(Chest. 2000;117:123S-126S.)
© 2000
American College of Chest Physicians
Locally Advanced, Unresectable Non-Small Cell Lung Cancer*
New Treatment Strategies
David H. Johnson, MD
*
From the Division of Medical Oncology, Vanderbilt Cancer Center, Nashville, TN.
Correspondence to: David H. Johnson, MD, Division of Medical Oncology, 1956 The Vanderbilt Clinic, Nashville, TN 37232-5536
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Abstract
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Approximately 40% of non-small cell lung cancer (NSCLC) patients
present with locally advanced, unresectable lesions. Treatment
with thoracic radiotherapy yields survivals averaging just 9 to 10
months, and long-term survival at 5 years is poor. Recent studies
indicate that chemotherapy followed by thoracic radiotherapy improves
5-year survival by three- to fourfold. Nevertheless, most patients do
ultimately die of the underlying disease. New strategies designed to
enhance local tumor controluse of radiation-sensitizing drugs,
three-dimensional treatment planning techniques, or altered radiation
fractionation schedulesmay further improve survival outcome. In
addition, newer cisplatin-based regimens containing either paclitaxel
or vinorelbine improve survival over that achieved with older vinca
alkaloid or podophyllotoxin combination regimens. Accordingly, the
newer drug regimens combined with radiotherapy can be expected to
further improve survival in this subset of NSCLC patients. Prospective
studies are underway to test this conjecture.
Key Words: distant metastases fractionation local control radiation sensitization radiotherapy three-dimensional planning
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Introduction
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Non
-small cell lung cancer (NSCLC) is a leading cause of cancer deaths
worldwide.1
The high death rate is due to the fact that
NSCLC is usually in an advanced stage not amenable to surgical
resection when first diagnosed. Although the outlook for NSCLC patients
remains fairly dismal, there is reason for guarded optimism, as modest
therapeutic advances have been realized in this disease over the course
of the past 2 decades. For example, in stage IV disease, survival can
be lengthened and symptom palliation is possible with cisplatin-based
chemotherapy.2
3
Similarly, survival for individuals with
locally advanced, stage III NSCLC has improved with combined-modality
therapy.4
5
6
Historically, patients with locally advanced
NSCLC were treated with thoracic radiotherapy alone. However, because
so many patients develop recurrent disease outside the chest,
chemotherapy was added to standard thoracic radiotherapy in an attempt
to diminish this problem with a resultant fourfold increase in 2-year
survival rates.4
5
6
Despite these noteworthy advances, the
overwhelming majority of NSCLC patients continue to die of their
underlying malignancy, leaving considerable room for further refinement
in the management of this disease. This review will focus on strategies
aimed at improving outcome in locally advanced NSCLC.
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Current Management of Locally Advanced, Unresectable NSCLC
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Approximately 40% of patients with newly diagnosed NSCLC first
present with locally advanced disease, and the majority are
inoperable.1
Traditionally, these patients were treated
with radiotherapy alone, resulting in a median survival of
approximately 9 to 10 months and a 5-year survival rate of
approximately 7%.7
These discouraging results were
largely due to the eventual development of extrathoracic metastases.
Several investigators have tried combining local therapy
(ie, radiotherapy) with systemic therapy (ie,
chemotherapy) in an attempt to overcome the obstacle of systemic
recurrence. Although the initial results with this approach were
somewhat disappointing,8
9
possibly due to the modest
activity of chemotherapy regimens initially employed, there appeared to
be a subset of patients with locally advanced disease who derived a
modest survival benefit,4
10
particularly those with good
performance status and little or no weight loss. Most thoracic
oncologists now advocate the routine use of chemotherapy plus
radiotherapy in this group of patients with locally advanced,
unresectable NSCLC.
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Improving Local Tumor Control
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Although combined-modality treatment with chemotherapy and
radiotherapy has improved survival in some patients with stage III
NSCLC, most still succumb to the underlying disease.1
Tumor progression remains problematic, both locally within the chest
and in extrathoracic sites. We will first examine the problem of local
tumor control.
