Cascinu Stefano, Rosati Gerardo, Nasti Guglielmo, Lonardi Sara, Zaniboni Alberto, Marchetti Paolo, Leone Francesco, Bilancia Domenico, Iaffaioli Rosario Vincenzo, Zagonel Vittorina, Giordano Monica, Corsi Domenico C, Ferraú Francesco, Labianca Roberto, Ronzoni Monica, Scartozzi Mario, Galli Francesca
Modena Cancer Center, Department of Oncology/Hematology, Università di Modena e Reggio Emilia, Italy.
Medical Oncology, S. Carlo Hospital, Potenza, Italy.
Eur J Cancer. 2017 Sep;83:106-115. doi: 10.1016/j.ejca.2017.06.029. Epub 2017 Jul 20.
The optimal treatment strategy for RAS wild type (WT) mCRC is controversial. Our phase III study investigated the effect of introducing earlier (second-line) or later (third-line) cetuximab in patients progressed after FOLFIRI/bevacizumab first-line.
mCRC patients progressing after FOLFIRI/bevacizumab first-line were randomised to receive second-line irinotecan/cetuximab followed by third-line FOLFOX-4 (arm A) or the reverse sequence (arm B). Primary end-point was progression-free survival (PFS).
About 54 and 56 patients were randomised in arm A and in arm B, respectively. After a median follow-up of 37.5 months, 100 PFS events were recorded. Median PFS was 9.9 months in arm A and 11.3 months in arm B (Hazard ratio [HR] 1.04, 95% confidence interval [CI]: 0.69-1.56, p = 0.854), while median overall survival was 12.3 months in arm A and 18.6 months in arm B (HR 0.84, 95% CI: 0.55-1.28; p = 0.411). No overall difference in side-effects were observed between the two treatment arms.
This trial did not meet the primary end-point (PFS). Like other preclinical and clinical evidences, our study seems to suggest a reduced activity of cetuximab after a first-line bevacizumab-based therapy.
RAS野生型(WT)转移性结直肠癌(mCRC)的最佳治疗策略存在争议。我们的III期研究调查了在一线FOLFIRI/贝伐单抗治疗后进展的患者中,早期(二线)或晚期(三线)引入西妥昔单抗的效果。
一线FOLFIRI/贝伐单抗治疗后进展的mCRC患者被随机分为两组,一组接受二线伊立替康/西妥昔单抗治疗,随后接受三线FOLFOX-4治疗(A组),另一组接受相反顺序的治疗(B组)。主要终点是无进展生存期(PFS)。
A组和B组分别随机入组约54例和56例患者。中位随访37.5个月后,记录到100例PFS事件。A组的中位PFS为9.9个月,B组为11.3个月(风险比[HR]1.04,95%置信区间[CI]:0.69-1.56,p = 0.854),而A组的中位总生存期为12.3个月,B组为18.6个月(HR 0.84,95%CI:0.55-1.28;p = 0.411)。两个治疗组之间未观察到副作用的总体差异。
该试验未达到主要终点(PFS)。与其他临床前和临床证据一样,我们的研究似乎表明,在一线基于贝伐单抗的治疗后,西妥昔单抗的活性降低。