Stem Cell Transplantation and Vinblastine Monotherapy for Relapsed Pediatric Anaplastic Large Cell Lymphoma: Results of the International, Prospective ALCL-Relapse Trial.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 12 2020
Historique:
pubmed: 31 7 2020
medline: 7 4 2021
entrez: 31 7 2020
Statut: ppublish

Résumé

To analyze the efficacy of a risk-stratified treatment of children with relapsed anaplastic large cell lymphoma (ALCL). The ALCL-Relapse trial (ClinicalTrials.gov identifier: NCT00317408) stratified patients according to the time of relapse and CD3 expression to prospectively test reinduction approaches combined with consolidation by allogeneic or autologous hematopoietic stem cell transplantation (SCT) and vinblastine monotherapy. Patients with progression during frontline therapy (very high risk) or a CD3-positive relapse (high risk) were scheduled for allogeneic SCT after reinduction chemotherapy. Patients with a CD3-negative relapse within 1 year after initial diagnosis or prior exposure to vinblastine (intermediate risk) received autologous SCT after carmustine-etoposide-cytarabine-melphalan. This arm was terminated prematurely, and subsequent patients received vinblastine monotherapy instead. Patients with a CD3-negative relapse > 1 year after initial diagnosis (low risk) received vinblastine monotherapy. One hundred sixteen patients met the inclusion criteria; 105 evaluable patients with CNS-negative disease had a 5-year event-free survival (EFS) of 53% ± 5% and a 5-year overall survival (OS) of 78% ± 4%. Before termination of autologous SCT, EFS rates of patients in the very-high- (n = 17), high- (n = 26), intermediate- (n = 32), and low- (n = 21) risk groups were 41% ± 12%, 62% ± 10%, 44% ± 9%, and 81% ± 9%; the respective OS rates were 59% ± 12%, 73% ± 9%, 78% ± 7%, and 90% ± 6%. Analyzing only the patients in the intermediate-risk group consolidated per protocol by autologous SCT, EFS and OS of 23 patients were 30% ± 10% and 78% ± 9%, respectively. All 5 patients with intermediate risk receiving vinblastine monotherapy after the amendment experienced relapse again. Shorter time to relapse was the strongest predictor of subsequent relapse. Allogeneic SCT offers a chance for cure in patients with high-risk ALCL relapse. For early relapsed ALCL autologous SCT was not effective. Vinblastine monotherapy achieved cure in patients with late relapse; however, it was not effective for early relapses.

Identifiants

pubmed: 32730187
doi: 10.1200/JCO.20.00157
doi:

Substances chimiques

Vinblastine 5V9KLZ54CY

Banques de données

ClinicalTrials.gov
['NCT00317408']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3999-4009

Commentaires et corrections

Type : CommentIn

Auteurs

Fabian Knörr (F)

Pediatric Hematology and Oncology, University Hospital Hamburg-Eppendorf, Germany.

Laurence Brugières (L)

Department of Children and Adolescents Oncology, Gustave Roussy University Hospital, Paris-Saclay University, Villejuif, France.

Marta Pillon (M)

Pediatric Hematology and Oncology, University Hospital of Padova, Italy.

Martin Zimmermann (M)

Department of Pediatric Hematology and Oncology, Hannover Medical School, Germany.

Stephanie Ruf (S)

Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.

Andishe Attarbaschi (A)

Pediatric Hematology and Oncology, St Anna Children's Hospital, Medical University of Vienna, Austria.

Karin Mellgren (K)

Department of Pediatric Oncology and Hematology, The Queen Silvia Children's Hospital, Göteborg, Sweden.

G Amos A Burke (GAA)

Department of Pediatric Hematology, Oncology and Palliative Care, Cambridge University Hospital NHS Trust, Cambridge, United Kingdom.

Anne Uyttebroeck (A)

Department of Pediatric Oncology & Hematology, University Hospitals Leuven, Belgium.

Grażyna Wróbel (G)

Department of Bone Marrow Transplantation, Children's Oncology and Hematology, Wroclaw Medical University, Poland.

Auke Beishuizen (A)

Princess Maxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Nathalie Aladjidi (N)

Department of Pediatric Hematology and Oncology, CIC1401, INSERM CICP, University Hospital of Bordeaux, France.

Alfred Reiter (A)

Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.

Wilhelm Woessmann (W)

Pediatric Hematology and Oncology, University Hospital Hamburg-Eppendorf, Germany.

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Classifications MeSH