Current revision |
Your text |
Line 10: |
Line 10: |
| **vagina | | **vagina |
| **trophoblastic | | **trophoblastic |
- |
| |
- |
| |
- | {|border=1
| |
- | !Cancer
| |
- | !Incidence
| |
- | !Kills (Rank)
| |
- | !Lifetime Risk
| |
- | !Risk Factors
| |
- | |-
| |
- | !Cervical
| |
- | |12.2k / year (#3)
| |
- | |'''#3 (#1 worldwide'''; 4.2k / year)
| |
- | |1/135
| |
- | |High Grade Dysplasia, smoking, a lifestyle cancer (early parity, early coitus, multiple partners)
| |
- | |-
| |
- | !Endometrial (Uterine)
| |
- | |'''41k / year (#1)'''
| |
- | |#2 (7.1k / year)
| |
- | |'''1/38'''
| |
- | |Obesity, HTN, Diabetes, Atypical Hyperplasia
| |
- | |-
| |
- | !Ovarian
| |
- | |23k / year (#2 at 23% of gyn ca)
| |
- | |'''#1''' (47% of gyn ca)
| |
- | |~1/70
| |
- | |BRCA1, BRCA2, HNPCC, (not smoking)
| |
- | |}
| |
| | | |
| ==Epidemiology== | | ==Epidemiology== |
- | *Who gets it and how many?
| |
- |
| |
- | ==Presentation - Differential Dx==
| |
- | *Common presentations of gyn cancers include:
| |
- | **Adnexal Mass
| |
- | **Abnormal Pap
| |
- | **Post Menopausal Bleeding
| |
- |
| |
- | ==Prevention==
| |
- | *Prevention
| |
- | **Screening: BRCA
| |
- | **Vaccines
| |
- | **Role of HRT
| |
- |
| |
- | ==Detection / Diagnosis==
| |
- | *Pathology
| |
- | *Staging
| |
- | *(Treatment)
| |
| | | |
| ==Adnexal mass and ovarian cancer== | | ==Adnexal mass and ovarian cancer== |
Line 65: |
Line 20: |
| *23% of gyn cancers are ovarian. | | *23% of gyn cancers are ovarian. |
| *47% of deaths are caused by ovarian | | *47% of deaths are caused by ovarian |
- | *1 / 70 lifetime risk in US
| |
| | | |
| ===Embryology / Oncology=== | | ===Embryology / Oncology=== |
- | *Epithelial adenocarcinoma: | + | *Gi-> ovary is a krukenburg |
- | **originate from the peritoneal mesothelium
| + | |
- | **make up 65% of Ovarian cancers
| + | |
- | *Germ Cell:
| + | |
- | **originiate from the yolk sac (dysgerminoma, teratoma)
| + | |
- | **make up 25% of ovarian cancers
| + | |
- | *Stromal:
| + | |
- | **Originate from the gonadal ridge –mesenchyme near protonephros (granulosa and theca cells)
| + | |
- | **Make up 8% of ovarian cancers
| + | |
- | *Metastatic:
| + | |
- | **Make up only 2% of ovarian cancers
| + | |
- | **Called Krukenburg tumors
| + | |
- | | + | |
- | ===Epithelial Ovarian Cancer: Histologic Types===
| + | |
- | *Histology (and the structure it recapitulates)
| + | |
- | **Serous (Tube)
| + | |
- | **Endometrioid (Endometrium)
| + | |
- | **Mucinous (Cervix)
| + | |
- | **Clear cell (Kidney)
| + | |
- | **'''Brenner (Transitional)'''
| + | |
- | | + | |
- | ===Ovarian Cancer: Pt History===
| + | |
- | *Epidemiology - Clinical
| + | |
- | *'''History: there is NO classic profile''':
| + | |
- | **Age / Parity
| + | |
- | **Menstrual history
| + | |
- | **Surgical Hx: hysterectomy or BTL
| + | |
- | **BCP / hormonal therapy history
| + | |
- | **Personal and family cancer history
| + | |
- | **Ethnicity
| + | |
- | | + | |
- | ===Ovarian Cancer: Risk Factors===
| + | |
- | | + | |
- | ====Factors that Decrease Risk====
| + | |
- | *Factor: Relative Risk
| + | |
- | *Nulliparous: 1.0
| + | |
- | *1 Full term pregnancy: 0.6
| + | |
- | *> 5 Full term pregnancies: 0.29
| + | |
- | *Use of Oral Contraceptions:
| + | |
- | **Never: 1.0
| + | |
- | **Ever 0.75
| + | |
- | **3 mo - 4 yrs: 0.6-0.7
| + | |
- | **> 10 years: 0.2
| + | |
- | *Bilateral Tubal Ligation: 0.5
| + | |
- | *Hysterectomy: 0.5
| + | |
- | *Breast feeding (linear with duration): 0.7
| + | |
| | | |
| + | ===EOC=== |
| + | *Brenner is transitional |
| | | |
| + | ===Decreased Risk=== |
| *Tying the tubes decreases one's risk, probably because there is decreased environmental exposure. | | *Tying the tubes decreases one's risk, probably because there is decreased environmental exposure. |
