Endometrial cancer Flashcards

1
Q

Stage I

A

Confined to the uterine corpus and ovary

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2
Q

IA

A

Disease limited to the endometrium OR non-aggressive histological type, i.e. low-grade endometroid, with invasion of less than half of myometrium with no or focal lymphovascular space involvement (LVSI) OR good prognosis disease

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3
Q

IA1

A

Non-aggressive histological type limited to an endometrial polyp OR confined to the endometrium

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4
Q

IA2

A

Non-aggressive histological types involving less than half of the myometrium with no or focal LVSI

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5
Q

IA3

A

Low-grade endometrioid carcinomas limited to the uterus and ovary

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6
Q

IB

A

Non-aggressive histological types with invasion of half or more of the myometrium, and with no or focal LVSI

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7
Q

IC

A

Aggressive histological typese limited to a polyp or confined to the endometrium

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8
Q

Stage II

A

Invasion of cervical stroma without extrauterine extension OR with substantial LVSI OR aggressive histological types with myometrial invasion

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9
Q

IIA

A

Invasion of the cervical stroma of non-aggressive histological types

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10
Q

IIB

A

Substantial LVSId of non-aggressive histological types

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11
Q

IIC

A

Aggressive histological typese with any myometrial involvement

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12
Q

Stage III

A

Local and/or regional spread of the tumor of any histological subtype

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13
Q

IIIA

A

Invasion of uterine serosa, adnexa, or both by direct extension or metastasis
IIIA1 Spread to ovary or fallopian tube (except when meeting stage IA3 criteria)c

IIIA2 Involvement of uterine subserosa or spread through the uterine serosa

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14
Q

IIIB

A

Metastasis or direct spread to the vagina and/or to the parametria or pelvic peritoneum
IIIB1 Metastasis or direct spread to the vagina and/or the parametria

IIIB2 Metastasis to the pelvic peritoneum

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15
Q

IIIC

A

Metastasis to the pelvic or para-aortic lymph nodes or bothf
IIIC1 Metastasis to the pelvic lymph nodes

IIIC1i Micrometastasis

IIIC1ii Macrometastasis

IIIC2 Metastasis to para-aortic lymph nodes up to the renal vessels, with or without metastasis to the pelvic lymph nodes

IIIC2i Micrometastasis

IIIC2ii Macrometastasis

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16
Q

Stage IV

A

Spread to the bladder mucosa and/or intestinal mucosa and/or distance metastasis

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17
Q

IVA

A

Invasion of the bladder mucosa and/or the intestinal/bowel mucosa

18
Q

IVB

A

Abdominal peritoneal metastasis beyond the pelvis

19
Q

IVC

A

Distant metastasis, including metastasis to any extra- or intra-abdominal lymph nodes above the renal vessels, lungs, liver, brain, or bone

20
Q

Treatment STAGE 1a GRADE-1

A

Lap TAH+BSO, no adjuvant RT

21
Q

VAGINAL BRACHYTHERAPY EBRT: for nodes positive with

A

For patients with high/intermediate risk factors (at least two of the factors:
a. age >60 years,
b. deep myometrial invasion,
c. grade 3,
d. serous or clear cell histology,
e. LVSI,

22
Q

STAGE 3 AND 4:

A

staging laparotomy and aim to debulk disease, with systemic lymphadenectomy.
* If both the para-aortic and pelvic nodes are negative use adjuvant vault radiotherapy + EBRT, which reduces
local recurrences
* Patients with clinical Stage III endometrial carcinoma in which surgical resection is not possible are treated
primarily by pelvic irradiation, with or without chemotherapy. Once therapy has been completed, exploratory
laparotomy should be considered for those patients whose disease now appears to be resectable

23
Q

STAGE 4

A

Treatment should be individualized to achieve local control. Pulmonary metastases are the most
common site of distant disease.
* A combination of surgery, radiotherapy for palliative local control, and chemotherapy for distant
control can be used.
* NCT :- poor candidates for surgery. Carboplatin+ paclitaxel
* Progestogens have been demonstrated to be useful for pulmonary metastases. (Response rates vary
from 0 to 53%).
* Pelvic radiotherapy in Stage IV disease is sometimes considered to provide local tumor control.
Similarly, it has also been suggested that patients with vaginal bleeding or pain from a local tumor
mass, or with leg edema due to lymph node involvement, should be treated with pelvic radiotherapy.
Palliation of brain or bone metastases can be effectively obtained with short courses (1–5fractions) of
radiotherapy

24
Q

RECURRENT DISEASE

A

7-18%

25
Q

Risk with obesity

A

3-10 fold

26
Q

diabetes risk

A

40-80%

27
Q

unapposed estrogen risk

A

6-8 fold risk

28
Q

tamoxifen risk

A

3-6 fold

29
Q

Continuous combined HRT effect

A

reduces risk by 76%

30
Q

Sequential HRT effect

A

70% increased risk

31
Q

estrogen-only HRT risk

A

50% increase PMB (risk of cancer is 10

32
Q

Endometrial sample(Pipelle)

A

False negative 10-15%

33
Q

Lynch type 2
syndrome with a wish for fertility preservation,

A

endometrial surveillance is performed by aspiration biopsy
and transvaginal ultrasonography starting from the age of 35 years (annually until hysterectomy).
Prophylactic surgery (hysterectomy and bilateral salpingo-oophorectomy), preferably using a
minimally invasive approach, should be discussed at the age of 40

34
Q

Risk of endometrial hyperplasia without atypia progressing to endometrial
cancer is

A

less than 5% over 20 years.

35
Q

Risk of progression to carcinoma-
* Hyperplasia without atypia

A

2%

36
Q

Risk of progression to carcinoma- Simple atypical hyperplasia

A

23%

37
Q

Risk of progression to carcinoma-Complex atypical hyperplasia

A

29%

38
Q

Adenocarcinoma co exists in what % atypical complex hyperplasia

A

25%

39
Q

Type 2 genetic factor

A

p53 mutation

40
Q

Type 1 genetic factor

A

PTEN , K-RAS