Outcomes of Adolescent LBCL Patients Treated With Adult Type Chemotherapy: A Single Center Experience.

IF 2.7 4区 医学 Q2 HEMATOLOGY
Riad El Fakih, Taimoor Hussain, Oudai Sahwan, Ghaith Meir, Abdulwahab A Albabtain, Saud Alhayli, Abdullah Alamer, Mhd Anas Alsibai, Shamayel Mohammed, Ali Nasser, Muhammad Shahzad Rauf, Haifa Abdulrahman Alsuwaine, Irfan Maghfoor, Saad Akhtar, Alfadel Alshaibani, Walid Rasheed, Mahmoud Aljurf
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引用次数: 0

Abstract

Background: Lymphoma is the most common cancer in adolescents. Outcome disparities based on the locus of care are increasingly recognized in this age group.

Materials and methods: We report outcomes of LBCL patients between 14 and 21 who were treated at an adult center using adult type chemotherapy.

Results: Sixty-four patients, median age 19 were analyzed. 82.8% were DLBCL, 17.2% were PMBCL; 21.9% stage I, 31.3% stage II, 7.8% stage III, and 39 % stage IV; 18.8% "very good", 62.5% "good" and 18.8% "poor" RIPI score. The median follow-up period was 68.8 months. The 5 years OS was 94.3%, and the 5 years EFS was 78.3%. High RIPI patients had a worse OS. High RIPI, B symptoms, ABC cell of origin and PMBCL had worse EFS.

Conclusion: Pediatric protocol use should be restricted to patients at higher risk of events rather than to all these patients.

青少年LBCL患者接受成人型化疗的结果:单中心经验。
背景:淋巴瘤是青少年中最常见的癌症。在这个年龄组中,基于护理地点的结果差异越来越被认识到。材料和方法:我们报道了14 - 21岁的LBCL患者在成人中心接受成人型化疗的结果。结果:64例患者,中位年龄19岁。DLBCL占82.8%,PMBCL占17.2%;I期21.9%,II期31.3%,III期7.8%,IV期39%;“非常好”占18.8%,“好”占62.5%,“差”占18.8%。中位随访时间为68.8个月。5年OS为94.3%,5年EFS为78.3%。高RIPI患者的OS较差。高RIPI、B症状、ABC细胞源性和PMBCL均加重EFS。结论:儿科方案的使用应仅限于事件风险较高的患者,而不是所有这些患者。
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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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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