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. Author manuscript; available in PMC: 2012 Oct 12.
Published in final edited form as: N Engl J Med. 2012 Apr 12;366(15):1371–1381. doi: 10.1056/NEJMoa1110169

Table 2.

Prognostic Factors for Survival, According to Hazard Ratio for Death.*

Prognostic Factor No. of Patients Hazard Ratio for Death (95% CI) P Value
B-cell lineage, t(9;22)(BCR-ABL1)–negative patients
M3 bone marrow at the end of induction 97 0.9 (0.6–1.3) 0.62
Leukocyte count ≥100×109 per liter 49 1.7 (1.1–2.5) 0.01
Age 6–9 yr 56 2.4 (1.5–3.8) 0.001
Age ≥10 yr 103 2.6 (1.8–4.0) <0.001
SCT with matched, related donor 35 1.0 (0.6–1.8) 0.97
Other allogeneic SCT 38 2.1 (1.3–3.5) 0.003
T-cell lineage, t(9;22)(BCR-ABL1)–negative patients§
M3 bone marrow at the end of induction 99 1.6 (1.1–2.2) 0.01
Male sex 143 1.4 (1.0–2.0) 0.05
Any allogeneic SCT 86 0.7 (0.5–1.0) 0.07
All patients with cytogenetic data
M3 bone marrow at the end of induction 163 1.5 (1.2–2.0) 0.002
MLL 43 1.9 (1.2–2.8) 0.004
T-ALL 165 1.6 (1.2–2.2) 0.001
Age ≥10 yr 150 1.4 (1.0–1.8) 0.03
High hyperdiploidy 51 0.7 (0.4–1.2) 0.23
SCT with matched, related donor 61 0.8 (0.5–1.2) 0.28
Other allogeneic SCT 43 1.3 (0.8–1.9) 0.27
*

Only patients with information on whether they had undergone stem-cell transplantation (SCT) are included. MLL-positive patients are excluded because the MLL status was available for less than 46% of the patients. In the Cox regression, the following features were explored as possible prognostic factors in the model: age (<1 year, 6 to 9 years, and ≥10 years), leukocyte count (<20×109 per liter, >50×109 per liter, and ≥100×109 per liter), sex, involvement of the central nervous system or lymph nodes, enlargement of liver and spleen, presence of mediastinal mass, presence of cytogenetic aberrations (MLL rearrangement, high hyperdiploidy with modal chromosomal number of 50 or more), treatment period (years during which patients were treated), study groups (in three strata according to treatment results), and time to transplantation as a time-dependent variable. CI denotes confidence interval.

In each case, the comparator group is the obverse of the noted criterion. For age 6 to 9 years and age 10 years or older, the comparison is with age 1 to 5 years. For SCT with matched, related donor, other allogeneic SCT, and any allogeneic SCT, the comparison is with chemotherapy.

A total of 297 patients had B-cell lineage, t(9;22)(BCR-ABL1)–negative status and known SCT status, with a 10-year-survival rate of 47±3%.

§

A total of 225 patients had T-cell lineage, t(9;22)(BCR-ABL1)–negative status and known SCT status, with a 10-year-survival rate of 28±3%.

A total of 448 patients had cytogenetic data and known SCT status, with a 10-year survival estimate (±SE) of 36±2%.