SEATTLE-Concurrent
chemoradiotherapy improves survival
time in non-small-cell lung
cancer (NSCLC) but toxicity is
higher, and survival worsens if
treatment breaks are required.
Approaches that limit radiationinduced
esophagitis and pneumonitis
might translate into better
outcomes for NSCLC patients.
Vivek Mehta, MD, a radiation
oncologist at the Swedish Cancer
Institute, Seattle, Washington, and
investigators in the Community
Trial Non-Small-Cell Lung Cancer
Group are launching an open-
label trial to test the effectiveness
of amifostine(Drug information on amifostine) (Ethyol) for preventing
these problems in patients with
unresectable stage IIIA/IIIB
NSCLC who are receiving weekly
chemotherapy plus daily radiotherapy.
"Without cytoprotection, the
V20-the percentage of lung receiving
over 20 Gy of radiation-
predicts the risk of radiation pneumonitis,
as does the volume
received over 30 Gy," Dr. Mehta
said (see Figure 1). "There is a line
you can draw such that the risk of
radiation pneumonitis is fourfold
higher if 18% or more of lung volume
receives over 30 Gy."
Cytoprotection With Amifostine
A study by Komaki et al suggested
benefit from the addition of
amifostine to chemoradiation with cisplatin(Drug information on cisplatin) (Platinol) and etoposide(Drug information on etoposide)
(VePesid) in patients with inoperable
stage II or III NSCLC.[1] Dr.
Mehta said the trend did not reach
significance, perhaps because the
patients were not followed for a
long enough period of time.
The new open-label multicenter
trial will enroll 350 patients with
metastatic, unresectable stage IIIA
or IIIB NSCLC. All patients will
receive 3D conformal radiotherapy
in conventional daily fractions
of 1.8 to 2.0 Gy/d to a total dose of
60 to 70 Gy. The chemotherapy
regimen during radiotherapy can
either be cisplatin/etoposide or car-
boplatin (Paraplatin)/paclitaxel.
Following completion of chemotherapy,
patients can then receive
adjuvant consolidative docetaxel(Drug information on docetaxel)
(Taxotere) at the investigators' dis-
cretion. Amifostine will be given
at 500 mg/d prior to radiation.
"Our primary objective is to
determine the incidence of acute
esophagitis, acute pneumonitis,
and chronic pneumonitis," Dr.
Mehta said. "A secondary objective
is to describe the changes in
pulmonary function as measured
by DLCO [carbon monoxide diffusing
capacity] and FEV1 [forced
expiratory volume in 1 second] in
patients treated with concurrent
chemoradiotherapy."