| *Anything that makes the ovary quiescent will decrease the risk of ovarian cancer. | | *Anything that makes the ovary quiescent will decrease the risk of ovarian cancer. |
| | | |
- | ====Factors that Increase Risk==== | + | ===Increased Risk=== |
- | *Factor: Relative Risk
| + | |
- | *Hx of Breast Cancer:
| + | |
- | **None: 1.0
| + | |
- | **1st Degree Relative: 2.1
| + | |
- | **Personal History: 10
| + | |
- | *Hx of Ovarian Cancer:
| + | |
- | **None: 1.0
| + | |
- | **One 1st Degree Relative: 3.1
| + | |
- | **>2 1st Degree Relatives: 4-15
| + | |
- | **Hereditary Cancer Syndrome: 12-30
| + | |
- | *Saturated Fat Diet: ?
| + | |
- | | + | |
- | | + | |
| *Family history of breast cancer increases the risk for ovarian cancer by 2 fold. | | *Family history of breast cancer increases the risk for ovarian cancer by 2 fold. |
| **A personal history makes the risk 10 fold higher! | | **A personal history makes the risk 10 fold higher! |
Line 138: |
Line 37: |
| | | |
| ===Adnexal Mass Ddx=== | | ===Adnexal Mass Ddx=== |
- | *The differential diagnosis for an adnexal mass should include all of the following:
| + | *PID can form a pretty big, complex mass on the ovary with fallopian tube involvement. |
- | **Physiologic
| + | *How do we tell between good and bad? |
- | **Gestational
| + | |
- | **Inflammatory
| + | |
- | ***PID can form a pretty big, complex mass on the ovary with fallopian tube involvement.
| + | |
- | **Congenital | + | |
- | **Traumatic
| + | |
- | **Neoplastic
| + | |
| | | |
| | | |
- | *How do we tell between good and bad?
| + | *Good: |
- | *Good indicators: | + | **fluid filled (not solid) |
- | **Asymptomatic
| + | **usually younger |
- | **Cystic
| + | **asymptomatic |
- | ***fluid filled (not solid)
| + | |
- | **Age between 15 and 45 | + | |
- | **Resolves | + | |
- | *Bad indicators:
| + | |
- | **Pain or other vague symptoms
| + | |
- | **Symptomatic: Ascites
| + | |
- | **Complex, Solid: Omental cake
| + | |
- | **Persists: Adenopathy
| + | |
| | | |
- | ===Detective work: Diagnosis===
| |
- | *ROS:
| |
- | **'''65% of ovarian cancer patients DO have sypmtoms; often vague and non-gynecologic'''
| |
- | ***Not really the ''"silent killer"''
| |
- | **Pain, GI symptoms, Fatigue, Weight change
| |
| | | |
| + | *Bad: |
| + | **pain or other vague symptoms |
| + | **ascites |
| + | **complex, solid |
| + | **omental cake |
| + | **adenopathy. |
| | | |
- | *Physical Exam: | + | ===Evaluate the pt=== |
- | **Lungs: dullness (Pleural effusion), ronchi, or wheezes? | + | *ROS: |
- | **Abdomen-mass or fluid wave? | + | **65% of ovarian pts do have sympstoms but often vague |
| + | **Pin, GI symptoms, fatigue, weight change |
| + | *PE: |
| + | **Pleural effusion is frequent, ronchi, wheezes |
| + | **abdominal mass or fluid wave |
| **Rectovaginal exam; mass, nodularity | | **Rectovaginal exam; mass, nodularity |
- | **General appearance
| |
| | | |
| + | ===Adnexal mass ddx=== |
| + | *Pelvic exam |
| + | *US > CT |
| | | |
- | *Pelvic Exam
| + | ===FIGO Staging=== |
- | *Labs | + | *Ovarian often goes to the lung. |
- | *Imaging | + | *Surface of the liver is stage 3 but parenchymal liver mets is stage 4. |
- | **Ultrasound
| + | |
- | **CT Scan
| + | |
- | **U/S > CT
| + | |
| | | |
- | | + | ===Survival=== |
- | *Operation
| + | *down |
- | | + | |
- | ===Surgical: FIGO Staging=== | + | |
- | *I = Limited to ovary (ies) | + | |
- | *II = Extension to uterus, tubes, other pelvic tissues
| + | |
- | *III = Peritoneal surface implants, nodes
| + | |
- | **Surface of the liver is stage 3 but parenchymal liver mets is stage 4.
