Heinz Schmidberger
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Heinz Schmidberger has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Robert Michael Hermann
Center for Radiotherapy and Radiooncology Bremen and Westerstede, 26655 Westerstede, Germany
3 shared publications - Carsten Gründker
University Medical Center Göttingen, Department of Gynecology and Obstetrics, Göttingen, Germany
2 shared publications - Hans Christiansen
University Medicine Göttingen
2 shared publications - Margret Rave-Fränk
Department of radiotherapy radiooncology, Universität Göttingen, Robert Koch Strasse 40, 37075 Göttingen, Germany
2 shared publications - Paul Thelen
Georg-August-University, Göttingen, Germany
2 shared publications - Andrea Hille
Department of Radiotherapy, University hospital, Robert-Koch-Str. 40, 37075 Göttingen, Germany
1 shared publication
Latest Publications
- 15 July 2011
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 80 (4) , 1214-1219
Fractionated External Beam Radiotherapy as a Suitable Preparative Regimen for Hepatocyte Transplantation After Partial Hepatectomy
- 15 July 2011
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 80 (4) , 1214-1219
Fractionated External Beam Radiotherapy as a Suitable Preparative Regimen for Hepatocyte Transplantation After Partial Hepatectomy
- Open Access
- 14 July 2008
- Published by Springer Nature in Radiation Oncology
- Vol. 3 (1) , 19
In vitro studies on the modification of low-dose hyper-radiosensitivity in prostate cancer cells by incubation with genistein and estradiol
As the majority of prostate cancers (PC) express estrogen receptors, we evaluated the combination of radiation and estrogenic stimulation (estrogen and genistein) on the radiosensitivity of PC cells in vitro.
- 14 July 2008
- Published by Springer Nature in Radiation Oncology
- Vol. 3 (1) , 19
Open AccessIn vitro studies on the modification of low-dose hyper-radiosensitivity in prostate cancer cells by incubation with genistein and estradiol
As the majority of prostate cancers (PC) express estrogen receptors, we evaluated the combination of radiation and estrogenic stimulation (estrogen and genistein) on the radiosensitivity of PC cells in vitro.
- 1 June 2008
- Published by Springer Nature in Der Onkologe
- Vol. 14 (6) , 618-624
Therapie des Seminoms im Stadium I
- 1 June 2008
- Published by Springer Nature in Der Onkologe
- Vol. 14 (6) , 618-624
Therapie des Seminoms im Stadium I
- Open Access
- 1 December 2007
- Published by Springer Nature in Radiation Oncology
- Vol. 2 (1) , 31
No supra-additive effects of goserelin and radiotherapy on clonogenic survival of prostate carcinoma cells in vitro
Oncological results of radiotherapy for locally advanced prostate cancer (PC) are significantly improved by simultaneous application of LHRH analoga (e.g. goserelin). As 85% of PC express LHRH receptors, we investigated the interaction of goserelin incubation with radiotherapy under androgen-deprived conditions in vitro.
- 1 December 2007
- Published by Springer Nature in Radiation Oncology
- Vol. 2 (1) , 31
Open AccessNo supra-additive effects of goserelin and radiotherapy on clonogenic survival of prostate carcinoma cells in vitro
Oncological results of radiotherapy for locally advanced prostate cancer (PC) are significantly improved by simultaneous application of LHRH analoga (e.g. goserelin). As 85% of PC express LHRH receptors, we investigated the interaction of goserelin incubation with radiotherapy under androgen-deprived conditions in vitro.
- 29 April 2005
- Published by S. Karger AG in Oncology Research and Treatment
- Vol. 28 (5) , 275-280
Combination of Anti-Estrogenic Therapy with Radiation in Breast Cancer: Simultaneous or Sequential Treatment?
Adjuvant radiotherapy and adjuvant endocrine therapy are commonly given to patients with invasive breast cancer or with ductal carcinoma in situ (DCIS). Although both therapies have been well established through a number of randomized studies, little is known about a possible interaction of both treatment modalities if they are given simultaneously. A number of in vitro studies indicated that tamoxifen treatment might reduce the intrinsic radiosensitivity of MCF-7 breast cancer cells. Conversely, estradiol treatment increased the intrinsic radiosensitivity of MCF-7 cells. This phenomenon has not been found in clinical studies. Retrospective analyses of prospectively randomized clinical studies did not indicate an antagonistic effect of tamoxifen on the effectiveness of ionizing radiation (XRT), since local control has been consistently higher when XRT was combined with tamoxifen, compared to treatment with XRT alone, regardless of whether tamoxifen was started simultaneously with radiotherapy or after completion of radiotherapy. Currently there are no clinical data available that would suggest an adverse effect of adjuvant tamoxifen treatment started prior to or simultaneously with radiotherapy in breast cancer or DCIS. However, since an antagonistic effect of tamoxifen and simultaneous chemotherapy has been reported recently, the issue of simultaneous.
- 29 April 2005
- Published by S. Karger AG in Oncology Research and Treatment
- Vol. 28 (5) , 275-280
Combination of Anti-Estrogenic Therapy with Radiation in Breast Cancer: Simultaneous or Sequential Treatment?
Adjuvant radiotherapy and adjuvant endocrine therapy are commonly given to patients with invasive breast cancer or with ductal carcinoma in situ (DCIS). Although both therapies have been well established through a number of randomized studies, little is known about a possible interaction of both treatment modalities if they are given simultaneously. A number of in vitro studies indicated that tamoxifen treatment might reduce the intrinsic radiosensitivity of MCF-7 breast cancer cells. Conversely, estradiol treatment increased the intrinsic radiosensitivity of MCF-7 cells. This phenomenon has not been found in clinical studies. Retrospective analyses of prospectively randomized clinical studies did not indicate an antagonistic effect of tamoxifen on the effectiveness of ionizing radiation (XRT), since local control has been consistently higher when XRT was combined with tamoxifen, compared to treatment with XRT alone, regardless of whether tamoxifen was started simultaneously with radiotherapy or after completion of radiotherapy. Currently there are no clinical data available that would suggest an adverse effect of adjuvant tamoxifen treatment started prior to or simultaneously with radiotherapy in breast cancer or DCIS. However, since an antagonistic effect of tamoxifen and simultaneous chemotherapy has been reported recently, the issue of simultaneous.