Lupattelli Marco, Palazzari Elisa, Polesel Jerry, Chiloiro Giuditta, Angelicone Ilaria, Panni Valeria, Caravatta Luciana, Di Biase Saide, Macchia Gabriella, Niespolo Rita Marina, Franco Pierfrancesco, Epifani Valeria, Meldolesi Elisa, de Giacomo Flavia, Lucarelli Marco, Montesi Giampaolo, Mantello Giovanna, Innocente Roberto, Osti Mattia Falchetto, Gambacorta Maria Antonietta, Aristei Cynthia, De Paoli Antonino
Radiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital, 06129 Perugia, Italy.
Radiation Oncology Department, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, 33081 Aviano, Italy.
Cancers (Basel). 2023 Dec 4;15(23):5702. doi: 10.3390/cancers15235702.
Despite the feasibility and promising activity data on intensity-modulated RT and simultaneous integrated boost (IMRT-SIB) dose escalation in preoperative chemoradiation (CRT) for locally advanced rectal cancer (LARC), few data are currently available on long-term outcomes.
A cohort of 288 LARC patients with cT3-T4, cN0-2, cM0 treated with IMRT-SIB and capecitabine from March 2013 to December 2019, followed by a total mesorectal excision (TME) or an organ-preserving strategy, was collected from a prospective database of 10 Italian institutions. A dose of 45 Gy in 25 fractions was prescribed to the tumor and elective nodes, while the SIB dose was prescribed according to the clinical practice of each institution on the gross tumor volume (GTV). Concurrent capecitabine was administered at a dose of 825 mg/m twice daily, 7 days a week. The primary objective of the study was to evaluate long-term outcomes in terms of local control (LC), progression-free survival (PFS) and overall survival (OS). The secondary objective was to confirm the previously reported feasibility, safety and efficacy (pCR, TRG1-2 and downstaging rates) of the treatment in a larger patient population.
All patients received a dose of 45 Gy to the tumor and elective nodes, while the SIB dose ranged from 52.5 Gy to 57.5 Gy (median 55 Gy). Acute gastrointestinal and hematologic toxicity rates of grade 3-4 were 5.7% and 1.8%, respectively. At preoperative restaging, 36 patients (12.5%) with complete or major clinical responses (cCR or mCR) were offered an organ-preserving approach with local excision (29 patients) or a watch and wait strategy (7 patients). The complete pathologic response rate (pCR) in radically operated patients was 25.8%. In addition, 4 TME patients had pT0N1 and 19 LE patients had pT0Nx, corresponding to an overall pT0 rate of 31.3%. Of the 36 patients selected for organ preservation, 7 (19.5%) required the completion of TME due to unfavorable pathologic features after LE or tumor regrowth during W-W resulting in long-term rectal preservation in 29 of 288 (10.1%) of the total patient population. Major postoperative complications occurred in 14.2% of all operated patients. At a median follow-up of 50 months, the 5-year PFS and OS rates were 72.3% (95% CI: 66.3-77.4) and 85.9% (95% CI: 80.2-90.1), respectively. The 5-year local recurrence (LR) rate was 9.2% (95% CI: 6.0-13.2), while the distant metastasis (DM) rate was 21.3% (95% CI: 16.5-26.5). The DM rate was 24.5% in the high-risk subset compared to 16.2% in the low-intermediate risk group ( = 0.062) with similar LR rates (10% and 8%, respectively). On multivariable analysis, cT4 and TRG3-5 were significantly associated with worse PFS, OS and metastasis-free survival.
Preoperative IMRT-SIB with the moderate dose intensification of 52.5-57.5 Gy (median 55 Gy) and the full dose of concurrent capecitabine confirmed to be feasible and effective in our real-life clinical practice. Organ preservation was shown to be feasible in carefully selected, responsive patients. The favorable long-term survival rates highlight the efficacy of this intensified treatment program. The incorporation of IMRT-SIB with a more effective systemic therapy component in high-risk patients could represent a new area of investigational interest.
尽管调强放疗(IMRT)联合同步整合加量(SIB)用于局部晚期直肠癌(LARC)术前放化疗(CRT)时剂量递增具有可行性且活性数据颇具前景,但目前关于长期预后的数据尚少。
从10家意大利机构的前瞻性数据库中收集了288例cT3 - T4、cN0 - 2、cM0的LARC患者,这些患者在2013年3月至2019年12月期间接受了IMRT - SIB联合卡培他滨治疗,随后接受了全直肠系膜切除术(TME)或保器官策略。肿瘤及选择性淋巴结的处方剂量为45 Gy,分25次给予,而SIB剂量根据各机构对大体肿瘤体积(GTV)的临床实践来确定。卡培他滨同步给药剂量为825 mg/m²,每日2次,每周7天。本研究的主要目的是评估局部控制(LC)、无进展生存期(PFS)和总生存期(OS)方面的长期预后。次要目的是在更大的患者群体中证实先前报道的该治疗的可行性、安全性和疗效(pCR、TRG1 - 2及降期率)。
所有患者肿瘤及选择性淋巴结均接受了45 Gy的剂量,而SIB剂量范围为52.5 Gy至57.5 Gy(中位剂量55 Gy)。3 - 4级急性胃肠道和血液学毒性发生率分别为5.7%和1.8%。术前重新分期时,36例(12.5%)有完全或主要临床缓解(cCR或mCR)的患者接受了保器官方法,包括局部切除(29例患者)或观察等待策略(7例患者)。根治性手术患者的完全病理缓解率(pCR)为25.8%。此外,4例TME患者为pT0N1,19例LE患者为pT0Nx,总体pT0率为31.3%。在36例选择保器官的患者中,7例(19.5%)因局部切除后病理特征不佳或观察等待期间肿瘤复发而需要完成TME,最终288例患者中有29例(10.1%)长期保留直肠。所有手术患者中主要术后并发症发生率为14.2%。中位随访50个月时,5年PFS率和OS率分别为72.3%(95%CI:66.3 - 77.4)和85.9%(95%CI:80.2 - 90.1)。5年局部复发(LR)率为9.2%(95%CI:6.0 - 13.2),远处转移(DM)率为21.3%(95%CI:16.5 - 26.5)。高危亚组的DM率为24.5%,而低 - 中危组为16.2%(P = 0.062),LR率相似(分别为10%和8%)。多变量分析显示,cT4和TRG3 - 5与更差的PFS、OS和无转移生存期显著相关。
术前IMRT - SIB联合52.5 - 57.5 Gy(中位剂量55 Gy)的适度剂量强化及全剂量卡培他滨在我们的实际临床实践中被证实是可行且有效的。在精心挑选的有反应的患者中,保器官是可行的。良好的长期生存率凸显了这种强化治疗方案的疗效。在高危患者中,将IMRT - SIB与更有效的全身治疗成分相结合可能代表一个新的研究热点领域。