Publications by authors named "Kreipe Hans"

The prognostication of individual disease trajectory and selection of optimal therapy in patients with localized, low-grade prostate cancer often presents significant difficulty. The phosphatase and tensin homolog on chromosome 10 (PTEN) has emerged as a potential novel biomarker in this clinical context, based on its demonstrated prognostic significance in multiple retrospective studies. Incorporation into standard clinical practice necessitates exceptional diagnostic accuracy, and PTEN's binary readout-retention or loss-suggests its suitability as a biomarker.

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The majority of mastocytosis cases are characterized by an activating mutation in the KIT gene in codon 816. The detection of this alteration is of importance for proper diagnostic workup. Therefore, reliable and sensitive methods for the detection of KIT Codon 816 hotspot mutations in various types of patient samples are required.

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  • The study examines how post-mortem examinations correlate with clinical diagnoses in neonatal deaths occurring within the first week of life, often linked to conditions like premature birth and lung diseases.
  • It involved analyzing 27 autopsy cases from 2006 to 2021, focusing on discrepancies between clinical findings and autopsy results, categorized into full agreement, additional findings, or diagnosis changes.
  • Results showed that lung issues were prevalent (56%), with 48% revealing additional findings and 11% of cases having their diagnosis altered by the autopsy, highlighting its importance for clinical improvement and potential genetic counseling.
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  • * A specialized next-generation sequencing (NGS) assay analyzed samples from 162 liquid biopsies and 25 metastatic sites, detecting mutations in important genes like ESR1, ERBB2, and TP53.
  • * Results showed that mutations in these genes could indicate necessary changes in therapy, suggesting that liquid biopsies are a valuable, noninvasive tool for guiding treatment in metastatic BC patients.
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  • Chronic myeloid leukemia (CML) is characterized by the Philadelphia translocation (t(9;22)) that creates the BCR::ABL1 fusion gene, which is key to its diagnosis.
  • Other myeloproliferative neoplasms (MPNs) also exhibit specific chromosomal abnormalities, but these are not unique to any one type and diagnosis relies on various cytological, histopathological, and molecular features.
  • The progression of CML and other MPNs can be influenced by additional mutations, particularly in key genes like JAK2, MPL, and CALR, as well as the order in which these mutations occur, making ongoing monitoring essential.
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Introduction: Each year the interdisciplinary AGO (Arbeitsgemeinschaft Gynäkologische Onkologie, German Gynecological Oncology Group) Breast Committee on Diagnosis and Treatment of Breast Cancer provides updated state-of-the-art recommendations for early and metastatic breast cancer.

Methods: The updated evidence-based treatment recommendations for early and metastatic breast cancer have been released in March 2024.

Results And Conclusion: This paper concisely captures the updated recommendations for early breast cancer chapter by chapter.

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Collagenous spherulosis (CS) is a rare breast lesion of unknown histogenesis. Adenoid cystic carcinoma (ACC) is a rare basal-like breast carcinoma with low histological grade. CS is a benign lesion but resembles ACC.

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Invasive lobular carcinoma (ILC) is a special breast cancer type characterized by noncohesive growth and E-cadherin loss. Focal activation of P-cadherin expression in tumor cells that are deficient for E-cadherin occurs in a subset of ILCs. Switching from an E-cadherin deficient to P-cadherin proficient status (EPS) partially restores cell-cell adhesion leading to the formation of cohesive tubular elements.

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Besides microscopic evaluation of smears, flow cytometric analysis, chromosomal and molecular studies, histological analysis of bone marrow biopsies (BMbx) is an important component of multiparameter diagnostics of cytopenias in hematology. More than in other fields of histopathology, correct interpretation of BMbx requires correlation with the results of these further studies and other clinical findings. Microcytic, normocytic and macrocytic anemia, isolated granulocytopenia and thromobocytopenia as well as pancytopenia represent frequent and recurrent diseases.

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  • Breast cancer rates have risen over the last 20 years, but survival has improved due to better detection and treatment, although some women still face relapses or metastases after initial treatment.
  • About 70% of breast cancers are HR+ and HER2-, with a 20-year risk of recurrence, prompting a review of patient characteristics, biomarkers, and genomic tools for assessing high-risk cases.
  • Accurate risk assessment is vital for treatment decisions, combining multiple prognostic tools and tailoring approaches to each patient’s situation to prevent over- or undertreatment.
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Phyllodes tumor (PT) of the breast is a biphasic neoplasia composed of mesenchymal and epithelial cells. PTs are graded as benign, borderline or malignant according to histological criteria. Invasive lobular carcinoma (ILC) is a special breast cancer subtype defined by non-cohesive growth and loss of E-cadherin.

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Background: Each year the interdisciplinary Arbeitsgemeinschaft Gynäkologische Onkologie (AGO), German Gynecological Oncology Group Breast Committee on Diagnosis and Treatment of Breast Cancer provides updated state-of-the-art recommendations for early and metastatic breast cancer.

Summary: The updated evidence-based treatment recommendation for early and metastatic breast cancer has been released in March 2023.

Key Messages: This paper concisely captures the updated recommendations for early breast cancer chapter by chapter.

