Park Kwonoh, Lee Hyun Jung, Kim Tae Un, Ryu Hwaseong, Ki Yong Kan, Hong Yun Jeong, Nam Jong Kil
Department of Internal Medicine, Medical Oncology and Hematology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, South Korea.
Department of Internal Medicine, Hanyang University Seoul Hospital, Hanyang University College of Medicine, Seoul, South Korea.
Asia Pac J Clin Oncol. 2023 Dec;19(6):739-746. doi: 10.1111/ajco.13996. Epub 2023 Jul 17.
While previous retrospective or phase II studies in Western populations showed that dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin (ddMVAC) as neoadjuvant chemotherapy (NAC) was beneficial, no studies have been reported in Asian populations. This prospective phase II study aimed to evaluate efficacy and safety of ddMVAC in Korean patients with muscle-invasive bladder cancer (MIBC) or locally advanced urothelial cancer (UC).
Patients with MIBC (cT2-4aN0M0) or locally advanced UC (cTanyN1-3M0) eligible for radical cystectomy (RC) were enrolled prospectively. The participants were treated with four cycles of ddMVAC with pegfilgrastim every 2 weeks. The primary endpoint was pathologic response rate (≤ypT1N0). Secondary endpoints were pathologic complete response (pCR, ypT0N0), relapse-free survival (RFS), overall survival (OS), and safety.
Among 24 patients enrolled between December 2019 and August 2021, 23 were evaluable (52%, cT2-4aN0; 48%, cTanyN1-3). Eighteen patients (78%) completed four cycles of ddMVAC, while remaining five patients experienced early discontinuation. Dose modification (91%) and dose delay (70%) occurred, and the dose intensity of ddMVAC was 79%. Nineteen patients underwent RC and four patients declined. Of 19 patients who underwent RC, eight patients (42%) achieved ≤ypT1N0. With a median follow-up of 22.8 months, the median RFS was 13.5 months (95% CI, not yet evaluable) and the median OS was 28.9 months (95% confidence interval, 19.9-37.9).
Our study showed substantial efficacy and safety of ddMVAC, even in patients with locally advanced UC. The ddMVAC still should be a promising option as NAC in Asian patients with UC.
虽然之前在西方人群中进行的回顾性研究或II期研究表明,剂量密集型甲氨蝶呤、长春花碱、阿霉素和顺铂(ddMVAC)作为新辅助化疗(NAC)是有益的,但亚洲人群中尚未有相关研究报道。这项前瞻性II期研究旨在评估ddMVAC在韩国肌肉浸润性膀胱癌(MIBC)或局部晚期尿路上皮癌(UC)患者中的疗效和安全性。
前瞻性纳入符合根治性膀胱切除术(RC)条件的MIBC(cT2 - 4aN0M0)或局部晚期UC(cTanyN1 - 3M0)患者。参与者每2周接受四个周期的ddMVAC联合培非格司亭治疗。主要终点是病理缓解率(≤ypT1N0)。次要终点是病理完全缓解(pCR,ypT0N0)、无复发生存期(RFS)、总生存期(OS)和安全性。
在2019年12月至2021年8月期间纳入的24例患者中,23例可评估(52%为cT2 - 4aN0;48%为cTanyN1 - 3)。18例患者(78%)完成了四个周期的ddMVAC治疗,其余5例患者提前停药。发生了剂量调整(91%)和剂量延迟(70%),ddMVAC的剂量强度为79%。19例患者接受了RC,4例患者拒绝。在接受RC的19例患者中,8例患者(42%)达到了≤ypT1N0。中位随访22.8个月,中位RFS为13.5个月(95%CI,尚未评估),中位OS为28.9个月(95%置信区间,19.9 - 37.9)。
我们的研究表明,即使在局部晚期UC患者中,ddMVAC也具有显著的疗效和安全性。ddMVAC作为亚洲UC患者的NAC仍然应该是一个有前景的选择。