In, J H~d,‘,,,,,nOn,,,,,,41 Pnntcd tn Ihc I b ,
H,,,, 411 r,ehl.
Ph,c Lul rcwrvcd
‘,pp
461
4h-
??Original Contribution RADIATION PNEUMONITIS FOLLOWING LARGE SINGLE DOSE IRRADIATION: A RE-EVALUATION BASED ON ABSOLUTE DOSE TO LUNG .I. VAN DYK, M.Sc., F.C.C.P.M.,* T.J. KEANE, M.B.. M.R.C.P.I., F.R.C.P.(C),t S. KAY, M.D..$ W.D. RIDER, M.B., F.R.C.P.(C), F.R.C.R.$ AND C.J.H. FRYER. L.R.C.P.. M.R.C.S.. F.R.C.P.(C)** The Ontario Cancer Institute. The Princess Margaret Hospital, 500 Sherbourne Street Toronto. Ontario M4X I K9 The acute radiption pnmunonitis syndrome is 8 major complic8tion for patients receiving tot81 tborrcie irrrdirtion in a brge single dose. Previous studies have evnlwted tk onset of rrdi8tion pkumonitis on tk ksis of r8dirtion doses c8krloted 8ssuming nnit density tissues. In tbis report, tk incidence of radintion pneumoniti is determined as a function of absolute dose to lung. A sintfde algorithm relating dose correction factor to 8nteriorposteriar patient di8meter ks been derived using a CT-aided trntment pl8tming system. This 8Igorithm ~8s used to determine, retrospectively, tk dose to lnng for a group of 303 patients who kd been trnted with hrge kid irrndiation tecbnques. Of tbis groop, 150 patients kd no previous lung disense and kd virtually no 8ddkonall~ irrndiation prior or sobsequent to their large kid treatment. Tk rctnnri8l i&dence of rndiation pMnmonitisver!utsdoseto lung was evnhmted using 8 simplified probit 8nrlysis. Tk rennR8nt host fit sigmoidal complkation curve demomstrrtlcsthe onset of ndbtiea pmeulnodtis to occur 8t about 750 md witb tk 5 46 8ctonrinl ioci&mx occuring 8t rpproritnntely 820 nd. Tk errors usocirted with tk dose determkntion procedure as well 8s tk ncttmri8l incidence akubtions 8re considered. Tbe time of onset of rndiition pneumonitis occnrs between 1 to 7 motWbs after irrndi8tion for 90% of the p8ticnts who developed pneutnonitis witb tk pook incii occnrring at 2 to 3 tnontk. No correlation ~8s found between time of onset and tk dose to hmg over a dose r8nge of 650 to 1250 r8d. R8diation
pneumonitis.
Large field radiotkmpy.
Tissue inhomogeneity,
INTRODUCTION Half
body
irradiation
Because treatment lung irradiation,
disseminated
this organ’s
from
this
Fryer er al.’ describing doses of radiation radiation dyspnea oped
pneumonitis
method
malignant
syndrome
available.
conjunction
was published
by
dures to determine
lung.
of increasing
radiographic patients
patient
In
to the entire
and characteristic
in 44 of the 245
become
a
with
the toxic effects of large single
given
The
studied.
The
with
a precision
recent study”
acute
actuarial
patients
and 1000 rad. respectively.
These doses were calculated
dosage correction
patients
consisted
of
unit
This
this
series of
tomography
density
information
inhomogeneity than
(CT)
information can
be
has
used
dose calculation
doses at any point greater
were studied
try
the
for
within
previously
in
proce-
the patient possible.