| + | |
- | *IV = Distant metastasis
| + | |
- | **Ovarian often goes to the lung.
| + | |
- | | + | |
- | ===Ovarian Cancer: Outcomes===
| + | |
- | *5 year survival:
| + | |
- | **Stage I: 75%
| + | |
- | **Stage II: 60%
| + | |
- | **Stage III: 30%
| + | |
- | **Stage IV: 15%
| + | |
| | | |
| ===Ovarianc cancer=== | | ===Ovarianc cancer=== |
| *usually requires histology to know it is cancer. | | *usually requires histology to know it is cancer. |
| | | |
- | ===Ovarian Cancer: Treatment=== | + | ===Ovarian cancer treatment=== |
- | *Goals of Operation:
| + | |
- | **Is this cancer?
| + | |
- | **Is this ovarian cancer?
| + | |
- | **What stage?
| + | |
- | *If apparently confined to ovary, do a “staging” operation.
| + | |
- | *If bulky disease, do a “debulking” operation
| + | |
- | | + | |
- | | + | |
- | *Operation
| + | |
- | **USO / BSO
| + | |
- | **Omentectomy
| + | |
- | **Lymphadenectomy
| + | |
- | **Peritoneal biopsies
| + | |
- | **Hysterectomy
| + | |
- | | + | |
- | | + | |
- | *Young patients, early stage: possibility of fertility-sparing surgery
| + | |
- | | + | |
- | ====Epithelial Cancers: Treatment====
| + | |
- | *Recall that epithelial is one origin of ovarian cancer.
| + | |
- | *Epitheilal ovarian cancer treatment is specifically treated with chemotherapy.
| + | |
- | *Platinum and taxane-based combination chemotherapy
| + | |
- | **Platinum: Cisplatin, carboplatin
| + | |
- | **Taxane: Paclitaxel, docetaxel
| + | |
- | | + | |
- | ===Ovarian Cancer: Familial Inheritance=== | + | |
- | *Ovarian Cancer Inheritance risks:
| + | |
- | **Lifetime risk in U.S.: 1.4%
| + | |
- | **One 1st-degree relative: 5%
| + | |
- | **> two 1st-degree relatives: 7%
| + | |
- | **HBOC: 6-50%
| + | |
- | *'''OF THESE, 3% WILL HAVE A HEREDITARY CANCER SYNDROME'''
| + | |
- | | + | |
- | | + | |
- | *Hereditary cancer syndromes are characterized by:
| + | |
- | **1/800 US BRCA and 1/600 HNPCC
| + | |
- | **Autosomal dominant inheritance
| + | |
- | **Early age of onset
| + | |
- | **Younger affected members in subsequent generations
| + | |
- | **Multiple cancers in individuals
| + | |
- | **Bilaterality of certain cancers
| + | |
- | **Male breast cancer (BRCA 2)
| + | |
| | | |
- | ===Cancer: Family History===
| |
- | *Obtaining a Family History of Cancer
| |
- | *3 + generation family history.
| |
- | *Update regularly
| |
- | *Maternal and paternal data
| |
- | *Race, ethnic background, all cancers, current age, age at diagnosis, age at death
| |
- | *Medical records review
| |
- | *Genetic counseling BEFORE TESTING!
