- Letter to the Editor
- Open Access
The clinical characteristics and prognosis in adult Ph negative acute lymphoblastic leukemia with TP53 aberrations
Experimental Hematology & Oncology volume 11, Article number: 22 (2022)
Very few reports elucidate the prognosis of patients with TP53 aberrations using both measurable residual disease (MRD) and the status of having undergone allogeneic hematopoietic stem cell transplantation (allo-SCT). In this study, aberrations of TP53 were analyzed using next-generation sequencing (NGS) and fluorescence in situ hybridization (FISH) in patients with Philadelphia chromosome-negative (Ph−) ALL enrolled in a prospective single-arm clinical trial at our leukemia center. We analyzed the survival of the patients grouped according to the MRD level at the third month and whether or not received allo-SCT. We found that allo-SCT could improve the OS in patients with TP53 aberrations; Patients having negative MRD at the third month still showed worse 3-year OS and 3-year DFS without undergoing allo-SCT, which is different from previous studies, moreover, the prognostic significance of TP53 deletions was as important as TP53 mutations, the importance of screening both TP53 deletions and mutations in adult Ph− ALL at diagnosis should be emphasized.
To the Editor,
TP53 aberrations are one of the most common genetic lesions associated with cancers in humans, particularly with hematological malignancies . Examples of genetic modifications include mutations, deletions, and insertions. Previous studies have found that the frequency of TP53 aberrations observed in acute lymphoblastic leukemia (ALL) was 16–19%, which is higher than that observed in acute myeloid leukemia and myelodysplastic syndrome [2, 3]. TP53 aberrations were strongly correlated with complex karyotype in ALL (45% of patients with complex karyotypes) and older age (25–36% of patients ≥ 60 years with TP53 aberrations) . Moreover, TP53 aberrations resulted in suboptimal treatment response and poor survival rates [lower event-free survival and overall survival (OS) rates] in pediatric and adult patients with ALL [4,5,6]. Very few reports elucidate the prognosis of patients with TP53 aberrations using both measurable residual disease (MRD) and the status of having undergone allogeneic hematopoietic stem cell transplantation (allo-SCT).
Aberrations of TP53 were analyzed using next-generation sequencing (NGS) (n = 309) and fluorescence in situ hybridization (FISH) (n = 242) in 309 patients with Philadelphia chromosome-negative (Ph−) ALL enrolled in a prospective single-arm clinical trial (ChiCTR-TNC-09000397) at our leukemia center . The results revealed that 45 patients (14.6%; 25 men and 20 women) had TP53 aberrations, which was lower than the proportions of patients reported in previous data. Of the 45 patients with TP53 aberrations, 35 cases were B-cell ALL and 10 cases were T-cell ALL. The median patient age was 27 years (range: 14–67 years), and the median white blood cell count at diagnosis was 5.35 × 109/L (range: 0.73–245 × 109/L). Among the 45 patients, fourteen patients (14/242, 5.8%) had only TP53 deletions (as per FISH), nine patients (9/242, 3.7%) had both TP53 deletions and mutations, and 22 patients (22/309, 7.1%) had only TP53 mutations (as per NGS). Detailed data of the patients with different TP53 aberrations are listed in Table 1 (the concomitant gene mutations observed in the patients with TP53 aberrations are listed in Additional file 1: Table S1). No significant differences were observed between the groups in terms of clinical characteristics. Median mutation frequency of TP53 was 45.1% (range: 2–89.6%). Mutation sites were mainly located in exons 3–9 and included hotspot residues of R280, R273, R282, E286, C257, R248, Y220, R196, R213, and L194. Specific mutation sites are shown in Fig. 1A.
All patients received scheduled therapy in accordance with the trial protocol described previously . Three patients died during induction therapy, and one patient was lost during follow-up. The complete remission (CR) rate achieved after one course of induction therapy was 85.4% (35/41), and the overall CR rate was 100% (41/41). Eight-color flow cytometry performed during the third month after induction therapy initiation revealed the MRD level of 35 patients, of whom 23 (65.5%) exhibited negative results (MRD level < 0.01%) and 11 (34.5%) exhibited positive results. Of the 41 patients who achieved CR, 30 patients underwent allo-SCT during the first CR period (CR1) and 11 did not undergo allo-SCT.