A
how CT was used to determine with a
precision of better than 23% for radiation qualities ranging from cobalt-60 to 25 MV X rays. Twenty-three
devel-
was found to increase from single doses to lung of 800
that
specific
illustrated
incidence of this syndrome 29% to 84% for uncorrected assuming
rates
the dose to lung for upper half body radiotherapy
cough with
changes
Dose
the advent of computerized
detailed
to radiation.
tolerance
institution
With more
total
has provided
tissues only.
pknning.
patients ranged from SO to 400 rad per minute.
for
disease.‘.’
of the upper half body involves
the half body technique
means of analyzing
1978. a report
waterlike
provides an excellent
the palliation of widely
Dose corrections, Tre8tment
and lung
normal
density.
healthy
density
to determine data
factors.
average
lung geome-
and corresponding For cobalt-60
lungs, corrected
radiation
mid-lung and for
doses were found
to be
**Radiation Oncologist, Assistant Professor of Paediatrics. Cancer Control Agency of British Columbia, 2656 Heather Street, Vancouver, B.C. Canada VSZ 353. Reprint requests to: J. Van Dyk, M.Sc. Acknowledgements-We appreciate the discussions with Dr. P.M.K. Leung and the statistical help of Theresa Chua. Accepted for publication I8 December 1980.
Supported by grants from the NCI (Canada) and The Ontario Cancer Treatment and Research Foundation. *Medical Physicist. *Radiation Oncologist. $Clinical Fellow, Radiation Oncology. $Head, Radiation Oncology Department and Professor of Radiology. 461
362
Radiation
greater
by
??Physics
Oncology 0 Biology
IO to 24% compared
to their
April
198
I,
Volume 7. Number
4
uncorrected
values. In this paper. absolute
we describe
a method
lung doses retrospectively.
be obtained
addition, with
analyzed
and a toxicity
group of 58 patients
half
body
to provide
Lung
or total
treated
body
2 0.6391
thltkncss
+QlC52
In
since 1977
irradiation
more comprehensive
111
thscknes
1 Oatlant
curve
on the basis of real dose to lung.
another
upper
Least slluares
such that the patients
of the Fryer study4 could be reviewed could
of determining
were
toxicity
data.
METHODS AND MATERIALS To determine
the dose to lung in a retrospective
sis. a dose calculation uses patient patient
procedure
specific data that has been recorded
at the time
posterior recorded
of their
analy-
must be developed treatment.
which
for every
Since
anterior-
patient diameters in the thorax region were for all patients in the Fryer study.’ an attempt
was made to relate these to the dose at the middle lung. Van Dyk ef al.” reported made on a group ment
planning
tions were calculated then making a ratio
first assuming
tissue inhomogeneity
of the corrected
dose correction
mid-lung
thickness In
By taking
Using
between
thickness
is plotted
patient
indicates
on the average,
is 0.64 of the total
lung thicknesses from this linear correction
deviate
thickness:
by as much
squares
factor
fields
using
the lung
however,
as 3 cm (or 23%)
between
thickness
the correlation
patient
thickness
between is much
pleural
Hermluation
illustrate
for 50 x 60 cm tissue-air
dose correction
factor
14
I6
182Q22242629~
thckncss (cm)
oj’Fryrr’s original
radiation
ratio
and
the correlation
discrepancies.
Even the data points for a 7 year-old child fall very close to the linear best fit curve. In summary, this data provides a very simple procedure to estimate, retrospectively. the dose correction factor for cobalt-60 radiation for patients wirh normal lungs who received large field radiotherapy. By knowing the patient thickness. the dose correction factor can be determined.
description
pneumonitis findings.
the
much greater
12
r.
thickness versus patient thickness. (b) Dose for large tield cobalt-60 radiation versus
For a detailed
This
deviation is 3.5%. The points for abnormal containing high density tumor masses or
effusions)
0
R ESU LTS
is illustrated.
than
6
patient thickness.
paper by Fryer
between lung thickness and patient thickness. In fact, for the data of Figure I b. more than 80% of the points for normal lungs lie within I.57 of the best fit straight line; the maximum lungs (mostly
Fig. I. (a) Lung correction factor
dose
equivalent
better
6
mid-lung
was calculated the
4
Pohent
some
(TAR) method as developed by Sontag and Cunningham.‘” A comparison of Figure I a and Figure I b reveals that
2
clinical
factor and patient
dose correction
0
fit
best tit.
