巩固放化疗可提高局部晚期GBC (LA-GBC)一线化疗(CT)应答者的生存率。

S. Agrawal, Nawed Alam, N. Rastogi, K. Das
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引用次数: 0

摘要

背景:CT是晚期GBC [LA-GBC和转移性GBC (M-GBC)]的标准治疗方法。LA-GBC的CT生存率高于M-GBC。表现良好的CT应答者是否应该给予巩固化疗放疗(cCTRT)以延缓进展和提高生存率?文献中关于这种方法的文献很少。我们介绍了我们在该地区以地方性比例呈现的LA-GBC中使用这种方法的经验。方法:回顾经伦理批准的连续3年(2014-2016)GBC患者的记录。在550名患者中,145名LA-GBC患者接受了根治性治疗。PS良好且对CT有反应(部分和稳定的疾病)但不能切除的患者接受cCTRT治疗。放疗于GB床、门静脉周围、肝总、腹腔、上正中和主动脉旁淋巴结(直至L2椎体),剂量为45-54 Gy,分为25至28份,同时使用卡培他滨@ 1250 mg/m2。根据基于CECT腹部的RECIST标准对治疗反应进行分类。采用Cox-Regression分析计算治疗毒性、OS及影响OS的因素。结果:疾病负担为[T3 (55%), T4 (45%), N1 (30%), N2(70%)]。65%的患者单独行CT, 35%的患者行CT后再行cCTRT。10例患者行根治性手术(CT后6例,cCTRT后3例)。2级毒性发生率为:胃炎(10%)和腹泻(5%)。65%的患者获得部分缓解(PR), 12%的患者获得静止疾病(SD), 10%的患者获得进展疾病(PD), 13%的患者无法评估(NE)[未完成6个周期CT或失去随访]。在中位随访8个月(IQR 5-15个月)时,所有患者的中位OS为9个月,CT组为7个月,cCTRT组为14个月(p=0.04)。中位生存期CR为57个月,PR和SD为12个月,PD为7个月,NE为5个月(p=0.008)。KPS≥80的生存期为10个月,KPS <80的生存期为5个月(p=0.008)。治疗类型和对治疗的反应被保留为影响OS的独立预后因素。结论:在PS良好的应答者中,CT和cCTRT的生存率提高了一倍。这种创新的方法应该在一项随机研究中进行测试。
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Consolidation chemoradiation improves survival in responders to first-line chemotherapy (CT) in locally advanced GBC (LA-GBC).
97 Background: CT is the standard of care in advanced GBC [LA-GBC and metastatic GBC (M-GBC)]. The survival rates with CT are better in LA-GBC than M-GBC. Should responders to CT with good performance status (PS) be offered consolidation chemo-radiation (cCTRT) to delay progression and improve survival? There is scarcity of literature on this approach in the literature. We present our experience with this approach in LA-GBC which presents in endemic proportions in this region. Methods: We reviewed the records of consecutive GBC patients over 3 year period (2014-2016) after ethics approval. Out of 550 patients, 145 were LA-GBC who were treated with radical intent. Patients with good PS and responders to CT (partial and stable disease) but unresectable, were treated with cCTRT. Radiotherapy was given to GB bed, peri-portal, common hepatic, coeliac, superior mesentric and para aortic lymph-nodes (upto L2 vertebra) upto a dose of 45-54 Gy in 25 to 28 fractions along with concurrent capecitabine @ 1250 mg/m2. Response to treatment was categorised according to RECIST criteria based on CECT abdomen. Treatment toxicity, OS and factors affecting OS were computed by Cox-Regression analysis. Results: Burden of disease was [T3 (55%), T4 (45%), N1 (30%), N2 (70%)]. 65% patients underwent CT alone and 35% received CT followed by cCTRT. 10 patients underwent Radical Surgery ( 6 after CT and 3 after cCTRT). The incidence of grade 2 toxicity were: gastritis (10%) and diarrhoea (5%). 65% patients achieved partial response (PR), 12% static disease (SD), 10% progressive disease (PD) and 13% were non-evaluable (NE) [ did not complete 6 cycles CT or lost to follow-up]. At a median follow-up of 8 months (IQR 5-15 months), the median OS was 9 months for all, 7 months with CT and 14 months with cCTRT arm (p=0.04).The median OS was 57 months for CR, 12 months for PR and SD, 7 months for PD and 5 months for NE (p=0.008). OS was 10 months for KPS >80 and 5 months for KPS <80 (p=0.008). Type of treatment and response to treatment were retained as independent prognostic factors affecting OS. Conclusions: CT followed by cCTRT doubles survival in responders with good PS. This innovative approach should be tested in a randomised study.
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期刊介绍: The Journal of Global Oncology (JGO) is an online only, open access journal focused on cancer care, research and care delivery issues unique to countries and settings with limited healthcare resources. JGO aims to provide a home for high-quality literature that fulfills a growing need for content describing the array of challenges health care professionals in resource-constrained settings face. Article types include original reports, review articles, commentaries, correspondence/replies, special articles and editorials.
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