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Table 1 Clinicopathologic features of published cases with de novo acute lymphoblastic leukemia-like disease of high grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements

From: De novo acute lymphoblastic leukemia-like disease of high grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements: a case report and literature review

Case (ref. n)

Age/sex

Extramedullary lesion at presentation

CNS

FAB criteria

Immunophenotype

Main cytogenetic abnormalities

FISH or gene analysis

Curative therapy

Survival

CD10

CD19

CD20

sIg

IGH-BCL2

MYC

 

1 (8)

57/F

bone

+

L3

+

+

–

ND

t(8;22)(q24;q12a),t(14;18)(q32;q21)

NA

NA

ALL regimen

7 mo

2 (9)

74/M

palate, L (cervical, pretracheal)

–

L3

NA

+

NA

μ

t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

NA

ALL regimen

3 mo

3 (9)

37/M

none

–

L2

–

+

+

IgMλ

t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

NA

ALL regimen

12 mo

4 (9)

73/M

none

+

L3

+

+

+

IgMκ

t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

NA

ALL regimen

8 mo

5 (10)

62/M

H, S

–

L3

+

+

+

ND

t(8;14)(q24;q32),t(14;18)(q32;q21)

NA

NA

ALL regimen

3 mo

6 (11)

35/M

none

–

L3

+

+

NA

ND

t(14;18)(q32;q21)

GR (+)

GR (+)

ALL regimen

0.3 mo

7 (12)

27/M

L (IP, RP)

+

L3

+

+

–

ND

t(8;22)(q24;q11),der(14)t(14;18)(q32;q21)

NA

NA

ALL regimen

5 mo

8 (13)

67/M

none

–

L3

NA

+

+

IgGκ

t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

NA

none

0.1 mo

9 (14)

71/M

none

–

L3

−/+

+

+

IgMλ

t(1;3;11)(q42.3;q27.1;q23.1),der(8)t(8;9)(q24.2;p13.3),t(14;18)(q32.3;q21.3),der(17)t(17;?)(p13;?)

GR (+)

GR (+)

none

0.1 mo

10 (15)

36/F

IP mass

–

NA

+

+

NA

ND

t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

GR (−)

ALL regimen

3 mo

11 (15)

60 M

none

+

L2

NA

NA

NA

NA

t(8;22)(q24;q11),t(14;18)(q32;q21),+der(14)t(14;18)(q32;q21)

NA

GR (−)

ALL regimen

6 mo

12 (16)

40/M

GL, paravertebral mass

–

L2

+

+

+

NA

der(6)t(6;8)(q1?;q24),add(8)(q24),der(9)t(8;9)(q24;p1?),t(14;18)(q32;q21),del(17)(p11)

NA

NA

ALL regimen

1 mo

13 (17)

69/M

H

–

L3

–

+

+

IgMκ

der(7;17)(q10;q10),+der(8)t(8;14;18)(q24;q32;q22),add(14)(q32),del(18)(q21)

GR (+)

NA

ALL regimen

5 mo

14 (18)

41/F

none

–

L3

+

+

+

NA

t(2;3)(p12;q27),del(8)(q24),t(14;18)(q32;q21)

GR (+)

GR (+)

ALL regimen

10 mo

15 (19)

50/F

GL

–

L2

+

+

+

IgMκ

t(3;4)(q27;p13),t(8;14;18)(q24;q32;q21),+ider(8)(q10)t(8;14;18)(q24;q32;q21)

GR (+)

GR (+)

ALL regimen

0.1 mo

16 (19)

44/M

GL, S

+

NA

+

+

+

IgMκ

t(3;13)(q27;q14),t(8;22)(q24;q11),t(14;18)(q32;q21),+der(18)t(14;18)(q32;q21)

GR (+)

GR (−)

NCVBP, IVAM, ASCT

7 mo

17 (19)

46/F

GL, S, Asc, PE

+

L2

+

+

+

IgMκ

t(2;3)(p12;q27),add(8)(q24),der(14)t(8;14)(q24;q32),der(18)t(14;18)(q32;q21)

GR (+)

GR (+)

ACVBP, allo-SCT

3 mo

18 (20)

62/F

none

NA

L3

NA

NA

NA

NA

t(2;8)(p12;q24),t(14;18)(q32;q21)

NA

NA

none

0.1 mo

19 (21)

48/M

GL

–

L2

NA

NA

NA

NA

t(8;9)(q24,p13),t(14;18)(q32;q21)

NA

NA

R-CHOP

3.5 mo

20 (22)