I b, the relationship
In Figure
cobalt-60
that.
least
was
these points is shown by the solid line. The slope curve
linear
between
thickness
through thickness
A
I.04 1
the same
against of this
thickness.
lung
I
I
,“/’
lC6
lung thickness
factor and patient la.
treattissues,
as well as the relationship
Figure
fucmf = thKkw%
mtmt
+QB075
dose, a mid-lung
was determined.
dose correction
determined.
corrections.
the relationship
Dose carfuctlan
dose distribu-
unit density
to uncorrected
factor
group of patients. and patient
using a CT-aided
For each patient,
IIt m nc+mat
O.Ol27l.
on specific measurements
of 23 patients
system.
of the
Least squares lunq data
syndrome
the reader
data
of the appearance is referred
et ui.” For comparison
sake of clarity
reviewed
in Table
incidence
of radiation
the original
of the
and the corresponding to the original purposes
incidence
and for
tigures
arc
I of this paper. This table gives the pneumonitis
rected dose 10 lung. No patients
as a function were excluded
of uncorbecause of
additional radiation treatments or because of known lung disease. The actuarial risk increased from 18’7 to 847 for uncorrected
doses of 600 to 1000 rad respectively.
By applying the appropriate dose correction factors using the procedure outlined above. corrected lung doses were determined for the same group of patients. Table 2 summarizes the results. Because of greater variability in lung
dose. the patients
now had to be subdivided
into
smaller groups according w ~1specitied dose interval. The 50 rad increment was a compromise between a large interval which includes many patients in one group and a smaller patients tainties.
interval which produces small numbers of in each group with resultant statistical unccr-
In Fryer’s mediastinum
study.’ btgnificant .’ radiation to lungs in addition to the half body treatment
and was
Radiation
pncumonitis
(rad)
Actuarial risk
Crude incidence
Number of patients
VAh
(o/o
(%)
Number of patients
Dose l/49 3124 281149 I2123 245
~600 600 800 1000 Total
found
order
to increase
to evaluate
risk of radiation
incidence
of pneumonitis, irradiation
for abnormal
2 were re-analyzed significant
data
are
the actuarial
(b)
pneumonitis
Using
Finney’
the data
number
of patients
location
on the sigmoidal
incidence
were
number
of
centered
at 850.
incidence
points
probit
per group
given
patients
zero
900 and
in
950
as their
Points
weight.
occurred
rad.
for these dose intervals
regression
as outlined according
as well
curve.
it
complication
analysis
were weighted
until
dose to lung. probit analysis
by a mathematical
the full
total
at about 800
rapidly
the best fit sigmoidal
can be determined
procedure.
lung
3. The
occurred
increased
reached 100% at about I 100 rad absolute This data was also evaluated using curve
by
to the relative
of 0% or 100%
Since the
the
dose
and since
occurred
largest intervals percent
on the rising
Table 2. The incidence of radiation pneumonitis for corrected dose to lung for all the patients in Fryer’s original study“
Dose -
(rad) o-574
Number of patients 47
575-624
3
Crude incidence (%,I
Actuarial risk (%)
0 1 4 5 I 120
2
3
3
0
0
0
I!
9
17
I5
675-724
I4
14
17
0 100 22 I6 28 0 50 57 77 67
0 100 33 28 49 0 100 100 74 100
II 0 0 17 7 I2 0 0 0 I5 0
I I I8 93 32 0 2 7 I3 3 245
Actuarial risk
(S)
(R)
0 0 0 0 0 100 I3 I6 20
0 0 0 0 0 100 I3 24 27
0 0 0 0 0 0 I2 8 I4
0 0 75 80 0
0 0 100 IO0 0
0 0 0 0 0
Standard deviation
part
of
the
weighted
dures while To
sigmoidal
very
avoid
procedure
curve,
heavily problem
0% and 100% incidence 99.9% the
incidence
analyses.
number
illustrates
they would
the percent
Those points with
were assumed each
ignored. regression
at 700 rad and including
to a probit.
