Low Survival Due to Higher Risk of Relapse and Nonrelapse Mortality After Allogeneic HSCT in ATL Compared with AML and ALL.

IF 3.6 3区 医学 Q2 HEMATOLOGY
Shohei Tomori, Satoko Morishima, Koji Kato, Hideki Nakasone, Nobuaki Nakano, Tetsuya Eto, Toshiro Kawakita, Youko Suehiro, Yasuhiko Miyazaki, Naoyuki Uchida, Yasushi Sawayama, Yasuo Mori, Hirohisa Nakamae, Koji Nagafuji, Yasufumi Uehara, Noriko Doki, Junya Kanda, Takahiro Fukuda, Yoshiko Atsuta, Makoto Yoshimitsu
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Abstract

Background: Patients with adult T-cell leukemia/lymphoma (ATL) are considered to have worse outcomes after allogeneic hematopoietic stem cell transplantation (allo-HSCT) than patients with other hematological malignancies, owing to high risk of relapse and immunocompromised status. However, no studies have compared transplant outcomes between patients with ATL and those with other hematological malignancies using a large-scale database.

Objectives: To compare transplant outcomes between patients with ATL and those with other leukemias and to identify factors contributing to worse transplant outcomes in ATL patients.

Study design: Using Japanese registry data, we retrospectively compared transplant outcomes between patients with ATL and those with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). As ATL often develops in patients in their 60s or older, patients with ATL, AML, or ALL aged ≥50 years were included in order to compare patients in the same age group. A total of 7764 patients (ATL, n = 1151; AML, n = 5393; ALL, n = 1220) who underwent their first allo-HSCT between January 1, 2006 and December 31, 2017 were included in this study.

Results: Compared with AML, ATL showed significantly worse overall survival (OS) (hazard ratio [HR], 1.24; 95% confidence interval [CI], 1.14 to 1.34; P < .001) and higher risk of relapse (HR, 1.33; 95% CI, 1.2 to 1.47; P < .001), while there were no significant differences between AML and ALL. Among patients in complete remission (CR) at transplantation, ATL showed worse OS (HR, 1.30; 95% CI, 1.08 to 1.56; P = .006), higher risk of relapse (HR, 1.78; 95% CI, 1.48 to 2.14; P < .001), and higher risk of nonrelapse mortality (NRM) (HR, 1.38; 95% CI, 1.14 to 1.33; P = .001) in comparison with AML, whereas there were no significant differences between AML and ALL.

Conclusion: We found that ATL patients have poor transplant outcomes compared with AML or ALL patients. In ATL patients, survival is poor, relapse is more frequent, and NRM is significantly higher, especially in cases of CR. These findings suggest that prevention of relapse and transplant-related complications is important for successful allo-HSCT in ATL.

与AML和ALL相比,同种异体造血干细胞移植后ATL患者的复发和非复发死亡率风险较高,生存率较低。
背景:成人t细胞白血病/淋巴瘤(ATL)患者接受同种异体造血干细胞移植(allogeneic hematopoietic stem cell transplantation, alloo - hsct)后的预后被认为比其他血液系统恶性肿瘤患者更差,因为其复发风险高且免疫功能低下。然而,没有研究使用大规模数据库比较ATL患者和其他血液系统恶性肿瘤患者的移植结果。目的:比较ATL患者和其他白血病患者的移植结果,并确定导致ATL患者移植结果较差的因素。研究设计:使用日本注册数据,我们回顾性比较了ATL患者与急性髓性白血病(AML)和急性淋巴细胞白血病(ALL)患者的移植结果。由于ATL通常发生在60岁或以上的患者中,为了比较同一年龄组的患者,我们将年龄≥50岁的ATL、AML或ALL患者纳入研究。共7764例患者(ATL, n = 1151;AML, n = 5393;在2006年1月1日至2017年12月31日期间接受首次同种异体造血干细胞移植的ALL患者(n = 1220)被纳入本研究。结果:与AML相比,ATL的总生存期(OS)明显差(风险比[HR], 1.24;95%置信区间[CI], 1.14-1.34;P < 0.001)和更高的复发风险(HR, 1.33;95% ci, 1.2-1.47;P < 0.001),而AML与ALL之间无显著差异。在移植完全缓解(CR)的患者中,ATL表现出更差的OS (HR, 1.30;95% ci, 1.08-1.56;P = 0.006),复发风险较高(HR, 1.78;95% ci, 1.48-2.14;P < 0.001),非复发死亡率(NRM)风险较高(HR, 1.38;95% ci, 1.14-1.33;P = 0.001),而AML与ALL之间无显著差异。结论:我们发现与AML或ALL患者相比,ATL患者的移植预后较差。在ATL患者中,生存率很低,复发更频繁,NRM明显更高,特别是在CR的情况下。这些研究结果表明,预防复发和移植相关并发症对于ATL移植成功至关重要。
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
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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