Inge-Marie Obdeijn
Erasmus University Rotterdam
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Inge-Marie Obdeijn.
Journal of Clinical Oncology | 2010
A.J. Rijnsburger; Inge-Marie Obdeijn; R. Kaas; Madeleine M. A. Tilanus-Linthorst; Carla Boetes; Claudette E. Loo; Martin N. J. M. Wasser; Elisabeth Bergers; Theo Kok; Sara H. Muller; Hans Peterse; Rob A. E. M. Tollenaar; Nicoline Hoogerbrugge; Sybren Meijer; C.C.M. Bartels; Caroline Seynaeve; Maartje J. Hooning; Mieke Kriege; P.I.M. Schmitz; Jan C. Oosterwijk; Harry J. de Koning; Emiel J. Th. Rutgers; J.G.M. Klijn
PURPOSE The Dutch MRI Screening Study on early detection of hereditary breast cancer started in 1999. We evaluated the long-term results including separate analyses of BRCA1 and BRCA2 mutation carriers and first results on survival. PATIENTS AND METHODS Women with higher than 15% cumulative lifetime risk (CLTR) of breast cancer were screened with biannual clinical breast examination and annual mammography and magnetic resonance imaging (MRI). Participants were divided into subgroups: carriers of a gene mutation (50% to 85% CLTR) and two familial groups with high (30% to 50% CLTR) or moderate risk (15% to 30% CLTR). RESULTS Our update contains 2,157 eligible women including 599 mutation carriers (median follow-up of 4.9 years from entry) with 97 primary breast cancers detected (median follow-up of 5.0 years from diagnosis). MRI sensitivity was superior to that of mammography for invasive cancer (77.4% v 35.5%; P<.00005), but not for ductal carcinoma in situ. Results in the BRCA1 group were worse compared to the BRCA2, the high-, and the moderate-risk groups, respectively, for mammography sensitivity (25.0% v 61.5%, 45.5%, 46.7%), tumor size at diagnosis≤1 cm (21.4% v 61.5%, 40.9%, 63.6%), proportion of DCIS (6.5% v 18.8%, 14.8%, 31.3%) and interval cancers (32.3% v 6.3%, 3.7%, 6.3%), and age at diagnosis younger than 30 years (9.7% v 0%). Cumulative distant metastasis-free and overall survival at 6 years in all 42 BRCA1/2 mutation carriers with invasive breast cancer were 83.9% (95% CI, 64.1% to 93.3%) and 92.7% (95% CI, 79.0% to 97.6%), respectively, and 100% in the familial groups (n=43). CONCLUSION Screening results were somewhat worse in BRCA1 mutation carriers, but 6-year survival was high in all risk groups.
Clinical Cancer Research | 2007
Madeleine M.A. Tilanus-Linthorst; Inge-Marie Obdeijn; Wim C. J. Hop; Petrina Causer; Martin O. Leach; Ellen Warner; Linda Pointon; Kimberley Hill; J.G.M. Klijn; Ruth Warren; Fiona J. Gilbert
Purpose: Magnetic resonance imaging (MRI) screening enables early detection of breast cancers in women with an inherited predisposition. Interval cancers occurred in women with a BRCA1 mutation, possibly due to fast tumor growth. We investigated the effect of a BRCA1 or BRCA2 mutation and age on the growth rate of breast cancers, as this may influence the optimal screening frequency. Experimental Design: We reviewed the invasive cancers from the United Kingdom, Dutch, and Canadian MRI screening trials for women at hereditary risk, measuring tumor size at diagnosis and on preceding MRI and/or mammography. We could assess tumor volume doubling time (DT) in 100 cancers. Results: Tumor DT was estimated for 43 women with a BRCA1 mutation, 16 women with a BRCA2 mutation, and 41 women at high risk without an identified mutation. Growth rate slowed continuously with increasing age (P = 0.004). Growth was twice as fast in BRCA1 (P = 0.003) or BRCA2 (P = 0.03) patients as in high-risk patients of the same age. The mean DT for women with BRCA1/2 mutations diagnosed at ages ≤40, 41 to 50, and >50 years was 28, 68, and 81 days, respectively, and 83, 121, and 173 days, respectively, in the high-risk group. Pathologic tumor size decreased with increasing age (P = 0.001). Median size was 15 mm for patients ages ≤40 years compared with 9 mm in older patients (P = 0.003); tumors were largest in young women with BRCA1 mutations. Conclusion: Tumors grow quickly in women with BRCA1 mutations and in young women. Age and risk group should be taken into account in screening protocols.
