Adamus Nicolas, Edeline Julien, Henriques Julie, Fares Nadim, Lecomte Thierry, Turpin Anthony, Vernerey Dewi, Vincens Mathilde, Chanez Brice, Tougeron David, Tournigand Christophe, Assenat Eric, Delaye Matthieu, Manfredi Sylvain, Bouché Olivier, Williet Nicolas, Vienot Angelique, Blaise Lorraine, Mas Léo, Neuzillet Cindy, Boilève Alice, Roth Gaël S
Univ. Grenoble Alpes, Department of Hepato-Gastroenterology and Digestive Oncology, CHU Grenoble Alpes, Grenoble; Association pour l'étude des Cancers et Affections des voies Biliaires (ACABi); GERCOR, Paris, France.
Department of Medical Oncology, Centre Eugène Marquis, Rennes, France and INSERM, Univ Rennes, COSS (Chemistry Oncogenesis Stress Signaling), UMR_S 1242, Rennes, France.
JHEP Rep. 2024 Nov 20;7(2):101279. doi: 10.1016/j.jhepr.2024.101279. eCollection 2025 Feb.
BACKGROUND & AIMS: Selective internal radiation therapy (SIRT) is a promising option for liver-only unresectable intrahepatic cholangiocarcinoma (iCCA). The Real-SIRTCCA study retrospectively assessed the benefit of adding SIRT to chemotherapy in this setting within the French nationwide observational cohort ACABi-GERCOR-PRONOBIL.
Inclusion criteria were advanced iCCA with limited or no extrahepatic disease, treated with first-line gemcitabine plus platinum chemotherapy +/- concurrent SIRT. All patients treated with chemotherapy and concurrent SIRT were included. To ensure groups' similarity, a rigorous selection was applied to the chemo-only group, with exclusion of patients with liver involvement >50% and extrahepatic metastases. The primary outcome was progression-free survival (PFS). Secondary outcomes were overall survival (OS), objective response rate (ORR) and tumor resection rate. Propensity score and inverse probability of treatment weighting (IPTW) propensity approaches were used to address confounding factors between groups.
Between July 2007 and December 2023, 277 patients met the Real-SIRTCCA inclusion criteria, with 88 in the chemo-SIRT group and 189 in chemo-only group. Chemo-SIRT was associated with longer PFS (median = 10.8 5.5 months, hazard ratio [HR] 0.54, 95% CI 0.41-0.71, 0.0001), a trend for longer OS (median = 22.5 15.1 months, HR 0.76, 95% CI 0.57-1.01), higher ORR (58.3% 28.5%, odds ratio [OR] 3.51, 95% CI 2.03-6.09, 0.0001), and resection rate (18.7% . 8.8%, = 0.0279) compared to chemo-alone. After IPTW, the superiority of chemo-SIRT was confirmed with better PFS (HR 0.55, 95% CI 0.45-0.66, 0,0001), OS (HR 0.70, 95% CI 0.58-0.85, = 0.0004), ORR (OR 3.17, 95% CI 2.18-4.49, 0.0001) and resection rate (OR 2.94, 95% CI 1.71-5.03, 0.0001).
Adding SIRT to first-line chemotherapy significantly improved survival outcomes, ORR, and secondary tumor resection rates in locally advanced iCCA. Prospective randomized data are needed to confirm these results.
Herein, we report the results of the Real-SIRTCCA study, comparing the efficacy of the gemcitabine-platinum systemic first-line chemotherapy with or without selective internal radiation therapy (SIRT) in 277 patients with locally advanced intrahepatic cholangiocarcinoma within the cohort ACABi-PRONOBIL. An improvement of progression-free survival, overall survival, tumor response and secondary surgical resection rate was observed in favor of chemo-SIRT, before adjustment and after inverse probability of treatment weighting propensity score analyses. Even though prospective randomized data would be needed to confirm these findings, we believe that this study constitutes new evidence of the potential benefit of combining SIRT with chemotherapy. The safety and efficacy of this strategy whether as a bridge to intent-to-cure strategies or in a palliative setting, should encourage its adoption in a larger panel of clinical centers, or at very least, prompt clinicians to refer their patients to centers where SIRT is performed.
NCT04935853.
选择性内照射治疗(SIRT)是仅局限于肝脏的不可切除肝内胆管癌(iCCA)的一种有前景的治疗选择。Real-SIRTCCA研究在法国全国性观察队列ACABi-GERCOR-PRONOBIL中,回顾性评估了在这种情况下SIRT联合化疗的益处。
纳入标准为晚期iCCA且肝外疾病局限或无肝外疾病,接受一线吉西他滨联合铂类化疗±同期SIRT治疗。纳入所有接受化疗及同期SIRT治疗的患者。为确保两组相似,对单纯化疗组进行了严格筛选,排除肝脏受累>50%及有肝外转移的患者。主要结局为无进展生存期(PFS)。次要结局为总生存期(OS)、客观缓解率(ORR)和肿瘤切除率。采用倾向评分和治疗权重逆概率(IPTW)倾向方法处理组间混杂因素。
2007年7月至2023年12月期间,277例患者符合Real-SIRTCCA纳入标准,其中化疗联合SIRT组88例,单纯化疗组189例。化疗联合SIRT组的PFS更长(中位值=10.8对5.5个月,风险比[HR]0.54,95%置信区间0.41-0.71,P<0.0001),OS有延长趋势(中位值=22.5对15.1个月,HR 0.76,95%置信区间0.57-1.01),ORR更高(58.3%对28.5%,优势比[OR]3.51,95%置信区间2.03-6.09,P<0.0001),与单纯化疗相比,肿瘤切除率也更高(18.7%对8.8%,P=0.0279)。IPTW后,化疗联合SIRT的优势得到确认,PFS更好(HR 0.55,95%置信区间0.45-0.66,P<0. 0001),OS(HR 0.70,95%置信区间0.58-0.85,P=0.0004),ORR(OR 3.17,95%置信区间2.18-4.49,P<0.0001)和肿瘤切除率(OR 2.94,95%置信区间1.71-5.03,P<0.0001)。
一线化疗联合SIRT可显著改善局部晚期iCCA的生存结局、ORR和二次肿瘤切除率。需要前瞻性随机数据来证实这些结果。
在此,我们报告了Real-SIRTCCA研究的结果,比较了吉西他滨-铂类一线全身化疗联合或不联合选择性内照射治疗(SIRT)在ACABi-PRONOBIL队列中277例局部晚期肝内胆管癌患者中的疗效。在调整前和治疗权重逆概率倾向评分分析后,均观察到化疗联合SIRT组的无进展生存期延长、总生存期延长、肿瘤缓解和二次手术切除率提高。尽管需要前瞻性随机数据来证实这些发现,但我们认为本研究构成了SIRT联合化疗潜在益处的确凿新证据。这种策略无论是作为根治性治疗策略的桥梁还是在姑息治疗环境中的安全性和有效性,都应促使其在更多临床中心被采用,或者至少促使临床医生将患者转诊至开展SIRT治疗的中心。
NCT04935853。