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Does the addition of oxaliplatin to preoperative chemoradiation benefit cT4 or fixed cT3 rectal cancer treatment? A subgroup analysis from a prospective study.
Wisniowska, K; Nasierowska-Guttmejer, A; Polkowski, W; Michalski, W; Wyrwicz, L; Pietrzak, L; Rutkowski, A; Malinowska, M; Krynski, J; Kosakowska, E; Zwolinski, J; Winiarek, M; Oledzki, J; Kusnierz, J; Zajac, L; Bednarczyk, M; Szczepkowski, M; Tarnowski, W; Pasnik, K; Radziszewski, J; Partycki, M; Beczkowska, K; Stylinski, R; Wierzbicki, R; Bury, P; Jankiewicz, M; Paprota, K; Lewicka, M; Cisel, B; Skórzewska, M; Mielko, J; Danek, A; Nawrocki, G; Sopylo, R; Kepka, L; Bujko, K.
Afiliación
  • Wisniowska K; I Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Nasierowska-Guttmejer A; Department of Pathology, Clinical Hospital of Ministry of Internal Affairs and Administration, Warsaw, Poland.
  • Polkowski W; Department of Surgical Oncology, Medical University of Lublin, Poland.
  • Michalski W; Bioinformatics and Biostatistics Unit, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Wyrwicz L; Bioinformatics and Biostatistics Unit, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Pietrzak L; I Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Rutkowski A; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Malinowska M; Department of Pathology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Krynski J; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Kosakowska E; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Zwolinski J; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Winiarek M; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Oledzki J; Department of Colorectal Surgery, Medical University, Warsaw, Poland; Medical Faculty, University of Rzeszów, Poland.
  • Kusnierz J; Department of Gynaecology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Zajac L; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Bednarczyk M; Department of Gastroenterological Oncology, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Szczepkowski M; Department of Rehabilitation, Józef Pilsudski University of Physical Education and Clinical Department of General and Colorectal Surgery, Bielanski Hospital, Warsaw, Poland.
  • Tarnowski W; Department of General, Oncologic and Digestive Tract Surgery, Medical Centre of Postgraduate Education, Orlowski Hospital Warsaw, Poland.
  • Pasnik K; Department of General, Oncological, Metabolic and Thoracic Surgery, Military Institute of Medicine, Warsaw, Poland.
  • Radziszewski J; Department of General and Vascular Surgery, Multidisciplinary Hospital, Warsaw-Miedzylesie, Poland.
  • Partycki M; I Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Beczkowska K; I Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Stylinski R; 1st Department of General Surgery, Transplantology and Nutritional Therapy, Medical University of Lublin, Poland.
  • Wierzbicki R; Department of Surgery, MSW Hospital, Lublin, Poland.
  • Bury P; Department of General and Gastrointestinal Surgery and Surgical Oncology of the Alimentary Tract, Medical University, Lublin, Poland.
  • Jankiewicz M; Department of Surgical Oncology, Medical University of Lublin, Poland; Department of Radiotherapy, St. John's Cancer Centre, Lublin, Poland.
  • Paprota K; Department of Radiotherapy, St. John's Cancer Centre, Lublin, Poland.
  • Lewicka M; Department of Surgical Oncology, Medical University of Lublin, Poland.
  • Cisel B; Department of Surgical Oncology, Medical University of Lublin, Poland.
  • Skórzewska M; Department of Surgical Oncology, Medical University of Lublin, Poland.
  • Mielko J; Department of Surgical Oncology, Medical University of Lublin, Poland.
  • Danek A; II Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Nawrocki G; Department of Surgery, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Sopylo R; Department of Surgery, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
  • Kepka L; Department Radiotherapy, Independent Public Health Care Facility of the Ministry of the Interior and Warmian-Masurian Oncology Centre, Olsztyn, Poland.
  • Bujko K; I Department of Radiotherapy, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland. Electronic address: bujko@coi.waw.pl.
Eur J Surg Oncol ; 42(12): 1859-1865, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27546011
ABSTRACT

BACKGROUND:

Whether there is any benefit derived from adding oxaliplatin to fluoropyrimidine-based preoperative chemoradiation is currently unknown in cases of advanced cT3 or cT4 tumours. Our aim was to evaluate this issue by analysing a randomized trial, which compared two schedules of preoperative treatment (chemoradiation vs. 5 × 5 Gy with 3 cycles of consolidation chemotherapy) for cT4 or fixed cT3 rectal cancer. PATIENTS AND

METHODS:

Delivery of oxaliplatin was mandatory to the first part of the study. For the second part, its delivery in both treatment-assigned groups was left to the discretion of the local investigator. We analysed a subgroup of 272 patients (136 in the oxaliplatin group and 136 in the fluorouracil-only group) from institutions that had omitted oxaliplatin in the second part of the study.

RESULTS:

Circumferential resection margin negative (CRM-) status rate was 68% in the oxaliplatin group and 70% in the fluorouracil-only group, p = 0.72. The pathological complete response rate (pCR) was correspondingly 14% vs. 7%, p = 0.10. Following multivariable analysis, when comparing the CRM- status in the oxaliplatin group to the fluorouracil-only group, the odds ratio was 0.79 (95 CI 0.35-1.74), p = 0.54; there being no interaction between concomitant chemoradiation and 5 × 5 Gy with consolidation chemotherapy; pinteraction = 0.073. For pCR, the corresponding results were 0.47 (95 CI 0.19-1.16), p = 0.10, pinteraction = 0.84.

CONCLUSION:

No benefit was found of adding oxaliplatin in terms of CRM nor pCR rates for either concomitant or sequential settings in preoperative radiochemotherapy for very advanced rectal cancer.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias del Recto / Procedimientos Quirúrgicos del Sistema Digestivo / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadyuvante / Quimioradioterapia Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Surg Oncol Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias del Recto / Procedimientos Quirúrgicos del Sistema Digestivo / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadyuvante / Quimioradioterapia Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Surg Oncol Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: Polonia