Examples of using Complete remission in English and their translations into German
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Complete remission.
Following Primary Systemic Therapy(PST) complete remission(CR) shown in imaging.
Complete remission, 50% partial remission. .
On average, it took 57 days for the patients to reach complete remission.
Complete remission means that after the treatment no tumour is detectable.
The aim of induction therapy is the achievement of a complete remission CR.
We have achieved complete remission in patients with advanced metastatic cancer.
In a phase-II pilot study all 36 patients reached complete remission after rituximab 24.
Complete remission(CR)1/Complete remission with partial haematological recovery(CRh*)2.
The total disappearance of symptoms and complete remission without signs of malignant cells.
CRp Complete Remission in the Absence of Total Platelet Recovery PR Partial Remission. .
This individual was then given allogeneic stem cell transplantation andremains in complete remission after 59 months.
Complete remission means the disorder is no longer detectable by any means, including brain maps.
In a study following subjects for ten years, agoraphobia without panic attacks was one of the most persistent disorders,with rare complete remission.
For acute leukemia, a complete remission that lasts five years after treatment often indicates cure.
In the main study, 60(97%) of 62 patients had either complete or partial remission, and 47(76%)had complete remission.
It is also recommended that responding patients who do not achieve a complete remission receive a total of 8 cycles of VELCADE therapy.
These drugs induce complete remission in nearly 80% of AML patients, though this percentage tends to decrease with increasing age and other factors, such as genetic abnormalities.
In the main study, 97% of the patients had either complete or partial remission(60 out of 62),and 76% had complete remission 47 out of 62.
Viewed overall, the new approach to this oncological treatment achieved one complete remission, 28 partial remissions and at least 40 times a temporary cessation of the illness.
CR complete remission; CRp complete remission with incomplete platelet recovery, EFS event-free survival, PFS progression-free survival, OR odds ratio, HR hazard ratio.
During the maintenance phase, 19 patientswere evaluated, with 17 patients achieving complete remission(89%), and 1 patient with therapeutic efficacy 5.
Overall survival and complete remission rates in pre-specified disease-related sub-groups(i.e., cytogenetic risk, Eastern Cooperative Oncology Group[ECOG] score, age, type of AML, and baseline bone marrow blast count) were consistent with results for the overall study population.
The first trial cohort enrolled 13 patients with untreated BPDCN, and seven patients(54%)achieved complete remission(CR) or CR with a skin abnormality not indicative of active disease CRc.
Evaluate Minimal Residual Disease(MRD) at baseline and follow-up in a clinical study or registry, as appropriate, for the assessment of the anti-leukaemic activity of Ceplene plus low dose Interleukin-2 in a sufficient number of adult patients stratifiedby age greater or less than 60 years with Acute Myeloid Leukemia in First Complete Remission.
Overall, from five studies analysed based on 65 ALL patients exposed to Oncaspar using thehighest therapeutic response during the entire study, complete remission were observed in 30 patients(46%), partial remission in 7 patients(11%) and haematological improvement in 1 patient 2.
Determine the feasibility of conducting, in conjunction with collaborative groups in Europe and/ or the United States, a Multicenter Randomized Open-Label Study to Evaluate the Safety and Efficacy of Ceplene plus Interleukin-2 to be determined in approximately 350 adult Patients(stratified by age greater or less than 60 years)with Acute Myeloid Leukemia in First Complete Remission by Q3, 2009.
Biotest: Pre-clinical studies demonstrate high efficacy ofBT-062 in solid tumours Immunoconjugate induces complete remission of human solid tumours in mouse models High anti-tumour activity against aggressive human breast, pancreas, bladder and lung carcinoma Data show efficacy in indications with a particularly great medical need Dreieich, Germany.
Clinical Study to evaluate the Biomarkers and Pharmacologic Endpoints of Ceplene plus low dose Interleukin-2 in approximately 100 Adult Patients stratified by age greater orless than 60 years with Acute Myeloid Leukemia in First Complete Remission(CR), with well characterized Morphologic, Cytogenetic and Molecular profiles First Patient In Q2, 2009 Final Study Results Q4, 2011.
The response was classified according to the WHO classification, which testifies complete remission when no further effusion is evident within four weeks of the last puncture, partial remission when further effusion is found within four weeks of the last puncture but no puncture is required, and failure(no change, progressive disease) when further effusion requiring puncture appears within four weeks.
