Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Sep 10:46:101062.
doi: 10.1016/j.lanepe.2024.101062. eCollection 2024 Nov.

Efficacy and safety of interim oncology treatments introduced for solid cancers during the COVID-19 pandemic in England: a retrospective evidence-based analysis

Affiliations

Efficacy and safety of interim oncology treatments introduced for solid cancers during the COVID-19 pandemic in England: a retrospective evidence-based analysis

Mark P Lythgoe et al. Lancet Reg Health Eur. .

Abstract

Background: The COVID-19 global pandemic placed unprecedented pressure on cancer services, requiring new interim Systemic Anti-Cancer Treatments (SACT) options to mitigate risks to patients and maintain cancer services. In this study we analyse interim COVID-19 SACT therapy options recommended in England, evaluating the evidence supporting inclusion and delineating how these have been integrated into routine cancer care.

Methods: We performed a retrospective analysis of interim Systemic Anti-Cancer Treatments endorsed by NHS England during the COVID-19 pandemic. Interim therapy options were compared to baseline (replacement) therapies by comparing data from the key pivotal trial(s) in terms of clinical efficacy and potential benefits (e.g., reduced immunosuppression or improved adverse effect profile) within the context of the pandemic. Furthermore, we evaluated the evolution of these interim SACT options, exploring if these have been integrated into current treatment pathways or are no longer accessible at the pandemic end.

Findings: 31 interim oncology treatment options, across 36 indications, for solid cancers were endorsed by NHS England between March 2020 and August 2021. Interim therapies focused on the metastatic setting (83%; 30/36), allowing greater utilisation of immune checkpoint inhibitors (45%; 14/31) and targeted therapies (26%; 8/31), in place of cytotoxic chemotherapy. Overall, 36% (13/36) of therapies could not have efficacy compared with baseline treatments due to a paucity of evidence. For those which could, 39% (9/23) had superior efficacy (e.g., overall survival), 26% (6/23) had equivocal efficacy and 35% (8/23) lower efficacy. 53% (19/36) of interim therapies had better or equivocal toxicity profiles (when assessable), and/or were associated with reduced immunosuppression. Almost half (47%; 17/36) of interim therapies did not have UK market authorisation, being classified as 'off label' use. Analysing access to interim options at the end of the pandemic (May 2023) identified 19 (53% 19/36) interim options were fully available, and a further four (11% 4/36) therapies were partially available.

Interpretation: Interim SACT options, introduced in England, across a range of solid cancers supported delivery of cancer services during the pandemic. Most interim therapies did not demonstrate superior efficacy, but provided other important benefits (e.g., reduced immunosuppression) in the context of the pandemic.

Funding: None.

Keywords: COVID-19; Cancer; Immune checkpoint inhibitors; Immunosuppression; Immunotherapy; NICE.

PubMed Disclaimer

Conflict of interest statement

ML, AE, RS, JK declare no conflicts of interest. HN reported receiving grants from the Commonwealth Fund, Health Foundation, UK Research and Innovation, and National Institute for Health and Care Research and personal fees from the World Health Organization, BMJ, and Pharmaceutical Group of the European Union outside the submitted work. AA is the recipient of an Advanced Fellowship NIHR300599 from the National Institute for Health Research. The views expressed in this publication are those of the author(s) and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health and Social Care.

Figures

Fig. 1
Fig. 1
A: Categorisation of Systemic Anti-Cancer Therapies (SACT) based on treatment intent and risk-benefit ratio. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 1). B: Number of therapies meeting each Selection Criteria for Interim Treatment Options During the COVID-19 Pandemic. ∗All therapies deemed to meet criteria 4 and 5 for inclusion. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 2). C: Number of therapies meeting each selection criteria for inclusion as an interim treatment options. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 2). D: UK Market Authorisation of Interim Treatment Options Approved During the COVID-19 Pandemic. E: Availability of Interim Treatment Options at the End of the COVID-19 Pandemic.
Fig. 1
Fig. 1
A: Categorisation of Systemic Anti-Cancer Therapies (SACT) based on treatment intent and risk-benefit ratio. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 1). B: Number of therapies meeting each Selection Criteria for Interim Treatment Options During the COVID-19 Pandemic. ∗All therapies deemed to meet criteria 4 and 5 for inclusion. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 2). C: Number of therapies meeting each selection criteria for inclusion as an interim treatment options. Treatments were classified based on NHS COVID-19 prioritisation guidance [NG161] (Table 2). D: UK Market Authorisation of Interim Treatment Options Approved During the COVID-19 Pandemic. E: Availability of Interim Treatment Options at the End of the COVID-19 Pandemic.

Similar articles

Cited by

References

    1. Holshue M.L., DeBolt C., Lindquist S., et al. First case of 2019 novel coronavirus in the United States. N Engl J Med. 2020;382:929–936. - PMC - PubMed
    1. Liang W., Guan W., Chen R., et al. Cancer patients in SARS-CoV-2 infection: a nationwide analysis in China. Lancet Oncol. 2020;21:335–337. - PMC - PubMed
    1. Zhang L., Zhu F., Xie L., et al. Clinical characteristics of COVID-19-infected cancer patients: a retrospective case study in three hospitals within Wuhan, China. Ann Oncol. 2020;31:894–901. - PMC - PubMed
    1. Desai A., Mohammed T.J., Duma N., et al. COVID-19 and cancer: a review of the registry-based pandemic response. JAMA Oncol. 2021;7:1882–1890. - PMC - PubMed
    1. Lythgoe M.P., Middleton P. Comparison of COVID-19 vaccine approvals at the US food and drug administration, European medicines agency, and health Canada. JAMA Netw Open. 2021;4:e2114531. - PMC - PubMed

LinkOut - more resources