| |
| | | |
| ===Familial Ovarian cancer=== | | ===Familial Ovarian cancer=== |
Line 262: |
Line 86: |
| *Male breast cancer is so rare that if seen, suspect brca(2) mutation. | | *Male breast cancer is so rare that if seen, suspect brca(2) mutation. |
| | | |
- | ===Clinical Use of Serum CA 125=== | + | ===CA125 Serum Testing=== |
- | *CA 125 can be used to '''following response to chemotherapy''' | + | *CA 125 does not detect ovarian cancer at an earlier stage. |
- | *CA 125 can be used for '''surveillance for patients with known genetic mutation or strong family history''' indicative of a hereditary inheritance pattern
| + | |
- | **+ rectovaginal exam, +/- transvaginal pelvic ultrasound
| + | |
| | | |
- | | + | ===Triage=== |
- | *'''CA 125 does not detect ovarian cancer at an earlier stage.'''
| + | |
- | | + | |
- | | + | |
- | *When NOT to Obtain a Serum CA 125 Level:
| + | |
- | **When a low-risk patient asks you for it!
| + | |
- | ***Requires extensive counseling
| + | |
- | ***Poor sensitivity and specificity
| + | |
- | *When operation is already indicated
| + | |
- | | + | |
- | | + | |
- | *Non-malignant conditions that may elevate the CA 125:
| + | |
- | **PID
| + | |
- | **Adenomyosis
| + | |
- | **Benign neoplasm
| + | |
- | **Endometriosis
| + | |
- | **Functional cyst
| + | |
- | **Menstruation
| + | |
- | **Infertility
| + | |
- | **Leiomyomata
| + | |
- | **Hepatitis
| + | |
- | **Pancreatitis
| + | |
- | **Cirrhosis
| + | |
- | **Colitis
| + | |
- | **CHF
| + | |
- | **Diverticulitis
| + | |
- | **Postoperative period
| + | |
- | **Renal disease
| + | |
- | **SLE
| + | |
- | **Pneumonia
| + | |
- | **Diabetes
| + | |
- | | + | |
- | ===Chemoprevention with Oral Contraceptives=== | + | |
- | *OC use for > 5 years reduces risk of ovarian cancer by 60% in the general population
| + | |
- | *Protective effect increases with increasing duration of use
| + | |
- | *Protection continues for 10 years following discontinuation
| + | |
| | | |
| ===Prophylactic Surgery=== | | ===Prophylactic Surgery=== |
- | *Oophorectomy: | + | *These prophylactic surgeries (breast and ovary) are not completely protective because we just can't find every cell. |
- | **Reduced ovarian cancer risk by 95-100%
| + | *After prophy, a 5% risk over 20 years for developing cancer (as a brca pt). |
- | **Reduced breast cancer risk by 53-68%
| + | |
- | **Reduced risk of fallopian tube cancer and primary peritoneal cancer
| + | |
- | **Evidence suggests that many BRCA-related ovarian cancers are actually fallopian tube primaries
| + | |
- | | + | |
- | | + | |
- | *Bilateral Mastectomy:
| + | |
- | **BRCA patients ~ 85-100% reduction in risk for breast cancer
| + | |
- | | + | |
- | | + | |
- | *'''These prophylactic surgeries (breast and ovary) are not completely protective because we just can't find every cell.'''
| + | |
- | *'''After prophy, a 5% risk over 20 years for developing cancer (as a brca pt).''' | + | |
| **But that's much better. | | **But that's much better. |
| | | |
| ==Abnormal Pap Smear and Cervical Cancer== | | ==Abnormal Pap Smear and Cervical Cancer== |
| + | * |
| | | |
- | ===Cervical Cancer Epidemiology=== | + | ===Cervical Cancer screening=== |
- | *12,200 new cases in the US per year | + | *Moved up to 21 b/c we were over treating. |
- | *4,210 deaths in the US per year
| + | *Coposcopy is magnifying the cervix to identify early microscopic changes. |
- | *180 new cases in Indiana
| + | |
- | *< 100 deaths in Indiana
| + | |
- | *Life time risk 1 / 135
| + | |
- | *2nd to breast cancer for cancer death in women ages 20-39
| + | |
- | *500,000 women die each year world wide
| + | |
- | *'''Number one cancer killer of women worldwide'''
| + | |
- | | + | |
- | | + | |
- | *In the US 60% are Stage I at diagnosis
| + | |
- | *More common in minorities, disadvantaged
| + | |
- | *Early coitus, early parity, multiple partners
| + | |
- | *Associated with / caused by HPV 16,18,31,33
| + | |
- | *Not all infected patients develop cancer
| + | |
- | *Smoking increases risk
| + | |
- | | + | |
- | ===Cervical Cancer: Prevention===
| + | |
- | *Randomized Double-Blind Clinical Trial:
| + | |
- | **2392 Young women vaccinated with 3 doses of placebo or HPV-16 virus-like particle vaccine
| + | |
- | **At a median of 17.4 months, 3.8 / 100 women of the placebo women and 0 / 100 of the treated women had persistent HPV infection
| + | |
- | *Nine CIN events were all the placebo group
| + | |
- | | + | |
- | ===Cervical Cancer: Screening===
| + | |
- | *Begin screening at age 21 regardless of age of onset of sexual intercourse
| + | |
- | **'''Moved up to 21 b/c we were over treating.'''
