Napolitano U, Imperato F, Mossa B, Framarino M L, Marziani R, Marzetti L
Division of Obstetrics and Gynecology, Sant'Andrea Hospital, II School of Medicine, University of Rome "La Sapienza," Italy.
Eur J Gynaecol Oncol. 2003;24(1):51-9.
to verify whether a regimen of preventive chemotherapy in the treatment of cervical carcinoma allows surgical treatment in a larger number of patients and whether cases treated with this combined neoadjuvant polychemotherapy/surgery regimen improves overall and disease-free survival rates.
prospective randomized clinical study.
Department of Gynaecology and Obstetrics, University of Rome "La Sapienza".
192 patients suffering from squamous cell carcinoma of the uterine cervix in Stages Ib-IIb were randomized to one of the following treatments: three courses of neoadjuvant chemotherapy with cisplatin, vincristine, bleomycin (NACT arm; n = 106); conventional surgery or radiotherapy alone (CO arm; n = 86). One hundred and fifty-six patients in Stage Ib-IIb (n = 86, NACT arm and n = 70, CO arm) and 16 patients in Stage III (NACT arm) who proved to be sensitive to the neoadjuvant chemotherapy, underwent radical hysterectomy. Four Stage III patients not sensitive to chemotherapy and 16 patients, Stage III, of the CO arm underwent radiotherapy.
the 5-year overall survival rates for the NACT and CO arm, respectively, were 78.6% and 73.2% in Stages Ib-IIa (p = NS), 68.7% and 64.3% in Stage IIb (p = NS). A 5-year disease-free survival rate for the NACT arm and CO arm, respectively, of 77.1% and 64.3% in Stages Ib-IIa (p < .05), 56.2% and 57.1% in Stage IIb (p = NS) was found.
the responsiveness of cervical cancer to neoadjuvant chemotherapy allows surgical treatment in a larger number of patients and results in longer overall and disease-free survival.
验证宫颈癌预防性化疗方案是否能使更多患者接受手术治疗,以及采用这种新辅助多药化疗/手术联合方案治疗的病例是否能提高总生存率和无病生存率。
前瞻性随机临床研究。
罗马“La Sapienza”大学妇产科。
192例Ib-IIb期子宫颈鳞状细胞癌患者被随机分为以下治疗组之一:顺铂、长春新碱、博来霉素新辅助化疗三个疗程(新辅助化疗组;n = 106);单纯传统手术或放疗(对照组;n = 86)。Ib-IIb期的156例患者(新辅助化疗组n = 86,对照组n = 70)和III期的16例患者(新辅助化疗组)对新辅助化疗敏感,接受了根治性子宫切除术。4例对化疗不敏感的III期患者和对照组的16例III期患者接受了放疗。
Ib-IIa期新辅助化疗组和对照组的5年总生存率分别为78.6%和73.2%(p = 无统计学意义),IIb期分别为68.7%和64.3%(p = 无统计学意义)。发现Ib-IIa期新辅助化疗组和对照组的5年无病生存率分别为77.1%和64.3%(p < 0.05),IIb期分别为56.2%和57.1%(p = 无统计学意义)。
宫颈癌对新辅助化疗的反应性使更多患者能够接受手术治疗,并能延长总生存期和无病生存期。