The dominant TP53 hotspot mutation in IDH-mutant astrocytoma, R273C, has distinctive pathologic features and sex-specific prognostic implications

Background Infiltrative astrocytic tumors with and without isocitrate dehydrogenase (IDH) mutation frequently contain mutations in the TP53 tumor suppressor gene. Disruption of normal p53 protein activity confers neoplastic cells with a number of oncogenic properties and is a common feature of aggressive malignancies. However, the high prevalence of TP53 mutation and its pathogenic role in IDH-mutant (IDHmut) astrocytoma is not well understood. Methods We performed a retrospective analysis of molecular and clinical data from patients with IDHmut astrocytoma at the University of Pittsburgh Medical Center between 2015 and 2019 as our initial cohort. We validated and expanded our findings using molecular and clinical data from The Cancer Genome Atlas. Results We show that the TP53 mutational spectrum in IDHmut astrocytomas is dominated by a single hotspot mutation that codes for the R273C amino acid change. This mutation is not enriched in IDH-wildtype astrocytomas. The high prevalence of TP53 R273C mutation is not readily explained by known mutagenic mechanisms, and TP53 R273C mutant tumors have lower transcriptional levels of proliferation-related genes compared to IDHmut astrocytomas harboring other forms of mutant p53. Despite lower proliferation, TP53 R273C mutant tumors tend to progress more quickly and have a shorter overall survival than those with other TP53 mutations, particularly in male patients. Conclusions Our findings suggest that compared to other TP53 mutations, IDHmut astrocytomas may select for TP53 R273C mutations during tumorigenesis. The genotype, sex, and mutation-specific findings are clinically relevant and should prompt further investigation of TP53 R273C.

Sensitivity to targeted therapy differs between HER2-amplified breast cancer cells harboring kinase and helical domain mutations in PIK3CA

Background HER2-amplified breast cancer is a clinically defined subtype of breast cancer for which there are multiple viable targeted therapies. Resistance to these targeted therapies is a common problem, but the mechanisms by which resistance occurs remain incompletely defined. One mechanism that has been proposed is through mutation of genes in the PI3-kinase pathway. Intracellular signaling from the HER2 pathway can occur through PI3-kinase, and mutations of the encoding gene PIK3CA are known to be oncogenic. Mutations in PIK3CA co-occur with HER2-amplification in ~ 20% of cases within the HER2-amplified subtype. Methods We generated isogenic knockin mutants of each PIK3CA hotspot mutation in HER2-amplified breast cancer cells using adeno-associated virus-mediated gene targeting. Isogenic clones were analyzed using a combinatorial drug screen to determine differential responses to HER2-targeted therapy. Western blot analysis and immunofluorescence uncovered unique intracellular signaling dynamics in cells resistant to HER2-targeted therapy. Subsequent combinatorial drug screens were used to explore neuregulin-1-mediated resistance to HER2-targeted therapy. Finally, results from in vitro experiments were extrapolated to publicly available datasets. Results Treatment with HER2-targeted therapy reveals that mutations in the kinase domain (H1047R) but not the helical domain (E545K) increase resistance to lapatinib. Mechanistically, sustained AKT signaling drives lapatinib resistance in cells with the kinase domain mutation, as demonstrated by staining for the intracellular product of PI3-kinase, PIP3. This resistance can be overcome by co-treatment with an inhibitor to the downstream kinase AKT. Additionally, knockout of the PIP3 phosphatase, PTEN, phenocopies this result. We also show that neuregulin-1, a ligand for HER-family receptors, confers resistance to cells harboring either hotspot mutation and modulates response to combinatorial therapy. Finally, we show clinical evidence that the hotspot mutations have distinct expression profiles related to therapeutic resistance through analysis of TCGA and METABRIC data cohorts. Conclusion Our results demonstrate unique intracellular signaling differences depending on which mutation in PIK3CA the cell harbors. Only mutations in the kinase domain fully activate the PI3-kinase signaling pathway and maintain downstream signaling in the presence of HER2 inhibition. Moreover, we show there is potentially clinical importance in understanding both the PIK3CA mutational status and levels of neuregulin-1 expression in patients with HER2-amplified breast cancer treated with targeted therapy and that these problems warrant further pre-clinical and clinical testing.