72/M

H, S

–

L2

+

NA

+

IgGκ

t(8;9)(q24;p13),t(14;18)(q32;q21)

NA

NA

R-EPOCH

4 mo

21 (23)

71/M

S (mild)

–

L2

–

+

+

γ

t(1;2)(q22–23;p13),t(8;14)(q24;q32),t(14;18)(q32;q22)

GR (+)

GR (+)

ALL regimen

2 mo

22 (24)

50/F

L (axillary), SC mass

–

L3

+

+

NA

ND

t(2;3)(p12;q27),t(8;22)(q24;q11),t(14;18)(q32;q21),-17

fusion (+)

split (+)

ALL regimen

7 mo

23 (25)

29/M

none

–

L3

+

+

+

NA

+8,t(8;22)(q24;q11),t(14;18)(q32;q21)

NA

split (+)

R-CHOP, R-ICE, R-hyper-CVAD/MA

5 mo

24 (25)

72/M

none

–

L3

+

+

+

NA

t(8;22)(q24;q11.2),t(14;18)(q32;q21)

NA

NA

R-hyper-CVAD/MA

11 mob

25 (25)

50/F

none

+

L3

+

+

+

NA

t(8;22)(q24;q11),t(14;18)(q32;q21)

fusion (+)

split (+)

R-hyper-CVAD/MA

3 mo

26 (25)

32/M

L (mesenteric)

+

L3

+

+

+

NA

t(1;3)(p32;q26.2),t(8;22)(q24;q11),add(14)(q32),t(14;18)(q32;q21)

fusion (+)

split (+)

hyper-CVAD/MA

8 mo

27 (25)

67/M

L (P), small intestine

+

L3

+

+

+

NA

t(8;14)(q24;q32),der(8)t(8;14)t(14;18)(q32;q21),der(14)t(8;14),+add(14)(q32),i(17)(q10)

fusion (+)

split (+)

R-hyper-CVAD/MA, velcade

9 mo

28 (25)

61/M

L (RP), colon, prostate

+

L3

NA

NA

NA

NA

t(8;22)(q24;q11),t(14;18)(q32;q21),+der(14)t(14;18)

fusion (+)

NA

hyper-CVAD/MA, MOAP

9 mo

29 (25)

42/F

small intestine, omentum, breast

–

L3

+

+

+

NA

t(8;14)(q24;q32),t(14;18)(q32;q21),der(17)t(10;17)(q22;q10)

fusion (+)

NA

proMACECytaBOM, CHOP, ESHAP, hyper-CVAD/MA, SCT, RT

12 mo

30 (25)

63/M

testis, lip

–

L3

+

+

+

NA

NA

fusion (+)

split (+)

hyper-CVAD

18 mo

31 (26)

57/F

none

NA

NA

+

+

–

NA

der(3)t(3;14;?)(q27;q32;?),t(8;14)(q24;q32),der(18)t(14;18)(q32;q21)

fusion (+)

split (+)

CODOX-M/IVAC

2.5 mo

32 (26)

60/M

none

NA

L3

+

+

+

D

t(2;8)(p12;q24),der(8)t(2;8)(p12;q24),t(14;18)(q32;q21),?i(17)(q10)

fusion (+)

split (+)

hyper-CVAD, CODOX-M

3 mo

33 (26)

63/M

GL, S (mild)

NA

L3

+

+

+

D

der(3)t(1;3)(q23;q27),t(8;22)(q24;q11),t(14;18)(q32;q21)

fusion (+)

split (+)

CODOX-M/IVAC

6 mo

34 (26)

76/F

none

NA

L3

–

+

NA

D

t(8;22)(q24,q11),t(14;18)(q32;q21)

fusion (+)

split (+)

VAD

6 mo

35 (26)

59/F

none

NA

L2

+

NA

NA

NA

t(8;9)(q24;p13),t(14;18)(q32;q21)

fusion (+)

split (+)

ALL regimen

1.5 mo

36 (26)

69/M

L (IP), H

NA

L3

+

+

+

D

t(14;18)(q32;q21)

fusion (+)

split (+)

ALL regimen

1.5 mo

37 (26)

86/F

none

NA

L2

+

+

+

ND

add(9)(p13),t(14;18)(q32;q21)

fusion (+)

split (+)

none

0.5 mo

38 (27)

43/F

pancreas

+

L3

+

+

+

IgMλ

t(8;14)(q24;q32),t(14;18)(q32;q21)

fusion (+)

split (+)

R-CODOX-M/IVAC

5 mo

39 (28)

