Assessment of response to total neoadjuvant therapy in carcinoma rectum: A real-world prospective observational study from eastern India.

IF 1.3
Priyanka Mukherjee, Sandip K Barik, Saroj K D Majumdar, Deepak K Das, Mathan K Ramasubbu, Sk S Ahmed, Dillip K Muduly, Prakash K Sasmal, Tushar S Mishra, Bramhadatta Pattnaik, Tanmay Dutta, Sunita Gupta, Sovan S Dhar, Ashutosh Pattanaik, Bikash R Mahapatra, Avinash Badajena, Minakshi Mishra, Satyabrata Kanungo, K M Nehla Haroon, U Poornima Devi, Anupam Muraleedharan, Ankur Mahajan, Shaha S Abdulla, Arnab Sarkar, Dillip K Parida
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Abstract

Background: Preoperative chemoradiotherapy and subsequent surgery is the standard of care for locally advanced rectal cancer. This has resulted in good local control, but without a significant survival benefit. Multiple randomised trials have utilised total neoadjuvant therapy (TNT) to improve survival outcomes. However, clinical experience in India is limited.

Methods: Patients with cT3/4 or N + rectal adenocarcinoma with ECOG 0-1 were included. Treatment course comprised Short-course radiotherapy (25 Gy in 5 fractions over 1 week), followed by 6 cycles of chemotherapy (Inj. oxaliplatin 130 mg/m2 on D1 and Tab capecitabine 1000 mg/m2 BID from D1-14, q21 days). Following the completion of neoadjuvant treatment, patients were assessed for surgery. Surgery involved Total Mesorectal Excision.

Results: 32 patients were enrolled. Males comprised 66% of the population, and the median age was 42 years. 75% of patients had distal rectal tumours. 18.8% were signet ring cell carcinoma (SRC). 43.8% of patients had mesorectal fascia involvement and lateral lymph nodes (LLN) were present in 28% patients. All patients completed the full course of TNT. 84.4% patients underwent definitive surgery. Pathological complete response was reported in 37% patients, with R0 resection in 96%. Sphincter preservation could be achieved in 29.2% of distal tumours. The incidence of acute grade 3 or higher adverse events was 40.6%, the most common being diarrhoea (15.6%), followed by anaemia (9.4%). Post-operative complications were seen in 22.2% of patients, the most frequent being delayed wound healing. The incidence of Clavien-Dindo grade IV complications was 3.7%. At a median follow-up of 2 years, OS and PFS were 75% and 59.4%, respectively. Absence of LLN and non-SRC histology was associated with significantly higher PFS and OS.

Conclusion: The TNT protocol we followed was well tolerated in our patient population. Excellent tumour and nodal regression rates were seen. It can be considered a viable alternative to preoperative conventional chemoradiation, particularly in a resource-limited setting. However, this treatment strategy was not optimal for patients with high-risk features such as the presence of LLNs and SRC histology.

评估对直肠癌新辅助治疗的反应:一项来自印度东部的真实世界前瞻性观察研究。
背景:术前放化疗及术后手术是局部晚期直肠癌的标准治疗方法。这导致了良好的局部控制,但没有显著的生存效益。多个随机试验已经使用总新辅助治疗(TNT)来改善生存结果。然而,印度的临床经验有限。方法:纳入ECOG 0-1的cT3/4或N +直肠腺癌患者。疗程包括短期放射治疗(25 Gy,分5次,1周),然后是6个周期的化疗(注射)。D1:奥沙利铂130 mg/m2, BID:卡培他滨1000 mg/m2 (D1-14, q21天)。完成新辅助治疗后,对患者进行手术评估。手术包括全直肠系膜切除术。结果:32例患者入组。男性占人口的66%,年龄中位数为42岁。75%的患者有直肠远端肿瘤。18.8%为印戒细胞癌(SRC)。43.8%的患者有直肠系膜筋膜受累,28%的患者有外侧淋巴结(LLN)。所有患者均完成了TNT的整个疗程。84.4%的患者接受了最终手术。37%的患者病理完全缓解,96%的患者R0切除。29.2%的远端肿瘤可保留括约肌。急性3级及以上不良事件发生率为40.6%,最常见的是腹泻(15.6%),其次是贫血(9.4%)。22.2%的患者出现术后并发症,最常见的是伤口愈合延迟。Clavien-Dindo IV级并发症发生率为3.7%。中位随访2年,OS和PFS分别为75%和59.4%。LLN和非src组织学的缺失与更高的PFS和OS相关。结论:我们所采用的TNT治疗方案在患者群体中耐受性良好。良好的肿瘤和淋巴结消退率。它可以被认为是术前常规放化疗的可行替代方案,特别是在资源有限的情况下。然而,对于存在lln和SRC组织学等高风险特征的患者,这种治疗策略并不理想。
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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