Genomic characteristics of breast cancer to predict response of neoadjuvant chemotherapy and long-term prognosis.

557 Background: To precisely predict neoadjuvant chemotherapy (NAC) response and long-term prognosis, we developed prediction model with clinical and genomic characteristics of breast cancer (BC). Methods: We included early and locally advanced BC that would be scheduled to receive standard NAC (four cycles of anthracycline and cyclophosphamide and four cycles of docetaxel or docetaxel plus trastuzumab for HER2+ BC) followed by curative surgery. For each patient, tumor tissue and matched blood were prospectively collected three times: at diagnosis (T1), three weeks after the first cycle of chemotherapy (T2), and curative surgery (T3). Whole exome sequencing (WES) was performed to detect somatic mutation, mutational signature and tumor mutational burden (TMB) while RNASeq with PAM50 prediction was to classify intrinsic subtype. In terms of clinical variables, clinical stage and IHC subtype at diagnosis, residual cancer burden (RCB) class and distant recurrence free survival (DRFS) were used. Logistic regression was used for predicting RCB class with clinical and genomic variables at T1. Univariate and multivariate Cox regression were performed to identify prognostic factors for DRFS. Results: In total, 210 patients were enrolled and treated with NAC as scheduled. We successfully conducted WES in 231 BC tissues (T1:117, T2:101 and T3:13) from 117 patients. In NAC response, 13 patients were in RCB class 3, 39 in class 2, 14 in class 1 and 46 in class 0. Median follow up duration was 44months and distant recurrence was observed in 13 patients. TP53 mutation (68%) was the most commonly detected genetic alteration. ARID1A, CDH1, CSMD3, LRP1B, PIK3CA, RUNX1 and TP53 were significantly mutated genes in driver gene analysis. Median TMB was 87 (range, 14-570) and signature 3 was most frequently observed. Among genetic characteristics, high TMB was significantly associated with better NAC response compared with low TMB (hazard ratio[HR] for RCB class III: 0.11, 95% confident interval[CI]: 0.01, 0.74, p = 0.05). In prediction model, combination of seven variables: intrinsic subtype, TMB, LRRK1, OPLAH, and PIK3CA hotspot mutation, ERBB2 amplification, and clinical stage had 0.83 in area under curve (AUC) and 0.75 in accuracy. High clinical stage, PTEN and PIK3CA hotspot mutation negatively affected to DRFS while high TMB had protective effect (all ps < 0.05). Prediction model made with five variables: intrinsic subtype, TMB, PTEN mutation, PIK3CA hotspot mutation and clinical stage had 0.88 in c-index (95% CI: 0.81, 0.95). Conclusions: TMB, PIK3CA hotspot mutation and clinical stage showed predictive roles on NAC response and distant recurrence of BC in NAC setting. In prediction model, intrinsic subtype, TMB, LRRK1, OPLAH, and PIK3CA hotspot mutation, ERBB2 amplification, and clinical stage affected to RCB class while intrinsic subtype, TMB, PTEN, PIK3CA hotspot mutation and clinical stage did to DRFS. Clinical trial information: NCT02591966.

Pleuropulmonary Blastoma with Hotspot Mutations in RNase IIIb Domain of DICER 1: Clinicopathologic Study of 10 Cases in a Single-Institute Experience

