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- Apr 16, 2004
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55F who presented with vaginal bleeding and abdominal cramps. Endometrial biopsy revealed adenocarcinoma. No pre-operative imaging.
Pt has TAH-BSO + b/l LND. Final path was 2.1 cm well-differentiated endometrial adenocarcinoma invading 1 mm into the myometrium. No LVI. 0/22 positive pelvic LN. 0/3 positive PA LN.
FIGO Stage IA
No adjuvant therapy recommend based on final pathology.
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16 months later, on routine gyn examination, a 1 cm fleshy mass was palpated in the vaginal apex. Biopsy revealed well-differentiated adenocarcinoma. PET/CT was done and was negative (including in the site of recurrence).
Pt is referred to you for treatment options. What do you do?
Choice #1: EBRT to pelvic LN + HDR boost; Evidence
Choice #2: HDR monotherapy; Evidence
Note: The data for #2 is based on PORTEC 2 which is not totally applicable because (a) this is a recurrence and (b) it is "technically" not high-intermediate risk based on pathology.
Concurrent chemoXRT was also discussed but dismissed due to lack of data.
Pt has TAH-BSO + b/l LND. Final path was 2.1 cm well-differentiated endometrial adenocarcinoma invading 1 mm into the myometrium. No LVI. 0/22 positive pelvic LN. 0/3 positive PA LN.
FIGO Stage IA
No adjuvant therapy recommend based on final pathology.
------------------------
16 months later, on routine gyn examination, a 1 cm fleshy mass was palpated in the vaginal apex. Biopsy revealed well-differentiated adenocarcinoma. PET/CT was done and was negative (including in the site of recurrence).
Pt is referred to you for treatment options. What do you do?
Choice #1: EBRT to pelvic LN + HDR boost; Evidence
Choice #2: HDR monotherapy; Evidence
Note: The data for #2 is based on PORTEC 2 which is not totally applicable because (a) this is a recurrence and (b) it is "technically" not high-intermediate risk based on pathology.
Concurrent chemoXRT was also discussed but dismissed due to lack of data.