Histopathologic Regression and Survival in RAS Wildtype Metastatic Colorectal Cancer Under First-Line Treatment – Subgroup Analysis of the VOLFI Trial (AIO-KRK-0109)

S. Noepel-Duennebacke, H. Juette, C. Lugnier, D. Modest, U. Martens, R. Klaassen-Mielke, V. Heinemann, T. Seufferlein, M. Geissler, A. Tannapfel, A. Reinacher-Schick, I. Tischoff
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引用次数: 1

Abstract

Aim: The VOLFI trial demonstrated an improved objective response rate through the addition of panitumumab to FOLFOXIRI in untreated all-RAS-wildtype mCRCs compared to FOLFOXIRI alone. In this subgroup analysis, we focused on histopathological response as a predictive marker for PFS. Additionally, we analyzed chemotherapy induced steatosis hepatitis (CASH) in both treatment arms. Methods: Histopathological response, CASH, sinusoidal obstructive syndrome, ballooning, steatosis, cholestasis, fibrosis and inflammation were determined in 14 resected liver metastasis. PFS was estimated using Kaplan-Meier method, the logrank test was used for the statistical comparison. The trial is registered with Clinical Trials. gov, NCT01328171. Results: Tissue of 14/18 resected pts. was evaluable. Median age was 57.5 yrs. (32–67), 7 male and 7 females. All primary tumors were located in the left colon. Molecular analysis detected one BRAF V600E mutation and one MSI-H tumor. Median treatment duration until resection were 7 cycles (3 – 12) panitumumab/mFOLFOXIRI and 9.5 cycles (7 - 11) FOLFOXIRI. 7 pts. achieved very good histopathological response corresponding to ≤20% vital tumor cells (panitumumab/ mFOLFOXIRI vs. FOLFOXIRI 2/5) and 7 pts. showed vital tumor cells >20% (panitumumab/mFOLFOXIRI vs. FOLFOXIRI 2/5). A very good histopathological response (residual tumor cells in proportion to the total tumor area ≤20%) showed a trend to an improved PFS in comparison to >20% (median PFS 12.40; 95% CI 6.43-51.22 vs. PFS 9.88; 95% CI 6.17-15.26 months). The severity of CASH was not increased by the addition of panitumumab or longer duration of chemotherapy. Discussion: In this analysis histopathological response seems to correlate with a better PFS after secondary metastasis resection. By analysis of liver toxicity, no relevant difference of CASH were detectable regarding panitumumab/mFOLFOXIRI vs. FOLFOXIRI or the duration of chemotherapy.
一线治疗下RAS野生型转移性结直肠癌的组织病理学退化和生存率——VOLFI试验的亚组分析(AIO-KRK-0109)
目的:VOLFI试验表明,与单独使用FOLFOXIRI相比,在未治疗的all-RAS-wildtype mccrcs中,通过将帕尼单抗加入FOLFOXIRI,客观缓解率有所提高。在这个亚组分析中,我们关注组织病理反应作为PFS的预测指标。此外,我们分析了两个治疗组中化疗诱导的脂肪变性肝炎(CASH)。方法:观察14例肝转移切除患者的组织病理反应、CASH、窦状动脉阻塞综合征、水肿、脂肪变性、胆汁淤积、纤维化和炎症。PFS采用Kaplan-Meier法估计,统计学比较采用logrank检验。该试验已在临床试验中注册。州长,NCT01328171。结果:14/18的组织被切除。可评价的。中位年龄为57.5岁。(32-67),男7名,女7名。所有原发肿瘤均位于左结肠。分子分析检测到1例BRAF V600E突变和1例MSI-H肿瘤。panitumumab/mFOLFOXIRI的中位治疗时间为7个周期(3 - 12),FOLFOXIRI为9.5个周期(7 - 11)。7分。获得了非常好的组织病理学反应,对应于≤20%的重要肿瘤细胞(panitumumab/ mFOLFOXIRI vs FOLFOXIRI 2/5)和7例。显示存活肿瘤细胞>20% (panitumumab/mFOLFOXIRI vs. FOLFOXIRI 2/5)。非常好的组织病理学反应(残余肿瘤细胞占肿瘤总面积的比例≤20%)表明,与>20%相比,PFS有改善的趋势(中位PFS 12.40;95% CI 6.43-51.22, PFS 9.88;95% CI 6.17-15.26个月)。CASH的严重程度不会因帕尼单抗的增加或化疗时间的延长而增加。讨论:在本分析中,组织病理反应似乎与继发性转移切除后较好的PFS相关。通过肝毒性分析,在panitumumab/mFOLFOXIRI与FOLFOXIRI或化疗时间方面,没有检测到CASH的相关差异。
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