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1.
Hematology, Oncology and Stem Cell Therapy. 2014; 7 (4): 142-148
in English | IMEMR | ID: emr-153848

ABSTRACT

To determine the frequency of PIK3CA mutations in a Peruvian cohort with HER2-amplified and triple negative breast cancers [TNBC]. We analyzed two cohorts of 134 primary non-metastatic breast cancer patients from Peru. Cohorts consisted of 51 hormone receptors [+]/HER2-amplified breast tumor patients surgically resected as first treatment included in the ALTTO trial [ALTTO cohort] and 81 TNBC patients with residual disease after neoadjuvant treatment [neoadjuvant cohort]. Genomic DNA was extracted from paraffin-embedded tumor samples. Samples from the ALTTO and neoadjuvant cohorts were taken at biopsies and from residual tumors, respectively. PIK3CA mutations were detected by sequencing DNA fragments obtained by PCR amplification of exons and their flanking introns. All of the detected PIK3CA mutations were confirmed in a second independent run of sample testing. PIK3CA mutations were present in 21/134 cases [15.7%]. Mutations in exon 9 and 20 were present in 10/134 [7.5%] and 11/134 [8.2%], respectively. No cases had mutations in both exons. Mutations in exon 9 consisted of E545A [seven cases], E545K [two cases] and E545Q [one case]; while in exon 20, mutations consisted of H1047R [10 cases] and H1047L [one case]. Compared to TNBC patients, HER2-amplified patients were more likely to have PIK3CA mutated [23% vs 9.6%; P = 0.034]. There were no associations between mutational status of PIK3CA with estrogen receptor status [P = 0.731], progesterone receptor status [P = 0.921], age [P = 0.646], nodal status [P = 0.240] or histological grade [P = 1.00]. No significant associations were found between PIK3CA mutational status and clinicopathological features. We found a similar frequency of PIK3CA mutations to that reported in other series. Although we did not include HR+/HER2 patients, those with HER2-amplified tumors were more likely to present PIK3CA mutations compared to patients with triple negative tumors


Subject(s)
Humans , Female , Phosphatidylinositol 3-Kinases , Breast Neoplasms/genetics , Genes, erbB-2 , Mutation
2.
Hematology, Oncology and Stem Cell Therapy. 2014; 7 (4): 149-156
in English | IMEMR | ID: emr-153849

ABSTRACT

Mammography is the cornerstone of breast cancer [BC] evaluation. This report investigates whether breast density [BD] and mammographic features of the tumor can provide information on both BC susceptibility to chemotherapy and other clinicopathologic features of locally advanced BC [LA BC]. We evaluated mammography films and clinicopathological information of patients with LA BC who received neoadjuvant chemotherapy [NAC] followed by tumor resection at the Instituto Nacional de Enfermedades Neoplasicas [INEN] from 2000 to 2011. We selected 494 LA BC cases. Most cases were at clinical tumor stage 4 [48.5%], node stage 1 [58.8%] and had high histologic grade [53.3%]. BI-RADS 1, 2, 3, and 4 BD were found in 16.9%, 22%, 35.7% and 25.1% of patients, respectively. High BD has been associated with younger age [p<0.001], obesity [p = 0.017] and no skin infiltration [T3 vs T4] [p = 0.018]. An association between dusty microcalcifications and HER2 group, as well as between casting microcalcifications and TN BC group [p = 0.05] was found. NAC included anthracyclines and taxanes in 422 [85.5%] cases. Miller-Payne pathologic responses 4 and 5 [pCR] in the primary lesion and absence of axillary lymph nodes involvement were found in 15.3% of cases and were associated with younger age [p < 0.001] and HG-3 lesions [p < 0.001], but not with mammographic images. Mammographic features are associated with specific clinicopathological features of pre-NAC BC lesions but do not predict pCR. The implications and biological reasons for these findings require further study


Subject(s)
Humans , Female , Mammography , Calcinosis , Chemotherapy, Adjuvant , Breast Neoplasms/diagnosis
3.
Hematology, Oncology and Stem Cell Therapy. 2010; 3 (3): 109-115
in English | IMEMR | ID: emr-129185

ABSTRACT

This study was conducted to determine the prognostic effect hormone receptor [HR] status in early HER2 positive [HER2+] breast cancer patients, since it has not yet been established whether HR status can be used in the prognosis of patients with [HER2+] breast cancer. We obtained data from 299 patients with early HER2+ breast cancer who underwent surgery and received standard adjuvant chemotherapy, hormonal therapy and/or radiation between 2000 and 2002 at the Instituto Nacional de Enfermedaldes Neoplasticas, Peru. Clinical and pathological features were compared. Endpoints analyzed were disease free survival [DFS] and overall survival [OS]. Overall, 155 patients were HR-positive [HR+] and 144 were negative [HR-]. The two groups had similar characteristics except for histologic grade and extracapsular extension. With a median follow-up of 93 months, 5-year DFS was statistically different between the two groups: 65.0% for [HER2+/HR-] and 74.6% for the [HER2+/HR+] patients [P=.045]. OS at 5 years was not statistically different between the two groups with 75.5% for [HER2+/HR-] patients and 82.4% for the [HER2+/HR+] [P=.140]. Patients with [HER2+/HR-] breast cancers treated with surgery and standard adjuvant chemotherapy exhibited a statistically worse DFS compared to those with [HER2+/HR+] tumors. However, OS was similar in both groups


Subject(s)
Humans , Female , Genes, erbB-2 , Prognosis , Disease-Free Survival , Hormones , Receptors, Cell Surface , Retrospective Studies
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