Transcript HPV
Cervical Cancer
Xin LU
OB/GYN Hospital
Fudan University
Contents
General information
CINs
Spread pattern
FIGO staging
Clinical signs
Diagnosis and differential diagnosis
Principle for treatment
Prevention
Surveillance
Key words
Cervical cancer (Cxca)
Human Papillomavirus (HPV)
Radical Hysterectomy (RH)
Radiotherapy (RT)
Chemotherapy (CT)
Neoadjuvant chemotherapy (NACT)
Concurrent chemo-radiotherapy (CCCR)
Radical Trachelectomy
Female Reproductive Anatomy
Cervical Cancer
子宫颈癌
World report:
Account for 1/3 female malignancies
New cases: 529 800
Death: 275 100
85% developing country
The 4th most common cause of death
from malignancy in women.
Cxca Progression
HPV infection
CINs
Carcinoma in situ
≈10-15yr
Cervical cancer
Etiology
High-risk factors
HR-HPV
Use of oral contraceptives
Smoking
Multiple sexual partners
History of herpes infection
History of STD
Human Papillomavirus , HPV
人乳头瘤状病毒
1972:Harald zur Hausen Zur
Hausen
1995:High-risk HPV by
International Agency for
Research on Cancer,IARC
90% cervical cancer with HPV
infection
HPV
High risk HPV(HR-HPV)
oncogenic HPV
HPV 16,18,31,33,35,39,45, 51,52,56,58,59,68,73,82
HSIL, Cxca
Low risk HPV(LR-HPV)
non-carcinogenic HPV
HPV 6,11,42,43,44,54,61,70,72,81
LSIL
Precursors
CIN: Cervical Intraepithielial Neoplasm
CIN I:mild dysplasia,1/3
CIN II:moderate dysplasia,1/3-2/3
CIN III:severe dysplasia , 3/3
CIS : carcinoma in situ
Precursors ---CINs
Cervical cancer
Histological Types
Squamous carcinoma 80-85%
Adenocaricinoma 15-20%
Endometrial carcinoma
Clear cell carcinoma
Adenosquamous 3-5%
Undifferentiated carcinoma
Minimal deviation adenocarcinoma (MDA)
Neuroendocrine tumor (small cell) <5%
Spread pattern
Transcelomic
most common
Lymphatic
retroperitoneal ( pelvic and paraaortic ) LN
spreading is common in advanced- stage
Hematogenous
uncommon
FIGO
stage
FIGO Staging
I The carcinoma is strictly confined to the cervix (extension to the uterine corpus should be disregarded).
IA Invasive cancer identified only microscopically. Invasion is limited to measured stromal invasion with a
maximum depth of 5mmb and no wider than 7mm. (All gross lesions even with superficial invasion are
Stage IB cancers.)
IA1: Measured invasion of stroma ≤3mm in depth and ≤7mm width.
IA2 : Measured invasion of stroma >3mm and <5mm in depth and ≤7mm width.
IB Clinical lesions confined to the cervix, or preclinical lesions greater than stage IA.
IB1: Clinical lesions no greater than 4cm in size.
IB2: Clinical lesions >4cm in size.
II The carcinoma extends beyond the uterus, but has not extended onto the pelvic wall or to the lower third of
vagina.
IIA Involvement of up to the upper 2/3 of the vagina. No obvious parametrial involvement.
IIA1: Clinically visible lesion ≤4cm
IIA2: Clinically visible lesion >4cm
IIB Obvious parametrial involvement but not onto the pelvic sidewall.
III The carcinoma has extended onto the pelvic sidewall. On rectal examination, there is no cancer-free space
between the tumor and pelvic sidewall. The tumor involves the lower third of the vagina. All cases of
hydronephrosis or non-functioning kidney should be included unless they are known to be due to other
causes.
IIIA Involvement of the lower vagina but no extension onto pelvic sidewall.
IIIB Extension onto the pelvic sidewall, or hydronephrosis/non-functioning kidney.
IV The carcinoma has extended beyond the true pelvis or has clinically involved the mucosa of the bladder
and/or rectum.
IVA Spread to adjacent pelvic organs.
IVB Spread to distant organs.
