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Carboplatin and Paclitaxel for Advanced Endometrial Cancer: Final Overall Survival and Adverse Event Analysis of a Phase III Trial (NRG Oncology/GOG0209).
Miller, David S; Filiaci, Virginia L; Mannel, Robert S; Cohn, David E; Matsumoto, Takashi; Tewari, Krishnansu S; DiSilvestro, Paul; Pearl, Michael L; Argenta, Peter A; Powell, Matthew A; Zweizig, Susan L; Warshal, David P; Hanjani, Parviz; Carney, Michael E; Huang, Helen; Cella, David; Zaino, Richard; Fleming, Gini F.
Afiliación
  • Miller DS; University of Texas Southwestern Medical Center, Dallas, TX.
  • Filiaci VL; NRG Oncology, Clinical Trial Development Division, Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Mannel RS; The Peggy and Charles Stephenson Cancer Center, The University of Oklahoma Health Sciences Center, Oklahoma City, OK.
  • Cohn DE; Arthur G. James Cancer Hospital and Solove Research Institute, Ohio State University, Columbus, OH.
  • Matsumoto T; Ehime University School of Medicine, Ehime, Japan.
  • Tewari KS; Division of Obstetrics and Gynecology, University of California, Irvine Medical Center, Orange, CA.
  • DiSilvestro P; Women and Infants Hospital, Providence, RI.
  • Pearl ML; Stony Brook University Hospital, Stony Brook, NY.
  • Argenta PA; University of Minnesota, Minneapolis, MN.
  • Powell MA; Gynecologic Oncology, Washington University School of Medicine, St Louis, MO.
  • Zweizig SL; University of Massachusetts Memorial Medical Center, Worcester, MA.
  • Warshal DP; Cooper Hospital/University Medical Center, Camden, NJ.
  • Hanjani P; Hanjani Institute for Gynecologic Oncology, Abington Memorial Hospital, Abington, PA.
  • Carney ME; John A. Burns School of Medicine, University of Hawaii Cancer Center, Honolulu, HI.
  • Huang H; NRG Oncology, Clinical Trial Development Division, Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Cella D; Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Zaino R; Penn State University, Hershey, PA.
  • Fleming GF; The University of Chicago Medicine, Chicago, IL.
J Clin Oncol ; 38(33): 3841-3850, 2020 11 20.
Article en En | MEDLINE | ID: mdl-33078978
ABSTRACT

PURPOSE:

Limitations of the paclitaxel-doxorubicin-cisplatin (TAP) regimen in the treatment of endometrial cancer include tolerability and cumbersome scheduling. The Gynecologic Oncology Group studied carboplatin plus paclitaxel (TC) as a noninferior alternative to TAP.

METHODS:

GOG0209 was a phase III, randomized, noninferiority, open-label trial. Inclusion criteria were stage III, stage IV, and recurrent endometrial cancers; performance status 0-2; and adequate renal, hepatic, and marrow function. Prior radiotherapy and/or hormonal therapy were permitted, but chemotherapy, including radiosensitization, was not. Patients were treated with doxorubicin 45 mg/m2 and cisplatin 50 mg/m2 (day 1), followed by paclitaxel 160 mg/m2 (day 2) with granulocyte colony-stimulating factor or paclitaxel 175 mg/m2 and carboplatin area under the curve 6 (day 1) every 21 days for seven cycles. The primary endpoint was overall survival (OS; modified intention to treat). Progression-free survival (PFS), health-related quality of life (HRQoL), and toxicity were secondary endpoints.

RESULTS:

From 2003 to 2009, 1,381 women were enrolled. Noninferiority of TC to TAP was concluded for OS (median, 37 v 41 months, respectively; hazard ratio [HR], 1.002; 90% CI, 0.9 to 1.12), and PFS (median, 13 v 14 months; HR, 1.032; 90% CI, 0.93 to 1.15). Neutropenic fever was reported in 7% of patients receiving TAP and 6% of those receiving TC. Grade > 2 sensory neuropathy was recorded in 26% of patients receiving TAP and 20% receiving TC (P = .40). More grade ≥ 3 thrombocytopenia (23% v 12%), vomiting (7% v 4%), diarrhea (6% v 2%), and metabolic (14% v 8%) toxicities were reported with TAP. Neutropenia (52% v 80%) was more common with TC. Small HRQoL differences favored TC.

CONCLUSION:

With demonstrated noninferiority to TAP, TC is the global first-line standard for advanced endometrial cancer.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Endometriales Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Female / Humans / Middle aged Idioma: En Revista: J Clin Oncol Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Endometriales Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Female / Humans / Middle aged Idioma: En Revista: J Clin Oncol Año: 2020 Tipo del documento: Article
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