Weighting
were proce-
to have 0. I o/r,and
also be included
point
according
a least squares fit was performed
back
in Figure
to a percent 2 was obtained.
an incidence
incidence,
in
to the
versus the log of the dose. By converting
best fit probits illustrated
so that
of patients,
the probits
probit
more than 3 patients,
was transformed
points
analysis
were virtually
a simplified
was used. Beginning with
data
probit
the other data points this
only those points incidence
these
in the full
of the
the curve
This best fit curve
of 1% at 800 rad and 7% at 850
rad.
Probit Regression Line
Standard deviation
625-674
725-?74 775-824 825-874 875-924 925-914 915- 1.024 I ,025-l .074 1.075-1.124 l,l25-1.174 1,175-1.224 Total
975-1.024 I ,025-l .074 I .075- I, I24 1.125-1.174 1.175-1.224 Total
I
Crude incidence
the lung. The
in the analysis was 120.
incidence
in which
is
who had (a)
previous
in Table
remaining
above
the data of Table
masses within
summarized
of patients
procedures
8 44 I5
significant
outlined
those patients
irradiation.
The onset of radiation rad;
method
33 I 3 4 0
O-514 575-624 625-674 675-724 725-774 775-824 825-874 875-924 925-974
In
from the analy-
lungs. Hence.
disease and (c) known tumor number
with
be removed
excluding
additional
adjusted
pneumonitis.
the patients
should
the dose correction
inaccurate
(rad)
the effect of a large single dose on the
additional sis. Also
3 18 36 84
2 13 19 52
the
463
DYk ef al.
Table 3. The incidence of radiation pncumonitis for corrected dose to lung for Fryer’s study’ excluding those patients with (a) significant previous and subsequent lung irradiation (b) previous lung disease and (c) tumours in lung
Table I. The incidence of radiation pncumonitis for uncorrected dose to lung. (Data taken from Fryer ef a/.‘)
Dose
??J.
rcKvaluated
Bawd on patients in
/
Dose to lung (rod)
arlqinol study (l960Encludino :
YI,
Fig. 2. Best fit sigmoidal complication curve using simplified probit regression analysis for the patients in Fryer’s study.’ The solid dots represent the points from Table 3 that were used to produce this curve. (Standard deviations do not apply for 0 or 100% incidence).
464
Radiation Oncology 0 Biology 0 Physrcs
Additional
analysis of patients treated since / 977
Fryer’s
original
study4 considered
patients
treated
up
to the end of 1976. During
1977 and 1978. another
of 58 patients
using large held radiotherapy.
were treated
Because of the toxicity
data provided
study.’ most of these patients rected
doses of
patients
who
marrow have
less than
received
tumor
dose region.
nally
by
in the
Fryer
held
et al.’ Also,
results of Table
incidence
irradiation
previous
with previous
with
the actuarial
incidence
the larger
rapidly.
simplified
probit
Figure
incidence
with
and large
patients
lung irradiation. in the lung have
which
Tables
the incidence
the results
of the
above. This best fit
of 3% at 800 rad and
3 and 5 as well as Figures
3, it will be noticed that only the dose interval 800
rad
shows
incidence patients
of
ial incidence. ered,
2 out
pneumonitis
difference
pneumonitis.
there
that patient
a marked
For
was only one patient
developed When of
original in that
pneumonitis-hence the additional
5 patients
resulting
in
this
in an actuarial
2 and
centered
in the
the
at
group interval
of and
are consid-
interval incidence
developed
Crude incidence
Actuarial
Number of
(rad)
patients
(S)
(S)
O-574 575-624 625-674 675-724 725-774 715-824 825-874 875-924 925-974 975-1.024 I ,025-I ,074 1,075-1,124 l,125-1,174 l,l75-1,225 Total
65 4 15 26 8 IO 23 93 32 0 2 7 I3 5 303
2 0 7 12 13 30 22 15 28 0 50 57 77 80
risk
2 0 II I3 I3 37 41 28 49 0 100 I00 74 100
(‘7)
(‘k)
Standard deviatron
0 0 0 0 0 10 20 I6 25 0
0 0 0 0 0 53
0 0 0 0 0 27
II
II
23 35 0
8 I4 0
I 4 5 3
0 75 80 67
0 100 100 100
0 0 0 0
I 50
Total
The
high
incidence
for this dose interval
concern
when it is considered
context
of the rest of the data,
statistically
the dose intervals
centered
much
show a lower incidence. that the high incidence of 2 out of 5 patients
in the
incidence
is
for example.
