Cancer Res Treat.  2023 Apr;55(2):684-692. 10.4143/crt.2022.1434.

Current Treatment Patterns and the Role of Upfront Autologous Stem Cell Transplantation in Patients with Peripheral T-Cell Lymphoma: A Korean Nationwide, Multicenter Prospective Registry Study (CISL 1404)

Affiliations
  • 1Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 2Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
  • 3Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
  • 4Department of Medicine, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea
  • 5Department of Internal Medicine, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, Jinju, Korea
  • 6Department of Internal Medicine, Jeonbuk National University Hospital, Jeonju, Korea
  • 7Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea
  • 8Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea
  • 9Department of Internal Medicine, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul, Korea
  • 10Department of Internal Medicine, Chung-Ang University Hospital, Seoul, Korea
  • 11Department of Internal Medicine, Gachon University of Gil Medical Center, Gachon University College of Medicine, Incheon, Korea
  • 12Department of Internal Medicine, Inje University Busan Paik Hospital, Busan, Korea
  • 13Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea
  • 14Department of Hematology and Oncology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea
  • 15Center for Hematologic Malignancies, National Cancer Center, Goyang, Korea
  • 16Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea
  • 17Department of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea
  • 18Department of Internal Medicine, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Korea
  • 19Department of Internal Medicine, Inje University Sanggye Paik Hospital, Seoul, Korea
  • 20Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea

Abstract

Purpose
We conducted a nationwide, multicenter, prospective registry study for newly diagnosed patients with peripheral T-cell lymphoma (PTCL) to better define the clinical characteristics, treatment patterns, survival outcomes, and the role of upfront autologous stem cell transplantation (ASCT) in these patients.
Materials and Methods
Patients with PTCL receiving chemotherapy with curative intent were registered and prospectively monitored. All patients were pathologically diagnosed with PTCL.
Results
A total of 191 patients with PTCL were enrolled in this prospective registry study. PTCL, not otherwise specified (PTCL-NOS) was the most common pathologic subtype (n=80, 41.9%), followed by angioimmunoblastic T-cell lymphoma (AITL) (n=60, 31.4%). With a median follow-up duration of 3.9 years, the 3-year progression-free survival (PFS) and overall survival (OS) rates were 39.5% and 60.4%, respectively. The role of upfront ASCT was evaluated in patients who were considered transplant-eligible (n=59). ASCT was performed as an upfront consolidative treatment in 32 (54.2%) of these patients. There were no significant differences in PFS and OS between the ASCT and non-ASCT groups for all patients (n=59) and for patients with PTCL-NOS (n=26). However, in patients with AITL, the ASCT group was associated with significantly better PFS than the non-ASCT group, although there was no significant difference in OS.
Conclusion
The current study demonstrated that the survival outcomes with the current treatment options remain poor for patients with PTCL-NOS. Upfront ASCT may provide a survival benefit for patients with AITL, but not PTCL-NOS.

Keyword

Peripheral T-cell lymphoma; Treatment pattern; Autologous stem cell transplantation

Figure

  • Fig. 1 Progression-free survival (A) and overall survival (B) of all patients (n=191). Progression-free survival (C) and overall survival (D) according to the five most common subtypes of PTCL (PTCL-NOS, AITL, ALK+ ALCL, ALK− ALCL, and MEITL) (n=184). AITL, angioimmunoblastic T-cell lymphoma; ALCL, anaplastic large cell lymphoma; ALK, anaplastic lymphoma kinase; MEITL, monomorphic epitheliotropic intestinal T-cell lymphoma; PTCL-NOS, peripheral T-cell lymphoma not otherwise specified.

  • Fig. 2 Progression-free survival (A) and overall survival (B) according to upfront autologous stem cell transplantation (ASCT) in transplant-eligible patients.

  • Fig. 3 Progression-free survival according to upfront autologous stem cell transplantation (ASCT) in patients who achieved complete remission (A) and partial remission (B) from first-line systemic chemotherapy. Progression-free survival according to upfront ASCT in patients with limited-stage disease (C), advanced-stage disease (D), low International Prognostic Index (IPI) score (E) (low or low-intermediate risk group), high IPI score (high-intermediate or high-risk group) (F), low Prognostic Index for peripheral T-cell lymphoma–unspecified (PIT) score (group 1 or 2) (G), high PIT score (group 3 or 4) (H).

  • Fig. 4 Progression-free survival (A) and overall survival (B) according to upfront autologous stem cell transplantation (ASCT) in peripheral T-cell lymphoma not otherwise specified patients. Progression-free survival (C) and overall survival (D) according to upfront ASCT in angioimmunoblastic T-cell lymphoma patients.


Reference

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