Katsurada Naoko, Tachihara Motoko, Hatakeyama Yukihisa, Koyama Kiyoko, Yumura Masako, Kiriu Tatsunori, Dokuni Ryota, Hazama Daisuke, Tokunaga Shuntaro, Tamura Daisuke, Nakata Kyosuke, Yamamoto Masatsugu, Kamiryo Hiroshi, Kobayashi Kazuyuki, Tanaka Yugo, Maniwa Yoshimasa, Nishimura Yoshihiro
Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Division of General Theocratic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Cancer Manag Res. 2020 Feb 3;12:777-782. doi: 10.2147/CMAR.S239647. eCollection 2020.
Adjuvant chemotherapy with cisplatin (CDDP) plus vinorelbine is the standard regimen for the treatment of non-small cell lung cancer (NSCLC). However, CDDP elicits severe toxic effects, including emesis, neurotoxicity, and renal damage; carboplatin (CBDCA) may be a feasible alternative for CDDP-unfit patients. CBDCA plus paclitaxel (PTX) adjuvant chemotherapy showed a survival benefit for patients with stage IB tumors >4 cm in size, while CBDCA plus nanoparticle albumin-bound (nab)-PTX showed greater efficacy and lower neurotoxicity than CBDCA plus PTX in advanced NSCLC. Here, we investigated the feasibility of using CBDCA plus nab-PTX as adjuvant chemotherapy for NSCLC.
Patients with completely resected stage II or III NSCLC, with an Eastern Cooperative Oncology Group performance status of 0-1 and adequate kidney function, received four cycles of postoperative adjuvant chemotherapy with CBDCA (AUC=5 mg/mL/min, on day 1) and nab-PTX (100 mg/m, on days 1, 8, and 15) administered every 4 weeks within 8 weeks after surgery. The study was designed as a prospective, single-center, Phase II study. The primary endpoint was the completion rate of chemotherapy; secondary endpoints were two-year relapse-free survival (RFS) and safety. The expected completion rate was 80%, with a 50% lower limit.
Of 21 enrolled patients, 18 (85.7%) were CDDP-unfit owing to age (≥75 years old [n=11, 52.4%]) or mild renal impairment (n=7, 33.3%). Nineteen of the 21 enrolled patients were assigned to the intervention. The most common grade 3 or 4 adverse events were neutropenia (n=15, 78.9%) and anemia (n=3, 15.8%). The completion rate for the four cycles was 63.2% (95% CI, 38.4-83.7). Two-year RFS was 56.8% (95% CI, 29.7-76.9).
The completion rate for CBDCA plus nab-PTX as adjuvant chemotherapy for CDDP-unfit NSCLC patients did not reach treatment feasibility. Further dose modifications may be required in future studies.
顺铂(CDDP)联合长春瑞滨的辅助化疗是治疗非小细胞肺癌(NSCLC)的标准方案。然而,CDDP会引发严重的毒性反应,包括呕吐、神经毒性和肾损伤;对于不适合使用CDDP的患者,卡铂(CBDCA)可能是一种可行的替代药物。CBDCA联合紫杉醇(PTX)辅助化疗对肿瘤大小>4 cm的IB期患者显示出生存获益,而在晚期NSCLC中,CBDCA联合纳米白蛋白结合型(nab)-PTX比CBDCA联合PTX疗效更佳且神经毒性更低。在此,我们研究了使用CBDCA联合nab-PTX作为NSCLC辅助化疗的可行性。
完全切除的II期或III期NSCLC患者,东部肿瘤协作组体能状态为0 - 1且肾功能正常,在术后8周内每4周接受4个周期的辅助化疗,使用CBDCA(曲线下面积=5 mg/mL/分钟,第1天)和nab-PTX(100 mg/m²,第1、8和15天)。该研究设计为一项前瞻性、单中心的II期研究。主要终点是化疗完成率;次要终点是两年无复发生存率(RFS)和安全性。预期完成率为80%,下限为50%。
在21例入组患者中,18例(8