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每周拓扑替康和顺铂(TOPOCIS)作为局部晚期宫颈鳞癌的新辅助化疗:一项多中心 II 期研究结果。

Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study.

机构信息

Gynecologic Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori, via Venezian no.1, Milan, Italy.

出版信息

Eur J Cancer. 2013 Mar;49(5):1065-72. doi: 10.1016/j.ejca.2012.10.008. Epub 2012 Nov 11.

Abstract

OBJECTIVES

The aim of this phase II multicentric study was to evaluate the efficacy and toxicity of neo-adjuvant chemotherapy with weekly topotecan and cisplatin in locally-advanced squamous cervical cancer.

PATIENTS AND METHODS

From November 2008 to January 2011, 92 patients met the inclusion criteria and were enrolled. Eligibility criteria were: squamous or adenosquamous cervical cancer; clinical stages IB2, IIA, IIB; Eastern Cooperative Oncology Group (ECOG) Performance Status (PS)≤ 2; neutrophils ≥1500/μL; platelets ≥100,000/μL, normal renal and liver function. Treatment consisted of six courses of weekly topotecan (2mg/m(2)) and cisplatin (40 mg/m(2)). All responsive and stable patients were submitted to radical surgery, while progressed cases underwent definitive radiotherapy±chemotherapy. Primary end-point was evaluation of efficacy and toxicity. All patients are evaluable for toxicity and efficacy.

RESULTS

Ninety-six percent of patients completed the six planned courses of chemotherapy, and 95% of courses were administered at a full dose and without interruption or delay. Mean age was 49 years (35-64 years). FIGO Stage distribution was 30 IB2, 13 IIA and 49 IIB. Treatment was well tolerated and no death occurred. G3-G4 haematological toxicity was observed in 28% of patients (5% out of cycles). Support therapies (blood transfusions and/or erythropoietin and/or Granocyte-Colony Stimulating Factor) were given to 24% of patients. Clinical response rate was 77%. The nine progressed cases were irradiated, while the remaining 83 patients were submitted to radical surgery. An overall pathologic response was observed in 67% of patients, with an optimal response rate of 32% and a disease downstage in 57% of patients. Nodal metastases occurred in 36% of patients. Adjuvant therapy (radiotherapy and or chemotherapy) was prescribed in 55% of patients, because of lymph node metastases, parametrial or vaginal involvement or cut-through margins. Median follow-up was 18 months: 76% of patients are alive and free from recurrence, 24% of patients relapsed and 13% died.

CONCLUSIONS

Weekly topotecan and cisplatin showed an acceptable toxicity profile; the promising response rate warrants further investigation.

摘要

目的

本 II 期多中心研究的目的是评估每周拓扑替康联合顺铂新辅助化疗在局部晚期宫颈鳞癌中的疗效和毒性。

患者和方法

2008 年 11 月至 2011 年 1 月,92 例患者符合纳入标准并被纳入研究。入选标准为:宫颈鳞癌或腺鳞癌;临床分期为 IB2、IIA、IIB;东部肿瘤协作组(ECOG)体力状态(PS)≤2;中性粒细胞≥1500/μL;血小板≥100000/μL,肝肾功能正常。治疗包括 6 个疗程的每周拓扑替康(2mg/m2)和顺铂(40mg/m2)。所有有反应和稳定的患者均接受根治性手术,进展患者接受根治性放疗±化疗。主要终点为疗效和毒性评估。所有患者均可评估毒性和疗效。

结果

96%的患者完成了 6 个计划疗程的化疗,95%的疗程按全剂量、无中断或延迟给药。平均年龄为 49 岁(35-64 岁)。FIGO 分期分布为 30 例 IB2、13 例 IIA 和 49 例 IIB。治疗耐受性良好,无死亡病例。28%的患者出现 3-4 级血液学毒性(5%的周期)。24%的患者接受了输血和/或促红细胞生成素和/或粒细胞集落刺激因子等支持治疗。临床缓解率为 77%。9 例进展患者接受放疗,其余 83 例患者接受根治性手术。67%的患者有总体病理缓解,最佳缓解率为 32%,57%的患者疾病降期。36%的患者出现淋巴结转移。55%的患者因淋巴结转移、宫旁或阴道受累或切缘穿透而接受辅助治疗(放疗和/或化疗)。中位随访时间为 18 个月:76%的患者存活且无复发,24%的患者复发,13%的患者死亡。

结论

每周拓扑替康联合顺铂的毒性谱可接受,有希望的缓解率值得进一步研究。

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