Table 1

Patient characteristics

PatientAge at APL diagnosis, yPrimary malignancyTreatment of primary malignancyCumulative dose of epirubicin, mg/m2Latency, mo*CytogeneticsPML breakpoint
RARA breakpoint
APL therapyCurrent status of APL
der(15)der(17)der(15)der(17)
UPN1 40 Breastcarcinoma 4 Cycles of epirubicin (165 mg), 6 cycles of CMF (cyclophosphamide 990 mg, methotrexate 65 mg, 5FU 990 mg) 400 48 t(15;17)(q22;q12-21) idem, del(5)(q?31q?35) 1186 1185 13463 13437 PETHEMA Alive in first CRm at 61 mo 
UPN2 47 Breastcarcinoma 4 Cycles of epirubicin (175 mg) + cyclophosphamide (1180 mg) DXT 400 28 t(7;14)(q32;q22), t(15;17)(q22;q21) 1270§ 1267§ 16192 16192 MRC Alive in first CRm at 43 mo; treatment complicated by anthracycline-related cardiomyopathy (ejection fraction 30%–40%) 
UPN3 41 Breastcarcinoma 6 Cycles of epirubicin (118 mg) + cyclophosphamide (940 mg) DXT 450 18 t(15;17)(q22;q21) 379-80§ 375-76§ 9291-92 9293-94 MRC Death in first CRm (fungal infection) at 5 mo 
UPN4 55 Breastcarcinoma 4 Cycles of epirubicin (200 mg), 4 cycles of CMF (cyclophosphamide 1200 mg, methotrexate 80 mg, 5FU 1200 mg) DXT 400 18 der(12), t(8;12)(q13;p13), t(15;17)(q22;q21) 1184-85 1187-1191 13332-33 13336-40 PETHEMA Alive in first CRm at 42 mo 
UPN5 60 Breastcarcinoma 6 Cycles of FEC (5FU 975 mg, epirubicin 98 mg, cyclophosphamide 980 mg), DXT 360 24 t(15;17)(q22;q21) 1968 1964-65 16196 16192-93 MRC Induction death (typhlitis) at 13 da 
UPN6 55 Breastcarcinoma 6 Cycles of FEC (5FU 1100 mg, epirubicin 110 mg, cyclophosphamide 1100 mg × 3; 5FU 1000 mg, epirubicin 100 mg, cyclophosphamide 1000 mg × 3) DXT 300 27 t(15;17)(q22;q21) 955-57 955-59 14882-84 14884-88 PETHEMA #1 ATO + ATRA consolidation Alive in first CRm at 15 mo 
PatientAge at APL diagnosis, yPrimary malignancyTreatment of primary malignancyCumulative dose of epirubicin, mg/m2Latency, mo*CytogeneticsPML breakpoint
RARA breakpoint
APL therapyCurrent status of APL
der(15)der(17)der(15)der(17)
UPN1 40 Breastcarcinoma 4 Cycles of epirubicin (165 mg), 6 cycles of CMF (cyclophosphamide 990 mg, methotrexate 65 mg, 5FU 990 mg) 400 48 t(15;17)(q22;q12-21) idem, del(5)(q?31q?35) 1186 1185 13463 13437 PETHEMA Alive in first CRm at 61 mo 
UPN2 47 Breastcarcinoma 4 Cycles of epirubicin (175 mg) + cyclophosphamide (1180 mg) DXT 400 28 t(7;14)(q32;q22), t(15;17)(q22;q21) 1270§ 1267§ 16192 16192 MRC Alive in first CRm at 43 mo; treatment complicated by anthracycline-related cardiomyopathy (ejection fraction 30%–40%) 
UPN3 41 Breastcarcinoma 6 Cycles of epirubicin (118 mg) + cyclophosphamide (940 mg) DXT 450 18 t(15;17)(q22;q21) 379-80§ 375-76§ 9291-92 9293-94 MRC Death in first CRm (fungal infection) at 5 mo 
UPN4 55 Breastcarcinoma 4 Cycles of epirubicin (200 mg), 4 cycles of CMF (cyclophosphamide 1200 mg, methotrexate 80 mg, 5FU 1200 mg) DXT 400 18 der(12), t(8;12)(q13;p13), t(15;17)(q22;q21) 1184-85 1187-1191 13332-33 13336-40 PETHEMA Alive in first CRm at 42 mo 
UPN5 60 Breastcarcinoma 6 Cycles of FEC (5FU 975 mg, epirubicin 98 mg, cyclophosphamide 980 mg), DXT 360 24 t(15;17)(q22;q21) 1968 1964-65 16196 16192-93 MRC Induction death (typhlitis) at 13 da 
UPN6 55 Breastcarcinoma 6 Cycles of FEC (5FU 1100 mg, epirubicin 110 mg, cyclophosphamide 1100 mg × 3; 5FU 1000 mg, epirubicin 100 mg, cyclophosphamide 1000 mg × 3) DXT 300 27 t(15;17)(q22;q21) 955-57 955-59 14882-84 14884-88 PETHEMA #1 ATO + ATRA consolidation Alive in first CRm at 15 mo 

APL indicates acute promyelocytic leukemia; CRm, molecular remission; DXT, radiotherapy; 5FU, fluorouracil; UPN: Unique patient number; and #1, course 1.

*

Length of time between first epirubicin exposure and presentation with therapy-related APL.

Breakpoint locations for PML intron 6 are numbered according to the GenBank accession no. S57791.

Patients were treated with an extended course of all-trans retinoic acid (ATRA) given simultaneously with induction chemotherapy. Medical Research Council (MRC) and PETHEMA treatment schedules were given as described.16  UPN6 received consolidation with arsenic trioxide (ATO) and ATRA according to the National Cancer Research Institute AML17 protocol (http://aml17.cardiff.ac.uk).

§

Breakpoint locations for PML intron 3 are numbered according to the GenBank accession no. S51489.

Breakpoint locations for PML exon 7 are numbered according to the GenBank accession no. S57791.

Breakpoint locations for RARA intron 2 are numbered according to the GenBank accession no. AJ297538.

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