61/M

GL, S, PE

–

L3

+

+

+

γ

t(3;5)(q27;q15),t(8;14;18)(q24;q32;q21),+der(8)t(8;14;18),+der(18)t(8;14;18)

fusion (+)

split (+)

R-hyper-CVAD,

NAc

40 (29)

42/M

L (IP), S

+

L2

+

+

+

κ

der(8)del(8)(q12.1q12.3)del(8)(q24.21q24.21)t(8;12)(q24.21;p12.1),der(12)del(12)(p12.1p12.1)t(8;12)(q24.21;p12.1),t(14;18)(q32;q21)

fusion (+)

split (+)

R-CHOP, ALL regimen

7 mo

41 (30)

72/M

bone, liver

+

NA

+

NA

+

NA

t(3;8)(q27;q24),t(14;18)(q32;q21)

fusion (+)

split (+)

ALL regimen

NAc

42 (31)

64/M

L (NA)

–

NA

+

NA

+

NA

NA

fusion (+)

split (+)

R-EPOCH

1.7 moc

43 (31)

72/M

L (NA)

–

NA

+

NA

+

NA

t(3;22)(q27;q11.2),t(8;14)(q24;q32),t(14;18)(q32;q21)

fusion (+)

split (+)

R-EPOCH

1.6 moc

44 (32)

74/F

none

+

L2

+

+

+

κ

–8,del(11)(q23q25),del(13)(q12q14),t(14;18)(q32;q21),+18

fusion (+)

split (+)

R-CHOP

3 mo

45 (32)

67/M

colon

–

L3

+

+

−/+

κ

NA

fusion (+)

split (+)

R-CHOP

11 mod

46 (32)

71/M

L (mediastinal)

–

L3

+

+

+

κ

der(8)t(8;14;18)(q24;q32;q21),der(14)t(8;14)(q24.1;q32),der(18)t(14;18)(q32;q21)

fusion (+)

split (+)

R-EPOCH, R-ICE, ASCT

14 mo

47 (33)

60/M

GL

NA

L2

+

+

+

λ

+8,inv(8)(p11.2q24)×2,t(14;18)(q32;q21),-17

fusion (+)

split (+)

R-hyperCVAD, ofatumumab + EPOCH

18 mo

48 (present case)

69/F

none

–

L2

+

+

+

IgMκ

add(8)(q24),t(14;18)(q32;q21),-17

fusion (+)

split (+), EC (+)

R-hyper-CVAD/MA, R-EPOCH

7 mo

  1. Abbreviations: Ref n reference number, FAB criteria blastoid cell morphology according to the French-American-British classification, CNS development of central nervous system involvement, sIg surface immunoglobulin, M male, F female, L lymphadenopathy, H hepatomegaly, S splenomegaly, SC subcutaneous, IP intraperitoneal, RP retroperitoneal, GL generalized lymphadenopathy, Asc ascites, PE pleural effusion, P pelvic, ND not detected, D detected, NA not available, GR gene rearrangement, EC extra copies, ALL regimen multidrug chemotherapy for acute lymphoblastic leukemia, NCVBP mitoxantrone, cyclophosphamide, vinblastine, bleomycin, and prednisone, IVAM ifosfamide, etoposide, cytarabine, and methotrexate, ASCT autologous stem cell transplantation, ACVBP doxorubicin, cyclophosphamide, vinblastine, bleomycin, and prednisone, allo-SCT allogeneic stem cell transplantation, R rituximab, CHOP cyclophosphamide, doxorubicin, vincristine, and prednisone, EPOCH etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin, ICE ifosfamide, carboplatin, and etoposide, hyper-CVAD/MA cyclophosphamide, vincristine, doxorubicin, dexamethasone alternating with methotrexate and cytarabine, MOAP methotrexate, vincristine, asparaginase, and prednisone, proMACEcytaBOM prednisone, vincristine, methotrexate, doxorubicin, cyclophosphamide, etoposide, cytarabine, and bleomycin, ESHAP etoposide, methylprednisolone, cytarabine, and cisplatin, RT radiation therapy, CODOX-M/IVAC cyclophosphamide, vincristine, doxorubicin, methotrexate alternating with ifosfamide, etoposide, and cytarabine, VAD vincristine, doxorubicin, and dexamethasone, POMP prednisone, vincristine, methotrexate, and mercaptopurine
  2. aThis description is according to original work [8]
  3. bAlive (disease status was not described)
  4. cAlive with disease at the time of publication
  5. dAlive with no evidence of disease at the time of publication