.36678', 'article-title': '"Nirmatrelvir-Ritonavir and COVID-19 Mortality and Hospitalization ' 'Among Patients With Vulnerability to COVID-19 Complications," (in eng)', 'volume': '6', 'author': 'Dormuth CR', 'year': '2023', 'unstructured': 'C. R. Dormuth, J. D. Kim, A. Fisher, J. Piszczek, and I. F. Kuo, ' '"Nirmatrelvir-Ritonavir and COVID-19 Mortality and Hospitalization Among ' 'Patients With Vulnerability to COVID-19 Complications," (in eng), JAMA ' 'Netw Open, vol. 6, no. 10, p. e2336678, Oct 2 2023, doi: ' '10.1001/jamanetworkopen.2023.36678.', 'journal-title': 'JAMA Netw Open'}, { 'issue': '6', 'key': 'ref22', 'doi-asserted-by': 'publisher', 'first-page': '787', 'DOI': '10.1016/j.annonc.2021.02.024', 'article-title': '"Association of clinical factors and recent anticancer therapy with ' 'COVID-19 severity among patients with cancer: a report from the ' 'COVID-19 and Cancer Consortium,"', 'volume': '32', 'author': 'Grivas P', 'year': '2021', 'unstructured': 'P. Grivas et al., "Association of clinical factors and recent anticancer ' 'therapy with COVID-19 severity among patients with cancer: a report from ' 'the COVID-19 and Cancer Consortium," Ann Oncol, vol. 32, no. 6, pp. ' '787–800, Jun 2021, doi: 10.1016/j.annonc.2021.02.024.', 'journal-title': 'Ann Oncol'}, { 'key': 'ref23', 'doi-asserted-by': 'publisher', 'first-page': '100445', 'DOI': '10.1016/j.lana.2023.100445', 'article-title': '"Breakthrough SARS-CoV-2 infections among patients with cancer ' 'following two and three doses of COVID-19 mRNA vaccines: a ' 'retrospective observational study from the COVID-19 and Cancer ' 'Consortium,"', 'volume': '19', 'author': 'Choueiri TK', 'year': '2023', 'unstructured': 'T. K. Choueiri et al., "Breakthrough SARS-CoV-2 infections among ' 'patients with cancer following two and three doses of COVID-19 mRNA ' 'vaccines: a retrospective observational study from the COVID-19 and ' 'Cancer Consortium," Lancet Reg Health Am, vol. 19, p. 100445, Mar 2023, ' 'doi: 10.1016/j.lana.2023.100445.', 'journal-title': 'Lancet Reg Health Am'}, { 'issue': '3', 'key': 'ref24', 'doi-asserted-by': 'publisher', 'first-page': '340', 'DOI': '10.1016/j.annonc.2021.12.006', 'article-title': '"COVID-19 vaccination and breakthrough infections in patients with ' 'cancer,"', 'volume': '33', 'author': 'Schmidt AL', 'year': '2022', 'unstructured': 'A. L. Schmidt et al., "COVID-19 vaccination and breakthrough infections ' 'in patients with cancer," Ann Oncol, vol. 33, no. 3, pp. 340–346, Mar ' '2022, doi: 10.1016/j.annonc.2021.12.006.', 'journal-title': 'Ann Oncol'}, { 'key': 'ref25', 'doi-asserted-by': 'publisher', 'author': 'Eng H', 'year': '2022', 'unstructured': 'H. Eng et al., "Disposition of Nirmatrelvir, an Orally Bioavailable ' 'Inhibitor of SARS-CoV-2 3C-Like Protease, across Animals and Humans," ' '(in eng), Drug Metab Dispos, vol. 50, no. 5, pp. 576–590, May 2022, doi: ' '10.1124/dmd.121.000801.', 'DOI': '10.1124/dmd.121.000801'}, { 'key': 'ref26', 'doi-asserted-by': 'publisher', 'author': 'Vaishampayan U', 'unstructured': 'U. Vaishampayan, R. E. Parchment, B. R. Jasti, and M. Hussain, "Taxanes: ' 'an overview of the pharmacokinetics and pharmacodynamics," (in eng), ' 'Urology, vol. 54, no. 6A Suppl, pp. 22\u2009–\u20099, Dec 1999, doi: ' '10.1016/s0090-4295(99)00451-3.', 'DOI': '10.1016/s0090-4295(99)00451-3'}, { 'key': 'ref27', 'author': 'Yao D', 'year': '2000', 'unstructured': 'D. Yao, S. Ding, B. Burchell, C. R. Wolf, and T. Friedberg, ' '"Detoxication of vinca alkaloids by human P450 CYP3A4-mediated ' 'metabolism: implications for the development of drug resistance," (in ' 'eng), J Pharmacol Exp Ther, vol. 294, no. 1, pp. 387\u2009–\u200995, Jul ' '2000.'