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BREAST CANCER IN PREGNANCY

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Presentation on theme: "BREAST CANCER IN PREGNANCY"— Presentation transcript:

1 BREAST CANCER IN PREGNANCY

2 Incidence 2nd most common cancer in pregnancy (after cervical cancer)
Accounts for 3% of total Ca breast in women Exact incidence- difficult to estimate Recorded incidence- 1: :50,000 (Smith et al, 2003) Recent studies- Incidence is 1:3000 Pregnancy associated breast Ca (PABC)- Ca diagnosed primarily during pregnancy or 1 year after it’s termination Causes of increased incidence Child bearing at late age Life style changes

3 Effect of Pregnancy on Breast Cancer
Not simply explained by high dose of estrogen Increased AFP and hCG are protective PABC are more likely to be advanced/ metastatic (due to increased blood/ lymphatic supply) Microscopic lymph node involvement more likely in pregnancy (60%) Stage I- 30%, Stage II- 30%, Stage III & IV- 40% Higher incidence of Inflammatory Cancers 80% lesions are ER/PR negative Interruption of pregnancy does not alter the prognosis

4 Does Pregnancy Affect The Prognosis?
Slight delay in diagnosis- mean delay 1-2 months 6 month delay increases chance of nodal involvement by 10% Post-pregnancy breast remodeling may favour tumour cell dissemination Breast cancer is always more aggressive in young women (so more common at advanced stage) NO difference in 5 year survival between pregnant and non-pregnant women when matched with age and stage (Bladstrom et al, 2003; Beadle et al, 2009)

5 Effect of Breast Cancer on Pregnancy
Disease itself- very little effect, if any Adverse effects due to Anaesthetic drugs Radiation Chemotherapy Hormonal agents Placental metastasis Seen occasionally in inter-villus space No transmission to the fetus due to immune rejection by the trophoblasts

6 Diagnosis Clinical Imaging
Any suspicious breast mass must be evaluated Physiological changes, especially in lactation makes diagnosis difficult Friction-free examination may help Imaging USG- Irregular borders with shadowing is highly suspicious Mammography Fetal exposure only 0.04 cGy False negative result 35-40% in pregnancy MRI More sensitive No ionizing radiation More false positive in pregnancy

7 Diagnosis (Contd.) Normal Pregnancy Invasive Cancer Tissue Diagnosis
If the mass is suspicious/ non-diagnostic in imaging Lactation should be suppressed to decrease vascularity and chance of milk-fistula Needs expert pathologist FNAC High rate of insufficient samples Pregnancy induced changes (lobular hyperplasia, galactostasis) Core biopsy Standard of diagnosis Normal Pregnancy Invasive Cancer

8 Metastatic Workup Chest X-ray- Alkaline Phosphatase- CT scan abdomen
Should be done (fetal exposure 0.08 cGy) Alkaline Phosphatase- Unreliable CT scan abdomen Usually avoided (fetal exposure <2 cGy) Bone scan Yield is low, selective use (fetal exposure 0.4 cGy) MRI abdomen- Safer alternative, when indicated clinicaly

9 Differential Diagnosis
Associated with pregnancy May undergo H/P changes due to hormonal stimulation Fibroadenoma Lipoma Papilloma Fibrocystic disease Peculiar to pregnancy Lactating adenoma Galactocele Mastitis Breast abscess (Wall should be biopsied) Bloody nipple discharge Cytology is always warranted Not a contraindication to breast-feeding Physiological Infection Duct papiloma Carcinoma

10 Management Multidisciplinary approach Respect patient’s wishes
Obstetricians Surgeons Neonatologists Medical Oncologists Anaesthetists Psychiatric Counselors Respect patient’s wishes If diagnosed post-partum- lactation to be suppressed and immediate treatment to be started

11 Surgery Treatment of choice for non-metastatic disease
Peri-operative hazards- position, anaesthesia, risk of preterm labour Modified radical mastectomy (MRM) with axillary clearance- done in most cases Breast Conserving Surgery (BCT) Lumpectomy/ Quadranectomy + Axillary Clearance Needs adjuvant RT after delivery (<8 weeks) Only for localized Tx diagnosed in 3rd trimester Sentinel LN biopsy Tc99sulphur colloid- NOT detrimental (fetal exposure 0.5 cGy)

12 Chemotherapy Indications- Axillary LN +ve, growth >1 cm, aneuploidy
Early pregnancy- Teratogenic (3-8 weeks of embryonic age) → needs MTP Late pregnancy- Can be given in late 2nd and 3rd trimester Breast feeding should be avoided during chemo CAF (Cyclophophamide, Adriamycin, 5-FU) is the preferred regime CMF- Methotrexate (Mtx) instead of Adriamycin- Controversial as Mtx can kill the trophoblasts

13 Other Therapies Radiotherapy Contraindicated- deferred till delivery
Maternal dose of 5000 cGy exposes the fetus to cGy Immunotherapy Trustuzumab-Herceptin (monoclonal Ab against HER2/neu) Limited experience in pregnancy May cause oligohydramnios (Shrim et al, 2008; Sekar and Stone, 2007) Hormonal therapy Tamoxifen is teratogenic (Cat D drug) Aromatase inhibitors- may cause ambiguous genitalia Oophorectomy- little help

14 Future Pregnancy ER/PR +ve breast Ca may be theoretically aggravated by future pregnancy (no evidence) Most of the recurrence- within 2-3 years Better to plan next pregnancy after 2-3 years of completion of therapy Chemo may cause POF No adverse effect on future obst outcome Survival is even BETTER! than those who don’t conceive Breast feeding possible even from the affected breast after BCT & RT

15 THANK YOU Thank You


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