It is commonly estimated that radiotherapy alone affords intrathoracic
control in up to 50% of NSCLC cases, provided a total dose
60 Gy
is employed.11
However, such estimates are based on
studies conducted > 20 years ago, which are probably not very
accurate. The signs and symptoms associated with an extrathoracic
lesion usually so dominate the clinical picture that even if local
progression is present, it is commonly overlooked. Indeed, a patient
who progresses outside of the chest rarely undergoes a thorough
restaging. Consequently, the true incidence of local failure is almost
certainly much higher than is commonly believed. In those rare
circumstances where a careful reevaluation has been performed, the
frequency of local control is disappointingly low, even when total
radiotherapy doses are > 60 Gy.12
Fewer than 20% of
irradiated patients undergoing repeat bronchoscopy have evidence of
complete tumor control at the site of the primary
lesion.12
13
Does this lack of local control really matter given our failure to
adequately control systemic disease? The available data suggest
improved local control is worthwhile. Strategies employed in recent
years to further improve local tumor control include the use of
radiation-sensitizing drugs, altered radiotherapy fractionation
schedules, and the use of three-dimensional treatment planning
techniques. Several antineoplastic agents including cisplatin,
topoisomerase-inhibiting agents, paclitaxel, and gemcitabine all have
radiation-sensitizing potential.14
15
16
17
This approach was
tested in a European randomized trial showing that concomitant
cisplatin and irradiation improved survival compared with radiotherapy
alone.18
The survival benefit was clearly attributable to
improved local tumor control because the rate of distant failure was
not affected (Table 1 ). Although this approach warrants additional study, it is worth noting
that the simultaneous use of radiation and drugs can be a double-edged
sword. Administering chemotherapy and radiotherapy concomitantly may
increase host toxicities, necessitating dose reductions in one or both
treatment modalities. Esophagitis and pulmonary toxicities are
particularly worrisome in this regard.19
20
21
There appears to be a linear correlation between radiotherapy dose and
local control of NSCLC.7
22
Accordingly, one theoretically
could improve control at the primary tumor merely by increasing the
dose of radiotherapy. However, it is difficult to increase the
radiation dose > 60 Gy, due to toxicities engendered in normal
tissues. Three-dimensional treatment planning may permit use of
increasing total radiation doses without causing excessive host
toxicity.23
Preliminary studies indicate radiotherapy
doses can be escalated to as high as 85 to 90 Gy without causing major
damage to normal tissues with this technique.24
25
26
27
Yet another means of increasing radiotherapy dose while minimizing
normal tissue toxicity is the use of multiple daily radiation
fractions.28
Pilot studies indicate this approach also is
feasible.29
30
In fact, the results of several studies
suggest hyperfractionated irradiation yields a survival benefit
comparable to that achieved with combined-modality therapy (Table 2
).29
31
32
These tantalizing data lend strong support to
the notion that improving local tumor control is a worthwhile goal,
even in the absence of improved control of extrathoracic disease.
In further support of this position are the results of a recently
completed British trial in which continuous hyperfractionated
accelerated radiotherapy (CHART) was compared with standard daily
radiotherapy (total dose, 60 Gy in 30 fractions) for the treatment of
patients with unresectable NSCLC.33
34
CHART consisted of
thrice-daily 1.5-Gy fractions of irradiation given for 12 consecutive
days to a total dose of 54 Gy (36 fractions). Median and long-term
survival favored the CHART-treated group (Table 3
), as did local control group rates. If these results are validated in
confirmatory trials, the impact on the practice of NSCLC treatment
could be profound.
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Improved Control of Systemic Disease
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Several meta-analyses clearly showed that cisplatin-based
chemotherapy can improve survival in patients with
NSCLC.2
35
36
The modest survival advantage benefits
primarily those patients treated with cisplatin-based combination
regimens, although there is a trend toward improved survival with
regimens containing vinca alkaloids or etoposide.2
Within
the past few years, several new drugs have shown excellent activity
against NSCLC, including the taxanes (paclitaxel and docetaxel),
vinorelbine, gemcitabine, and irinotecan.37
Importantly,
some of these agents possess unique mechanisms of action and, with rare
exception, appear to be less toxic than many of the older agents used
in the management of NSCLC.
In recently completed randomized studies, the combinations of
cisplatin plus paclitaxel or cisplatin plus vinorelbine yielded modest
survival advantages over older cisplatin-based combination
regimens.38
39
Given these observations, it is
reasonable to anticipate these newer regimens will provide similar (or
greater) survival benefit in locally advanced NSCLC. Already there is
considerable preliminary data to suggest this is likely to be true, and
randomized trials are in progress. Furthermore, combining chemotherapy
with newer techniques of thoracic radiotherapy may well provide
additional survival benefit as suggested by the results of several
pilot studies 19
and at least one recently reported
randomized trial.40
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Summary
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In summary, better local control, as well as greater control of
extrathoracic micrometastases, should result in improved survival among
patients with locally advanced NSCLC. The methods of improving local
control are quite varied, and each merits continued investigation.
Potentially, these techniques will lead to further improvement in the
survival of NSCLC patients with locally advanced disease.
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Footnotes
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Abbreviations: CHART = continuous
hyperfractionated accelerated radiotherapy; NSCLC = non-small cell
lung cancer
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