Initial Panitumumab Plus Fluorouracil, Leucovorin, and Oxaliplatin or Plus Fluorouracil and Leucovorin in Elderly Patients With RAS and BRAF Wild-Type Metastatic Colorectal Cancer: The PANDA Trial by the GONO Foundation.

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2023-12-01 Epub Date: 2023-08-03 DOI:10.1200/JCO.23.00506
Sara Lonardi, Cosimo Rasola, Riccardo Lobefaro, Daniele Rossini, Vincenzo Formica, Mario Scartozzi, Giovanni Luca Frassineti, Giorgia Boscolo, Saverio Cinieri, Samantha Di Donato, Nicoletta Pella, Francesca Bergamo, Alessandra Raimondi, Ermenegildo Arnoldi, Lorenzo Antonuzzo, Cristina Granetto, Fable Zustovich, Monica Ronzoni, Silvana Leo, Federica Morano, Fotios Loupakis, Federica Buggin, Vittorina Zagonel, Matteo Fassan, Chiara Cremolini, Luca Boni, Filippo Pietrantonio
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引用次数: 0

Abstract

Purpose: To verify whether both doublet chemotherapy with a modified schedule of fluorouracil, leucovorin, and oxaliplatin (mFOLFOX) and monochemotherapy with fluorouracil plus leucovorin (5-FU + LV) achieve satisfactory efficacy when both regimens are combined with panitumumab (PAN) as initial treatment of elderly patients with RAS/BRAF wild-type metastatic colorectal cancer (mCRC).

Patients and methods: PANDA (ClinicalTrials.gov identifier: NCT02904031) was an open-label, randomized phase II noncomparative trial in previously untreated patients age 70 years and older with unresectable RAS/BRAF wild-type mCRC. Patients were randomly assigned 1:1 to mFOLFOX + PAN (arm A) or 5-FU + LV + PAN (arm B) for up to 12 cycles, followed by PAN maintenance. The primary end point was progression-free survival (PFS). In each arm, assuming a null hypothesis of median PFS time 6 months and target PFS ≥9.65, 90 patients per arm were needed to achieve 90% power and 5% type I error (one-sided Brookmeyer-Crowley test).

Results: Between July 2016 and April 2019, 91 patients were randomly assigned to arm A and 92 to arm B. At a median follow-up of 50.0 months (IQR, 45.6-56.4), median PFS was 9.6 and 9.0 months for arm A and B, respectively (P < .001 in each arm). Overall response rate was 69% and 52%, whereas median overall survival was 23.5 and 22.0 months in arm A and B, respectively. The overall rate of grade >2 chemotherapy-related adverse events was 60% and 37%, respectively. Baseline G8 and Chemotherapy Risk Assessment Scale for High-Age Patients scores were prognostic, but they were not associated with efficacy and safety of the two arms.

Conclusion: Both mFOLFOX and 5-FU + LV + PAN are reasonable options as initial therapy of elderly patients with RAS/BRAF wild-type mCRC. 5-FU + LV + PAN is associated with a better safety profile.

帕尼单抗联合氟尿嘧啶、亚叶酸钙和奥沙利铂或联合氟尿嘧啶和亚叶酸钙治疗RAS和BRAF野生型转移性结直肠癌的老年患者:GONO基金会的PANDA试验
目的:验证改良方案的氟尿嘧啶+亚叶酸钙+奥沙利铂双重化疗(mFOLFOX)和氟尿嘧啶+亚叶酸钙(5-FU + LV)单化疗(5-FU + LV)联合帕尼单抗(PAN)作为老年RAS/BRAF野生型转移性结直肠癌(mCRC)患者的初始治疗是否能获得满意的疗效。患者和方法:PANDA (ClinicalTrials.gov标识符:NCT02904031)是一项开放标签,随机II期非比较试验,在70岁及以上未经治疗的不可切除RAS/BRAF野生型mCRC患者中进行。患者按1:1的比例随机分配到mFOLFOX + PAN (A组)或5-FU + LV + PAN (B组),持续12个周期,随后进行PAN维持。主要终点为无进展生存期(PFS)。在每组中,假设中位PFS时间≤6个月,目标PFS≥9.65的零假设,每组需要90例患者才能达到90%的有效性和5%的I型误差(单侧Brookmeyer-Crowley检验)。结果:在2016年7月至2019年4月期间,91名患者被随机分配到A组,92名患者被随机分配到B组。中位随访时间为50.0个月(IQR, 45.6-56.4), A组和B组的中位PFS分别为9.6和9.0个月(每组P < 0.001)。总有效率为69%和52%,而A组和B组的中位总生存期分别为23.5个月和22.0个月。2级以上化疗相关不良事件的总发生率分别为60%和37%。基线G8和高龄患者化疗风险评估量表评分具有预后作用,但与两组的疗效和安全性无关。结论:mFOLFOX和5-FU + LV + PAN均是老年RAS/BRAF野生型mCRC患者初始治疗的合理选择。5-FU + LV + PAN具有更好的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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