Chang A Y, Kim K, Boucher H, Bonomi P, Stewart J A, Karp D D, Blum R H
Interlakes Oncology & Hematology, P.C., Rochester, New York 14623, USA.
Cancer. 1998 Jan 15;82(2):292-300. doi: 10.1002/(SICI)1097-0142(19980115)82:2<301::AID-CNCR8>3.0.CO;2-T.
Patients with metastatic nonsmall cell lung carcinoma (NSCLC) usually have a poor prognosis. A chemotherapy regimen containing cisplatin is commonly used for symptom palliation. Echinomycin is a potent bifunctional intercalator of double-strand DNA; trimetrexate is a new derivative of methotrexate and is active against methotrexate-resistant tumor cells in vitro.
The Eastern Cooperative Oncology Group conducted a randomized Phase II study. Eligible patients were assigned to receive echinomycin 1200 microg/m2 by intravenous (i.v.) infusion over 30-60 minutes once a week for 4 weeks, repeated every 6 weeks; trimetrexate 12 mg/m2 i.v. bolus on Days 1-5 every 3 weeks, or 8 mg/m2 i.v. bolus on Days 1-5 for patients who had prior radiation to greater than 30% of their bone marrow; or cisplatin 60 mg/m2 i.v. on Day 1 and etoposide 120 mg/m2 i.v. on Days 1-3 every 4 weeks. Patients were evaluated before each cycle for tumor response, toxicity, and quality-of-life measurements.
One hundred thirty-six patients were entered on the study, and 118 were evaluable for toxicity and response. The response rates were 16%, 5%, and 5% in patients treated with cisplatin and etoposide, echinomycin, and trimetrexate, respectively. There were no complete responses. The median survival was 37.9, 24.3, and 28.0 weeks for patients who received cisplatin and etoposide, echinomycin, and trimetrexate, respectively. Although cisplatin and etoposide appeared to give better therapeutic results, the response rate or survival did not reach statistical significance. This may have been due to inadequate sample size. Neither did quality-of-life measurement show any significant differences among treatments.
Echinomycin and trimetrexate had minimal antitumor activity in patients with metastatic NSCLC: Response rate and survival remained poor in all three treatment arms. Patients should be encouraged to participate in clinical trials so that more effective therapy can be identified.
转移性非小细胞肺癌(NSCLC)患者通常预后较差。含顺铂的化疗方案常用于缓解症状。棘霉素是一种有效的双链DNA双功能嵌入剂;三甲曲沙是甲氨蝶呤的一种新衍生物,在体外对耐甲氨蝶呤的肿瘤细胞具有活性。
东部肿瘤协作组进行了一项随机II期研究。符合条件的患者被分配接受以下治疗:棘霉素1200微克/平方米,静脉输注30 - 60分钟,每周一次,共4周,每6周重复一次;三甲曲沙12毫克/平方米,静脉推注,每3周的第1 - 5天给药,对于骨髓照射超过30%的患者,每3周的第1 - 5天静脉推注8毫克/平方米;或顺铂60毫克/平方米,静脉滴注,第1天给药,依托泊苷120毫克/平方米,静脉滴注,第1 - 3天给药,每4周重复一次。在每个周期前对患者进行肿瘤反应、毒性和生活质量评估。
136例患者进入该研究,118例可评估毒性和反应。接受顺铂和依托泊苷、棘霉素、三甲曲沙治疗的患者的缓解率分别为16%、5%和5%。无完全缓解病例。接受顺铂和依托泊苷、棘霉素、三甲曲沙治疗的患者的中位生存期分别为37.9周、24.3周和28.0周。虽然顺铂和依托泊苷似乎产生了更好的治疗效果,但缓解率或生存期未达到统计学显著性。这可能是由于样本量不足。生活质量评估在各治疗组之间也未显示出任何显著差异。
棘霉素和三甲曲沙对转移性NSCLC患者的抗肿瘤活性极小:所有三个治疗组的缓解率和生存期仍然较差。应鼓励患者参加临床试验,以便确定更有效的治疗方法。