European Radiology | 2008
J. Veltman; R. Mann; Theo Kok; Inge-Marie Obdeijn; Nicoline Hoogerbrugge; Johan G. Blickman; Carla Boetes
The appearance of malignant lesions in BRCA1 and BRCA2 mutation carriers (BRCA-MCs) on mammography and magnetic resonance imaging (MRI) was evaluated. Thus, 29 BRCA-MCs with breast cancer were retrospectively evaluated and the results compared with an age, tumor size and tumor type matched control group of 29 sporadic breast cancer cases. Detection rates on both modalities were evaluated. Tumors were analyzed on morphology, density (mammography), enhancement pattern and kinetics (MRI). Overall detection was significantly better with MRI than with mammography (55/58 vs 44/57, P = 0.021). On mammography, lesions in the BRCA-MC group were significantly more described as rounded (12//19 vs 3/13, P = 0.036) and with sharp margins (9/19 vs 1/13, P = 0.024). On MRI lesions in the BRCA-MC group were significantly more described as rounded (16/27 vs 7/28, P = 0.010), with sharp margins (20/27 vs 7/28, P < 0.001) and with rim enhancement (7/27 vs 1/28, P = 0.025). No significant difference was found for enhancement kinetics (P = 0.667). Malignant lesions in BRCA-MC frequently have morphological characteristics commonly seen in benign lesions, like a rounded shape or sharp margins. This applies for both mammography and MRI. However the possibility of MRI to evaluate the enhancement pattern and kinetics enables the detection of characteristics suggestive for a malignancy.
American Journal of Roentgenology | 2013
Inge-Marie Obdeijn; Madeleine M.A. Tilanus-Linthorst; Sandra Spronk; Carolien H.M. van Deurzen; Cécile de Monyé; M. G. Myriam Hunink; Marian B. E. Menke
OBJECTIVE In breast cancer patients eligible for breast-conserving surgery, we evaluated whether the information provided by preoperative MRI of the breast would result in fewer tumor-positive resection margins and fewer reoperations. SUBJECTS AND METHODS The study group consisted of 123 consecutive patients diagnosed with either breast cancer or ductal carcinoma in situ eligible for breast-conserving surgery between April 2007 and July 2010. For these patients, a first plan for breast-conserving surgery was made on the basis of clinical examination and conventional imaging. The final surgical plan was made with knowledge of the preoperative breast MRI. The rates of tumor-positive resection margins and reoperations were compared with those of a historical control group consisting of 119 patients who underwent 123 breast-conserving procedures between January 2005 and December 2006. The percentage of change in the surgical plan was recorded. RESULTS Preoperative breast MRI changed the surgical plan to more extensive surgery in 42 patients (34.1%), mainly to mastectomy (29 patients, 23.6%). Ninety-four patients underwent 95 breast-conserving procedures. Significantly fewer patients had tumor-positive resection margins than in the control group (15.8%, 15/95 versus 29.3%, 36/123; p < 0.01). Patients in the study group underwent significantly fewer reoperations compared with the historical control group (18.9%, 18/95 vs 37.4%, 46/123; p < 0.01). CONCLUSION Preoperative breast MRI can substantially decrease the rate of tumor-positive resection margins and reoperations in breast cancer patients eligible for breast-conserving surgery.
Journal of the National Cancer Institute | 2013
Sepideh Saadatmand; Madeleine M.A. Tilanus-Linthorst; Emiel J. Th. Rutgers; Nicoline Hoogerbrugge; Jan C. Oosterwijk; Rob A. E. M. Tollenaar; Maartje J. Hooning; Claudette E. Loo; Inge-Marie Obdeijn; Eveline A.M. Heijnsdijk; Harry J. de Koning
BACKGROUND To reduce mortality, women with a family history of breast cancer are often screened with mammography before age 50 years. Additional magnetic resonance imaging (MRI) improves sensitivity and is cost-effective for BRCA1/2 mutation carriers. However, for women with a family history without a proven mutation, cost-effectiveness is unclear. METHODS We evaluated data of the largest prospective MRI screening study (MRISC). Between 1999 and 2007, 1597 women (8370 woman-years at risk) aged 25 to 70 years with an estimated cumulative lifetime risk of 15% to 50% for breast cancer were screened with clinical breast examination every 6 months and with annual mammography and MRI. We calculated the cost per detected and treated breast cancer. After incorporating MRISC data into a microsimulation screening analysis model (MISCAN), different schemes were evaluated, and cost per life-year gained (LYG) was estimated in comparison with the Dutch nationwide breast cancer screening program (biennial mammography from age 50 to 75 years). All statistical tests were two-sided. RESULTS Forty-seven breast cancers (9 ductal carcinoma in situ) were detected. Screening with additional MRI costs
International Journal of Cancer | 2015
Sepideh Saadatmand; Inge-Marie Obdeijn; Emiel J. Rutgers; Jan C. Oosterwijk; Rob A. E. M. Tollenaar; Gwendolyn H. Woldringh; Elisabeth Bergers; Cornelis Verhoef; Eveline A.M. Heijnsdijk; Maartje J. Hooning; Harry J. de Koning; Madeleine M.A. Tilanus-Linthorst
123 672 (€93 639) per detected breast cancer. In increasing age-cohorts, costs per detected and treated breast cancer decreased, but, unexpectedly, the percentage of MRI-only detected cancers increased. Screening under the MRISC-scheme from age 35 to 50 years was estimated to reduce breast cancer mortality by 25% at
BMC Cancer | 2012
Sepideh Saadatmand; Emiel J. Th. Rutgers; Rob A. E. M. Tollenaar; Hermien M. Zonderland; Margreet G. E. M. Ausems; Kristien Keymeulen; Margreet S. Schlooz-Vries; Linetta B. Koppert; Eveline A.M. Heijnsdijk; Caroline Seynaeve; Cees Verhoef; Jan C. Oosterwijk; Inge-Marie Obdeijn; Harry J. de Koning; Madeleine M.A. Tilanus-Linthorst
134 932 (€102 164) per LYG (3.5% discounting) compared with 17% mortality reduction at
Journal of Surgical Oncology | 2015
Elvira L. Vos; A. H. Koning; Inge-Marie Obdeijn; Victorien M.T. van Verschuer; Cornelis Verhoef; Peter J. van der Spek; Marian B. E. Menke-Pluijmers; Linetta B. Koppert
54 665 (€41 390) per LYG with mammography only. CONCLUSIONS Screening with MRI may improve survival for women with familial risk for breast cancer but is expensive, especially in the youngest age categories.