| + | |
- | *Repeat every 2 years if normal and lowrisk from age 21-29 | + | |
- | *After age 30, and 3 consecutive negatives, and low-risk, screen every 3 years
| + | |
- | *May stop after age 70
| + | |
- | *No need for Pap after total hysterectomy
| + | |
- | | + | |
- | | + | |
- | *Low risk: No history of high grade dysplasia, HIV, or other immunosuppression
| + | |
- | *Remember the pap is a screening test
| + | |
- | **If abnormal, or if the cervix appears or feels abnormal, proceed with diagnostic test
| + | |
- | *Colposcopy
| + | |
- | *Directed Biopsy
| + | |
- | | + | |
- | | + | |
| *ASCUS = atypica squamous cells of undetermined significance | | *ASCUS = atypica squamous cells of undetermined significance |
| + | *AGUS = atypical ? |
| | | |
- | ====Interpreting Results==== | + | ===Colposcopy=== |
- | *The Bethesda system: | + | *Use acetic acid to highlight abnormal spots; biopsy them. |
- | **LGSIL
| + | *Must do a cone biopsy if you have an inadequate simple (cervical) biopsy. |
- | **HGSIL
| + | |
- | **AGUS/ASCUS
| + | |
| | | |
| + | ===Pyramid=== |
| + | *Treat red and yellow, wait on blue and green. |
| | | |
- | *Histologic diagnoses:
| + | ===Cervical Cancer Staging=== |
- | **CIN 1
| + | |
- | **CIN 2
| + | |
- | **CIN 3/CIS
| + | |
- | **Invasive cancer
| + | |
- | | + | |
- | ====Classification Terminology for Cervical Cytology====
| + | |
- | *The 2001 Bethesda System
| + | |
- | | + | |
- | | + | |
- | *Two types of atypical squamous cells (ASC)
| + | |
- | **'''Atypical squamous cells of undetermined significance (ASCUS)'''
| + | |
- | **'''Atypical squamous cells, cannot exclude high-grade squamous intraepithelial lesions (ASC-H)'''
| + | |
- | | + | |
- | | + | |
- | *Squamous intraepithelial lesions (SIL)
| + | |
- | **'''Low-grade SIL (LSIL)''': Mild dysplasia, cervical intraepithelial neoplasia 1 (CIN 1)
| + | |
- | **'''High-grade SIL (HSIL)''': Moderate and severe dysplasia, CIN 2/3, carcinoma in situ (CIS)
| + | |
- | | + | |
- | | + | |
- | *Cervical intraepithelial neoplasia (CIN)
| + | |
- | **'''CIN 1''': Mild dysplasia; includes condyloma (anogenital warts)
| + | |
- | **CIN 2: Moderate dysplasia
| + | |
- | **CIN 3: Severe dysplasia; includes CIS
| + | |
- | *'''CIN caused by HPV can clear without treatment.'''
| + | |
- | | + | |
- | ===Cervical Cancer: Diagnosis=== | + | |
- | *Inadequate Colposcopy:
| + | |
- | **T-Zone not fully visualized
| + | |
- | **Can’t see the entire lesion
| + | |
- | **Lesion extends into canal
| + | |
- | **Discordance
| + | |
- | **Positive endocervical curettage (ECC)
| + | |
- | **Suspect invasion
| + | |
- | | + | |
- | ====What is a colposcopy?====
| + | |
- | *Use of a magnifying instrument
| + | |
- | *Application of a vinegar-like solution onto the cervix
| + | |
- | **Use acetic acid to highlight abnormal spots; biopsy them.
