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Event free survival at 24 months: A new endpoint in diffuse large B-cell lymphoma

医学 美罗华 弥漫性大B细胞淋巴瘤 淋巴瘤 内科学 临床终点 人口 无进展生存期 肿瘤科 外科 总体生存率 临床试验 环境卫生
作者
Blanca Cantos,Juan Cristóbal Sánchez,V. Calvo de Juan,M. Méndez García,C. Maximiano Alonso,D. Callejo,F. Franco,Lourdes Sanz,Aldo López,Beatriz Núñez,M. Provencio Pulla
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:28: v361-v361
标识
DOI:10.1093/annonc/mdx373.016
摘要

Background: The monoclonal antibody rituximab has changed the natural history of Diffuse Large B-cell Lymphoma (DLBCL). Recent data show that patients with DLBCL achieving EFS24 (event-free survival at 24 months) after treatment with immunochemotherapy have a normal life expectancy. We have explored what happens in our patient population. Methods: We reviewed our database of patients with lymphoma treated between 1987 and 2011. We selected DLBCL patients who had received a minimum follow up of 5 years. We included 228 patients in the analysis; 100 had received rituximab based treatment and 128 did not receive any antibody. We studied the pattern of relapse and event-free survival at 12 and 24 months from diagnosis in both populations. Results: Our data show that the pattern of relapse in DLBCL patients has changed in the post-rituximab era. There are fewer relapses (24% versus 33%, p = 0,04) but those who relapse do so earlier: 75% of relapse occur in the first two years and late relapse (after 5 years) are rare (less than 8%) in rituximab treated patients. Patients who achieve EFS12 have a better prognosis than patients who did not achieve it (80% OS 5 years versus 15%, p < 0,001) but patients who achieve EFS24 have a very good prognosis compared to patients who do not achieve EFS24 (p < 0,001), regardless of the treatment received (90% versus 15% OS at 5 years, p < 0,001). Comparing EFS12 and ESF24, ESF24 is a better prognostic tool to determine long term survival. Conclusions: Most of the patients who relapse after immunochemotherapy do so early, probably linked to a different biological behavior of the tumor. Patients who achieve EFS24 have a very good prognosis. We need to perform an accurate follow up with patients in the first 2 years after diagnosis to detect early relapses and focus on studying the molecular biology of these tumours to detect differences in relapsed patients. Follow up after 5 years from diagnosis will detect only a small account of relapses and probably will not impact on survival. Legal entity responsible for the study: Hospital Puerta de Hierro Majadahonda Funding: None Disclosure: All authors have declared no conflicts of interest.

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