Cancer Biology & Therapy | 2014
Victorien M.T. van Verschuer; Bernadette A. M. Heemskerk-Gerritsen; Carolien H.M. van Deurzen; Inge-Marie Obdeijn; Madeleine M.A. Tilanus-Linthorst; Cornelis Verhoef; Marjanka K. Schmidt; Linetta B. Koppert; Maartje J. Hooning; Caroline Seynaeve
Adding MRI to annual mammography screening improves early breast cancer detection in women with familial risk or BRCA1/2 mutation, but breast cancer specific metastasis free survival (MFS) remains unknown. We compared MFS of patients from the largest prospective MRI Screening Study (MRISC) with 1:1 matched controls. Controls, unscreened if<50 years, and screened with biennial mammography if ≥50 years, were matched on risk category (BRCA1, BRCA2, familial risk), year and age of diagnosis. Of 2,308 MRISC participants, breast cancer was detected in 93 (97 breast cancers), who received MRI <2 years before breast cancer diagnosis; 33 BRCA1 mutation carriers, 18 BRCA2 mutation carriers, and 42 with familial risk. MRISC patients had smaller (87% vs. 52%
European Journal of Cancer | 2005
Madeleine M.A. Tilanus-Linthorst; Mieke Kriege; Carla Boetes; Wim C. J. Hop; Inge-Marie Obdeijn; Jan C. Oosterwijk; Hans Peterse; Harmine M. Zonderland; Sybren Meijer; Alexander M.M. Eggermont; Harry J. de Koning; J.G.M. Klijn; Cecile T.M. Brekelmans
BackgroundTo reduce mortality, women with a family history of breast cancer often start mammography screening at a younger age than the general population. Breast density is high in over 50% of women younger than 50 years. With high breast density, breast cancer incidence increases, but sensitivity of mammography decreases. Therefore, mammography might not be the optimal method for breast cancer screening in young women. Adding MRI increases sensitivity, but also the risk of false-positive results. The limitation of all previous MRI screening studies is that they do not contain a comparison group; all participants received both MRI and mammography. Therefore, we cannot empirically assess in which stage tumours would have been detected by either test.The aim of the Familial MRI Screening Study (FaMRIsc) is to compare the efficacy of MRI screening to mammography for women with a familial risk. Furthermore, we will assess the influence of breast density.Methods/DesignThis Dutch multicentre, randomized controlled trial, with balanced randomisation (1:1) has a parallel grouped design. Women with a cumulative lifetime risk for breast cancer due to their family history of ≥20%, aged 30–55 years are eligible. Identified BRCA1/2 mutation carriers or women with 50% risk of carrying a mutation are excluded. Group 1 receives yearly mammography and clinical breast examination (n = 1000), and group 2 yearly MRI and clinical breast examination, and mammography biennially (n = 1000).Primary endpoints are the number and stage of the detected breast cancers in each arm. Secondary endpoints are the number of false-positive results in both screening arms. Furthermore, sensitivity and positive predictive value of both screening strategies will be assessed. Cost-effectiveness of both strategies will be assessed. Analyses will also be performed with mammographic density as stratification factor.DiscussionPersonalized breast cancer screening might optimize mortality reduction with less over diagnosis. Breast density may be a key discriminator for selecting the optimal screening strategy for women < 55 years with familial breast cancer risk; mammography or MRI. These issues are addressed in the FaMRIsc study including high risk women due to a familial predisposition.Trial registrationNetherland Trial Register NTR2789