Prognostic Index for Acute- and Lymphoma-Type Adult T-Cell Leukemia/Lymphoma

Author:

Katsuya Hiroo1,Yamanaka Takeharu1,Ishitsuka Kenji1,Utsunomiya Atae1,Sasaki Hidenori1,Hanada Shuichi1,Eto Tetsuya1,Moriuchi Yukiyoshi1,Saburi Yoshio1,Miyahara Masaharu1,Sueoka Eisaburo1,Uike Naokuni1,Yoshida Shinichiro1,Yamashita Kiyoshi1,Tsukasaki Kunihiro1,Suzushima Hitoshi1,Ohno Yuju1,Matsuoka Hitoshi1,Jo Tatsuro1,Suzumiya Junji1,Tamura Kazuo1

Affiliation:

1. Hiroo Katsuya, Kenji Ishitsuka, Hidenori Sasaki, and Kazuo Tamura, Fukuoka University; Tetsuya Eto, Hamanomachi Hospital; Naokuni Uike, National Kyushu Cancer Center, Fukuoka; Takeharu Yamanaka, National Cancer Center Hospital East; Atae Utsunomiya, Imamura Bun-in Hospital, Kagoshima; Shuichi Hanada, National Hospital Organization Kagoshima Medical Center, Kagoshima; Yukiyoshi Moriuchi, Sasebo City General Hospital, Sasebo; Yoshio Saburi, Oita Prefectural Hospital, Oita; Masaharu Miyahara, Karatsu Red...

Abstract

Purpose The prognosis of acute- and lymphoma-type adult T-cell leukemia/lymphoma (ATL) is poor, but there is marked diversity in survival outcomes. The aim of this study was to develop a prognostic index (PI) for acute- and lymphoma-type ATL (ATL-PI). Patients and Methods In a retrospective review, data from 807 patients newly diagnosed with acute- and lymphoma-type ATL between January 2000 and May 2009 were evaluated. We randomly divided subjects into training (n = 404) and validation (n = 403) samples, and developed a PI using a multivariable fractional polynomial model. Results Median overall survival time (MST) for the 807 patients was 7.7 months. The Ann Arbor stage (I and II v III and IV), performance status (0 to 1 v 2 to 4), and three continuous variables (age, serum albumin, and soluble interleukin-2 receptor [sIL-2R]) were identified as independent prognostic factors in the training sample. Using these variables, a prognostic model was devised to identify different levels of risk. In the validation sample, MSTs were 3.6, 7.3, and 16.2 months for patients at high, intermediate, and low risk, respectively (P < .001; χ2 = 89.7, 2 df; log-rank test). We also simplified the original ATL-PI according to dichotomizing age at 70 years, serum albumin at 3.5 g/dL, and sIL-2R at 20,000 U/mL and developed an easily calculable PI with prognostic discrimination power (P < .001; χ2 = 74.2, 2 df; log-rank test). Conclusion The ATL-PI is a promising new tool for identifying patients with acute- and lymphoma-type ATL at different risks.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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