Figure 2.
Figure 2. Landscape of CCA/Ph− in patients with chronic-phase chronic myeloid leukemia. (A) Distribution of CCA/Ph− according to the year after treatment start it is first detected. (B) Number of times CCA/Ph− is detected in independent cytogenetic analyses per patient, done every 3 months during the first year, then every 6 to 12 months while on study. (C) Maximum number of metaphases containing CCA/Ph− in a cytogenetic analysis per patient. (D) Distribution of CCA/Ph− by chromosome. Each row represents the chromosomes numbered from 1 to 22 with additional rows for the sex chromosomes and a row labeled “C” for patients with a complex karyotype defined as ≥3 chromosomal abnormalities in 1 metaphase. Each column represents a patient with CCA/Ph−. Red. deletion or loss; blue. gain; D, dasatinib; I, imatinib; N, nilotinib; P, ponatinib. Some of the CCA/Ph− metaphases were translocations not shown in this figure. Additional details are provided in supplemental Table 1.

Landscape of CCA/Ph in patients with chronic-phase chronic myeloid leukemia. (A) Distribution of CCA/Ph according to the year after treatment start it is first detected. (B) Number of times CCA/Ph is detected in independent cytogenetic analyses per patient, done every 3 months during the first year, then every 6 to 12 months while on study. (C) Maximum number of metaphases containing CCA/Ph in a cytogenetic analysis per patient. (D) Distribution of CCA/Ph by chromosome. Each row represents the chromosomes numbered from 1 to 22 with additional rows for the sex chromosomes and a row labeled “C” for patients with a complex karyotype defined as ≥3 chromosomal abnormalities in 1 metaphase. Each column represents a patient with CCA/Ph. Red. deletion or loss; blue. gain; D, dasatinib; I, imatinib; N, nilotinib; P, ponatinib. Some of the CCA/Ph metaphases were translocations not shown in this figure. Additional details are provided in supplemental Table 1.

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