Concurrent Radiotherapy and Panitumumab after Lymph Node Dissection and Induction Chemotherapy for Invasive Bladder Cancer.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 16 10 2018
medline: 11 4 2019
entrez: 16 10 2018
Statut: ppublish

Résumé

In this prospective study we evaluated the safety and efficacy of concurrent radiotherapy and panitumumab following neoadjuvant/induction chemotherapy and pelvic lymph node dissection as a bladder preserving therapy for invasive bladder cancer. Patients with cT1-4N0-2M0 bladder cancer were treated with pelvic lymph node dissection and 4 cycles of platinum based induction chemotherapy followed by a 6½-week schedule of weekly panitumumab (2.5 mg/kg) and concurrent radiotherapy to the bladder (33 × 2 Gy). As the primary objective we compared concurrent radiotherapy and panitumumab toxicity to a historical control toxicity rate of concurrent cisplatin/radiotherapy (less than 35% of patients with Grade 3-5 toxicity). A sample size of 31 patients was estimated. Secondary end points included complete remission at 3-month followup, the bladder preservation rate, EGFR (epidermal growth factor receptor) expression and RAS mutational status. Of the 38 cases initially included in this study 34 were staged cN0. After pelvic lymph node dissection 7 cases (21%) were up staged to pN+. Of the 38 patients 31 started concurrent radiotherapy and panitumumab. During concurrent radiotherapy and panitumumab 5 patients (16%, 95% CI 0-31) experienced systemic or local grade 3-4 toxicity. Four patients did not complete treatment due to adverse events. Complete remission was achieved in 29 of 31 patients (94%, 95% CI 83-100). At a median followup of 34 months 4 patients had local recurrence, for which 3 (10%) underwent salvage cystectomy. Two tumors showed EGFR or RAS mutation while 84% showed positive EGFR expression. Concurrent radiotherapy and panitumumab following induction chemotherapy and pelvic lymph node dissection has a safety profile that is noninferior to the historical profile of concurrent cisplatin/radiotherapy. The high complete remission and bladder preservation rates are promising and warrant further study.

Identifiants

pubmed: 30321552
pii: S0022-5347(18)43985-7
doi: 10.1016/j.juro.2018.10.007
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Panitumumab 6A901E312A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

478-485

Auteurs

Elisabeth E Fransen van de Putte (EE)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Floris Pos (F)

Department of Radiotherapy, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Barry Doodeman (B)

Department of Radiotherapy, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Bas W G van Rhijn (BWG)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Elsbeth van der Laan (E)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Petra Nederlof (P)

Department of Molecular Diagnostics, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Michiel S van der Heijden (MS)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Jolanda Bloos-van der Hulst (J)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Joyce Sanders (J)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Annegien Broeks (A)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

J Martijn Kerst (JM)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Vincent van der Noort (V)

Department of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Simon Horenblas (S)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Andries M Bergman (AM)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

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Classifications MeSH