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通过体外药敏试验选择个体化化疗方案治疗的局限期小细胞肺癌患者的生存情况。

Survival of patients with limited-stage small cell lung cancer treated with individualized chemotherapy selected by in vitro drug sensitivity testing.

作者信息

Cortazar P, Gazdar A F, Woods E, Russell E, Steinberg S M, Williams J, Ihde D C, Johnson B E

机构信息

National Cancer Institute-Navy Medical Oncology Branch, Biostatistics and Data Management Section, National Naval Medical Center, Bethesda, Maryland 20889-5105, USA.

出版信息

Clin Cancer Res. 1997 May;3(5):741-7.

PMID:9815744
Abstract

Our purpose was to study the feasibility of determining individualized chemotherapy regimens by in vitro drug sensitivity testing (DST) for patients with limited-stage small cell lung cancer (SCLC) and to evaluate patient response and survival. Fifty-four previously untreated patients with limited-stage small cell cancer were studied. Fresh tumor specimens for DST were collected, when possible, from patients' biopsies before the start of treatment. The differential staining cytotoxicity assay was used to determine the in vitro sensitivity of the tumor cells to different drugs. From these results, an in vitro best regimen (IVBR), a three-drug combination of previously proven efficacy of seven active drugs in SCLC, was selected. Patients were initially treated with four cycles of etoposide/cisplatin and concurrent radiotherapy. This was followed by four cycles of either individualized chemotherapy regimens based on the results of DST or, when DST results were not available, four cycles of vincristine, doxorubicin, and cyclophosphamide. Eighteen patients (33%) underwent biopsy procedures that provided tissue specimens for DST. The biopsy specimens contained tumor cells in 16 of 18 patients. The median duration from diagnosis to start of treatment was 22 days (range, 4-58 days) for the 18 patients who underwent elective thoracic biopsies compared to 21 days (range, 2-74 days) for members of the group that did not (P2 = 0.58). Time from thoracic biopsy to initiation of chemotherapy was a median of 4 days (range, 2-22 days). DST was done in 10 patients, and IVBR was administered to 8 patients. The median actuarial survival of 8 patients treated with their IVBR was 38.5 months compared to 19 months for the 46 patients treated with empiric chemotherapy. Selection of individualized chemotherapy regimens is labor intensive but feasible in limited-stage SCLC. Treatment with an individualized IVBR in our patients was associated with prolonged patient survival; however, because of the nature of our study design, other factors could have affected the results.

摘要

我们的目的是研究通过体外药敏试验(DST)为局限期小细胞肺癌(SCLC)患者确定个体化化疗方案的可行性,并评估患者的反应和生存情况。对54例既往未接受过治疗的局限期小细胞癌患者进行了研究。尽可能在治疗开始前从患者活检中收集用于DST的新鲜肿瘤标本。采用差异染色细胞毒性试验来确定肿瘤细胞对不同药物的体外敏感性。根据这些结果,选择了一种体外最佳方案(IVBR),即由七种已证实对SCLC有效的活性药物组成的三联药物组合。患者最初接受四个周期的依托泊苷/顺铂及同步放疗。随后,根据DST结果接受四个周期的个体化化疗方案,若无法获得DST结果,则接受四个周期的长春新碱、多柔比星和环磷酰胺治疗。18例患者(33%)接受了活检程序,获得了用于DST的组织标本。18例患者中有16例的活检标本含有肿瘤细胞。接受选择性胸部活检的18例患者从诊断到开始治疗的中位时间为22天(范围4 - 58天),未接受活检的患者组为21天(范围2 - 74天)(P2 = 0.58)。从胸部活检到开始化疗的时间中位为4天(范围2 - 22天)。10例患者进行了DST,8例患者接受了IVBR治疗。接受IVBR治疗的8例患者的中位精算生存时间为38.5个月,而接受经验性化疗的46例患者为19个月。在局限期SCLC中选择个体化化疗方案虽耗费人力,但可行。在我们的患者中,采用个体化IVBR治疗可延长患者生存期;然而,由于我们研究设计的性质,其他因素可能影响了结果。

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