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Bone Marrow-sparing Intensity Modulated Radiation Therapy With Concurrent Cisplatin For Stage IB-IVA Cervical Cancer: An International Multicenter Phase II Clinical Trial (INTERTECC-2).
Mell, Loren K; Sirák, Igor; Wei, Lichun; Tarnawski, Rafal; Mahantshetty, Umesh; Yashar, Catheryn M; McHale, Michael T; Xu, Ronghui; Honerkamp-Smith, Gordon; Carmona, Ruben; Wright, Mary; Williamson, Casey W; Kasaová, Linda; Li, Nan; Kry, Stephen; Michalski, Jeff; Bosch, Walter; Straube, William; Schwarz, Julie; Lowenstein, Jessica; Jiang, Steve B; Saenz, Cheryl C; Plaxe, Steve; Einck, John; Khorprasert, Chonlakiet; Koonings, Paul; Harrison, Terry; Shi, Mei; Mundt, A J.
Afiliação
  • Mell LK; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California. Electronic address: lmell@ucsd.edu.
  • Sirák I; Department of Oncology and Radiotherapy, University Hospital, Hradec Kralove, Czech Republic.
  • Wei L; Xijing Hospital, Xian, China.
  • Tarnawski R; Marie Sklodowska Cancer Center and Institute of Oncology, Gliwice, Poland.
  • Mahantshetty U; Tata Memorial Centre, Parel, Mumbai, India.
  • Yashar CM; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.
  • McHale MT; University of California, San Diego, La Jolla, California.
  • Xu R; University of California, San Diego, La Jolla, California.
  • Honerkamp-Smith G; University of California, San Diego, La Jolla, California.
  • Carmona R; University of California, San Diego, La Jolla, California.
  • Wright M; University of California, San Diego, La Jolla, California.
  • Williamson CW; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.
  • Kasaová L; Department of Oncology and Radiotherapy, University Hospital, Hradec Kralove, Czech Republic.
  • Li N; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.
  • Kry S; Department of Radiation Oncology, Washington University, St Louis, Missouri.
  • Michalski J; MD Anderson Cancer Center, Houston, Texas.
  • Bosch W; MD Anderson Cancer Center, Houston, Texas.
  • Straube W; MD Anderson Cancer Center, Houston, Texas.
  • Schwarz J; Washington University, St Louis, Missouri.
  • Lowenstein J; University of California, San Diego, La Jolla, California.
  • Jiang SB; University of California, San Diego, La Jolla, California.
  • Saenz CC; University of California, San Diego, La Jolla, California.
  • Plaxe S; University of California, San Diego, La Jolla, California.
  • Einck J; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.
  • Khorprasert C; Kaiser Permanente Medical Center, San Diego, California.
  • Koonings P; Chulalongkorn Hospital, Bangkok, Thailand.
  • Harrison T; Chulalongkorn Hospital, Bangkok, Thailand.
  • Shi M; Xijing Hospital, Xian, China.
  • Mundt AJ; Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.
Int J Radiat Oncol Biol Phys ; 97(3): 536-545, 2017 03 01.
Article em En | MEDLINE | ID: mdl-28126303
PURPOSE: To test the hypothesis that intensity modulated radiation therapy (IMRT) reduces acute hematologic and gastrointestinal (GI) toxicity for patients with locoregionally advanced cervical cancer. METHODS AND MATERIALS: We enrolled patients with stage IB-IVA cervical carcinoma in a single-arm phase II trial involving 8 centers internationally. All patients received weekly cisplatin concurrently with once-daily IMRT, followed by intracavitary brachytherapy, as indicated. The primary endpoint was the occurrence of either acute grade ≥3 neutropenia or clinically significant GI toxicity within 30 days of completing chemoradiation therapy. A preplanned subgroup analysis tested the hypothesis that positron emission tomography-based image-guided IMRT (IG-IMRT) would lower the risk of acute neutropenia. We also longitudinally assessed patients' changes in quality of life. RESULTS: From October 2011 to April 2015, 83 patients met the eligibility criteria and initiated protocol therapy. The median follow-up was 26.0 months. The incidence of any primary event was 26.5% (95% confidence interval [CI] 18.2%-36.9%), significantly lower than the 40% incidence hypothesized a priori from historical data (P=.012). The incidence of grade ≥3 neutropenia and clinically significant GI toxicity was 19.3% (95% CI 12.2%-29.0%) and 12.0% (95% CI 6.7%-20.8%), respectively. Compared with patients treated without IG-IMRT (n=48), those treated with IG-IMRT (n=35) had a significantly lower incidence of grade ≥3 neutropenia (8.6% vs 27.1%; 2-sided χ2P=.035) and nonsignificantly lower incidence of grade ≥3 leukopenia (25.7% vs 41.7%; P=.13) and any grade ≥3 hematologic toxicity (31.4% vs 43.8%; P=.25). CONCLUSIONS: IMRT reduces acute hematologic and GI toxicity compared with standard treatment, with promising therapeutic outcomes. Positron emission tomography IG-IMRT reduces the incidence of acute neutropenia.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiossensibilizantes / Medula Óssea / Neoplasias do Colo do Útero / Cisplatino / Radioterapia de Intensidade Modulada / Quimiorradioterapia / Tratamentos com Preservação do Órgão / Radioterapia Guiada por Imagem / Neutropenia Tipo de estudo: Clinical_trials / Guideline / Incidence_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiossensibilizantes / Medula Óssea / Neoplasias do Colo do Útero / Cisplatino / Radioterapia de Intensidade Modulada / Quimiorradioterapia / Tratamentos com Preservação do Órgão / Radioterapia Guiada por Imagem / Neutropenia Tipo de estudo: Clinical_trials / Guideline / Incidence_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2017 Tipo de documento: Article