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(Gyne) Endometrial Cancer (Dr. Dueñas) 2022
(Gyne) Endometrial Cancer (Dr. Dueñas) 2022
Obesity (due to: increased conversion of estrogen to Diagnostics Used for Endometrial Malignancy (EMCA)
estrone(E1), decreased SHBG, insulin resistance) 2-5
Primarily for patients with a BMI of 30 (2-3 fold inc. risk) TRANSVAGINAL -Maybe used to triage patients for endometrial
ULTRASOUND sampling
Diabetes (especially the obese diabetic) 2-3 -Endometrial thickness of >4mm has a sensitivity of
(For symptomatic 95%-100% for endometrial cancer in women with
Nulliparity (3.5x more risk than fertile women) 2-3 postmenopausal postmenopausal bleeding
women; it cannot -International Endometrial Tumor Analysis (IETA)
Menstrual factors (Early menarche [12 years old], Late 1.5-3.0 be done if the px. maybe included in the evaluation of women with
menopause [>/= 52 years old]) If asymptomatic!) postmenopausal bleeding.
STRUCTURAL NON-STRUCTURAL
-Patients with LYNCH SYNDROME are at risk for several malignancies
either endometrial, colonic or breast cancer.
P POLYP C COAGULOPATHY
A ADENOMYOSIS O OVULATORY
DYSFUNCTION
Enumerated are the Protective Factors for Relative
Endometrial Hyperplasia Risk (RR)
L LEIOMYOMA I IATROGENIC
1/5 Sources: PPT 2021 + Compre Gyne 7th Ed. + Gyne Manual + Transes from Previous Batches
Best for focal lesion [direct visualization of the Tumor Grade G1 TO G2 (moderate) G3 (poor)
(For symptomatic lesion in the uterine cavity via the instrument used]
postmenopausal Myometrial SUPERFICIAL DEEP
women) SISH (Hydrosonography) can be used as the INITIAL Invasion
STEP of investigation to disclose the presence of a
focal lesion Stage I/II III/IV
Office endometrial biopsy using a PIPELLE device Receptor HIGH sensitivity LOW sensitivity
has a sensitivity of 99.6% in the detection of Positivity to progestins to progestins
endometrial cancer in PMW.
ENDOMETRIAL PTEN (m/c) Tp53 (m/c)
Using Pipelle POST-MW PRE-MW
SAMPLING ARID1A (regular chromatin) Aneuploidy( common
Mutated PIK3CA also)
Sn (EMCA) 99.6% (Higher) 91%
(For symptomatic KRAS mutation PIK3CA
genes/Genetic
postmenopasual FGF2(growth factor) FBXW7 (regulator of myc,
Sn (Atypical 81% (Same) abnormalities
MSI cyclin E)
women) Hyperplasia) CTNNB1 (Wnt signaling) CHD4 (regulator of
[An OPD p53 chromatin)
procedure] Endometrial biopsy and D&C have a comparable
PPP2R1A (PP2A)
accuracy in diagnosing EMCA, the latter more
accurately reflecting FINAL TUMOR GRADE.
INDOLENT AGGRESSIVE
Behaviour Spread via the Spread via the
Additional Notes:
LYMPHATICS ONLY LYMPHATICS and
● For patients who have undergone D&C: they are admitted and
INTRAPERITONEALLY
anesthesia is applied. But looking at the comparison to
Endometrial biopsy, they have COMPARABLE ACCURACY Additional Notes:
● The advantage of D&C is on the GRADING of the tumor sample. ● As you can see in the HER-2-NEU amplification seen in the uterine
● Sampling can be done either at the OPD (via Pipelle) or serous carcinoma → associated with advanced stage and poor
Admitting the patient (via D&C) prognosis
● Remember you have to get in the way in the so-called
Diagnostics: PRE-OPERATIVE ENDOMETRIAL CANCER
“FRACTIONAL D&C” so it is no longer necessary for getting the
sample from the endocervix just to diagnose EMCA. So ang
sample lang na manggagaling ay sa loob lang ng matres / Imaging Parameter Sensitivity (%) Specificity(%)
bahay-bata (uterus) at hindi na kailangan ng sample galing sa Modality Measured
cervix. Enough na yung sa endometrial sampling.
Deep myometrial 83 72
invasion
ULTRASOUND
(UTZ) Cervical involvement 49 72
(m/c
available) LN Involvement 33 100
Deep myometrial 83 42
● These are the instruments used for endometrial sampling: invasion
CT SCAN
(Left) Pipelle cannula which is flexible (Middle) Randall
curette (Right) Novak curette [more serrated than the Randall] Cervical involvement 25 70
● MVA -> Manual Vacuum Aspirator ; can also be used in
endometrial sampling which is an OPD procedure. LN Involvement 45 88
Must know!!!
