Rosine Guimbaud, Centre Hospitalier Universitaire Toulouse, Toulouse; Christophe Louvet, Institut Mutualiste Montsouris; Thierry André, Hôpital Saint Antoine; Jean-Marc Gornet, Centre Hospitalier Universitaire Saint Louis (Assistance Publique-Hôpitaux de Paris); Pascal Hammel, Hôpital Beaujon; Philippe Rougier, Hôpital Européen Georges Pompidou, Paris; Pauline Ries, Institut Paoli Calmettes, Marseille; Marc Ychou, Institut Régional du Cancer Val d'Aurelle, Montpellier; Emilie Maillard, Fédération Francophone de Cancérologie Digestive; Laurent Bedenne, Centre Hospitalier Universitaire, Dijon; Thomas Aparicio, Hôpital Avicenne, Bobigny; Suzanne Nguyen, Hôpital Général, Beauvais; Ahmed Azzedine, Hôpital Général, Montélimard; Pierre-Luc Etienne, Clinique Armoricaine, Saint-Brieuc; Eveline Boucher, Centre Eugène Marquis, Rennes; Christine Rebischung, Hôpital A. Michallon, Grenoble; Olivier Bouché, Centre Hospitalier Universitaire Robert Debré, Reims, France.
J Clin Oncol. 2014 Nov 1;32(31):3520-6. doi: 10.1200/JCO.2013.54.1011. Epub 2014 Oct 6.
To compare epirubicin, cisplatin, and capecitabine (ECX) with fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatments in patients with advanced gastric or esophagogastric junction (EGJ) adenocarcinoma.
This open, randomized, phase III study was carried out in 71 centers. Patients with locally advanced or metastatic gastric or EGJ cancer were randomly assigned to receive either ECX as first-line treatment (ECX arm) or FOLFIRI (FOLFIRI arm). Second-line treatment was predefined (FOLFIRI for the ECX arm and ECX for the FOLFIRI arm). The primary criterion was time-to-treatment failure (TTF) of the first-line therapy. Secondary criteria were progression-free survival (PFS), overall survival (OS), toxicity, and quality of life.
In all, 416 patients were included (median age, 61.4 years; 74% male). After a median follow-up of 31 months, median TTF was significantly longer with FOLFIRI than with ECX (5.1 v 4.2 months; P = .008). There was no significant difference between the two groups in median PFS (5.3 v 5.8 months; P = .96), median OS (9.5 v 9.7 months; P = .95), or response rate (39.2% v 37.8%). First-line FOLFIRI was better tolerated (overall rate of grade 3 to 4 toxicity, 69% v 84%; P < .001; hematologic adverse events [AEs], 38% v 64.5%; P < .001; nonhematologic AEs: 53% v 53.5%; P = .81).
FOLFIRI as first-line treatment for advanced gastric and EGJ cancer demonstrated significantly better TTF than did ECX. Other outcome results indicate that FOLFIRI is an acceptable first-line regimen in this setting and should be explored as a backbone regimen for targeted agents.
比较表柔比星、顺铂和卡培他滨(ECX)与氟尿嘧啶、亚叶酸钙和伊立替康(FOLFIRI)作为晚期胃或胃食管交界(EGJ)腺癌患者的一线治疗。
这项开放、随机、III 期研究在 71 个中心进行。局部晚期或转移性胃或 EGJ 癌患者被随机分配接受一线治疗 ECX(ECX 组)或 FOLFIRI(FOLFIRI 组)。二线治疗是预先设定的(ECX 组的 FOLFIRI 和 FOLFIRI 组的 ECX)。主要标准是一线治疗的治疗失败时间(TTF)。次要标准是无进展生存期(PFS)、总生存期(OS)、毒性和生活质量。
共纳入 416 例患者(中位年龄 61.4 岁;74%为男性)。中位随访 31 个月后,FOLFIRI 的 TTF 明显长于 ECX(5.1 与 4.2 个月;P =.008)。两组中位 PFS(5.3 与 5.8 个月;P =.96)、中位 OS(9.5 与 9.7 个月;P =.95)或缓解率(39.2%与 37.8%)无显著差异。一线 FOLFIRI 耐受性更好(总 3-4 级毒性发生率,69%与 84%;P <.001;血液学不良事件[AE],38%与 64.5%;P <.001;非血液学 AE:53%与 53.5%;P =.81)。
FOLFIRI 作为晚期胃和 EGJ 癌的一线治疗,TTF 明显优于 ECX。其他结果表明,FOLFIRI 是该治疗环境下可接受的一线方案,应作为靶向药物的骨干方案进行探索。