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ConCerv: a prospective trial of conservative surgery for low-risk early-stage cervical cancer.
Schmeler, Kathleen M; Pareja, Rene; Lopez Blanco, Aldo; Humberto Fregnani, Jose; Lopes, Andre; Perrotta, Myriam; Tsunoda, Audrey T; Cantú-de-León, David F; Ramondetta, Lois M; Manchana, Tarinee; Crotzer, David R; McNally, Orla M; Riege, Martin; Scambia, Giovanni; Carvajal, Juan Manuel; Di Guilmi, Julian; Rendon, Gabriel J; Ramalingam, Preetha; Fellman, Bryan M; Coleman, Robert L; Frumovitz, Michael; Ramirez, Pedro T.
Afiliação
  • Schmeler KM; Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA KSchmele@mdanderson.org.
  • Pareja R; Instituto Nacional de Cancerología, Bogotá, and Clínica de Oncología Astorga, Medellin, Colombia.
  • Lopez Blanco A; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Humberto Fregnani J; A.C. Camargo Cancer Center, A.C. Camargo Cancer Center, Sao Paulo, Brazil.
  • Lopes A; Instituto Brasileiro de Controle do Cancer, Sao Paulo, Brazil.
  • Perrotta M; Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
  • Tsunoda AT; Hospital Erasto Gaertner, Curitiba, Brazil.
  • Cantú-de-León DF; Instituto Nacional de Cancerologia, Mexico, Mexico.
  • Ramondetta LM; Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Manchana T; Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Crotzer DR; Nebraska Methodist Health System, Omaha, Nebraska, USA.
  • McNally OM; Royal Women's Hospital and University of Melbourne, Melbourne, Victoria, Australia.
  • Riege M; Instituto de Ginecología de Rosario, Rosario, Argentina.
  • Scambia G; Fondazione Policlinico Universitario A. Gemelli IRCCS and Catholic University of the Sacred Heart, Rome, Italy.
  • Carvajal JM; Matamoros General Hospital Alfredo Pumarejo, Matamoros, Mexico.
  • Di Guilmi J; Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
  • Rendon GJ; Instituto de Cancerologia - Las Américas - AUNA, Medellin, Colombia.
  • Ramalingam P; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Fellman BM; Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Coleman RL; US Oncology Research, The Woodlands, Texas, USA.
  • Frumovitz M; Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ramirez PT; Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Int J Gynecol Cancer ; 31(10): 1317-1325, 2021 10.
Article em En | MEDLINE | ID: mdl-34493587
ABSTRACT

OBJECTIVE:

The objective of the ConCerv Trial was to prospectively evaluate the feasibility of conservative surgery in women with early-stage, low-risk cervical cancer.

METHODS:

From April 2010 to March 2019, a prospective, single-arm, multicenter study evaluated conservative surgery in participants from 16 sites in nine countries. Eligibility criteria included (1) FIGO 2009 stage IA2-IB1 cervical carcinoma; (2) squamous cell (any grade) or adenocarcinoma (grade 1 or 2 only) histology; (3) tumor size <2 cm; (4) no lymphovascular space invasion; (5) depth of invasion <10 mm; (6) negative imaging for metastatic disease; and (7) negative conization margins. Cervical conization was performed to determine eligibility, with one repeat cone permitted. Eligible women desiring fertility preservation underwent a second surgery with pelvic lymph node assessment, consisting of sentinel lymph node biopsy and/or full pelvic lymph node dissection. Those not desiring fertility preservation underwent simple hysterectomy with lymph node assessment. Women who had undergone an 'inadvertent' simple hysterectomy with an unexpected post-operative diagnosis of cancer were also eligible if they met the above inclusion criteria and underwent a second surgery with pelvic lymph node dissection only.

RESULTS:

100 evaluable patients were enrolled. Median age at surgery was 38 years (range 23-67). Stage was IA2 (33%) and IB1 (67%). Surgery included conization followed by lymph node assessment in 44 women, conization followed by simple hysterectomy with lymph node assessment in 40 women, and inadvertent simple hysterectomy followed by lymph node dissection in 16 women. Positive lymph nodes were noted in 5 patients (5%). Residual disease in the post-conization hysterectomy specimen was noted in 1/40 patients-that is, an immediate failure rate of 2.5%. Median follow-up was 36.3 months (range 0.0-68.3). Three patients developed recurrent disease within 2 years of surgery-that is, a cumulative incidence of 3.5% (95% CI 0.9% to 9.0%).

DISCUSSION:

Our prospective data show that select patients with early-stage, low-risk cervical carcinoma may be offered conservative surgery.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Adenocarcinoma / Neoplasias do Colo do Útero / Tratamento Conservador Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Adenocarcinoma / Neoplasias do Colo do Útero / Tratamento Conservador Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article