Deep myometrial 92 90
Histogenic Types of Endometrial Cancer invasion
MRI
TYPE I TYPE II Cervical involvement 86 97
LN Involvement 72 97
Age Pre and post MW Post MW
2/5 Sources: PPT 2021 + Compre Gyne 7th Ed. + Gyne Manual + Transes from Previous
Batches
tailor the management. But remember these are not used for
○ It is an Integral part of comprehensive staging
pre-operative staging.
procedure and allow tailoring of adjuvant
● Deep myometrial Invasion: the highest SN is requesting an MRI
treatment
and SP also
○ LN palpation is NOT ACCEPTABLE
● Cervical Involvement: MRI (both Sn and Sp)
○ The decision to omit LN Dissection must be made
● Lymph Node metastasis: UTZ (highest Sn) and PET/CT(highest
with a Gynecologic oncologist
also Sn)
○ LAN does not improve survival nor decrease
○ But comparing the availability and affordability of the
disease recurrence in women with early stage, low
two: Ultrasound is the best choice
grade EMCA
○ Not all institutions have a PET-CT scan
● But comparing the specificity for LN involvement: the highest will INDICATIONS FOR AORTIC NODE SAMPLING (Must Know!)
still be the MRI
○ It depends on the availability and affordability. ★ Suspicious ★ GROSSLY POSITIVE
● If you are entertaining a possible Distant metastasis (an extension para-aortic or ADNEXA
of the malignancy in other parts of the body eg. pelvis): the common iliac node ★ High grade tumors
PET-CT scan is the modality of choice (high Sn and Sp) ★ Grossly positive pelvic (G3)
Preoperative Work Up in Endometrial Cancer LN ★ Lymphovascular
★ Clear cell or Papillary space invasion (LVSI)
serous or ★ Lower Uterine
Complete Blood Count, Renal Routinely tested in corpus uteri
Carcinosarcoma segment Involvement
and Liver function test
★ Cervical Involvement
More than or equal to
Chest X-ray Universally available, low cost,
50% of myometrial
rarely positive in early disease
invasion
Cystoscopy and/or Proctoscopy Maybe helpful if direct extension to Conservative management must be done by Multidisciplinary team
the bladder or rectum is suspected
● Pretreatment ★ Endometrioid
Evaluation Adenocarcinoma
Definitive Management of Endometrial Cancer ● Patient ★ Confined to the UTERUS!
understands and ○ No myometrial
Extrafascial Hysterectomy Type 1 extended hysterectomy accepts that this is Invasion
(remove the uterus) not the standard ○ No adnexal
of care involvement
Bilateral Salpingo-oophorectomy Take out the FT and Ovaries ● Reasonable ○ No extrauterine
chance of fertility spread
Peritoneal Fluid Cytology (PFC) During surgery, you also collect (dapat may ○ No cervical
peritoneal fluid for analysis in the partner) involvement
laboratory. ● No medical ○ No LVSI
contraindication ○ No vaginal
Pelvic LN Dissection (PLND) Assess/ Evaluate the Lymph nodes to progesterone Involvement
involved
Para-aortic LN Sampling (PALS) To check for all the parameters mentioned, you have to utilize MRI! :D
Additional Notes: Exceptions to Initial Surgery (There are certain patient who cannot
● Ovarian Preservation in EMCA receive the standard treatment which is surgery
○ Feasible in young women with EMCA but it is
INDIVIDUALIZED
○ However, this is still controversial*
Option 1: Primary RT Option 2: High dose Progestin
○ This is not recommended in: (Remember!)
with/without Chemo followed by
■ Non-endometrioid Histology
appropriate surgery
■ Deep Myometrial Invasion
■ Cervical Stromal Invasion
-Poor surgical risk patients -Grade 1 Lesion (applied to well
■ Family Hx of HNPCC or Genetic Cancer
-Non-resectable disease (IE differentiated tumors)
● Lymphadenectomy (LAN) in EMCA
3/5 Sources: PPT 2021 + Compre Gyne 7th Ed. + Gyne Manual + Transes from Previous
Batches
mucosa
revealed parametria is nodular -For patients who are
and the fixed to the pelvic contraindicated for Anesthesia
IVB Distant metastasis, including intra-abdominal
sidewalls) -For patients who are unsuited
metastases, and/or inguinal Lymph Nodes
for Radiotherapy (RT)
Memorize!
Note: If these cases might happen (those who are exempted to undergo surgery) ,
you cannot apply the 2009 FIGO staging for Endometrial Cancer [since it was
mentioned that the lesions are surgico-pathologically staged
Instead, what you will use is the staging presented below for patients who
cannot undergo surgery! Stratification and Management (or Adjuvant TX.) of EMCA
1988 CLINICAL STAGING FOR ENDOMETRIAL CANCER Stage 1A G1 G2 no LVSI [very early stage]
(Surgico-pathologically staged) -Myometrial invasion of less than 50%; the
grading is well-moderately differentiated.
Stage I Confined to the corpus LOW RISK -The size is < 2cm; <60 years old.
-No LVSI
Stage II With cervical extension -Not need any form of adjuvant tx, but
surveillance after administration of
Stage III With extrauterine spread surgery.
STAGE II Stage 1B G3
HIGH RISK
Tumor invades the cervical STROMA, but does not extend beyond the Stage 2 G3
uterus
Note: The glandular involvement as what was the staging before is no longer a Stage 2 Any grade (+)LVSI
Stage 2 disease but rather a Stage 1!
IIIA Tumor invades serosa and/or adnexa Stage III and Stage IV Combination of RT and Chemotherapy
4/5 Sources: PPT 2021 + Compre Gyne 7th Ed. + Gyne Manual + Transes from Previous
Batches
with the Endometrial Hyperplasia
Updates!]
Must Know!
IA 90.9%
IB 88.2%
IC 81.0%
II 71.6%
III 51.4%
IV 8.9%
5/5 Sources: PPT 2021 + Compre Gyne 7th Ed. + Gyne Manual + Transes from Previous
Batches