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About 20%-30% of breast cancer (BC) patients will develop distant metastases, preferentially in bones, liver, lung, and brain. BCs with different intrinsic subtypes prefer different sites for metastasis. These subtypes vary in the abundance of genetic alterations which may influence the localization of metastases.

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Aims: Invasive lobular carcinoma (ILC) has distinct morphology and association with loss of E-cadherin function. It has special clinical and imaging features, and its proper recognition is important. Following a recent proposal, we tested the value of the routine use of E-cadherin immunohistochemistry (IHC) in recognizing ILC.

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Invasive lobular carcinoma (ILC) is a common breast cancer subtype that is often diagnosed at advanced stages and causes significant morbidity. Late-onset secondary tumor recurrence affects up to 30% of ILC patients, posing a therapeutic challenge if resistance to systemic therapy develops. Nonetheless, there is a lack of preclinical models for ILC, and the current models do not accurately reproduce the complete range of the disease.

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Background: Microsatellite instability (MSI) occurs in several cancer types and is commonly used for prognosis and as a predictive biomarker for immune checkpoint therapy.

Methods: We analyzed n = 263 formalin-fixed paraffin-embedded (FFPE) tumor specimens (127 colorectal cancer (CRC), 55 endometrial cancer (EC), 33 stomach adenocarcinoma (STAD), and 48 solid tumor specimens of other tumor types) with a capillary electrophoresis based multiplex monomorphic marker MSI-PCR panel and an amplicon-based NGS assay for microsatellite instability (MSI+). In total, n = 103 (39.

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Importance: Combination of chemotherapy with (dual) ERBB2 blockade is considered standard in hormone receptor (HR)-positive/ERBB2-positive early breast cancer (EBC). Despite some promising data on endocrine therapy (ET) combination with dual ERBB2 blockade in HR-positive/ERBB2-positive BC, to our knowledge, no prospective comparison of neoadjuvant chemotherapy vs ET plus ERBB2 blockade in particular with focus on molecular markers has yet been performed.

Objective: To determine whether neoadjuvant de-escalated chemotherapy is superior to endocrine therapy, both in combination with pertuzumab and trastuzumab, in a highly heterogeneous HR-positive/ERBB2-positive EBC.

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In cases of intrauterine fetal death (IUFD), autopsy and placenta pathology can provide additional information to sonographic findings. We assessed the frequency of prenatally missed relevant diagnoses. A retrospective evaluation of fetal autopsies from 2006 to 2021 was performed and were classified as: i) agreement, ii) cases where autopsy revealed additional findings, or iii) postmortem findings which changed the diagnosis.

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Purpose: Neoadjuvant chemotherapy is standard of care in human epidermal growth factor receptor 2-positive (HER2+) early breast cancer (EBC), irrespective of the hormone receptor status. Trastuzumab-emtansine (T-DM1), antibody-drug conjugate, is highly effective in HER2+ EBC; however, no survival data are available for de-escalated antibody-drug conjugate-based neoadjuvant therapy without conventional chemotherapy.

Patients And Methods: In the WSG-ADAPT-TP (ClinicalTrials.

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TP53 mutation is associated with primary endocrine resistance in luminal breast cancer (BC). Nuclear accumulation of p53, as determined by immunohistochemistry (IHC), is a surrogate marker for TP53 mutation. The immunohistochemical p53 index that defines a p53-positive status is not well established.

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  • * A round robin test was conducted across multiple academic centers in Germany to evaluate the performance of RNA-based next-generation sequencing (NGS) and fluorescence in situ hybridization (FISH) for detecting these fusions.
  • * The results indicated that RNA-based NGS is effective for FGFR2 fusion detection, but more adaptable methods that can identify unknown fusion partners are needed, alongside addressing bioinformatic challenges in analysis.
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Purpose: To identify associations of biological signatures and stromal tumor-infiltrating lymphocytes (sTIL) with pathological complete response (pCR; ypT0 ypN0) and survival in the Phase II WSG-ADAPT HER2+/HR- trial (NCT01817452).

Experimental Design: Patients with cT1-cT4c, cN0-3 HER2+/HR- early breast cancer (EBC) were randomized to pertuzumab+trastuzumab (P+T, n = 92) or P+T+paclitaxel (n = 42). Gene expression signatures were analyzed in baseline biopsies using NanoString Breast Cancer 360 panel (n = 117); baseline and on-treatment (week 3) sTIL levels were available in 119 and 76 patients, respectively.

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Second opinion in pathology recruits expert knowledge for the diagnosis in difficult cases and has a tradition in Germany with generation of a network between primarily diagnostic and academic institutes of pathology, active in research. The term reference pathology does mean a label for a class of institutes for pathology but rather specifies a function within prospective clinical trials with defined endpoints and a central pathology, which will derive expert knowledge from this function. On either way generated collection of samples and expertise will enable diagnostic support in difficult cases.

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Second opinions in pathology require expert knowledge for diagnosis in difficult cases and in Germany have a tradition that has grown into a network between primarily diagnostic care institutions and university-associated institutes of pathology that are active in research. The term reference pathology is not a designation for a class of institutes for pathology but rather indicates a function within prospective clinical trials with defined endpoints and a central pathology, which derives expert knowledge from this function. The thus generated collection of samples and expertise enable diagnostic support in difficult cases.

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