at 650. 700 and 750 rad. The for a total
5 demonstrates
Also. the dose intervals
950 tad contain
high
Consider.
3 shows 0 incidence
the data of Table
patients.
this
not very significant.
data of Table
is of serious
on its own. However.
larger
0 incidence
centered numbers
Therefore,
for I9
at 850.900
and
of patients
and
when it is considered
in this particular
developing
of 7 patients
point
pneumonitis
is a result
and when it
of 53F.
Table 4. The incidence of radiation pneumonitis for corrected dose to lung for Fryer’s study’ plus additional group of patients treated since 1977. all inclusive.
Dose
.4ctuarial risk
39 3 6 IO 3 5 IO 45 16 0
1.075-1.124 1.125-1.174 1.175-1.224
while
actuarial
100% actuar-
patients
Crude incidence
zero up to
12% at 850 rad. In comparing
o-574 575-624 625-674 675-724 725-774 775-824 825-874 875-924 925-974 975-I .024 1.025.- 1,074
of patients
remains
as described
curve gives an actuarial
the crude
number
3 illustrates
analysis
above.
data. The
5. those
of pneumonitis
a dose level of about 750 rad beyond increases
dose correction
treated
In Table
and subsequent
Even with
of 58 patients
described
lung disease, or with tumor
been excluded.
uncorrected
Number of patients
Dose (rad)
bone
to those origi-
4 illustrate
Table 5. The incidence of radiation pneumonitis for corrected dose to lung for Fryer‘s study’ plus additional group of patients treated since 1977. Excluded are those patients with ~a) significant previous and subsequent lung irradiation (b) previous lung disease (c) tumour in lung.
two
for
the original
of 303 patients
techniques.
with signiticant
group
identical
4
uncor-
addition.
1000 rad
using the method
This new data was combined accumulated
In
irradiation
This additional
were obtained
actuarial
body
using procedures
outlined
factors
rad.
7. Numhr
original
with
(at a dose rate near 5 radjmin)
also been included
was reviewed
750
total
transplantation
by Fryer’s
were treated
group
April 198 I. Volume
Probit
Regression
Line
Standard deviation
2 0
II 7 12 17 I6 7 12 0 0 0 I5 0
so0
700
Boo 900 1000 1100 1200 Dose to lung (rod1
1011,
Fig. 3. Best tit sigmoidal complication curve using simplified probit regression analysis for the patients in Fryer’s study as well as the additional patients treated since 1977. The solid dots represent the points from Table 5 that were used to produce this curve. (Standard deviations do not apply for 0 or 100% incidence).
is placed
in the context
significance Figure
pneumomtts
data.
its statistical
of the other
is not very high.
3 demonstrates
Radiation
In fact. the smooth
re-evaluared
??.I.
VA\
D\ h ef al
465
curve of
the best tit to ail the data. StOtldOrd
Time
of msel
pneunwniris
qf
after
The ttme of onset of radiation reported six
previously
months
~y.‘.‘.‘.‘~
after
s
l40-
to be in the neighborhood
of two to
$ E t
I20
-
100
-
of onset for the group The
the
peak
months.
of
course
the frequency
of 52 patients
acute the
radiation
of radiotheraversus the time
in this study
pneumonitis
distribution
occurs
while 90% of these patients
who
syndrome.
between
developed
2 to 3
pneumoni-
8 ‘0 2 g ‘a u f c
1 and 7 months.
tis between
meon
has been
a fractionated
the
about
pneumonitis
Figure 4 illustrates
developed
dewotlon
irradiation
Me0n
so-
60.
