Your browser doesn't support javascript.
loading
Active Surveillance of Papillary Thyroid Cancer: Frequency and Time Course of the Six Most Common Tumor Volume Kinetic Patterns.
Tuttle, Robert Michael; Fagin, James; Minkowitz, Gerald; Wong, Richard; Roman, Benjamin; Patel, Snehal; Untch, Brian; Ganly, Ian; Shaha, Ashok; Shah, Jatin; Li, Duan; Bach, Ariadne; Girshman, Jeffrey; Lin, Oscar; Cohen, Marc; Cohen, Jean-Marc; Cracchiolo, Jennifer; Ghossein, Ronald; Sabra, Mona; Boucai, Laura; Fish, Stephanie; Morris, Luc.
Afiliação
  • Tuttle RM; Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Fagin J; Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Minkowitz G; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Wong R; Department of Surgery Education, Columbia University Irving Medical Center, New York, New York, USA.
  • Roman B; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Patel S; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Untch B; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Ganly I; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Shaha A; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Shah J; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Li D; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Bach A; Radiology and Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Girshman J; Radiology and Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Lin O; Radiology and Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Cohen M; Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Cohen JM; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Cracchiolo J; Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Ghossein R; Head and Neck Service, Department of Surgery, Departments of Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Sabra M; Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Boucai L; Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Fish S; Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Morris L; Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Thyroid ; 32(11): 1337-1345, 2022 11.
Article em En | MEDLINE | ID: mdl-36178355
Background: The change in size of the papillary thyroid cancer (PTC) nodule during active surveillance has traditionally been characterized as either stable, increasing, or decreasing based on changes in maximal tumor diameter or tumor volume. More recently, it has been observed that the changes in tumor size observed during observation are more complex with tumor volume kinetic patterns that can be characterized either as stable (Pattern I), early increase in volume (Pattern II), later increase in volume (Pattern III), early increase in volume followed by stability (Pattern IV), stability followed by an increase in volume (Pattern V), or a decrease in tumor volume (Pattern VI). Methods: The frequency, time course, and clinical correlates of these six tumor volume kinetic patterns were analyzed in a cohort of 483 patients with low-risk PTC up to 1.5 cm in maximal diameter followed with active surveillance at our center for a median of 3.7 years. Results: The cumulative incidence of an increase in tumor volume for the entire cohort was 15.9% [confidence interval (CI) 11.8-20.0] at 5 years. At 5 years, most tumors demonstrated stability (78.8%, Pattern I) with 10.0% showing early growth (Pattern II), 4.1% late growth (Pattern III), 1.9% growth then stability (Pattern IV), 0.6% stability then growth (Pattern V), and 5.6% with a decrease in tumor volume (Pattern VI). Tumor volume doubling time during exponential growth significantly differed across the kinetic patterns, with median values of 2.4, 7.1, and 3.3 years for Patterns II, III, and IV, respectively (p < 0.01). Similarly, the time to a change in tumor volume was significantly different across the kinetic patterns, with median values of 1.5, 3, 1.6, 4.7, and 4.1 years for Patterns II, III, IV, V, and VI, respectively (analysis of variance, p < 0.01). Clinical correlates at baseline were not associated with tumor volume kinetic pattern. Conclusions: These six kinetic tumor volume patterns provide a comprehensive description of the changes in PTC tumor volume observed during the first 5 years of active surveillance.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Carcinoma Papilar Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Carcinoma Papilar Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article