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  • 1
    Online Resource
    Online Resource
    Philadelphia, Pa. : Lippincott Williams & Wilkins | [Erscheinungsort nicht ermittelbar] : Ovid ; 1.1989 -
    UID:
    (DE-627)324455887
    Format: Online-Ressource
    ISSN: 1531-703X
    Note: Gesehen am 14.12.2017 , Volltext auch als Teil einer Datenbank verfügbar
    Additional Edition: 1040-8746
    Additional Edition: Erscheint auch als Druck-Ausgabe Current opinion in oncology Hagerstown, Md. : Lippincott Williams & Wilkins, 1989 1040-8746
    Language: English
    Keywords: Zeitschrift
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  • 2
    Journal/Serial
    Journal/Serial
    Hagerstown, Md. : Lippincott Williams & Wilkins | Philadelphia, Pa. : Current Science ; 1.1989 -
    UID:
    (DE-627)170382265
    ISSN: 1040-8746
    Note: Ungezählte Beil.: Bibliography current world literature
    Additional Edition: 1531-703X
    Additional Edition: Erscheint auch als Online-Ausg. Current opinion in oncology Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989 1531-703X
    Language: English
    Keywords: Onkologie ; Bibliografie ; Onkologie ; Zeitschrift ; Zeitschrift
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  • 3
    UID:
    (DE-627)1806749297
    Format: 6
    ISSN: 1531-703X
    Content: Purpose of review - Desmoid-type fibromatosis, a rare locally aggressive fibroblastic proliferation, is a treatment challenge. This review aimed to explore recent data about the management of desmoid-type fibromatosis. - Recent findings - New data underline the role of kinases and ɣ-secretase in stimulating cell proliferation and invasiveness in desmoid-type fibromatosis. This explains the proven activity of multikinase inhibitors (sorafenib or pazopanib) in the management of desmoid-type fibromatosis or the emerging role of a ɣ-secretase inhibitor. An international guideline for management was recently published, and this guideline take into account patient point of view. Lastly, recent studies highlight the multidimensional burden of desmoid-type fibromatosis, particularly health-related quality of life (HRQoL). - Summary - Active surveillance with planned MRI is the first-line management in desmoid-type fibromatosis. A site-specific and stepwise approach should be considered for progressive desmoid-type fibromatosis. Further, a risk-benefit analysis that considers the side effects and long-term sequelae should be conducted before deciding to start any treatment. A less aggressive approach should be considered. Multikinase inhibitors are effective, but their tolerability and side effects should be discussed with the patients. The symptoms and HRQoL should be integrated in decision-making. Desmoid-type fibromatosis patients should be offered support to address their needs supportive care.
    Note: Gesehen am 10.06.2022
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 33(2021), 4 vom: Juli, Seite 309-314, 1531-703X
    In: volume:33
    In: year:2021
    In: number:4
    In: month:07
    In: pages:309-314
    In: extent:6
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 4
    UID:
    (DE-627)1664490884
    ISSN: 1531-703X
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 31(2019), 1, Seite 1-7, 1531-703X
    In: volume:31
    In: year:2019
    In: number:1
    In: pages:1-7
    Language: English
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  • 5
    UID:
    (DE-627)1818383462
    Format: 7
    ISSN: 1531-703X
    Content: Purpose of review - Human epidermal growth factor receptor 2 (HER2) amplification and overexpression play a central role in initiation, progression and metastasis of some common cancers, including breast and gastric cancer. About 20% of gastric and esophagogastric junction (EGJ) tumors overexpress HER2, providing a rationale to investigate trastuzumab, a monoclonal antibody directed against HER2, in this setting. This review focuses on the current role of HER2 inhibition as a new treatment option for gastric and EGJ cancer and discusses the optimization of gastric cancer-specific HER2 testing and analysis. - Recent findings - In the phase III ToGA trial, the addition of trastuzumab to chemotherapy significantly improved overall survival without compromising safety in patients with HER2-positive metastatic gastric or EGJ cancer. This improvement was mainly the result of the survival advantage conferred to patients with high expression of the HER2 protein, defined as immunohistochemistry (IHC) 3+ or IHC 2+/fluorescent in-situ hybridization (FISH) +. - Summary - On the basis of the results of the ToGA trial, HER2 status should now be included in the diagnostic workup of patients presenting with advanced gastric and EGJ cancer. The addition of trastuzumab to chemotherapy is a new standard treatment for patients with locally advanced and irresectable, recurrent or metastatic HER2-positive disease.