40 t
There
are only
a few
evaluate
the relationship
to lung.
Michaelson
clinical
pulmonary
proportional
toxicity with
treatment
insufficiency with
the 52 patients
though
in dogs to be inversely
increase
in time
of onset of
in dose has also been
fractionation in human
used
subjects.’
in
who developed
between
pneumonitis
in Figure
in our study.
5 and shows no obvious
time of onset and dose to lung even
cobalt-60
radiation
radiotherapy
using
XXI
800
Fig. 5. Time
to
lOO0
I I200
Imp
1 1300
)
(rod
*Is,
of onset of radiation
pneumonitis
lung for all 52 patients who developed radiation
versus dose 10 pneumonitis.
Error bars represent standard deviations.
patient
is about
tissues although to 24% depending 16% increase rad assuming an absolute
anterior-posterior
fields. the dose to lung for the average
on lung geometry
for 928 rad to lung
of the dose administered in the lung
method
fields.”
of a dose correction
factor
patient
2 I .5%
differences
for
the midpiane within
factor
lung,
are
using
especially
the
patients
is defined
corrections than
23%
for
the determination earlier
is accurate
studied,
for a point
Although
mid-lung
although
near
this
dose. there the anterior
the determination study is related actual treatment
of lung
the
in lung near point
may
are regions and posterior
that receive a 2 to 4% higher and probably
in the
on the basis of the anterioras described
the dose distributions
I?). Fourthiy,
difficult
Secondly.
of the patient.
an average
lung surfaces, example,
procedure to better
a few
error
as large as 3.5% have been noted. Thirdly.
dose correction represent
diameter 80%, of
curve, of
for inhomogeneity
to be accurate
is nearly
to lung. Because
sources
the dose computation TAR
of
curve requires
complication
possible
these large radiation
to
the incidence
such a steep complication
has been shown
dose of 800
for 800 rad to lung is only 38, the
regarding
posterior
A
tissues. the lungs would receive
incidence
First.
IO
unit density
control
comments
density
and lung density.”
dose of 928 rad. Although
50%. Obviously,
equivalent
it is to unit
for an uncorrected
pneumonitis
careful
than
in dose can vary between
means that
corresponding
order.
16% higher this increase
of this steepness
0123456709 Time
900
Oose
radiation
DlSCUSSlON heid
600
the
We have
the dose to lung varies from 650 to 1250 rad.
For large
L 1100
20
of onset of
the time of onset versus dose to lung for all
This data is illustrated correlation
the time
decrease
conventional
that
time of onset and dose
cl al.” found
of lung cancer
also evaluated
in the literature
between
to dose. This
pulmonary observed
reports
dose (see, for
of Figure
I. reference
the largest source of error dose for the patients
in
of this
to the inaccuracies associated with the of the patient. Although this error is
to determine
precisely.
an estimate
of ~54,
in
the delivery of tumor dose is probably reasonable. Combining these possible sources of error, the determinaof onset of pneumonitis
(months)
Fig. 4. The frequency distribution of the time of onset for ail 52 patients who developed radiation pneumonitis.
tion of lung dose for the patients
in this study is accurate
to 25%’ at best and -t 10% at worst. Errors in the determination of the actuarial
incidence
Radiation Oncology ??Biology 0 Physics
466
$
‘1
I
I
P .
1
I
1
zar’s study
1
would
Regression Line with Error Estimates
Probit
April 1981, Volume 7. Number 4
is 880 rad.
ment with Salazar’s
!!
From
yield an incidence
the data
of Figure
of 23% which
estimates
6. this
is in good agree-
of IO to 20%.