}, { 'key': 'ref28', 'doi-asserted-by': 'publisher', 'author': 'Lin DD', 'year': '2020', 'unstructured': 'D. D. Lin et al., "Chemotherapy Treatment Modifications During the ' 'COVID-19 Outbreak at a Community Cancer Center in New York City," (in ' 'eng), JCO Glob Oncol, vol. 6, pp. 1298–1305, Aug 2020, doi: ' '10.1200/go.20.00309.', 'DOI': '10.1200/go.20.00309'}, { 'key': 'ref29', 'doi-asserted-by': 'publisher', 'author': 'Butler CC', 'unstructured': 'C. C. Butler et al., "Molnupiravir plus usual care versus usual care ' 'alone as early treatment for adults with COVID-19 at increased risk of ' 'adverse outcomes (PANORAMIC): an open-label, platform-adaptive ' 'randomised controlled trial," Lancet, vol. 401, no. 10373, pp. 281–293, ' 'Jan 28 2023, doi: 10.1016/S0140-6736(22)02597-1.', 'DOI': '10.1016/S0140-6736(22)02597-1'}, { 'key': 'ref30', 'doi-asserted-by': 'publisher', 'DOI': '10.1093/cid/ciad504', 'article-title': 'Characteristics and outcomes of US Veterans with immunocompromised ' 'conditions at high risk of severe SARS-CoV-2 infection with or without ' 'receipt of oral antiviral agents,"', 'volume': '24', 'author': 'Gentry CA', 'year': '2023', 'unstructured': 'C. A. Gentry, P. N. Nguyen, S. K. Thind, G. Kurdgelashvili, and R. J. ' 'Williams, "Characteristics and outcomes of US Veterans with ' 'immunocompromised conditions at high risk of severe SARS-CoV-2 infection ' 'with or without receipt of oral antiviral agents," Clin Infect Dis, Aug ' '24 2023, doi: 10.1093/cid/ciad504.', 'journal-title': 'Clin Infect Dis, Aug'}, { 'issue': '3', 'key': 'ref31', 'doi-asserted-by': 'publisher', 'first-page': '749', 'DOI': '10.1007/s15010-022-01914-8', 'article-title': '"Outcome of lung transplant recipients infected with ' 'SARS-CoV-2/Omicron/B.1.1.529: a Nationwide German study," (in eng), ' 'Infection', 'volume': '51', 'author': 'Kneidinger N', 'year': '2023', 'unstructured': 'N. Kneidinger et al., "Outcome of lung transplant recipients infected ' 'with SARS-CoV-2/Omicron/B.1.1.529: a Nationwide German study," (in eng), ' 'Infection, vol. 51, no. 3, pp. 749–757, Jun 2023, doi: ' '10.1007/s15010-022-01914-8.'}, { 'key': 'ref32', 'doi-asserted-by': 'publisher', 'first-page': '1572', 'DOI': '10.1056/NEJMc2102446', 'article-title': '"Platform Trials - Beware the Noncomparable Control Group,"', 'volume': '384', 'author': 'Dodd LE', 'year': '2021', 'unstructured': 'L. E. Dodd, B. Freidlin, and E. L. Korn, "Platform Trials - Beware the ' 'Noncomparable Control Group," N Engl J Med, vol. 384, no. 16, pp. ' '1572–1573, Apr 22 2021, doi: 10.1056/NEJMc2102446.', 'journal-title': 'N Engl J Med'}], 'container-title': [], 'original-title': [], 'link': [ { 'URL': 'https://www.researchsquare.com/article/rs-3876022/v1', 'content-type': 'text/html', 'content-version': 'vor', 'intended-application': 'text-mining'}, { 'URL': 'https://www.researchsquare.com/article/rs-3876022/v1.html', 'content-type': 'unspecified', 'content-version': 'vor', 'intended-application': 'similarity-checking'}], 'deposited': { 'date-parts': [[2024, 1, 24]], 'date-time': '2024-01-24T18:57:59Z', 'timestamp': 1706122679000}, 'score': 1, 'resource': {'primary': {'URL': 'https://www.researchsquare.com/article/rs-3876022/v1'}}, 'subtitle': [], 'short-title': [], 'issued': {'date-parts': [[2024, 1, 24]]}, 'references-count': 32, 'URL': 'http://dx.doi.org/10.21203/rs.3.rs-3876022/v1', 'relation': {}, 'published': {'date-parts': [[2024, 1, 24]]}, 'subtype': 'preprint'}
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