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Supplementary Material for: Tolerability and Efficacy of Neoadjuvant Chemotherapy with a Tri-Weekly Interval Methotrexate, Doxorubicin, Vinblastine, and Cisplatin Regimen for Patients with Locally Advanced Bladder Cancer

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DataCite Commons2020-08-28 更新2024-07-27 收录
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https://karger.figshare.com/articles/Supplementary_Material_for_Tolerability_and_Efficacy_of_Neoadjuvant_Chemotherapy_with_a_Tri-Weekly_Interval_Methotrexate_Doxorubicin_Vinblastine_and_Cisplatin_Regimen_for_Patients_with_Locally_Advanced_Bladder_Cancer/6743267
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<b><i>Objective:</i></b> Compared with standard treatment, a modified tri-weekly MVAC (methotrexate, doxorubicin, vinblastine, and cisplatin) treatment regimen with a high cisplatin dose intensity shows good efficacy and lower toxicity. Thus, we retrospectively investigated the tolerability and efficacy of a modified tri-weekly MVAC neoadjuvant regimen. <b><i>Methods:</i></b> We analyzed 25 patients with locally advanced bladder cancer medicated by a modified tri-weekly MVAC neoadjuvant regimen that omits treatment on days 15 and 22. The efficacy and tolerability were assessed retrospectively. <b><i>Results:</i></b> The numbers of patients in clinical stages 2, 3, and 4 were 13 (52.0%), 1 (4.0%), and 11 (44.0%), respectively. Surgery could be performed on all patients. Five patients (20.0%) had no cancer remaining in their surgical specimens. Remaining non-muscle-invasive cancer without metastasis was observed in 7 patients (28.0%), and the total downstaging rate was 44.0%. The 5-year overall and relapse-free survival rates were 79.0 and 75.0%, respectively. The overall relative dose intensity was 0.90. Serious hematologic toxicities rated grade 3 or greater were leukopenia in 6 patients (24.0%) and anemia in 1 patient (4.0%). <b><i>Conclusions:</i></b> Sufficient efficacy and tolerability of a modified tri-weekly MVAC neoadjuvant regimen were suggested. Thus, tri-weekly modified MVAC may be an option for neoadjuvant chemotherapy of advanced bladder cancer.

**研究目的:** 相较于标准治疗方案,提升顺铂剂量强度的改良型每三周一次MVAC(甲氨蝶呤、多柔比星、长春碱和顺铂)化疗方案展现出更优异的疗效与更低的毒性。为此,本研究回顾性探讨了该改良型每三周一次MVAC新辅助化疗方案的耐受性与疗效。 **方法:** 本研究回顾性分析了25例局部晚期膀胱癌患者,所有患者均接受了省略第15天与第22天给药的改良型每三周一次MVAC新辅助化疗方案,本研究对该方案的疗效与耐受性进行了回顾性评估。 **结果:** 临床分期为2期、3期、4期的患者分别为13例(52.0%)、1例(4.0%)与11例(44.0%)。所有患者均顺利完成手术。其中5例患者(20.0%)的手术标本中未检出残留癌组织;7例患者(28.0%)检出残留非肌层浸润性癌且无远处转移;整体降期率为44.0%。患者的5年总生存率与无复发生存率分别为79.0%与75.0%。整体相对剂量强度为0.90。≥3级的严重血液学毒性包括6例(24.0%)白细胞减少与1例(4.0%)贫血。 **结论:** 本研究提示改良型每三周一次MVAC新辅助化疗方案具备充足的疗效与良好的耐受性。因此,该每三周一次的改良MVAC方案可作为晚期膀胱癌新辅助化疗的可选方案之一。
提供机构:
Karger Publishers
创建时间:
2018-07-05
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