Conte P F, Alama A, Bertelli G, Canavese G, Carnino F, Catturich A, Di Marco E, Gardin G, Jacomuzzi A, Monzeglio C
Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy.
Int J Cancer. 1987 Oct 15;40(4):490-4. doi: 10.1002/ijc.2910400410.
Thirty-nine patients with locally advanced breast cancer (T3b-4, N1-3 or inflammatory carcinoma) received 3 cycles of induction chemotherapy with estrogenic recruitment before surgery. The therapeutic regimen consisted of diethylstilbestrol (DES) orally on days 1-3, 5-Fluorouracil + Doxorubicin + Cyclophosphamide on day 4 q 21 days (DES-FAC). After surgery 6 additional cycles of chemotherapy (3 DES-FAC alternating with 3 DES-CMF with Methotrexate + F and C as in FAC) were administered. The objective response rate was 71.8% with 15.4% CR, and 56.4% PR; after surgery 36/39 (92.3%) patients were rendered disease-free. So far, 13 of 26 patients in stage IIIb have relapsed (9 of 13 with inflammatory carcinomas). Three-year survival and progression-free survival are 60% and 53.5%, respectively. Twenty-three of the 39 patients were subjected to serial tumor biopsies during the first DES-FAC regimen to allow for tumor-cell kinetic studies during DES and chemotherapy. A significant estrogenic recruitment occurred in 16 patients (69.6%), irrespective of estrogen-receptor status. At surgery, 3-4 weeks after induction chemotherapy, tumor proliferative activity was significantly depressed in comparison to basal values. These results indicate that breast cancer cells can be recruited in vivo with DES and that chemotherapy following estrogenic stimulation is effective and feasible with acceptable toxicity.
39例局部晚期乳腺癌(T3b - 4、N1 - 3或炎性癌)患者在手术前接受了3个周期的雌激素募集诱导化疗。治疗方案包括第1 - 3天口服己烯雌酚(DES),第4天给予5 - 氟尿嘧啶 + 阿霉素 + 环磷酰胺,每21天重复(DES - FAC)。术后给予另外6个周期的化疗(3个DES - FAC周期与3个DES - CMF周期交替,其中甲氨蝶呤 + 氟尿嘧啶和环磷酰胺同FAC方案)。客观缓解率为71.8%,完全缓解率为15.4%,部分缓解率为56.4%;术后39例患者中有36例(92.3%)无疾病进展。目前,Ⅲb期的26例患者中有13例复发(13例炎性癌患者中有9例复发)。三年生存率和无进展生存率分别为60%和53.5%。39例患者中有23例在首个DES - FAC方案期间接受了系列肿瘤活检,以便在DES和化疗期间进行肿瘤细胞动力学研究。16例患者(69.6%)出现了显著的雌激素募集,与雌激素受体状态无关。在诱导化疗后3 - 4周手术时,与基础值相比,肿瘤增殖活性显著降低。这些结果表明,DES可在体内募集乳腺癌细胞,雌激素刺激后的化疗有效且可行,毒性可接受。