Save
ONCOL 310
Gyne
Vaginal
Save
Share
Learn
Content
Leaderboard
Learn
Created by
MK
Visit profile
Cards (27)
True / False: most malignancies of vagina are due to invasion from nearby tumours (cervix, vulva)
true
:
most
malignancies are due to invasion from
nearby
tumours (
cervix
,
vulva
)
Peak incidence:
50
-
60
years (
sixth
-
seventh
decade)
Epidemiology:
mean age:
65
+/-
14
years
increasing incidence in younger women due to
HPV
vaginal
or utero - vaginal
prolapse
True / False: vaginal cancer incidence rates were highest for African American women
true
: incidence rates were
highest
for
African American
women
Etiology:
most common cause:
HPV
previous
cervical
cancer
in utero exposure to
DES
(diethylstilbestrol)
previous
hysterectomy
smoking
→
2
x risk of vaginal cancer
HIV
Pathology:
squamous cell
= most common
adenocarcinoma
more likely to spread than
squamous
cell carcinoma
Natural history:
commonly involves
superior
1
/ 3 of
vaginal
canal
exophytic
,
infiltrating
growth pattern
anterior wall →
vesicovaginal septum
or
urethra
posterior wall →
rectovaginal septum
or
rectal mucosa
advanced:
parametrium
,
levator ani muscles
, pelvic fascia, pelvic sidewall
distant mets:
lung
,
liver
,
bone
vaginal intraepithelial neoplasia (VAIN)→
precursor
lesion to
SCC
of vagina
VAIN 1:
low
grade, changes limited to
upper
1
/ 3 epithelium
VAIN 2: changes to
lower
2
/ 3 epithelium
VAIN 3: changes to
full thickness
of epithelium, carcinoma
in situ
True / False: in vaginal cancers, the lateral walls are less frequently involved
true
: the
lateral walls
are
less
frequently involved
Presentation:
abnormal
bleeding
from vagina (between
menstrual
periods)
abnormal vaginal
discharge
(smells
foul
,
blood
)
lump
in vagina
changes in
bladder
and
bowel
habits
Diagnostic tests:
history
and
physical
:
pelvic exam
may do DRE and Pap test
colposcopy
biopsy
= gold standard for diagnosis
imaging
(may use endovaginal gel)
CT
MRI
Prognostic indicators:
most important:
stage
early
stage = more
favourable
SCC
- most
favourable
location of tumour
middle
and
lower 1
/
3 vagina
+
back wall
=
less favourable
prognosis
present with symptoms =
less favourable
younger
age = more
favourable
advantage with
earlier hysterectomy
Routes of spread:
local
bladder
cervix
rectum
paracolpial
tissues =
vascular
and
connective
tissues along vagina
lymphatics
hematogenous:
lung
,
liver
,
bone
after
lymph node
involvement - rare and late
Lymphatics:
upper 1 / 3
vagina →
para cervical
nodes →
internal iliac
→
common iliac
→
para
aortic
→
cisterna chyli
→
thoracic
duct
middle 1 / 3
vagina →
internal iliac
→
common iliac
→ para
aortic nodes
→
cisterna
chyli
→
thoracic
duct
lower 1 / 3
vagina →
superficial inguinal nodes
→
external iliac
→
common iliac
→
para aortic
→
cisterna chyli
→
thoracic
duct
Staging FIGO:
stage
0
:
carcinoma
in
situ
stage
1
: confined to
vagina
stage 2:
paravaginal
tissues,
no
extension
beyond
pelvic side
walls
stage 3: extension to
pelvic side walls
stage 4: spread beyond
true pelvis
4A
:
bladder
and
rectal
mucosa
, extension beyond true pelvis
4B
:
distant
mets
N stage:
N0(I+):
isolated cells
in
regional node
(<
0.2
mm)
N1:
pelvic
or
inguinal
lymph nodes mets
Management overview:
goals
: cure, vaginal preservation
chemo
: used as primary if unfavourable factors
cervix
is primary site
large
lesion
downstage
before radical surgery
Stage 1 and 2 management (early stage):
RT:
brachy
(small and superficial) -
interstitial
or
intracavitary
EBRT
(large) +
intracavitary brachy
surgery:
radical hysterectomy
+
lymphadenectomy
may preserve
ovarian
and
sexual
function
Stage 3 and 4 management (late stage):
definitive RT =
primary
treatment
Stage 3 and 4A:
unresectable:
interstitial
+
intracavitary brachy
+
EBRT
if resectable: primary
pelvic exenteration
+ pelvic
lymphadenectomy
or neoadjuvant
chemo RT
stage 4B:
palliative
EBRT
+
concurrent
chemo
Concurrent chemo RT:
chemo =
cisplatin
or
5 FU
overall survival benefit of chemo -
minimal
greatest in stage
2
-
4
Surgery:
early stage (limited to
vaginal mucosa
): definitive
surgery
preserve
ovarian
and
sexual
function
eliminate risk for
radiation induced
malignancy
if upper vagina:
if intact uterus:
radical hysterectomy
,
vaginectomy
+
1
cm margin,
pelvic lymphadenectomy
if lower vagina:
radical wide local excision
+
1
cm margin,
bilateral groin
node dissection
if stage 4 + vesical or rectal vaginal fistula:
bilateral inguinofemoral lymphadenectomy
if distal 1 / 3 vagina involved
relapse (central after RT):
salvage surgery
Radiation:
benefit: organ
preservation
volume: entire
vagina
,
paravaginal
area to
pelvic side
wall,
common iliac
,
internal iliac
,
external iliac
,
obturator
,
presacral
,
inguinal
(if distal 1 / 3 vagina)
dose:
45
-
50.4
Gy /
25
-
28
fr
primary tumour receives total:
70
-
80
Gy
if no brachy for boost, can use IMRT to boost
energy:
15
MV
fields:
4
field or
AP
/
PA
EBRT upper 1 / 3 vagina field borders:
AP / PA:
sup:
L5
/
S1
inf:
bottom
of
obturator foramen
lat:
1.5
cm lat of
pelvic brim
Lat:
ant:
mid pubic symphysis
post:
S2
/
S3
if lower 1 / 3 vagina:
length extended
inferiorly
to include
inguinal nodes
Brachy:
indicated:
primary
and
recurrent
vaginal cancer
HDR: Ir -
192
intracavitary:
60
-
65
Gy +
1
-
2
Gy boost
interstitial:
70
-
85
Gy total
side effect:
radiation vaginitis
Acute RT toxicity:
diarrhea
anal mucositis
vaginal mucositis
radiation vaginitis
Chronic RT toxicity:
rectovaginal
or
vesicovaginal
fistula
stricture
in
rectum
or
vagina
vaginal stenosis
and
shortening
cystitis
proctitis
Prognosis: average =
47
%
localized = 67%
regional = 52%
distant = 19%