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1.
Radiat Oncol ; 14(1): 207, 2019 Nov 21.
Article in English | MEDLINE | ID: mdl-31752932

ABSTRACT

PURPOSE: The purpose of this study was to compare carbon-ion (C-ion), proton and photon radiotherapy (RT) plans with regard to dose reduction of the gastrointestinal (GI) tract by using a greater omentum spacer (GO spacer). METHODS: We retrospectively retrieved data for ten patients who received the GO spacer as surgical spacer placement for abdominal and pelvic tumors. Simulation plans were created on pre-spacer Computed Tomography (CT) and post-spacer CT for C-ion RT, proton RT and photon RT to compare the dose of the GI tract. The plans were normalized so that at least 95% of the planning target volume (PTV) received 70 Gy (relative biological effectiveness equivalent) delivered in 35 fractions. All plans were created with the lowest possible dose to the GI tract under conditions that meet the dose constraints for the PTV and spinal cord (maximum dose < 45 Gy). The part of the GI tract to be evaluated was defined as that most adjacent to the PTV. C-ion RT plans and proton RT plans were calculated by a spot scanning technique, and photon RT plans were calculated employing by fixed-field intensity-modulated radiation therapy. RESULTS: D2 cc and V10-70 of the GI tract were significantly lower on post-spacer plans than on pre-spacer plans for all three RT modalities. Regarding post-spacer plans, D2 cc of the GI tract was significantly lower on C-ion RT plans and proton RT plans than on photon RT plans (C-ion vs photon p = 0.001, proton vs photon p = 0.002). However, there was no significant difference between C-ion RT plans and proton RT plans for D2 cc of the GI tract (C-ion vs proton p = 0.992). In the photon RT plan for one patient, D2 cc of the GI tract did not meet < 50 Gy. CONCLUSIONS: The GO spacer shows a significant dose reduction effect on the GI tract.


Subject(s)
Abdominal Neoplasms/radiotherapy , Heavy Ion Radiotherapy/methods , Omentum/radiation effects , Pelvic Neoplasms/radiotherapy , Proton Therapy/methods , Radiotherapy, Intensity-Modulated/methods , Abdominal Neoplasms/surgery , Computer Simulation , Female , Gastrointestinal Tract/radiation effects , Humans , Male , Pelvic Neoplasms/surgery , Photons , Radiometry , Radiotherapy Dosage , Radiotherapy Planning, Computer-Assisted , Retrospective Studies , Tomography, X-Ray Computed
2.
Exp Hematol ; 3(3): 187-96, 1975 Jun.
Article in English | MEDLINE | ID: mdl-239853

ABSTRACT

Whole body irradiation of the recipients of syngeneic splenic implants into the omentum greatly enchances hematopoiesis and permits survial of and repopulation by stem cells of donor origin. Donor hematopioetic stem cells do not survive in spleen implants of the nonirradiated host; irradiated hosts were therfore used in the bulk of the experiments. Differentiation in the implants of splenic fragments is predominantly erythrocytic at 10 days and shifts to predominantly granulocytic differentiation at 21 days. Suspensions of spleen cells injected into the ometntum are predominantly granulocytopioetic at 10 days. The differntiation in fragments of spleen depleted of stem cells by irradtion, seeded with bone marrow cells and implanted into the omentum results in mixed erythocytic and granulocytic hematopoiesis, with granulocytic predominance. Lymphocytic cells appeared late in the implants of irrdiated recipients even at a time of prolific lymphocytopoiesis in the host's own spleens. The cause of the delay in the implants is not clear. The data are consisent with the concept that differntiation of hematopioetic stem cells is influenced by the stromal cells of the parent organ. The erythrocytic inductive capacity of the stromal cells may be lost by mechanical disruption or modified by irraidation or a prolonged period of implantation.


Subject(s)
Hematopoiesis/radiation effects , Omentum/radiation effects , Radiation Effects , Spleen/transplantation , Animals , Bone Marrow Cells , Bone Marrow Transplantation , Cell Division , Female , Graft Rejection , Hematopoietic Stem Cell Transplantation , Hematopoietic Stem Cells/radiation effects , Karyotyping , Mice , Mice, Inbred C57BL , Pregnancy , Spleen/cytology , Spleen/radiation effects , Time Factors , Transplantation, Homologous
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