    Note: Gesehen am 10.10.2022
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 23(2011), 4, Seite 396-402, 1531-703X
    In: volume:23
    In: year:2011
    In: number:4
    In: pages:396-402
    In: extent:7
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 6
    UID:
    (DE-627)1581218125
    Format: 9
    ISSN: 1531-703X
    Content: Purpose of review: Merkel cell carcinoma (MCC) is a highly aggressive neuroendocrine carcinoma of the skin demonstrating a high propensity of recurrence and metastasis. Its 5-year disease-specific survival rate is only about 60%. Although MCC is still regarded as a very rare tumor entity, its incidence is rapidly increasing. In this regard, the American Cancer Society estimated almost 1500 new cases in the United States in 2008. Recent findings: The newly identified Merkel cell polyomavirus (MCV) has been found associated to most MCC cases. Nevertheless, the distinct molecular pathogenesis of MCC and its link to MCV is not yet fully understood. Moreover, the impact of MCV positivity on the course of disease and prognosis of MCC patients is controversially discussed. Summary: This review summarizes recent findings on MCC pathogenesis with a special emphasis on the impact of MCV, presents an overview of clinical aspects, and discusses treatment options.
    Note: Gesehen am 24.09.2018
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 24(2012), 2, Seite 141-149, 1531-703X
    In: volume:24
    In: year:2012
    In: number:2
    In: pages:141-149
    In: extent:9
    Language: English
    URL: Volltext  (Pay-per-use)
    URL: Volltext  (Pay-per-use)
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  • 7
    UID:
    (DE-627)1756923213
    Format: 10
    ISSN: 1531-703X
    Content: Purpose of review: To discuss recent advances in the meningioma biology and their clinical implications. - Recent findings: Meningioma is the most common primary intracranial tumor. Mostly benign, 20% of cases display an aggressive behavior despite best standard of care. The genetic landscape of meningiomas is divided according to NF2 mutational status. Although about 60% of meningiomas display NF2 mutations, the other share is more heterogenous. Mutations in TRAF7, SMO, v-akt murine thymoma viral oncogene homolog 1 (AKT1), PI3KCA and KLF4 are seen mostly in WHO grade 1 meningiomas. In higher grade meningiomas, mutations of the TERT promoter and deletions of CDKN2A/B emerge and have prognostic value. Moreover, mutations in DMD, BAP1 and PBRM1 have recently been discovered and are being further explored. DNA methylation subgroups offer valuable insight into meningioma prognosis and its implementation in clinical setting is under evaluation. Moreover, the study of distinct meningioma populations such as radiation-induced meningioma and progestin-associated meningioma may provide further insight into meningioma oncogenesis and potential therapeutic targets. - Summary: The mutational landscape of meningioma has expanded following the use of the new genetic sequencing approaches. Novel mutations have been characterized and reveal their prognostic and therapeutic applications. This improved understanding of meningioma biology has promising implications for novel treatment strategies.
    Note: Gesehen am 03.05.2021
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 32(2020), 6, Seite 613-622, 1531-703X
    In: volume:32
    In: year:2020
    In: number:6
    In: pages:613-622
    In: extent:10
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 8
    UID:
    (DE-627)1854639692
    Format: 4
    ISSN: 1531-703X
    Content: Purpose of review - Desmoid tumor is a rare disease of intermediate malignancy characterized by a locally aggressive monoclonal, fibroblastic proliferation and accompanied by a variable and often unpredictable clinical course. The purpose of this review is to give an overview on the emerging new systemic treatment options for this intriguing disease for which no established or approved drugs are available yet. - Recent findings - Over decades, surgical resection has been the established initial treatment approach; however, more recently, a paradigm shift has been introduced towards a more conservative treatment strategy. Almost 10 years ago, The Desmoid Tumor Working Group has initiated a consensus process initially in Europe and then globally with the intention to harmonize the therapeutic strategy amongst clinicians and set up management recommendations for desmoid tumor patients. - Summary - This review will summarize and focus on the latest emerging impressive data on the use of gamma secretase inhibitors in this disease paving a possible future perspective in the treatment armamentarium for desmoid tumor patients.
