Department of Medical Oncology, AC Camargo Cancer Center, Sao Paulo, Brazil.
Department of Medical Oncology, AC Camargo Cancer Center, Sao Paulo, Brazil.
Clin Colorectal Cancer. 2017 Dec;16(4):316-323. doi: 10.1016/j.clcc.2017.03.002. Epub 2017 Mar 16.
Treatment of metastatic colorectal adenocarcinoma (mCRC) has evolved, and survival is over 30 months in contemporary trials. Nevertheless, there is a paucity of effective regimes after the first or second-line treatment. Thus, reexposure to previously used drugs has become a treatment strategy for some patients. We aimed to evaluate the efficacy of retreatment with an oxaliplatin-containing regimen in mCRC and correlate this with clinicopathologic features.
We retrospectively analyzed 83 patients with mCRC who underwent reexposure to oxaliplatin (REOX). REOX was defined as a second trial of an oxaliplatin-containing regimen after a previous failure. Primary endpoint was time to treatment failure (TTF).
The median age was 53.5 years, and the female/male ratio was 51.8%/48.2%. The site of the primary tumor was colon (67.5%) and rectal (32.5%). KRAS was mutated in 39.8%. Liver-limited metastasis was found in 19.3% of patients. The main regimen was 5-fluorouracil, levoleucovorin, and oxaliplatin (mFOLFOX6) (84.3%). Bevacizumab and cetuximab were used in 42.2% and 6% of patients, respectively. REOX was used in the third and fourth lines in 48.2% and 25.3% of patients, respectively. The median TTF after REOX was 6.04 months. Overall survival (OS) was 10.04 months. Disease control (complete response + partial response + stable disease) was observed in 56.6%, whereas 42.2% had progressive disease. Partial response + complete response to previous oxaliplatin was predictive of prolonged OS. Patients who attained disease control had better median OS compared with those with progressive disease (14.5 vs. 6.24 months; P < .0001).
In the setting of heavily pretreated patients with mCRC, REOX was an effective treatment, with mTTF of 6.04 months in our cohort. Selection of patients with the longest time since previous oxaliplatin can translate in better outcome. Further studies should be conducted to confirm our data.
转移性结直肠癌(mCRC)的治疗已经发展,在当代试验中,生存时间超过 30 个月。然而,在一线或二线治疗后,有效的治疗方案仍然有限。因此,重新使用以前使用过的药物已成为一些患者的治疗策略。我们旨在评估 mCRC 患者再次使用含奥沙利铂方案的疗效,并将其与临床病理特征相关联。
我们回顾性分析了 83 例接受奥沙利铂(REOX)再暴露治疗的 mCRC 患者。REOX 定义为先前失败后再次使用含奥沙利铂方案的第二次试验。主要终点是治疗失败时间(TTF)。
中位年龄为 53.5 岁,女性/男性比例为 51.8%/48.2%。原发肿瘤部位为结肠(67.5%)和直肠(32.5%)。KRAS 突变率为 39.8%。肝转移局限于 19.3%的患者。主要方案为 5-氟尿嘧啶、左亚叶酸钙和奥沙利铂(mFOLFOX6)(84.3%)。贝伐单抗和西妥昔单抗分别在 42.2%和 6%的患者中使用。REOX 在 48.2%和 25.3%的患者中分别用于三线和四线治疗。REOX 后的中位 TTF 为 6.04 个月。总生存期(OS)为 10.04 个月。观察到疾病控制(完全缓解+部分缓解+稳定疾病)为 56.6%,而 42.2%的患者疾病进展。对先前奥沙利铂有部分缓解+完全缓解的患者 OS 延长。与疾病进展的患者相比,达到疾病控制的患者中位 OS 更好(14.5 与 6.24 个月;P<0.0001)。
在 mCRC 患者进行大量预处理的情况下,REOX 是一种有效的治疗方法,本队列 mTTF 为 6.04 个月。选择上次使用奥沙利铂后时间最长的患者可以获得更好的结果。应进行进一步的研究来证实我们的数据。