We analyzed the data from several different perspectives (Additional file 1: Data S1, Tables S2, S3, Fig. S1) and confirmed that TP53 aberration is a poor independent prognostic factor for Ph− ALL. The median follow-up time was 38.57 months (range: 17.77–51.35 months). The 3-year OS rate of the 45 patients was 49.4% ± 8.6%, and the 3-year disease-free survival (DFS) rate was 50.7% ± 9.6%. For patients with different TP53 aberrations, the 3-year OS and 3-year DFS rates showed no significant difference (deletion only vs. mutation only vs. deletion and mutation: 3-year OS: 48.9% ± 15.6% vs. 53% ± 12% vs. 40% ± 20.3%, p = 0.948; 3-year DFS: 47.7% ± 9.1% vs. 55.7% ± 13.2% vs. 41.7% ± 17.3%, p = 0.387). We determined the survival of the patients grouped according to their MRD level during the third month and investigated whether they had undergone allo-SCT (the survival rates of the patients grouped according to their MRD level on days 14 and 28 after induction therapy initiation were also analyzed, and the outcomes are listed in Additional file 1: Data S2, Fig. S2). The 3-year OS and 3-year DFS of the patients who underwent allo-SCT were much better than those of the patients who did not undergo allo-SCT (3-year OS: 77.8% ± 8.9% vs. 6.7% ± 6.4%, p < 0.01; 3-year DFS: 67.4% ± 11% vs. 10% ± 9.5%, p < 0.01) (Fig. 1B, C). The 3-year OS and 3-year DFS rates of 27 patients who underwent allo-SCT were different when the patients were grouped according to their third month MRD level (nine positive cases vs. 18 negative cases; 3-year OS: 75.8% ± 12.5% vs. 87.5% ± 11.7%, p = 0.567; 3-year DFS: 56.7% ± 15.4% vs. 77.8% ± 13.9%, p = 0.753). However, there was no identifiable statistical significance because of the small sample size. In the MRD-negative group, the 3-year OS and 3-year DFS rates were better for the patients who underwent allo-SCT, whereas those who did not undergo allo-SCT still had poor survival rates. According to landmark analysis, there was an obvious significant difference between patients (five cases) who did not undergo allo-SCT and those (18 cases) who underwent allo-SCT in terms of 3-year OS and 3-year DFS (3-year OS: 20% ± 17.9% vs. 75.8% ± 12.5%, p = 0.034; 3-year DFS: 20% ± 17.9% vs. 56.7% ± 15.4%, p = 0.03) (Fig. 1D, E). Four of the five patients who did not undergo allo-SCT died due to disease relapse.
Overall, our data provide evidence that TP53 aberrations are critical prognostic factors in adult Ph− ALL and highlight the importance of allo-SCT in the management of ALL patients with TP53 aberrations. A comparison of the overall remission rates (ORRs) and CR rates after one course of induction therapy did not show substantial differences between patients with and without TP53 aberrations. Along with previous studies showing MRD level and allo-SCT are crucial prognostic factors in adult ALL patients [8,9,10,11,12], we also analyzed the prognostic value of the third month MRD level and allo-SCT in patients with TP53 aberrations. Our data showed that allo-SCT could improve the OS of patients with TP53 aberrations, regardless of aberration types. We also found that avoidance of allo-SCT was associated with a worse 3-year OS and DFS in the patients who achieved an early MRD-negative status. This however differs from a recent study from Ribera et al.  where omitting allo-HSCT did not hamper the outcomes of high-risk Ph− ALL patients with adequate MRD response. Moreover, our study first showed TP53 deletion was of as good prognostic value as the better-studied TP53 mutaion, which can be incorporated into an improved risk stratification system for adult Ph−ALL. Based on these findings, we suggest evaluation of both TP53 deletion and mutation status in adult patients with Ph−ALL at diagnosis and recommend that patients with ALL and any type of TP53 aberrations should consider allo-SCT.
Availability of data and materials
The clinical trial related information was obtained from public databases.
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Basic Scientific Research Project of National Universities (332021059); Tianjin Municipal Science and Technology Commission Grant (20JCZDJC00120).
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Ethics Review Board approval was obtained prior to study initiation. The procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008. All participants gave written informed consent.
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The concomitant gene mutations of patients with TP53 aberrations. Table S2. The clinical characteristics in patients with TP53 aberrations and without TP53 aberrations. Table S3. The COX regression analysis of the Ph− ALL patients, the covariate including TP53 aberrations, WBC count, age and whether or not they underwent allo-SCT. Figure S1. The 3-year OS (A) and 3-year DFS (B) of patients with TP53 aberrations compared with patients without TP53 aberrations in the 137 patients who didn’t undergo allo-SCT. The 3-year OS (C) and 3-year DFS (D) of the 4 different groups (MLL rearrangement, E2A/PBX1, TP53 aberrations, other-types) in the 137 patients who didn’t undergo allo-SCT. Figure S2. The 3-year OS and 3-year DFS of the patients with TP53 aberrations who underwent allo-SCT vs. the patients who did not undergo allo-SCT grouped according to MRD level on day 14 (A, B) and day 28 (C, D) from the therapy initiation.
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Fang, Q., Gong, X., Liu, K. et al. The clinical characteristics and prognosis in adult Ph negative acute lymphoblastic leukemia with TP53 aberrations. Exp Hematol Oncol 11, 22 (2022). https://doi.org/10.1186/s40164-022-00274-1
- Clinical characteristics
- TP53 aberrations
- Ph negative acute lymphoblastic leukemia