Does A Longer Waiting Period After Neoadjuvant Radio-chemotherapy Improve the Oncological Prognosis of Rectal Cancer?: Three Years' Follow-up Results of the Greccar-6 Randomized Multicenter Trial.


Journal

Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354

Informations de publication

Date de publication:
11 2019
Historique:
entrez: 22 10 2019
pubmed: 22 10 2019
medline: 17 3 2020
Statut: ppublish

Résumé

The aim of this study was to report the 3-year survival results of the GRECCAR-6 trial. Current data on the effect of an extended interval between radiochemotherapy (RCT) and resection for rectal cancer on the rate of complete pathological response (pCR = ypT0N0) is controversial. Furthermore, its effect on oncological outcomes is unknown. The GRECCAR-6 trial was a phase III, multicenter, randomized, open-label, parallel-group, controlled trial. Patients with cT3/T4 or TxN+ tumors of the mid or lower rectum who had received RCT (45-50 Gy with 5-fluorouracil or capecitabine) were included and randomized into a 7- or 11-week waiting period. Primary endpoint was the pCR rate. Secondary endpoints were 3-year overall (OS), disease-free survival (DFS), and recurrence rates. A total of 265 patients from 24 participating centers were enrolled. A total of 253 patients underwent a mesorectal excision. Overall pCR rate was 17% (43/253). Mean follow-up from surgical resection was 32 ± 8 months. Twenty-four deaths occurred with an 89% OS at 3 years. DFS was 68.7% at 3 years (75 recurrences). Three-year local and distant recurrences were 7.9% and 23.8%, respectively. The randomization group had no impact on the 3-year OS (P = 0.8868) or DFS (P = 0.9409). Distant (P = 0.7432) and local (P = 0.3944) recurrences were also not influenced by the waiting period. DFS was independently influenced by 3 factors: circumferential radial margin (CRM) ≤1 mm [hazard ratio (HR) = 2.03; 95% confidence interval (CI), 1.17-3.51], ypT3-T4 (HR = 2.69; 95% CI, 1.19-6.08) and positive lymph nodes (HR = 3.62; 95% CI, 1.89-6.91). Extending the waiting period by 4 weeks following RCT has no influence on the oncological outcomes of T3/T4 rectal cancers.

Sections du résumé

OBJECTIVE
The aim of this study was to report the 3-year survival results of the GRECCAR-6 trial.
SUMMARY BACKGROUND DATA
Current data on the effect of an extended interval between radiochemotherapy (RCT) and resection for rectal cancer on the rate of complete pathological response (pCR = ypT0N0) is controversial. Furthermore, its effect on oncological outcomes is unknown.
METHODS
The GRECCAR-6 trial was a phase III, multicenter, randomized, open-label, parallel-group, controlled trial. Patients with cT3/T4 or TxN+ tumors of the mid or lower rectum who had received RCT (45-50 Gy with 5-fluorouracil or capecitabine) were included and randomized into a 7- or 11-week waiting period. Primary endpoint was the pCR rate. Secondary endpoints were 3-year overall (OS), disease-free survival (DFS), and recurrence rates.
RESULTS
A total of 265 patients from 24 participating centers were enrolled. A total of 253 patients underwent a mesorectal excision. Overall pCR rate was 17% (43/253). Mean follow-up from surgical resection was 32 ± 8 months. Twenty-four deaths occurred with an 89% OS at 3 years. DFS was 68.7% at 3 years (75 recurrences). Three-year local and distant recurrences were 7.9% and 23.8%, respectively. The randomization group had no impact on the 3-year OS (P = 0.8868) or DFS (P = 0.9409). Distant (P = 0.7432) and local (P = 0.3944) recurrences were also not influenced by the waiting period. DFS was independently influenced by 3 factors: circumferential radial margin (CRM) ≤1 mm [hazard ratio (HR) = 2.03; 95% confidence interval (CI), 1.17-3.51], ypT3-T4 (HR = 2.69; 95% CI, 1.19-6.08) and positive lymph nodes (HR = 3.62; 95% CI, 1.89-6.91).
CONCLUSION
Extending the waiting period by 4 weeks following RCT has no influence on the oncological outcomes of T3/T4 rectal cancers.

