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Dive into the research topics where Frédéric Kridelka is active.

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Featured researches published by Frédéric Kridelka.


Cancer | 1999

Adjuvant small field pelvic radiation for patients with high risk, Stage IB lymph node negative cervix carcinoma after radical hysterectomy and pelvic lymph node dissection : A pilot study

Frédéric Kridelka; Derek O. Berg; Menahem Neuman; Lyndal S. Edwards; Greg Robertson; Peter Grant; Neville F. Hacker

After radical hysterectomy and pelvic lymph node dissection, an identifiable subgroup of patients with International Federation of Gynecology and Obstetrics Stage IB lymph node negative cervix carcinoma remains at high risk of pelvic recurrence. This study attempted to determine whether postoperative small field of pelvic radiation can improve the disease free survival (DFS) of this high risk group of patients without producing significant morbidity.


European Journal of Radiology | 1997

Stereotaxic Needle-Core Biopsy and Fine-Needle Aspiration Biopsy in the Diagnosis of Nonpalpable Breast Lesions: Controversies and Future Prospects

Eric Lifrange; Frédéric Kridelka; Claude Colin

OBJECTIVEnTo determine the advantages and limitations of a combined stereotaxic fine-needle aspiration biopsy and needle-core biopsy in the diagnosis of 353 nonpalpable breast lesions with special attention given to the collection of follow-up data.nnnMETHODS AND MATERIALn353 nonpalpable breast lesions underwent one pass stereotaxic fine-needle aspiration (21 gauge needle) and needle-core biopsy (18 gauge needle) at our institution from January 1990 to October 1993. Stereotaxic biopsies were carried out by means of an add-on unit. Surgical biopsy was usually recommended for highly suspicious radiologic patterns and/or needle biopsy reports classified as atypical or malignant. In all other cases mammographic follow-up was advised at 6 months and then annually for 3 years. The data were collected retrospectively during September 1995 (theoretical average follow-up of greater than 3 years).nnnRESULTSnFollowing the combined needle biopsy technique procedure, surgery was recommended for 83 lesions. Fifty-four cancers were associated to these suspicious lesions. Because of changing radiological or clinical pattern during follow-up (mean follow-up: 22 months), 11 cancers were detected among the 270 lesions initially considered not to need surgery. Forty-three percent of the 65 malignant lesions were initially read as having less than highly suspicious mammographic features. There was no significant difference between the sensitivity and the specificity of one pass fine-needle aspiration biopsy (57% and 96% respectively) and needle-core biopsy (60% and 97% respectively), but noncontributive samples were not included in the false negative diagnoses and atypical samples were included in the true positive diagnoses. Of the 11 missed cancers, nine were manifested initially by clusters of calcifications. Our diagnostic approach was significantly less sensitive (P = 0.006) and less specific (P = 0.032) in cases of clusters of calcifications (31% false negative diagnoses) than in cases of soft-tissue masses (5.5% false negative diagnoses). In this study, an average delay in diagnoses of 22 months was responsible for a significantly increased percentage of axillary node positive invasive cancer (P < 0.001) and six of the 11 missed cancers were palpable at the time of the delayed diagnosis. For the nine cancers initially manifested by calcifications, the 22 months delay in diagnosis was responsible for a nonsignificant increase of microinvasive type at the expense of carcinoma in situ.nnnCONCLUSIONnOur enthusiasm with the sensitivity of this double stereotaxic needle sampling has been tempered by the results of this reanalysis in the light of a mean theoretical follow-up of three years. Our diagnostic approach was adequate in the presence of soft-tissue masses but not valid in the presence of clustered calcifications. When dealing with calcifications, multiple samplings must be done in order to improve the sensitivity of the diagnosis. Furthermore, this study does not favour the theory that the majority of mammographically detected cancers are indolent and highlights the poor sensitivity of the mammographic follow-up of nonpalpable lesions.


Critical Reviews in Oncology Hematology | 2003

Staging of primary cervical cancers: the role of nuclear medicine

Tarik Belhocine; Frédéric Kridelka; Alain Thille; Caroline De Barsy; Jacqueline Foidart-Willems; Roland Hustinx; Pierre Rigo

In nuclear medicine, [18F]-fluorodeoxyglucose positron emission tomography (18FDG PET) and lymphatic mapping and sentinel lymphadenectomy (LM/SL) may significantly improve the staging of primary cervical cancers. Indeed, the disease progresses in a level by level fashion to regional nodes through the lymphatic channels, and also to extra-nodal sites via the hematogenous stream. Additionally, the sub-optimal efficacy of routine radiological protocols, while new combined therapies are proving to be more efficient, stresses the need for alternative staging procedures. Current data suggest that LM/SL accurately reflects the regional lymph node status in early stage cervical cancers, and thus could avoid unnecessary complete lymphadenectomies. Also, whole body 18FDG PET may provide valuable insights on extra-pelvic and distant tumor spreading, with a significant impact on treatment choices. If these promising results are confirmed on large controlled trials, LM/SL and 18FDG PET imaging could be incorporated in the routine staging work-up of primary cervical cancers.


Gynecologic Oncology | 2002

Contribution of whole-body (18)FDG PET imaging in the management of cervical cancer

Tarik Belhocine; Alain Thille; Viviana Fridman; Adelin Albert; Laurence Seidel; Philippe Nickers; Frédéric Kridelka; Pierre Rigo


Journal De Gynecologie Obstetrique Et Biologie De La Reproduction | 1994

Hématome extradural cervical spontané de la femme enceinte

X. Mahieu; Frédéric Kridelka; Axelle Pintiaux; Pol Hans; Jean-François Brichant; Jacques Born; H. Thoumsin


International Journal of Gynecological Cancer | 1999

CD44v6 expression is an independent prognostic factor in node-negative FIGO stage IB cervical carcinoma

P. Speiser; Frédéric Kridelka; C. Tempfer; Lyndall Edwards; Sepp Leodolter; C. Kainz; Neville F. Hacker


Hormone and Metabolic Research | 1989

RU-486 inhibits rat gonadal steroidogenesis

P. Sanchez; Mary Ryan; Frédéric Kridelka; Isabelle Gielen; S. Ren; B. Albertson; S. Malozowski; Lynnette Nieman; F. Cassorla


Revue médicale de Liège | 2003

Le depistage du cancer du col de l'uterus en Belgique: le point en 2003

Philippe Delvenne; Nathalie Jacobs; Chantal Lambert; Jean Doyen; Frédéric Kridelka


European Journal of Nuclear Medicine and Molecular Imaging | 2003

Added value of whole body 18FDG PET imaging in monitoring uterine cancers.

Tarik Belhocine; Alain Thille; C. De Barsy; Frédéric Kridelka; Roland Hustinx; Jacqueline Foidart-Willems


The Journal of Nuclear Medicine | 2001

Usefulness of FDG-PET imaging in the management of cervical carcinoma.

Tarik Belhocine; Roland Hustinx; Frédéric Kridelka; Alain Thille; Frédéric Daenen; Caroline De Barsy; Pierre Rigo

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Neville F. Hacker

University of New South Wales

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