Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Alvida M. Cain"'
Autor:
D. Ashley Hill, Catherine A. Billups, Alvida M. Cain, Bhaskar N. Rao, Shannon E. Riedley, Wayne L. Furman, Charles B. Pratt, Sheri L. Spunt
Publikováno v:
Journal of Clinical Oncology. 25:5808-5814
Purpose Pediatric colorectal carcinoma (CRC) is rare, but the available data suggest that it is more likely than adult CRC to be advanced at presentation and to have a poor outcome. We sought to better characterize pediatric CRC. Patients and Methods
Autor:
Wayne L. Furman, Fariba Navid, Sheri L. Spunt, Alberto S. Pappo, Alvida M. Cain, Catherine A. Billups, Bhaskar N. Rao, Thomas E. Merchant, Victor M. Santana, Gregory A. Hale
Publikováno v:
Cancer. 106:1846-1856
BACKGROUND Intensified chemotherapy may improve the outcome of patients with high-risk pediatric sarcomas. Vincristine, doxorubicin, cyclophosphamide, ifosfamide, and etoposide are highly effective against pediatric sarcomas. The authors investigated
Autor:
M. Beth McCarville, Alvida M. Cain, Carlos Rodriguez-Galindo, Catherine A. Billups, William H. Meyer, Bhaskar N. Rao, Najat C. Daw, Michael D. Neel, Jesse J. Jenkins
Publikováno v:
Cancer. 106:403-412
BACKGROUND. The outcome of patients with metastatic osteosarcoma treated in two consecutive trials from 1986 to 1997 was analyzed to evaluate the efficacy of carboplatin-based multiagent chemotherapy and to identify prognostic factors. The initial st
Autor:
Beverly Raney, Alp Ozkan, Adrian C. Mattke, Alvida M. Cain, Mark F. Munsell, Mehmet Fatih Okcu, Alberto S. Pappo, Michela Casanova, Andrea Ferrari, Joern Treuner
Publikováno v:
Journal of Clinical Oncology. 21:1602-1611
Purpose: To identify prognostic factors related to outcome in 219 children and adolescents with synovial sarcoma. Patients and Methods: We combined the experiences of the four following research groups: Cooperative Weichteilsarkomastudie Group, Germa
Autor:
Anami Patel, Jennifer Hyer, Alberto S. Pappo, D. Ashley Hill, Sheila A. Shurtleff, Catherine A. Billups, James R. Downing, Alvida M. Cain, Shannon E. Riedley
Publikováno v:
Pediatric and Developmental Pathology. 6:24-34
Synovial sarcoma is the most common nonrhabdomyosarcomatous soft tissue sarcoma in children and adolescents and is characterized by a reciprocal t(X;18)(p11;q11) which results in the fusion of the SYT gene on chromosome 18q11 to either of two closely
Autor:
Alberto S. Pappo, Sheri L. Spunt, Catherine A. Poquette, Alvida M. Cain, Larry E. Kun, Leonardo Brandao, M. McCarville
Publikováno v:
Journal of Pediatric Hematology/Oncology. 23:93-98
The benefit of whole-lung irradiation (WLI) for patients who have pulmonary metastases (PM) of Ewing sarcoma family tumors (ESFT) is unclear. At our institution, WLI is reserved for patients with PM that do not respond completely to induction chemoth
Autor:
M. Beth McCarville, Charles B. Pratt, Olga Goloubeva, C D O Sue Kaste, Bhaskar N. Rao, Alvida M. Cain Ccra
Publikováno v:
Cancer. 91:1170-1176
BACKGROUND In children with osteosarcoma who have undergone thoracotomy, it often is difficult to distinguish metastatic from benign recurrent pulmonary nodules. The authors of this study sought to identify any computed tomography (CT) imaging patter
Autor:
Catherine A. Poquette, Thomas E. Merchant, Jesse J. Jenkins, Alberto S. Pappo, Yasmeen S. Hurt, Victor M. Santana, Sheri L. Spunt, Charles B. Pratt, Bhaskar N. Rao, Alvida M. Cain
Publikováno v:
Journal of Clinical Oncology. 17:3697-3705
PURPOSE: The rarity and heterogeneity of pediatric nonrhabdomyosarcoma soft tissue sarcoma (NRSTS) has precluded meaningful analysis of prognostic factors associated with surgically resected disease. To define a population of patients at high risk of
Publikováno v:
Cancer. 86:1602-1608
BACKGROUND The authors performed a retrospective study to estimate the incidence rate of metastatic disease at the time of diagnosis of extremity osteosarcoma (OS), to characterize its pattern of presentation, and to identify factors predictive of su
Autor:
Alvida M. Cain, Alberto S. Pappo, Jesse J. Jenkins, Catherine A. Poquette, Bhaskar N. Rao, Charles B. Pratt, Thomas E. Merchant
Publikováno v:
Medical and Pediatric Oncology. 33:76-82
Background Because the natural history of pediatric patients with metastatic nonrhabdomyosarcomatous soft-tissue sarcomas (NRSTS) had not been well described, we retrospectively reviewed our single-institution experience with these tumors. Procedure