SUMMARY The
use of
standard
half
is also being therapy
evaluated
body irradiation
more frequently leukemic
600*900 1000 1100 1200 Iu)o Dose to lung (rod )
111s.I
Fig. 6. Error estimates superimposed on the sigmoidal curve of Fig. 3. Both the minimum and maximum error estimates are demonstrated.
pneumonitis
ial statistical
method
for small
less than 6 patients illustrate
are mainly
related
groups
of patients
per dose interval).
an incidence
of
Tables
nitis
these points contain
patients
though
without
even
a diagnosis
the actuarial last remaining having
patients
Tables
between
actuarial
risk values. is mainly
the
patients
the
were diagnosed
actuarial
figures
the crude
The mag’nitude
figures
minimum
and maximum
on the sigmoidal Salazar
the
estimated
complication
of patients
tion pneumonitis
to be between
using
IO MV data
X
rays.
as derived
Using from
IO and
magnitude
errors
On
in the 1.5%. of the
superimposed
Our experience
is a serious
of radia-
IO and 20%# for 800 rad half body irradiation
average
geometric
and
estimated
average
dose to lung for the patients
in Sala-
these
This is a unique toxicity
data.
toxicity
treatment
planning
the AP patient accounting
treated
with partial
rad.
at relating
and. because of the resultant Using
a CT-aided between factor
has been obtained. retrospec-
dose to lung of a series of patients or total body irradiation These patients
giving
fraction
pneumonitis
occurring
demonstrating
the onset of
750 rad with
at approximately
this dose the sigmoidal
rises dramatically.
pneumonitis
treatments,
occurs at about
incidence
large
were evaluated,
with respect to the radiation
For single
Above
the incidence dose to lung.
and the dose correction
doses in a single fraction.
5% actuarial
tech-
levels.
was then used lo determine.
the absolute
retrospectively.
pneumo-
data such that the dose to
for lung inhomogeneities
syndrome.
lungs of the
system. a simple relationship
tively,
for
involves
that radiation
be repeated.
diameter
This relationship
radiation
transplantation techniques
to the absolute
experience cannot
sarco-
are also being used
use of total lung irradia-
to non-toxic
pneumonitis
of radical
of these treatment
is a first attempt
of radiation
this technique form
to the total
indicates
the increased
detailed
This report
complication
the 820
curve
a 50 and 95 incidence
at 930 and 1060 rad. respectively.
In addition.
the time of
onset
pneumonitis
syndrome
of
the
months.
clinical
between
treatment
with
radiation
I to 7 months
the peak
No distinct
incidence
correlation
after
the
occurring
was found
radiation at 2 lo 3
between
the
time of onset and the dose to lung even over the large dose range of 650 to I250 rad. Certainly.
CT scan measurements”
(i.e. 22 cm A-P diameter, 14 cm of lung with relative electron density of 0.24). and previously published central ray data for IO MV X rays,” a mid-lung dose correction factor of I. IO has been calculated. Thus the
of
complication
lung can be limited
occurred
3.
the incidence
dose to lung for upper
density
279.
error
curve of Figure
PI ~1.~ have estimated
uncorrected
between
graphically
in the
of these standard
on the number
lies somewhere
6 illustrates
figures.
deviations
a group and is. at best, 8% and at worst.
Figure
as are
figures
and actuarial
standard
the basis of all the data points, the estimated incidence
died
because the
and the real incidence
dependent
of
(see crude incidence).
of the group
3 and 5 also illustrate
deviations
of
than
small groups
100%’ incidence
Hence.
an overestimate
are somewhere
within
yields
pneumonitis.
probably
some
of pneumonitis
method
3 and 5
Each
niques. Certainly,
(e.g.
100% for doses greater
1100 rad. However, and
to the actuar-
procedures
a
metas-
as well as Ewing’s
large single doses administered patient.
tion requires of radiation
Hospital,
prior to bone marrow
patients.
has become
of widespread
as an adjuvant
for oat cell carcinoma
ma. Total 700
radiotherapy
for palliation
tases. At the Princess Margaret
c--( Mmtmum error estlmote b-4 Mowmum error estimate
600
body
procedure
the data
of this study
indicate
that
lung
complications can only be avoided by precise individualized dosage calculations which include corrections for lung inhomogeneities. The corresponding absolute dose to lung should then single fraction.
be limited
to less than
800 rad in a
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