| + | |
- | *See abnormalities that can’t be seen with the naked eye
| + | |
- | *Feels like getting a Pap test, but lasts longer
| + | |
- | *'''Must do a cone biopsy if you have an inadequate simple (cervical) biopsy.'''
| + | |
- | | + | |
- | ====Cervical Biopsy====
| + | |
- | *Removal of a small piece of tissue from the cervix
| + | |
- | *Endocervical curettage is often performed to evaluate lesions within the cervical canal
| + | |
- | | + | |
- | ====Biopsy Results and Management====
| + | |
- | *CIN I
| + | |
- | **Observation
| + | |
- | *CIN II and III
| + | |
- | **Laser
| + | |
- | **Cryotherapy
| + | |
- | **Cone Biopsy: LEEP, laser cone, or cold-knife cone
| + | |
- | **Hysterectomy may be recommended
| + | |
- | | + | |
- | | + | |
- | *Cancer: Gynecologic Oncology Consultation
| + | |
- | | + | |
- | | + | |
- | *If the colposcopy is inadequate, or invasion is suspected, proceed with definitive diagnostic test:
| + | |
- | **LEEP Excision
| + | |
- | **Cold Knife Cone
| + | |
- | | + | |
- | | + | |
- | *If lesion is visible, biopsy can be diagnostic without cone
| + | |
- | | + | |
- | ====What is a cervical conization?====
| + | |
- | *Removes a coneshaped piece of tissue
| + | |
- | *Often allows for diagnosis and treatment
| + | |
- | *Performed with local anesthesia in the office or under general anesthesia in the operating room
| + | |
- | | + | |
- | ===Abnormal Pap: Epidemiology===
| + | |
- | *12,210 cancers
| + | |
- | **Treat
| + | |
- | *300,000 HSIL
| + | |
- | **Treat
| + | |
- | *1.25 million LSIL
| + | |
- | **Wait and see
| + | |
- | *2-3 million ASC
| + | |
- | **Wait and see
| + | |
- | *50-60 million women screened
| + | |
- | | + | |
- | ===Clinical Staging of Cervical Cancer===
| + | |
- | *Stage I: Disease confined to the cervix
| + | |
- | *Stage II: Vagina or parametrial extension
| + | |
- | *Stage III: Distal vagina, lateral pelvic wall, or hydronephrosis
| + | |
- | *Stage IV: Mucosa of bowel / bladder, or distant disease
| + | |
- | | + | |
- | | + | |
- | *Estimates of 5 year survival:
| + | |
- | **Stage I: 82-85%
| + | |
- | **Stage II: 61-66%
| + | |
- | **Stage III: 37-39%
| + | |
- | **Stage IV: 11-12%
| + | |
- | | + | |
- | ===Cervix Cancer: Treatment===
| + | |
| *Goal is to get a negative margin. | | *Goal is to get a negative margin. |
| *Will irradiate the entire tumor. | | *Will irradiate the entire tumor. |
Line 473: |
Line 118: |
| *Even radical hysterectomy leaves the ovaries. | | *Even radical hysterectomy leaves the ovaries. |
| **Cervical cancer very rarely involves the ovaries. | | **Cervical cancer very rarely involves the ovaries. |
- |
| |
- | ====Chemotherapy====
| |
- | *Stage IA1 (microinvasive): Cone vs. Simple Hysterectomy
| |
- | *Stage IA2-IB1: Radical Hysterectomy vs. Radiation
| |
- | *>Stage IB2: Concurrent platinum-based chemotherapy and radiation
| |
- |
| |
- | ====Surgical Treatment====
| |
- | *'''Only indicated if “negative margin” can be achieved'''
| |
- | *Advantages:
| |
- | **Permits More Accurate Assessment
| |
- | **Preserves Ovarian Function
| |
- | **Preserves Vaginal Function
| |
- | **Less Long-Term Morbidity
| |
- |
| |
- | ====Radiation Therapy====
| |
- | *'''Appropriate for all stages and patients with high surgical risk'''
| |
