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Dive into the research topics where Øyvin P. Solheim is active.

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Featured researches published by Øyvin P. Solheim.


Acta Oncologica | 1996

Targeted Radiotherapy of Osteosarcoma Using 153Sm-Edtmp: A new promising approach

Øyvind S. Bruland; Arne Skretting; Øyvin P. Solheim; Magne Aas

We report a case where targeted radionuclide therapy using 153Sm-EDTMP gave substantial palliative effect. A 35-year-old male with a primary osteosarcoma located in the first lumbar vertebra relapsed with progressive back pain after conventional treatment modalities had failed. He became bedridden, and developed paraparesis and impaired bladder function. On a diagnostic bone-scan intense radioactivity was localized in the tumor. He therefore was given 153Sm-EDTMP treatment twice, 8 weeks apart, 35 and 32 MBq/kg body weight respectively. After a few days the pain was significantly relieved and by the second radionuclide treatment the pareses subsided. For six months he was able to be up and about without any neurological signs or detectable metastases. Eventually, however, he experienced increasing local pain, developed paraparesis, was re-operated but died 4 months later. The dramatic transient improvement observed in this case warrants further exploration using 153Sm-EDTMP as a boost technique, supplementary to conventional external radiotherapy.


Cancer Chemotherapy and Pharmacology | 1995

Treatment of advanced, high-grade soft-tissue sarcoma with ifosfamide and continuous-infusion etoposide

Gunnar Sæter; Kristian Talle; Øyvin P. Solheim

A total of 33 patients (median age, 44 years) with high-grade, adult soft-tissue sarcoma were treated with etoposide given at 600 mg/m2 in a 72-h continuous infusion and ifosfamide given at 1500 mg/m2 per day for 3 days every 3 weeks. Dose escalation/reduction was protocolled depending on the level of hematological toxicity observed in the preceding course. Overall, 90% of patients had metastatic disease, and the most common histologies were malignant fibrous histiocytoma and leiomyosarcoma. A median of 5 (range, 1–9) courses were given. Of 30 patients who were evaluable for response, 12 (40%) obtained a partial remission, and the median time to progression was 8 (range, 4–13) months. Grade 3–4 leukopenia and thrombocytopenia were seen after 89% and 8% of the courses, respectively; neutropenic fever was seen in half of the patients (15% of courses); and 32% of courses had to be postponed by 7 days or more due to myelosuppression. Dose reduction to below the standard had to be performed in 46% of courses, and dose escalation was achieved in only 13%. The reduced toxicity seen after the addition of granulocyte colony-stimulating factor (G-CSF) in five patients indicates that growth-factor support may enhance the dose intensity of the regimen. The results indicate significant activity for this regimen in adult softtissue sarcoma, which may in part be a result of the escalated dose and prolonged mode of administration of the phasespecific agent etoposide. As a result of this pilot series, a phase II study with ifosfamide, etoposide, and G-CSF in advanced adult soft-tissue sarcoma has been initiated by the Scandinavian Sarcoma Group.


Pathology Research and Practice | 1997

SYNOVIAL SARCOMA : IMMUNOHISTOCHEMICAL EXPRESSION OF P-GLYCOPROTEIN AND GLUTATHIONE S TRANSFERASE-PI AND CLINICAL DRUG RESISTANCE

José Manuel Lopes; Øyvind S. Bruland; Bodil Bjerkehagen; M. Carolina Silva; Ruth Holm; Erik O. Pettersen; Øyvin P. Solheim; Manuel Sobrinho-Simões; Jahn M. Nesland