Platform of diagnosis for
cervical diseases
Pap
smear
TBS classification
TCT
HPV
Colposcopy--biopsy
LEEP
Cervical cancer
Symptoms
No symptoms
Abnormal pap smear
Leukorrhea
Postcoital bleeding
Pelvic pain
Cervical cancer
Diagnosis
History
Physical examination
Cytology (pap smear, TCT)
Biopsy (colposcopy)
Conization
Imaging
Principle for treat
cervical cancer
Evidence based medicine
FIGO ( International Federation of Gynecology and Obstetrics)
NCCN (National Comprehensive Cancer Network)
Individualized therapy;
Cervical Cancer Treatment
Precursor- CINs
Micro-invasive cancer
Invasive cancer
Treatment for CINs
CIN I: follow up 3—6months
CIN II:
local therapy
conization
CIN III:
conization
hysterectomy
Treatment for micro-invasive
cervical cancer
Ia1: hysterectomy
Ia2: modified hysterectomy
Ia with positive margin (Ia or CIS):
radical hysterectomy
Treatment for invasive
cervical cancer
Surgical threatment Ib-IIa
Radiotherapy
Chemotherapy
Combined therapy
Cervical cancer(Ⅰb1/Ⅱa1)
1. RH+PLND+/- PALND
Radical hysterectomy+ pelvic lymph
node dissection ±para-aortic lymph
node dissection;
2. RT
Pelvic RT+ Brachytherapy
±concurrent cisplatin-containing
chemotherapy
Cervical cancer(Ⅰb2/Ⅱa2)
1. RT
Pelvic RT+concurrent cisplatin-containing chemotherapy +
Brachytherapy
2. RH+PLND+/- PALND
Radical hysterectomy+ pelvic lymph node dissection ±paraaortic lymph node dissection;
3. RT+ Hysterectomy
Pelvic RT+concurrent cisplatin-containing chemotherapy +
Brachytherapy +adjuvant hysterectomy
Flow-chat for management
( IB, IIA cervical cancer)
IB2, IIA2
>4cm
IB1, IIA1
<4cm
CCRT
RH+PLND+PALND
NACT+RH+PLND +PALND
RH+PLND+/-PALND
RT
Adjuvant Therapy
(according to high-risk factors)
RT+CT
LN positive
positive margin
RT+/- CT
poor differentiated
deep myometrial invasion
LVSI
Complications of RH
Vesicovaginal fistula
Ureterovaginal fistula
Severe bladder atomy
Bowel obstruction
Lymphocyst
Thrombophlebtis
Pulmonary embolus
Post-surgical treatment
(high risk factors)
poor differentiated
deep myometrial invasion
LVSI
LN positive
positive margin (Vaginal, parametrium)
Advanced stage(Ⅱb,Ⅲ,Ⅳ)
Radiotherapy (RT)
NACT + Radiotherapy
Concurrent chemo-radiotherapy;
Combined RT and CT
Radical Trachelectomy
Fertility sparing
Ib <4cm
Evaluation of infertility factor
Procedure of trachelectomy
Vaginal
Laparoscopic
Abdominal
Complications
Outcome
Prognosis
5yr survival rate
patients with RT (RH)
Stage I: 91.5% (86.3%)
Stage IIa: 83.5% (75%)
Stage IIb: 66.5% (58.9%)
Stage IIIa: 45% (43%)
Stage IIIb: 36%
Stage IV: 14%
recurrent rate
Data from MD Anderson Hospital
1.5%
5%
7.5%
17%
Pregnant with cervical cancer
<20w, operation;
>20w, evaluation, Ia-Ib1 observation;
>24w, 32-34w CS+RH;
Prevention
Primary prevention
1. Health care
2. Sexual behavior
3. Dual protection
4. HPV vaccines
4. Cancer screening
5. Treat precursors
Secondary prevention
1.Early screening
2. Early treatment
Surveillance
Interval H & P
Every 3-6months for 2yr;
Every 6-12months fro 3-5yr
Cytology/yr
Imaging : PET, PET-CT, MRI, CT
Lab oratory assessment
Patient education
Take home message
HPV (HR)
CINs
FIGO stage
Surgery: Radical hysterectomy and PLND
Post-operation treatment: high risk factors
RT and CT
Fertility sparing trachelectomy
HPV Vaccine
THANKS
OB/GYN Hospital of Fudan University