- | *Indicated when negative surgical margin cannot be achieved
| |
- | **Advanced disease >IB2
| |
- | **Obesity (BMI>30)
| |
| | | |
| ==Post-Menopausal Bleeding and Endometrial Carcinoma== | | ==Post-Menopausal Bleeding and Endometrial Carcinoma== |
- | *Incidence in US women:
| |
- | **41,000 cases / year
| |
- | *'''Most common gynecologic cancer'''
| |
- | *1 / 38 lifetime risk
| |
- | *7,100 deaths / year
| |
- | *'''2nd most common cause of death due to gynecologic cancer'''
| |
- |
| |
- | ===Endometrial Pt Profile===
| |
- | *Age: 75% post-menopausal
| |
- | *Etiology: Prolonged unopposed estrogen stimulation
| |
- | *Clinical Presentation:
| |
- | **Abnormal bleeding, post-menopausal
| |
- | **Associated factors: obesity, hypertension, diabetes
| |
- | *HNPCC (Lynch)
| |
- |
| |
- | ===Endometrial Cancer: Risk Factors===
| |
- |
| |
- | ===Endometrial Cancer: Two Types===
| |
- | *Type I
| |
- | **Estrogen Related
| |
- | **'''Younger and heavier patients'''
| |
- | **Low grade
| |
- | **Perimenopausal
| |
- | **Exogenous estrogen
| |
- | **Insulin resistance
| |
- |
| |
- | *Type II
| |
- | **Aggressive
| |
- | **Unrelated to estrogen stimulation
| |
- | **'''Occurs in older & thinner women'''
| |
- | **'''Potential genetic basis'''
| |
- | ***Lynch syndrome
| |
- | ***Familial trend
| |
- |
| |
- |
| |
- | ===Endometrial Carcinoma===
| |
- | *Pathology
| |
- | **> '''70% adenocarcinomas'''
| |
- | **Histologic ''grade important''
| |
- | **Poor prognosis cell types: papillary serous and clear cell carcinomas, mixed tumors
| |
- |
| |
- |
| |
- | *FIGO Stage - Surgical Findings:
| |
- | **Stage 1: Confined to uterus
| |
- | **Stage 2: Extension to cervix
| |
- | **Stage 3: Regional spread (serosa, adnexa, vagina, parametria, pelvic / aortic nodes)
| |
- | **Stage 4: Metastases (Bladder / rectum, inguinal nodes, distant metastases)
| |
- |
| |
- |
| |
- | *Stage: Frequency; Survival
| |
- | **Stage 1: 75%; 90%
| |
- | **Stage 2: 13%; 60%
| |
- | **Stage 3: 9%; 40%
| |
- | **Stage 4: 3%; <10%
| |
- |
| |
- | ===Endometrial (uterine) Cancer: Diagnosis===
| |
- | *Pts with uterine cancer often present with AUB / PMB:
| |
- | **Abnormal Uterine Bleeding
| |
- | **Postmenopausal bleeding
| |
- |
| |
- |
| |
- | *Office biopsy (Pipelle)
| |
- | *Dilation and curettage (D&C)
| |
- | *Hysteroscopy
| |
- |
| |
- | ===Endometrial (uterine) Cancer: Treatment===
| |
- | *Mainstay is surgical
| |
- | **Total hysterectomy
| |
- | **BSO
| |
- | **Pelvic & PA Nodes
| |
- |
| |
- | ===Endometrial (uterine) Cancer: Surgical Staging===
| |
- | *Conceptual rationale:
| |
- | **Defines extent of disease
| |
- | **Minimizes over / under treatment
| |
- | **Minimally increases perioperative morbidity / mortality
| |
- | **Decreases overall Rx risks and costs
| |
- | **Allows comparison of therapeutic results
| |
- |
| |
- | ===Endometrial (uterine) Cancer: Adjuvant Therapy===
| |
- | *Options:
| |
- | **Brachytherapy
| |
- | **External beam radiotherapy
| |
- | **Hormonal therapy
| |
- | **Cytotoxic chemotherapy
| |
- | **Combination therapy
| |
- |
| |
| | | |
- | *Determining Factors:
| + | Did not cover all topics. |
- | **Stage
| + | |
- | **Histologic subtype
| + | |
- | **Staging completeness
| + | |
- | **Tumor biology
| + | |
- | **Medical conditions
| + | |