Despite many advances in pulmonary medicine over the years, lung
cancer remains a major ongoing concern. Mortality due to lung cancer
is high, with the 5-year survival of advanced disease being very close
to zero. Early disease has better survival rates, with tumours <1 cm
having up to 92% 5-year survival, but larger tumours and nodal spread
rapidly decrease the prospect of cure.[[1]] Approximately 25% of patients
present with potentially curable disease in Europe and USA;[[2]] this
figure is very much lower in Western Cape Province, South Africa
(SA), with 14.5% in 2009[[3]] and 6.3% reported by Parker et al.
[[4]] in
this issue.Staging is an essential component in the decision-making process
in the management of lung cancer because accurate staging allows
more precise determination of effective therapy and minimises
morbidity due to unnecessary surgical procedures. Traditional
staging has been with computed tomography (CT) and lymph
node sampling by procedures such as mediastinoscopy. The article
by Parker et al.
[[4]] elegantly describes the utility of newer modes of
assessment including positron emission tomography combined
with CT (PET-CT) and endobronchial ultrasound transbronchial
needle aspiration (EBUS-TBNA). These non-invasive or relatively
well-tolerated procedures were effective in improving the accuracy
of staging with both up- and downgrading of clinical staging. Only
1.2% of patients were ultimately thought to be suitable for surgical
resection, with >80% having advanced disease.The role of new techniques in refining staging is commendable
in decreasing morbidity and even unnecessary surgical mortality.
However, the majority of patients present with advanced disease, and
palliative care is usually the only recourse. The decline over 10 years
in the number of patients presenting with potentially curable disease
is very worrying.Much of the delay in identifying early disease is likely to be due
to problems in the healthcare system, with several potential choke-points
along the way. Measures implemented at the tertiary level, such as
expedited clinic bookings and arrangements whereby CT scans and
biopsy procedures are performed within 3 weeks of request, are effective
only when early referral into these pathways is possible.The major problem is how to get patients referred who have
early disease. There are two main routes for case detection: clinical
case-finding or population screening. Unfortunately, cough, weight loss,
slowly resolving infections and other nonspecific symptoms are all too
common in an area where there is a very high prevalence of tuberculosis,
HIV reactivity and cigarette smoking. Crowded primary healthcare
facilities, with limited time for clinical interaction, exacerbate the
problem. Increased awareness of lung cancer is essential, but probably
inadequate alone. Clinical detection of lung cancer often occurs when
disease is quite advanced.Clinical and chest X-ray screening for lung cancer have been shown
to be ineffective.[[5]] Low-dose CT (LDCT) has been shown to be able
to detect early lung cancers and to reduce lung cancer mortality.[[6]]
The SA Thoracic Society has published firm recommendations for
the use of LDCT screening in SA, targeting high-risk individuals
(aged 55 - 74 years, current or ex-smokers with >30 pack-years
smoking history). A conservative threshold for invasive sampling was
recommended because of the high prevalence of TB and post-TB lung
disease.[[6]] Limitations to the widespread implementation of LDCT
screening include the need for expertise, and cost, but this remains one
of the very few real interventions for facilitating early intervention in
lung cancer.The ideal approach to lung cancer management should include
increased societal, patient and clinician awareness of the problem
and the need for early diagnosis. This, coupled with all of the modern
technologies described, including LDCT screening, PET-CT and
EBUS-FNAB, should result in far better outcomes for patients with
lung cancer.
Authors: Aldoph B Nanguzgambo; Kushroo Aubeelack; Florian von Groote-Bidlingmaier; Susanna M Hattingh; Mercia Louw; Coenraad F N Koegelenberg; Chris T Bolliger Journal: J Thorac Oncol Date: 2011-02 Impact factor: 15.609