
58 AJTCCM VOL. 30 NO. 2 2024
ORIGINAL RESEARCH: ARTICLES
status (75.0% v. 25.0% with performance status 0 - 2; p=0.01) and
were more likely to have adenocarcinoma (49.7% v. 41.1%; p=0.02).
However, the potential cure rate at presentation did not dier between
the two cohorts.
e reduction observed in new lung cancer diagnoses is very similar
to the results reported by other investigators from our institution, who
reported a 36.2% decline in the number of all new cancers diagnosed
during the rst wave of the COVID-19 pandemic.[9] ese authors
noted an overall reduction in the cytopathological diagnosis of cancer of
61.1%. Substantial declines were seen for prostate (58.2%), oesophageal
(44.1%), breast (32.9%), gastric (32.6%) and colorectal cancer (29.2%).
e smallest decline was for cervical cancer (7%).[9] A study from Spain
also reported a 38% reduction in new lung cancer cases.[4]
In a pulse survey conducted by the WHO in 2020,[3] disruptions
of essential health services were reported by nearly all countries,
especially lower-income countries. e disruptions were caused by
a combination of factors including lockdowns impeding access to
healthcare, nancial diculties during lockdowns, cancellation of
elective services, reductions in attendance of outpatient services, sta
redeployment to provide COVID-19 relief, unavailability of services
owing to closures of health facilities or health services, and supply-
chain diculties. Cancer diagnosis and treatment was one of the
services most frequently reported to be disrupted globally.[3] At our
institution, pulmonology services were markedly de-escalated owing
to the need to use sta and other hospital resources in the COVID-19
response. Patients did not come to hospital because they were afraid
of contracting the disease. Outpatient services were also de-escalated.
Furthermore, COVID-19 may have caused increased mortality in
patients with lung cancer prior to presentation.
e rate of potentially curable cancer (stages I - IIIA) was similar
in the two groups, with no statistically signicant dierence (p=0.59).
is nding is in contrast to some international studies that showed
a reduction in early-stage lung cancer during the COVID pandemic.
[6] e most likely explanation for this observation internationally
is the suspension of lung cancer screening in the developed world
during the start of the pandemic.[7] SA did not have a lung cancer
screening programme at the time, and patients historically present to
our institution late in the disease course.
Our study showed that patients who presented during the
COVID-19 pandemic had better performance status than those who
presented pre-pandemic. e most plausible explanation for this
nding is selection bias, as referring doctors were arguably more
likely to refer patients who could benet from oncology services. It
contrasts with international data, where most countries found patients
who presented during the pandemic to be more symptomatic.[4]
Adenocarcinoma is well known to be the predominant tissue
type in new lung cancer diagnoses, both globally and locally.[10]
However, the statistically signicant increase in the proportion of
adenocarcinoma during the pandemic was an unexpected nding.
One possible explanation is that lung cancer in younger adults tends
to be adenocarcinoma and to be stage IV at presentation, which may
have contributed to a selection bias.[11]
One of the strengths of our study is that it was performed in a
high-volume tertiary referral centre with access to all relevant staging
and diagnostic modalities. Potential limitations may include major
selection bias during the peaks of the pandemic, when patients with
perceived advanced disease or with very poor performance status
were considered for palliation without referral.
Conclusion
During the COVID-19 pandemic there was a relative reduction
of 46% in the incidence of lung cancer observed in a high-volume
tertiary referral centre, and patients who were referred and diagnosed
with lung cancer had statistically better performance status and were
more likely to have adenocarcinoma than those in the pre-pandemic
period. No impact on the proportion of potentially curable disease
was noted.
Declaration. EMI, BWA and CFNK are members of the editorial
board. The research for this study was done in partial fulfilment of the
requirements for IF’s MMed (Int Med) degree at Stellenbosch
University.
Acknowledgements. None.
Author contributions. CFNK and IF conceived and designed the study;
IF was responsible for data collection; all authors were involved with
analysis and interpretation of data; IF drafted the manuscript, which was
critically revised by all authors; and all authors approved the final version.
Funding. None.
Conflicts of interest. None.
1. World Health Organization. Cancer. 3 February 2022. https://www.who.int/news-
room/fact-sheets/detail/cancer (accessed 7 February 2023).
2. Moynihan R, Sanders S, Michale ZA, et al. Impact of COVID-19 pandemic on
utilisation of healthcare services: A systematic review. BMJ Open 2021;11(3):e045343.
https://doi.org/10.1136/bmjopen-2020-045343
3. World Health Organization. Pulse survey on continuity of essential health services
during the COVID-19 pandemic: Interim report, 27 August 2020. Geneva: WHO,
2020. https://www.who.int/publications/i/item/WHO-2019-nCoV-EHS_continuity-
survey-2020.1 (accessed 3 February 2022).
4. Reyes R, López-Castro R, Auclin E, et al. Impact of COVID-19 pandemic in the
diagnosis and prognosis of lung cancer. J orac Oncol 2021;16(3):S141. https://doi.
org/10.1016/j.jtho.2021.01.219
5. Serra Mitjà P, Àvila M, García-Olivé I. Impact of the COVID-19 pandemic on lung
cancer diagnosis and treatment. Med Clin (Engl Ed) 2022;158(3):138-139. https://doi.
org/10.1016/j.medcle.2021.07.009
6. Jajbhay D, Arberry J, Gates J, et al. e impact of Covid-19 pandemic on lung cancer
diagnosis and treatment at St George’s Hospital. orax2021;76 (Suppl 2):A127-A128.
https://doi.org/10.1136/thorax-2021-BTSabstracts.221
7. Van Haren RM, Delman AM, Turner KM, et al. Impact of the COVID-19 pandemic
on lung cancer screening program and subsequent lung cancer. J Am Coll Surg
2021;232(4):600-605. https://doi.org/10.1016/j.jamcollsurg.2020.12.002
8. Detterbeck FC, Boa DJ, Kim AW, Tanoue LT. e eighth edition lung cancer stage
classication. Chest 2017;151(1):193-203. https://doi.org/10.1016/j.chest.2016.10.010
9. Van Wyk A, de Jager J, Razack R, et al. e initial impact of the COVID-19 pandemic
on the diagnosis of new cancers at a large pathology laboratory in the public health
sector, Western Cape Province, South Africa. S Afr Med J 2021;111(6):570-574.
https://doi.org/10.7196/SAMJ.2021.v111i6.15580
10. Koegelenberg CF, Aubeelack K, Nanguzgambo AB, et al. Adenocarcinoma the most
common cell type in patients presenting with primary lung cancer in the Western
Cape. S Afr Med J 2011;101(5):321. https://doi.org/10.7196/SAMJ.4554
11. Liu B, Quan X, Xu C, et al. Lung cancer in young adults aged 35 years or younger:
A full-scale analysis and review. J Cancer 2019;10(15):3553-3559. https://doi.
org/10.7150/jca.27490
Received 1 May 2023. Accepted 25 March 2024. Published 4 July 2024.