Hunt K J, Longton G, Williams M A, Livingston R B
Department of Medicine, University of Washington Medical Center, Seattle, USA.
Chest. 1996 May;109(5):1239-42. doi: 10.1378/chest.109.5.1239.
To determine the efficacy of methotrexate, vinblastine, and platinum chemotherapy in patients with diffuse unresectable malignant mesothelioma.
Patients with histologically confirmed malignant mesothelioma were evaluated for treatment with methotrexate, vinblastine, and cisplatin chemotherapy. If the patient had preexisting hearing loss or neuropathy, or was significantly disabled (eg, spending greater than half of the day in bed or a chair), cisplatin therapy was withheld.
All patients were initially evaluated at the University of Washington Medical Center and received chemotherapy at the University of Washington or in the community.
Between 1990 and 1994, 17 patients received this chemotherapy. Ten patients received cisplatin, 100 mg/m2 IV on day 1, methotrexate, 30 mg/m2 IV on days 8, 15, and 22, and vinblastine, 3 mg/m2 IV on days 8, 15, and 22, in 28-day cycles. One patient had carboplatin substituted for cisplatin due to preexisting hearing loss. Six patients received weekly methotrexate and vinblastine at the same doses without platinum.
Nine of the 17 (53%; 95% confidence interval [CI], 28 to 77%) patients responded, including two complete remissions, two partial remissions, and five regressions. Median time to progression is 8 months. The median survival time for all patients is 14 months. Projected 2-year survival is 35% (95% CI, 12 to 60%).
Although the number of the patients in this study is small, the response rate and projected 2-year survival of 35% are better than those typically reported for unresectable malignant mesothelioma. Further investigation is warranted in confirmatory trials.
确定甲氨蝶呤、长春碱和顺铂化疗对弥漫性不可切除恶性间皮瘤患者的疗效。
对组织学确诊的恶性间皮瘤患者进行甲氨蝶呤、长春碱和顺铂化疗评估。如果患者已有听力丧失或神经病变,或有严重残疾(如每天卧床或坐椅时间超过半天),则不进行顺铂治疗。
所有患者最初在华盛顿大学医学中心接受评估,并在华盛顿大学或社区接受化疗。
1990年至1994年间,17例患者接受了这种化疗。10例患者接受顺铂治疗,第1天静脉注射100mg/m²,甲氨蝶呤在第8、15和22天静脉注射30mg/m²,长春碱在第8、15和22天静脉注射3mg/m²,每28天为一个周期。1例患者因已有听力丧失而用卡铂替代顺铂。6例患者接受每周一次相同剂量的甲氨蝶呤和长春碱治疗,不使用铂类药物。
17例患者中有9例(53%;95%置信区间[CI],28%至77%)有反应,包括2例完全缓解、2例部分缓解和5例病情稳定。疾病进展的中位时间为8个月。所有患者的中位生存时间为14个月。预计2年生存率为35%(95%CI,12%至60%)。
尽管本研究中的患者数量较少,但35%的缓解率和预计2年生存率优于不可切除恶性间皮瘤通常报告的结果。有必要在验证性试验中进行进一步研究。