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. 2014 Feb 16;6(1):e2014020. doi: 10.4084/MJHID.2014.020

Table 1.

Patients’ series details (diagnosis, treatment response and follow-up data).

Patient Sex Age (years) Disease status at Aza beginning Karyotype MDAPS BM blasts (%) ECOG TD Response Aza cycles at response Loss of response (months of response duration) FU (months) Status Cause of death Disease status at FU Total Aza cycles at FU
1 M 83 AML Normal NA 30 2 Yes NE NA NA 2 Death MOF NE 2
2 M 76 CMML-2 (MPR)* Normal Int-2 19 1 No PR°° 6 No 19 Alive NA PR 13
3 M 72 CMML-1 (MPR) ** Normal Low 3 1 No SD°° 6 No 12 Death Sudden cardiac death SD 12
4 F 72 CMML-2 (MD) *** Normal Int-1 11 1 No SD 4 No 27 Alive NA SD 20
5 M 80 CMML-1 (MD) Normal Int-1 8 0 Yes PR 6 No 18 Alive NA PR 14
6 M 86 CMML-2 (MPR) * Normal Int-2 18 1 No PR°° 6 No 16 Alive NA PR 12
7 M 75 AML 46, XY, Inv12 NA 30 1 Yes CR 6 Yes (5) 13 Death AML AML 14
8 M 62 CMML-2 (MD) Normal High 16 1 No CR 4 Yes (1) 8 Death AML AML 6
9 F 62 CMML-2 (MPR) * Normal Int-2 16 0 No CR°° 6 No 10 Alive NA CR 9
10 M 82 CMML-2 (MD) 45, X, -Y Int-2 12 1 Yes CR 4 No 10 Alive NA CR 10

Aza: azacitidine; AML: acute myeloid leukemia; CMML: chronic myelomonocytic leukemia; MPR: myeloproliferative; MD: myelodysplastic; ECOG: Eastern Cooperative Oncology score, TD: transfusion dependence; NA: not applicable; NE: not evaluated; PR: partial response; SD: stable disease; CR: complete response; FU: follow-up; MOF: multi-organ failure.

*

Indication for treatment was high bone marrow blasts count (16–19%);

**

Indication for treatment was severe symptomatic thrombocytopenia;

***

Indication for treatment was severe symptomatic neutropenia;

°Response criteria: Responses were classified according to the modified IWG response criteria in myelodysplasia9 for MD-CMML and IWG consensus criteria for treatment response in myelofibrosis10 for MPR-CMML;

°°In MPR-CMML patients, ongoing cytoreductive treatment was discontinued at the moment of azacitidine start; no cytoreduction was added during treatment and at response assessment.