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Mutational profiling of acute lymphoblastic leukemia with testicular relapse.

  • Author(s): Ding, Ling-Wen
  • Sun, Qiao-Yang
  • Mayakonda, Anand
  • Tan, Kar-Tong
  • Chien, Wenwen
  • Lin, De-Chen
  • Jiang, Yan-Yi
  • Xu, Liang
  • Garg, Manoj
  • Lao, Zhen-Tang
  • Lill, Michael
  • Yang, Henry
  • Yeoh, Allen Eng Juh
  • Koeffler, H Phillip
  • et al.
Abstract

Relapsed acute lymphoblastic leukemia (ALL) is the leading cause of deaths of childhood cancer. Although relapse usually happens in the bone marrow, extramedullary relapse occasionally occurs including either the central nervous system or testis (<1-2%). We selected two pediatric ALL patients who experienced testicular relapse and interrogated their leukemic cells with exome sequencing. The sequencing results and clonality analyses suggest that relapse of patient D483 directly evolved from the leukemic clone at diagnosis which survived chemotherapy. In contrast, relapse leukemia cells (both bone marrow and testis) of patient D727 were likely derived from a common ancestral clone, and testicular relapse likely arose independently from the bone marrow relapsed leukemia. Our findings decipher the mutational spectra and shed light on the clonal evolution of two cases of pediatric ALL with testicular relapse. Presence of CREBBP/NT5C2 mutations suggests that a personalized therapeutic approach should be applied to these two patients.

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