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吉西他滨用于复发或顺铂难治性睾丸癌患者。

Gemcitabine in patients with relapsed or cisplatin-refractory testicular cancer.

作者信息

Bokemeyer C, Gerl A, Schöffski P, Harstrick A, Niederle N, Beyer J, Casper J, Schmoll H J, Kanz L

机构信息

Department of Hematology/Oncology, Internal Medicine II, Eberhard Karls University, Tübingen, Germany.

出版信息

J Clin Oncol. 1999 Feb;17(2):512-6. doi: 10.1200/JCO.1999.17.2.512.

Abstract

PURPOSE

Despite generally high cure rates in patients with metastatic testicular germ cell tumors, patients with incomplete response to cisplatin-based first-line therapy or with relapsed disease after high-dose salvage chemotherapy have a very poor prognosis. This phase II study evaluates the use of gemcitabine in patients with intensively pretreated or cisplatin-refractory testicular germ cell cancers.

PATIENTS AND METHODS

Thirty-five patients (median age, 33 years) were enrolled; 31 patients were fully assessable. All patients had metastatic nonseminomatous germ cell tumors; eight patients had extragonadal primary tumors. Twenty patients (63%) had lung metastases, and 12 patients (39%) had liver metastases. The median number of prior cisplatin-based chemotherapy cycles was seven; 22 patients (71%) had received high-dose chemotherapy with autologous stem-cell transplantation, and 19 patients (61%) had received treatment with paclitaxel. Seventeen patients (54%) were considered refractory or absolutely refractory to chemotherapy.

RESULTS

Six of 31 assessable patients (19%) responded favorably to gemcitabine, 11 patients (35%) displayed no change, and 14 patients (45%) had disease progression. The median time to treatment failure was 4 months (range, 2 to 9+ months), and the median survival was 6 months (range, 2 to 23 months). Patients received a median of six gemcitabine applications. Ten patients (32%) required dose reductions, mainly owing to hematologic toxicity. Grade 3/4 granulocytopenia occurred in four patients (13%) and grade 3/4 thrombocytopenia in seven patients (22%). One case of severe sepsis was observed.

CONCLUSION

Gemcitabine displays antitumor activity in intensively pretreated and refractory germ cell tumors. Responses were observed in approximately 20% of patients, including three of 22 patients after previous high-dose chemotherapy and one of four patients with mediastinal tumors. Gemcitabine may be a reasonable palliative option for intensively pretreated patients and should be further investigated to define its role in the risk-adapted treatment strategies for germ cell tumors.

摘要

目的

尽管转移性睾丸生殖细胞肿瘤患者的治愈率总体较高,但对基于顺铂的一线治疗反应不完全或在大剂量挽救化疗后复发的患者预后非常差。这项II期研究评估了吉西他滨在经过强化预处理或对顺铂耐药的睾丸生殖细胞癌患者中的应用。

患者与方法

招募了35例患者(中位年龄33岁);31例患者可进行全面评估。所有患者均患有转移性非精原细胞性生殖细胞肿瘤;8例患者有性腺外原发性肿瘤。20例患者(63%)有肺转移,12例患者(39%)有肝转移。既往基于顺铂的化疗周期中位数为7个;22例患者(71%)接受了大剂量化疗及自体干细胞移植,19例患者(61%)接受了紫杉醇治疗。17例患者(54%)被认为对化疗耐药或绝对耐药。

结果

31例可评估患者中有6例(19%)对吉西他滨反应良好,11例患者(35%)病情无变化,14例患者(45%)疾病进展。治疗失败的中位时间为4个月(范围2至9 +个月),中位生存期为6个月(范围2至23个月)。患者接受吉西他滨治疗的中位数为6次。10例患者(32%)需要降低剂量,主要是由于血液学毒性。4例患者(13%)发生3/4级粒细胞减少,7例患者(22%)发生3/4级血小板减少。观察到1例严重脓毒症病例。

结论

吉西他滨在经过强化预处理和耐药的生殖细胞肿瘤中显示出抗肿瘤活性。约20%的患者出现反应,包括22例既往接受大剂量化疗的患者中的3例以及4例纵隔肿瘤患者中的1例。对于经过强化预处理的患者,吉西他滨可能是一种合理的姑息治疗选择,应进一步研究以确定其在生殖细胞肿瘤风险适应性治疗策略中的作用。

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