Significant pelvic recurrence in high-risk pathologic stage I-IV endometrial carcinoma patients after adjuvant chemotherapy alone: Implications for adjuvant radiation therapy

被引:107
作者
Mundt, AJ
McBride, R
Rotmensch, J
Waggoner, SE
Yamada, SD
Connell, PP
机构
[1] Univ Chicago Hosp, Dept Radiat & Cellular Oncol, Gynecol Oncol Sect, Chicago, IL 60637 USA
[2] Univ Chicago Hosp, Dept Obstet & Gynecol, Gynecol Oncol Sect, Chicago, IL 60637 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2001年 / 50卷 / 05期
关键词
endometrial cancer; adjuvant chemotherapy; pattern of failure;
D O I
10.1016/S0360-3016(01)01566-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To evaluate the risk of pelvic recurrence (PVR) in high-risk pathologic Stage I-IV endometrial carcinoma patients after adjuvant chemotherapy alone. Methods: Between 1992 and 1998, 43 high-risk endometrial cancer patients received adjuvant chemotherapy. All patients underwent primary surgery consisting of total abdominal hysterectomy and bilateral salpingo-oophorectomy. No patients received preoperative radiation therapy (AT). Regional lymph nodes and peritoneal cytology were sampled in 62.8% and 83.7% of cases, respectively. Most patients had Stage III-IV disease (83.7%) or unfavorable histology tumors (74.4%). None had evidence of extra-abdominal disease. All patients received 4-6 cycles of chemotherapy as the sole adjuvant therapy, consisting primarily of cisplatin and doxorubicin. Recurrent disease sites were divided into pelvic (vaginal, nonvaginal) and extrapelvic (para-aortic, upper abdomen, liver, and extra-abdominal). Median follow-up was 27 months (range, 2-96 months). Results: Twenty-nine women (67.4%) relapsed. Seventeen (39.5%) recurred in the pelvis and 23 (55.5%) in extrapelvic sites. The 3-year actuarial PVR rate was 46.5%. The most significant factors correlated with PVR were cervical involvement (CI) (p = 0.01) and adnexal (p = 0.05) involvement. Of the 17 women who developed a PVR, 8 relapsed in the vagina, 3 in the nonvaginal pelvis, and 6 in both. The 3-year vaginal and nonvaginal PVR rates were 37.8% and 26%, respectively. The most significant factor correlated with vaginal PVR was CI (p = 0.0007). Deep myometrial invasion (p = 0.02) and lymph nodal involvement (p = 0.03) were both correlated with nonvaginal PVR. Nine of the 29 relapsed patients (31%) developed PVR as their only (6) ar first site (3) of recurrence. Factors associated with a higher rate of PVR (as the first or only site) were CI and Stage I-II disease. Conclusions: PVR is common in high-risk pathologic Stage I-IV endometrial cancer patients after adjuvant chemotherapy alone. These results support the continued use of locoregional RT in patients undergoing adjuvant chemotherapy. Further studies are needed to test the addition of chemotherapy to locoregional RT. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:1145 / 1153
页数:9
相关论文
共 54 条
[1]  
AALDERS J, 1980, OBSTET GYNECOL, V56, P419
[2]   SEROUS PAPILLARY CARCINOMA OF THE ENDOMETRIUM - A HISTOPATHOLOGICAL STUDY OF 22 CASES [J].
ABELER, VM ;
KJORSTAD, KE .
GYNECOLOGIC ONCOLOGY, 1990, 39 (03) :266-271
[3]   DOXORUBICIN CISPLATIN VINBLASTINE COMBINATION CHEMOTHERAPY OF ADVANCED ENDOMETRIAL CARCINOMA - A SOUTHWEST ONCOLOGY GROUP-STUDY [J].
ALBERTS, DS ;
MASON, NL ;
OTOOLE, RV ;
HILGERS, RD ;
RIVKIN, SE ;
BOUTSELIS, JG ;
PUGH, RP ;
VAITKEVICIUS, VK ;
GREEN, JB ;
OISHI, N .
GYNECOLOGIC ONCOLOGY, 1987, 26 (02) :193-201
[4]  
ALGAN O, 1998, INT J RADIAT ONCOL, V35, P925
[5]  
BURKE TW, 1991, GYNECOL ONCOL, V40, P264
[6]   POSTOPERATIVE ADJUVANT CISPLATIN, DOXORUBICIN, AND CYCLOPHOSPHAMIDE (PAC) CHEMOTHERAPY IN WOMEN WITH HIGH-RISK ENDOMETRIAL CARCINOMA [J].
BURKE, TW ;
GERSHENSON, DM ;
MORRIS, M ;
STRINGER, CA ;
LEVENBACK, C ;
TORTOLEROLUNA, G ;
BAKER, VV .
GYNECOLOGIC ONCOLOGY, 1994, 55 (01) :47-50
[7]   Chemotherapy as adjuvant and salvage treatment in women with endometrial carcinoma [J].
Burke, TW ;
Gershenson, DM .
CLINICAL OBSTETRICS AND GYNECOLOGY, 1996, 39 (03) :716-727
[8]   Surgery and postoperative radiation therapy in stage II endometrial carcinoma [J].
Calvin, DP ;
Connell, PP ;
Rotmensch, J ;
Waggoner, S ;
Mundt, AJ .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1999, 22 (04) :338-343
[9]  
CREASMAN WT, 1987, CANCER, V60, P2035, DOI 10.1002/1097-0142(19901015)60:8+<2035::AID-CNCR2820601515>3.0.CO
[10]  
2-8