    Note: Gesehen am 08.08.2023
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 35(2023), 4 vom: Juli, Seite 292-295, 1531-703X
    In: volume:35
    In: year:2023
    In: number:4
    In: month:07
    In: pages:292-295
    In: extent:4
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 9
    UID:
    (DE-627)167003187X
    Format: 7
    ISSN: 1531-703X
    Content: Purpose of review The present review introduces recent progress in eliciting the role of mutant isocitrate dehydrogenase (IDH) in gliomas, especially regarding its mode of action as a modulator of antitumor immune response, and provides rationales for targeting mutant IDH in glioma immunotherapy. Both the development of small molecule inhibitors repressing the enzymatic activity of mutant IDH and novel, mechanism-led combination immunotherapies are discussed. - Recent findings Since the discovery of highly frequent IDH mutations in low-grade gliomas and nonsolid malignancies, its tumor cell-intrinsic effects have been intensively investigated. Tumor cells expressing mutant IDH display profound alterations of redox control capacity, phospholipid profile, and ATP supply. Recent findings suggest that IDH mutations - via intricate, yet druggable pathways - cause immunological alterations, highlighting the importance of oncogenic drivers as modulators of antitumor immunity and targets for immunotherapy. - Summary Mutant IDH is not only a disease-defining biomarker and oncogenic driver in glioma, but is also a neoantigen and a regulator of glioma immune evasion. Effective and specific strategies targeting the immunomodulatory properties of mutant IDH may complement current (immuno-)therapeutic strategies and approved antiglioma treatments to improve outcome.
    Note: Gesehen am 25.07.2019 , Doi funktioniert nicht
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 30(2018), 6, Seite 368-374, 1531-703X
    In: volume:30
    In: year:2018
    In: number:6
    In: pages:368-374
    In: extent:7
    Language: English
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  • 10
    UID:
    (DE-627)1577867998
    Format: 7
    ISSN: 1531-703X
    Content: Purpose of review To discuss the recent developments of multimodal treatment for patients with local advanced rectal cancer, including incorporation of new chemotherapeutic and targeted agents, and the optimal sequence and timing of treatment components. Recent findings Five randomized trials have been completed to determine whether the addition of oxaliplatin to preoperative, fluorouracil-based chemoradiotherapy (CRT) offers an advantage compared to single-agent fluorouracil CRT. Early results from the ACCORD 12, STAR-01, and NSAPB R-04 trials did not confirm a significant improvement of early efficacy endpoints with the addition of oxaliplatin, whereas the German CAO/ARO/AIO-04 did. Most of the phase II trials incorporating cetuximab into CRT reported disappointingly low rates of pathologic complete response (pCR); the combination of CRT with VEGF inhibition showed encouraging pCR rates; however, it was associated with increased surgical complications. Novel clinical trials address the role of induction chemotherapy, of delayed, minimal or omitted surgery following CRT, or the omission of radiotherapy for selected patients. Summary At this time, the use of oxaliplatin or targeted agents as component of multimodality treatment for rectal cancer outside of a clinical trial is not recommended. The inclusion of different treatment options, according to tumor stage, location, imaging features, and response, will render the multimodal treatment approach of rectal cancer more risk-adapted.
    Note: Gesehen am 24.07.2018
    In: Current opinion in oncology, Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989, 24(2012), 4, Seite 441-447, 1531-703X
    In: volume:24
    In: year:2012
    In: number:4
    In: pages:441-447
    In: extent:7
    Language: English
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