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Clique para editar o título mestre Are there benefits from chemotherapy to early endometrial cancer? Ursula Matulonis, M.D. Associate Professor of Medicine, Harvard Medical School Director/Program Leader, Medical Gynecologic Oncology Dana-Farber Cancer Institute Boston MA Email: [email protected] Risk categories for recurrence • • • Low Risk no poor prognostic features Intermediate Risk deep myometrial invasion presence of lymphovascular invasion high grade or rare tumor histology High Risk positive nodes extrauterine disease • • • • • • Creasman WT, et al. AJ Obstet Gynecol 1999;181:31-34. Type I vs. Type II endometrial cancer Type II: Serous --Lack of unopposed estrogen (atrophy) -- High grade, often with -- Low to moderate grade, metastases minimal myometrial --Poorer prognosis (more invasion rare but causes a -- Good prognosis disproportionate number of deaths) Type I: Endometrioid --Unopposed estrogen (hyperplasia) NCCN guidelines for surgically staged stage I cancer Stage IA (<50% myometrial invasion) Stage IB (≥ 50% myometrial invasion) +/- adverse factors Grade 1 Grade 2 Grade 3 Adverse risk factors not present observe Observe or brachy Observe or brachy Adverse risk factors present obs or brachy Obs or brachy +/- pelvic RT Obs or brachy +/pelvic RT Adverse risk factors not present obs or brachy Observe or brachy Obs or brachy +/pelvic RT Adverse factors present Obs or brachy +/- pelvic RT Obs or brachy +/- pelvic RT Obs or pelvic RT and/or brachy +/chemotherapy (cat 2B for chemotherapy) Adverse risk features: age, +LVI, tumor size, lower uterine (cervical/gland involvement) www.nccn.org NCCN guidelines for stage II and IIIA IIIA: Tumor invades the serosa of the uterus and/or adnexae Grade 1 Grade 2 Grade 3 All Stage II Vag Brachy +/- pelvic RT Pelvic RT + vaginal brachy Pelvic RT + vag brachy +/- chemotherapy (category 2B) Stage IIIA Chemotherapy +/-RT or involved field RT +/chemotherapy or pelvic RT +/- brachy Chemotherapy +/-RT or involved field RT +/chemotherapy or pelvic RT +/- brachy Chemotherapy +/-RT or involved field RT +/chemotherapy or pelvic RT +/- brachy Is +Peritoneal cytology an independent risk factor? In the absence of adverse pathological features (high grade tumors, deep invasion, serous or clear cell path or extrauterine disease spread), + cytology is not generally treated. Is intraluminal fallopian tube spread considered stage III? www.nccn.org Surgically staged Stage IIIB or higher Stage Treatment Stage IIIB Chemotherapy +/- RT Stage IIIC1 (+ pelvic Chemotherapy +/- RT nodes) Stage IIIC2 (+para-aortic Chemotherapy +/- RT nodes) Stage IVA, IVB (no gross Chemotherapy +/- RT residual cancer) www.nccn.org Addition of chemotherapy to RT versus RT alone Results of 2 pooled studies: NSGO-EC-9501/EORTC-55991 (Nordic study) and MaNGO ILIADE-III 540 patients enrolled; 534 evaluable. Eur J of Cancer 46:2422, 2010 NSGO-EC-9501/EORTC-55991 and MaNGO ILIADE-III (pooled data) **Nordic trial showed that addition of CT to RT was associated with a significant 36% reduction in the risk of relapse or death and a sig 49% reduction in the risk of death from endometrial cancer; MaNGO trial showed same direction but not significant. Eur J of Cancer 46:2422, 2010 Problems with these studies Nordic trial - study closed early because of poor accrual - chemotherapy could be given either before or after RT - RT is lower than standard of care (44Gy) - serous and clear cell cancers were allowed. - no standard chemotherapy regimen prescribed. MaNGO trial - higher staged cancers included - serous and clear cell excluded Other problems: pooled data of different stages, histologies, treatments. Eur J of Cancer 46:2422, 2010 Phase III study: GOG 122 Endometrial cancer: GOG 122 for advanced III/IV cancer Doxorubicin 60 mg/m2 Cisplatin 50 mg/m2 every 3 weeks x 8 cycles Primary endpoint: PFS Secondary endpoint: OS Median F/u: 60 months - 73% were stage III WART (AP/PA) 30 Gy x 20 = 150 Gy 15 Gy boost to pelvic +/- PA Maximum Doxorubicin total dose = 420 mg/m2 Randall et al, JCO 2006 Progression-free survival improved with chemotherapy: GOG 122 HR 0.71 (95% CI, 0.55 to 0.91; P = .007) J Clin Oncol; 24:36-44 2006 Survival better with chemotherapy: GOG 122 HR 0.68 (0.52-0.89; p<0.01) J Clin Oncol; 24:36-44 2006 Survival by treatment and stage Randall, M. E. et al. J Clin Oncol; 24:36-44 2006 Ongoing studies of adjuvant therapy for endometrial cancer Danish study, n=678 (AGO, EORTC, MaNGO, and others) Stage I and II endometrial cancer treated with surgery. Phase III study, n = 678 Eligibility: Stage I grade 3 endometrioid adenocarcinoma Stage II endometrioid adenocarcinoma Stage I and II type 2 histology (clear cell, serous, squamous cell carcinoma, or undifferentiated carcinoma) Randomized to: 1) observation 2) 6 cycles of carboplatin and paclitaxel. NCT01244789 GOG 249: Phase III Endometrial cancer 1) stage I with high-intermediate risks with +/- cytology 2) stage II (any histology), +/risk factors 3) stage I/II serous or clear cell cancers with neg cytology n= 562 High-intermediate risks: age ≥ 70 yrs with one risk factor age ≥ 50 yrs with 2 risk factors age ≥ 18 yrs with 3 risk factors Pelvic RT optional vaginal cuff boost Vaginal cuff brachy + 3 cycles of paclitaxel 175 mg/m2 + carboplatin AUC 6 Risk factors: grade 2 or 3 tumor +LVI outer ½ myometrial invasion NCT00807768 NCT00411138 Clique paraGOG editar258 o título mestre GOG 258 Endometrial cancer stage I-IV Opened: 6/29/09 Phase III N=804 Paclitaxel 175 mg/m2 Carboplatin AUC 6 q21 days x 6 cycles Volume directed RT + cisplatin 50 mg/m2 days 1, 28 followed by: Paclitaxel 175 mg/m2 Carboplatin AUC 5 q21 days x 4 cycles NCT00942357 Incorporation of bevacizumab into early stage endometrial cancer treatment No extrauterine disease outside of the pelvis NCT01005329 Conclusions • When does our group use adjuvant chemotherapy for endometrial cancer and What type of chemotherapy? 1) Use IV carboplatin and paclitaxel 2) Sequential therapy 3) Clinical situations: Stage III or higher regardless of histology, Type II tumors (serous, clear cell) (any stage) Uterine carcinosarcomas As part of a clinical trial Follow the NCCN guidelines