Sclafani Francesco, Corrò Claudia, Koessler Thibaud
Department of Medical Oncology, Institut Jules Bordet, Rue Meylemeersch 90, 1070 Anderlecht, Belgium.
Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, Belgium.
Cancers (Basel). 2021 Dec 18;13(24):6361. doi: 10.3390/cancers13246361.
Recently, two large, randomised phase III clinical trials of total neoadjuvant therapy (TNT) in locally advanced rectal cancer were published (RAPIDO and PRODIGE 23). These two trials compared short-course radiotherapy (SCRT) followed by chemotherapy with standard chemoradiotherapy (CRT) and chemotherapy followed by CRT with standard CRT, respectively. They showed improvement in some of the outcomes such as distant recurrence and pathological complete response (pCR). No improvement, however, was observed in local disease control or the de-escalation of surgical procedures. Although it seems lawful to integrate TNT within the treatment algorithm of localised stage II and III rectal cancer, many questions remain unanswered, including which are the optimal criteria to identify patients who are most likely to benefit from this intensive treatment. Instead of providing a sterile summary of trial results, we put these in perspective in a pros and cons manner. Moreover, we discuss some biological aspects of rectal cancer, which may provide some insights into the current decision-making process, and represent the basis for the future development of alternative, more effective treatment strategies.
最近,两项关于局部晚期直肠癌全新辅助治疗(TNT)的大型随机III期临床试验(RAPIDO和PRODIGE 23)发表了。这两项试验分别比较了短程放疗(SCRT)后化疗与标准放化疗(CRT),以及化疗后CRT与标准CRT。它们显示出在一些结局方面有所改善,如远处复发和病理完全缓解(pCR)。然而,在局部疾病控制或手术程序的降期方面未观察到改善。尽管将TNT纳入局部II期和III期直肠癌的治疗方案似乎是合理的,但许多问题仍未得到解答,包括哪些是识别最可能从这种强化治疗中获益的患者的最佳标准。我们并非提供对试验结果的生硬总结,而是以利弊的方式对这些结果进行审视。此外,我们讨论了直肠癌的一些生物学方面,这可能为当前的决策过程提供一些见解,并为未来开发替代的、更有效的治疗策略奠定基础。