Our purpose was to study the role of the expression of P-glycoprotein (Pgp) and glutathione S transferase-pi (GST-pi) in predicting the response to chemotherapy, relapse-free interval, and survival of patients with synovial sarcoma (SS). Thirty-seven cases of primary SS, without regional lymph node or distant metastases, were studied. There were 17 females and 20 males, ranging in age from 7 to 81 years (median, 31 years) with tumors located in the lower extremity (n = 24) upper extremity (n = 5) and trunchus (n = 8). The cases were retrospectively studied without knowledge of clinical course to compare the immunohistochemical expression of Pgp and GST-pi, flow cytometry parameters (ploidy and % of cells in S+G2 phases), and PCNA and Ki-67 labeling of primary tumors before any therapy, with that observed in local recurrences and metastases after chemotherapy. The relationship of the aforementioned parameters with clinicopathological features (gender, age, and histo-blood group of the patients, size, location, histological subtype. TNM stage, and clinical response to chemotherapy of the tumors) was also evaluated. Results revealed that Pgp and GST-pi were expressed in 29.7% and 40.5% of the cases, respectively. In 48.6% of the tumors there was expression of a least one of the drug resistance markers. The markers were coexpressed in 25.0% of the tumors. The prevalence of Pgp expression was lower, but not significantly, in stage I-II (17.6%) than in stage III (40.0%) tumors, and also in cases without clinical progression (16.7%), than in cases with (36.0%). No such differences were observed for GST-pi expression. Pgp and GST-pi expressions were significantly associated with biphasic SS and were particularly noticeable in solid/glandular areas of biphasic SS. The expression of the drug resistance markers was not significantly associated with gender, age, and histo-blood group of the patients, dimension, location, and proliferative activity of the tumors; it was also not significantly related to relapse-free interval and survival of the patients. The expression of Pgp and GST-pi was not significantly associated either to response to chemotherapy or influenced by chemotherapy. We conclude that Pgp and GST-pi expressions are not good predictors response to of the chemotherapy in patients with localized SS. Other drug resistance mechanisms may be active in SS.


Acta Orthopaedica Scandinavica | 1999

Dynamic bone scintigraphy for evaluation of tumor response after preoperative chemotherapy : A retrospective study of osteosarcoma and Ewing's sarcoma patients

Mette Winderen; A. E. Stenwig; Øyvin P. Solheim; Gunnar Sæter; Magne Aas

Dynamic bone scintigraphy with 2-second scintigrams for 6 minutes after the injection of Tc-99m-MDP, may be regarded as a kind of angiography. We investigated the vascularity and early uptake of MD...


European Journal of Cancer | 1995

868 Impact of local recurrences in soft tissue sarcoma surgery

J. Høie; Øyvin P. Solheim; A. E. Stenwig

Primary surgery in soft tissue sarcomas may be a dilemma between saving functions, abstain of mutilation and the potential of local recurrence. Material: 394 consecutive patients treated before 1990 have been analyzed. Results 100 patients presented with 150 recurrences; 79 patients with one recurrence only. In these 79, distant spread were seen concomitant with the local recurrence in 27, another 25 patients are free of disease following treatment of their recurrence, in 15 wide primary excisions were impracticable, and 6 patients were above their 80-ties. In 6 patients only, more extensive primary surgery should be advocated. In 7 patients with 4 to 8 episodes of recurrence, 2 died of distant disease, 1 of the local disease and 4 are free of disease. Conclusion impact of local recurrence is moderate and may be accepted in lieu of mutilating surgery.


International Journal of Cancer | 1986

Characteristics of a cell line established from a patient with multiple osteosarcoma, appearing 13 years after treatment for bilateral retinoblastoma

Øystein Fodstad; Anton Brøgger; Øyvind S. Bruland; Øyvin P. Solheim; Jahn M. Nesland; Alexander Pihl


Radiology | 1999

Malignant pleural mesothelioma: US-guided histologic core-needle biopsy.

Arne Heilo; A. E. Stenwig; Øyvin P. Solheim


Acta Medica Scandinavica | 2009

Osteosclerotic Myeloma with Polyneuropathy

Jon B. Reitan; Eivind Pape; Sophie D. Fosså; Ole‐Jørgen ‐J Julsrud; Olav N. Slettnes; Øyvin P. Solheim


Radiology | 1991

Osteogenic sarcoma: MR signal abnormalities of the brain in asymptomatic patients treated with high-dose methotrexate.

Hans H. Lien; Viggo Blomlie; Gunnar Sæter; Øyvin P. Solheim; Sophie D. Fosså


European Journal of Cancer | 1994

Immunoscintigraphy of bone sarcomas--results in 5 patients.

Øyvind S. Bruland; Øystein Fodstad; Magne Aas; Øyvin P. Solheim; Johan Høie; Arne Skretting; Mette Winderen; T. Michaelsen; A. Pihl

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