<b><i>Introduction:</i></b> Pleuropulmonary blastoma (PPB) is a rare sarcomatous malignancy involving the lung and pleura which occurs in early childhood. Cystic PPB in the early stage can be misdiagnosed as other cystic diseases. Early detection of this entity is important for appropriate treatment and prevention of disease progression. Hotspot mutations in the ribonuclease IIIb (RNase IIIb) domain of <i>DICER1</i> have been reported to have a crucial role as genetic factors of PPB and <i>DICER1</i> familial syndrome. We reviewed the clinicopathologic findings of PPB and the status of <i>DICER1</i> hotspot mutation and patients’ clinical course. <b><i>Methods:</i></b> We retrospectively reviewed all patients with histologically confirmed PPB at Asan Medical Center between 2000 and 2017. Ten cases were identified in the database, and their clinicopathologic parameters were evaluated. PPB was classified into the following 3 pathologic subtypes: type I (purely cystic), type II (mixed cystic and solid), and type III (entirely solid). The status of <i>DICER1</i> mutation in 2 hotspot regions of the RNase IIIb domain was evaluated by Sanger sequencing. <b><i>Results:</i></b> The most frequent PPB type was II (6 cases), followed by I and III (2 cases each). The age at diagnosis ranged from 16 months to 15 years. All patients underwent surgery, and all patients received adjuvant or neoadjuvant chemotherapy. Four of 7 patients had missense mutations in the RNase IIIb hotspot; the base and predicted corresponding amino acid changes were c.5113 G&#x3e;A (p.E1705K), c.5407 G&#x3e;A (p.E1803K), c.5425 G&#x3e;A (p.G1809R), and c.5428 G&#x3e;T (p.D1810Y). There was no particular association between the presence of the hotspot mutation and histologic type. Nine patients survived with no evidence of disease for a median interval of 93 (range, 13–199) months. Only 1 patient diagnosed with type III PPB at the age of 18 years had recurrence after 20.8 months and eventually died 66 months after the initial diagnosis. <b><i>Conclusions:</i></b> Late detection of solid PPB is associated with poor prognosis. Considering the rarity of PPB disease and the importance of <i>DICER1</i> hotspot mutation in pathogenesis, <i>DICER1</i> hotspot mutation testing and identification in the early cystic stage can improve patient outcomes.

Co-Occurrence of Hotspot Point Mutation and Novel Deletion Mutation of TERT Promoter in Solid Variant Papillary Thyroid Carcinoma in a Patient with Synchronous Esophageal Cancer

(1) Introduction: Telomerase reverse transcriptase (TERT) promoter mutations are associated with unfavorable clinical outcomes in papillary thyroid carcinomas (PTCs). Two substitution mutations, C228T (c.1-124C>T) and C250T (c.1-146C>T), make up most of the mutations and occur in a mutually exclusive manner. (2) Case presentation: A 72-year-old man was initially referred to a tertiary hospital for treatment of esophageal cancer. Preoperative imaging revealed a 3.2 cm thyroid nodule pathologically diagnosed as PTC on needle biopsy. The patient underwent thyroid lobectomy with esophagectomy and was finally diagnosed with synchronous solid variant PTC (SVPTC) and esophageal squamous cell carcinoma. Sanger sequencing using DNA from the thyroid tumor showed an indel mutation, c.1-132_1-124delinsT, composed of a deletion (c.1-132_1-125del) as well as a hotspot mutation (c.1-124C>T(C228T)) in the TERT promoter. (3) Conclusions: This is the first report of PTC harboring a novel deletion along with a hotspot mutation in the TERT promoter in a patient with synchronous esophageal squamous cell carcinoma.

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

Deficiency of the transcription factor GATA2 is a highly penetrant genetic disorder predisposing to myelodysplastic syndromes (MDS) and immunodeficiency. It has been recognized as the most common cause underlying primary MDS in children. Triggered by the discovery of a recurrent synonymous GATA2 variant, we systematically investigated 911 patients with phenotype of pediatric MDS or cellular deficiencies for the presence of synonymous alterations in GATA2. In total, we identified nine individuals with five heterozygous synonymous mutations: c.351C>G, p.T117T (N = 4); c.649C>T, p.L217L; c.981G>A, p.G327G; c.1023C>T, p.A341A; and c.1416G>A, p.P472P (N = 2). They accounted for 8.2% (9/110) of cases with GATA2 deficiency in our cohort and resulted in selective loss of mutant RNA. While for the hotspot mutation (c.351C>G) a splicing error leading to RNA and protein reduction was identified, severe, likely late stage RNA loss without splicing disruption was found for other mutations. Finally, the synonymous mutations did not alter protein function or stability. In summary, synonymous GATA2 substitutions are a new common cause of GATA2 deficiency. These findings have broad implications for genetic counseling and pathogenic variant discovery in Mendelian disorders.