Identifiants

pubmed: 31634178
doi: 10.1097/SLA.0000000000003530
pii: 00000658-201911000-00005
doi:

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

747-754

Auteurs

Jérémie H Lefèvre (JH)

Sorbonne Université, Department of Digestive Surgery, AP-HP, Hôpital Saint Antoine, Paris, France.

Laurent Mineur (L)

Oncology, Radiotherapy, Sainte-Camille Institut, 250 Chemin de Baigne Pieds, Avignon, France.

Marine Cachanado (M)

Department of Clinical Pharmacology and Clinical Research Platform of East of Paris (URCEST-CRC-CRB), APHP, Hôpital Saint Antoine, Paris France.

Quentin Denost (Q)

Department of Surgery, CHU Saint-André, 1 Rue Jean Burguet, Bordeaux, France.

Philippe Rouanet (P)

Department of Oncological Surgery, Val d'Aurelle Institut, Montpellier, France.

Cécile de Chaisemartin (C)

Department of Oncological Surgery, Paoli-Calmettes Institut, 232 Boulevard de Sainte-Marguerite, Marseille CHU, France.

Bernard Meunier (B)

Department of Hepatobiliary and Digestive Surgery, CHU, Rennes, France.

Jafari Mehrdad (J)

Department of Oncological Surgery, Oscar Lambret Center, 3 Rue Frédéric Combemale, Lille, France.

Eddy Cotte (E)

Department of Digestive Surgery, CHU Lyon-Sud, 165 Chemin du Grand Revoyet, Pierre-Bénite, France.

Jérome Desrame (J)

Department of Gastrology and Hepatology, Jean Mermoz Institut, 55 Avenue Jean Mermoz, Lyon, France.

Mehdi Karoui (M)

Department of Digestive and Hepatobiliary Surgery, CHU Pitié-Salpétrière, 91 Boulevard de l'Hopital, Paris, France.

Stéphane Benoist (S)

Department of Digestive and Oncological Surgery, CHU Bicètre, 78 Rue du Général Leclerc, Le Kremlin-Bicêtre, France.

Sylvain Kirzin (S)

Department of Surgery, CHU Purpan, Place du Dr Joseph Baylac, Toulouse, France.

Anne Berger (A)

Department of Digestive, Oncological and General Surgery, CHU HEGP, Paris, France.

Yves Panis (Y)

Department of Colorectal Surgery, Hôpital Beaujon, Université Paris VII, 100 Boulevard du Général Leclerc, Clichy, France.

Guillaume Piessen (G)

Department of Digestive Surgery, CHRU, Lille, France.

Alain Saudemont (A)

Department of Digestive Surgery and Transplant Surgery, CHRU, Lille, France.

Michel Prudhomme (M)

Department of Digestive and Oncological Surgery, CHU Carémeau, 4 Rue du Professeur Robert Debré, Nîmes, France.

Frédérique Peschaud (F)

Department of Digestive Surgery, CHU Ambroise-Paré, 9 Avenue Charles de Gaulle, Boulogne-Billancourt, France.

Anne Dubois (A)

Department of Digestive Surgery, CHU Estaing, Clermont-Ferrand, France.

Jérome Loriau (J)

Department of Digestive Surgery, St-Joseph Hospital, 185 Rue Raymond Losserand, Paris, France.

Jean-Jacques Tuech (JJ)

Department of Digestive Surgery, CHU, 1 Rue de Germont, 76000 Rouen, France.

Guillaume Meurette (G)

Department of Digestive Surgery, CHU Hôtel-Dieu, 1 Place Alexis-Ricordeau, Nantes, France.

Renato Lupinacci (R)

Department of Digestive Surgery, Croix Saint-Simon Hospital, 12-18 Rue du Sergent Bauchat, Paris, France.

Nicolas Goasguen (N)

Department of Digestive Surgery, Croix Saint-Simon Hospital, 12-18 Rue du Sergent Bauchat, Paris, France.

Ben Creavin (B)

Department of Surgery, St Vincent's University Hospital, Elm Park, Dublin, Ireland.

Tabassome Simon (T)

Department of Clinical Pharmacology and Clinical Research Platform of East of Paris (URCEST-CRC-CRB), APHP, Hôpital Saint Antoine, Paris France.

Yann Parc (Y)

Sorbonne Université, Department of Digestive Surgery, AP-HP, Hôpital Saint Antoine, Paris, France.

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