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首页> 外文期刊>Gynecologic Oncology: An International Journal >Treatment of recurrent or persistent platinum-refractory ovarian, fallopian tube or primary peritoneal cancer with gemcitabine and topotecan: a phase II trial of the Puget Sound Oncology Consortium.
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Treatment of recurrent or persistent platinum-refractory ovarian, fallopian tube or primary peritoneal cancer with gemcitabine and topotecan: a phase II trial of the Puget Sound Oncology Consortium.

机译:吉西他滨和拓扑替康治疗复发性或持续性铂难治性卵巢,输卵管或原发性腹膜癌:Puget Sound Oncology Consortium的II期试验。

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OBJECTIVE: To determine the nature and degree of toxicity, response rate, quality of life (QOL), and progression-free interval in women with platinum-resistant refractory ovarian or peritoneal cancer receiving weekly topotecan and gemcitabine. METHODS: A Phase II trial of gemcitabine 800 mg/m(2) and topotecan 3.0 or 2.5 mg/m(2) administered on days 1 and 8 of a 21-day cycle was conducted. Response was assessed by RECIST criteria. Quality of life was assessed with FACT-O. RESULTS: Twenty-three patients were enrolled in the study and all were evaluable. One patient was later found to be ineligible due to a concurrent endometrial malignancy, but remains part of the analysis. Sixteen patients (70%) had measurable disease at baseline and 7 (30%) had elevated CA125 only. The median number of prior regimens was 1, range 1-4 and median number of prior cycles was 8, range 3-39. The first 6 patients received topotecan at a dose of 3.0 mg/m(2), but because of dose delays and need for GCSF the dose of topotecan was lowered to 2.5 mg/m(2). There were 4 (17%) partial responses, but only two (9%) were confirmed prior to progression; and 8 (35%) had stable disease. Toxicity was acceptable with only 8 of the 107 cycles given requiring a dose reduction. Four patients (17%) were taken off the study for toxicity, two at the higher dose and two at the lower dose. Median time to recurrence was 3.0 months and median overall survival was 12.6 months. QOL did not differ with subsequent cycles as compared to baseline. CONCLUSION: The combination of weekly topotecan and gemcitabine is well tolerated, but best response rate is 17%, and confirmed response is only 9%, which is not significantly better than single agent gemcitabine or topotecan. These results do not provide compelling evidence for the combination of weekly gemcitabine and topotecan as a promising therapy.
机译:目的:确定每周接受拓扑替康和吉西他滨治疗的铂耐药性难治性卵巢或腹膜癌女性的毒性,反应率,生活质量(QOL)和无进展间隔的性质和程度。方法:进行了吉西他滨800 mg / m(2)和拓扑替康3.0或2.5 mg / m(2)在21天周期的第1天和第8天进行的II期试验。通过RECIST标准评估反应。使用FACT-O评估生活质量。结果:23名患者被纳入研究,所有患者均可评估。后来发现一名患者由于并发子宫内膜恶性肿瘤不合格,但仍属于分析的一部分。 16名患者(70%)在基线时可测量疾病,而7名(30%)仅CA125升高。先前方案的中位数为1,范围为1-4,先前周期的中位数为8,范围为3-39。前6名患者接受3.0 mg / m(2)的拓扑替康剂量,但由于剂量延迟和对GCSF的需要,拓扑替康的剂量降低至2.5 mg / m(2)。有4例(17%)局部缓解,但只有2例(9%)在进展前被确认; 8名(35%)病情稳定。如果需要减少剂量,在107个周期中只有8个周期的毒性是可以接受的。有4名患者(17%)因毒性而退出研究,其中2名使用较高剂量,另2名使用较低剂量。复发中位时间为3.0个月,中位总生存期为12.6个月。与基线相比,QOL在随后的周期中没有差异。结论:每周一次拓扑替康和吉西他滨的组合耐受性良好,但最佳缓解率为17%,确定的响应仅为9%,这并不比单药吉西他滨或拓扑替康更好。这些结果并未提供每周吉西他滨和拓扑替康联合治疗的有力证据。

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