Skip to main content

Table 1 Clinical characteristics of 53 T-MN patients and comparison with other study groups

From: Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea

Characteristic

SNUH (n = 53)

Singhal (n = 129)

SEER (n = 1093)

Nishiyama (n = 13)

Age at diagnosis (years)

Inclusion of pediatric patients*

Yes: 56.5 (1.8–82.4)

No: 60.3 (20.7–82.4)

71.1 (20.7–89.9)

65 (20–97)

65 (24–76)

Age group

    

 < 20

7 (13.2)

0

 

0

 20–39

5 (9.4)

NA

68 (6.2)

4 (30.8)

 40–59

18 (34.0)

NA

317 (29.0)

2 (15.4)

 60–79

20 (37.7)

NA

606 (55.4)

7 (53.8)

 ≥ 80

3 (5.7)

NA

102 (9.3)

0

Sex

    

 Male

28 (52.8)

73 (56.6)

486 (44.5)

NA

 Female

25 (47.2)

56 (43.4)

607 (55.5)

NA

Race

Korean: 51 (96.2)

Others: 2 (3.8)

NA

White: 963 (88.1)

Black: 69 (6.3)

Other: 61 (5.6)

NA

Primary disease

    

 Non-Hodgkin lymphoma

16 (30.2)

49 (40.0)

341 (33.8)

6 (46.2)

  Plasma cell dyscrasia (plasma cell myeloma, etc.)

4 (7.5)

11 (8.5)

52 (5.2)

2 (15.4)

  Chronic lymphocytic leukemia

1 (1.9)

5 (3.9)

31 (3.0)

0

 Breast cancer

8 (15.1)

16 (12.4)

208 (20.6)

0

 Others

7 (13.2)

10 (7.8)

313 (30.6)

3 (23.1)

 Acute myeloid leukemia

5 (9.4)

1 (0.8)

NA

0

 Bone/soft tissue neoplasm

5 (9.4)

3 (2.3)

43 (4.3)

2 (15.4)

 Germ cell tumor

5 (9.4)

1 (0.8)

NA

2 (15.4)

 Colorectal cancer

4 (7.5)

9 (7.0)

NA

0

 Multiple primary tumors

2 (3.8)

6 (4.7)

NA

0

 Acute lymphoblastic leukemia

1 (1.9)

4 (3.1)

36 (3.6)

0

 Sole autoimmune disease

0

13 (10.1)

NA

0

 Hodgkin lymphoma

0

3 (2.3)

30 (2.9)

0

 Prostate cancer

0

14 (10.9)

43 (4.2)

0

Latency (months)

52.0 (12.0–309.7)

NA

NA

12 (4–48)

Duration of past cytotoxic therapy (months)

18.6 (1.2–122.8)

NA

NA

NA

Past cytotoxic therapy

  

Chemotherapy

Yes: 750 (68.6)

No/unknown: 343 (31.4)

 

 Sole chemotherapy

35 (66.0)

59 (45.7)

NA

NA

 Sole radiotherapy

0

28 (21.7)

NA

NA

 Chemotherapy and radiotherapy

18 (34.0)

42 (32.6)

NA

NA

 Alkylating agent

45 (84.9)

NA

NA

12 (92.3)

 Topoisomerase II inhibitor

36 (67.9)

NA

NA

2 (15.4)

 Antimetabolite

9 (17.0)

NA

NA

NA

 Antitubulin agent

25 (47.2)

NA

NA

NA

 Autologous PBSCT

9 (17.0)

21 (16.3)

NA

NA

 Allogenic PBSCT

3 (5.7)

NA

NA

NA

T-MN subtype

    

 MDS

28 (52.8)

83 (64.3)

NA

9 (69.2)

 MDS/MPN

1 (1.9)

11 (8.5)

NA

2 (15.4)

 AML

24 (45.3)

34 (26.4)

NA

2 (15.4)

 Cytogenetic abnormalities

    

 −5/del(5q)

15 (28.3)

5 (3.9)

NA

4 (30.8)

 −7/del(7q)

23 (43.4)

23 (17.8)

NA

4 (30.8)

 −17/del(17p)

5 (9.4)

NA

NA

1 (7.7)

 PML-RARA

4 (7.5)

2 (1.6)

NA

0

 KMT2A rearrangement§

4 (7.5)

4 (3.1)

NA

0

 RUNX1 rearrangement

1 (1.9)

NA

NA

0

 MECOM rearrangement

3 (5.7)

NA

NA

1 (7.7)

 Chromosome 3 abnormalities§

0

2 (1.6)

NA

0

 Complex karyotype (≥ 3 abnormalities)

25 (47.2)

36 (27.9)

NA

8 (61.5)

 Normal karyotype

6 (11.3)

NA

NA

2 (15.4)

 Not assessed

2 (3.8)

NA

NA

0

Overall survival (months)

Inclusion of pediatric patients*

Yes: 10.6 (0.2–102.4)

No: 9.2 (0.2–102.4)

10.6 (9.1–13.6)

NA

NA

  1. Data are presented as numbers (percentages) or median values (ranges)
  2. T-MN Therapy-related myeloid neoplasm; PBSCT Peripheral blood stem cell transplantation; AML Acute myeloid leukemia; MDS Myelodysplastic syndrome; MDS/MPN Myelodysplastic/myeloproliferative neoplasm; NA Not assessed; −5/del(5q) Chromosome 5 or 5q deletion; −7/del(7q) Chromosome 7 or 7q deletion; −17/del(17p) Chromosome 17 or 17p deletion
  3. *The seven pediatric patients aged below 20 years old
  4. Non-Hodgkin lymphoma includes plasma cell dyscrasia and chronic lymphocytic leukemia
  5. Several cytogenetic abnormalities coexisted in some patients. In particular, −5/del(5q) and −7/del(7q) tended to coexist
  6. §Chromosome 3 abnormalities and 11q23 translocations are presented which occur alone or in combination with other chromosomal abnormalities excluding −5/del(5q), −7/del(7q), or complex karyotype