scholarly journals An unusual response with long term survival using erlotinib in NSCLC lung with brain metastases

2016 ◽  
pp. bcr2015213239 ◽  
Author(s):  
Madhup Rastogi ◽  
Sambit Swarup Nanda ◽  
Chandra Prakash ◽  
Dinkar Kulshreshtha
2016 ◽  
pp. bcr2015213824
Author(s):  
Daniela Guelho ◽  
Cristina Ribeiro ◽  
Miguel Melo ◽  
Francisco Carrilho

Author(s):  
Izabella Czajka-Oraniec ◽  
Maria Stelmachowska-Banas ◽  
Arnika Szostek ◽  
Agnieszka Baranowska-Bik ◽  
Wojciech Zgliczynski

2018 ◽  
Vol 194 (12) ◽  
pp. 1144-1151 ◽  
Author(s):  
Heinz Schmidberger ◽  
Matthias Rapp ◽  
Anne Ebersberger ◽  
Silla Hey-Koch ◽  
Carmen Loquai ◽  
...  

Neurosurgery ◽  
1997 ◽  
Vol 41 (3) ◽  
pp. 735-735
Author(s):  
Walter Hall ◽  
Hamid Djalilian ◽  
Eric Nussbaum ◽  
Kwan Cho

2002 ◽  
Vol 128 (8) ◽  
pp. 417-425 ◽  
Author(s):  
Johannes Lutterbach ◽  
Susanne Bartelt ◽  
Christoph Ostertag

1997 ◽  
Vol 15 (4) ◽  
pp. 1449-1454 ◽  
Author(s):  
C Bokemeyer ◽  
P Nowak ◽  
A Haupt ◽  
B Metzner ◽  
H Köhne ◽  
...  

PURPOSE Despite improved cure rates for patients with metastatic testicular cancer with cisplatin-based combination chemotherapy, patients who develop brain metastases are generally considered to possess a poor prognosis. This report summarizes the long-term results in 44 patients with brain metastases from testicular cancer treated between 1978 and 1995 at Hannover University Medical School. PATIENTS AND METHODS Histologically, 42 patients (95%) had a nonseminomatous germ cell cancer and two patients (5%) a seminoma. Thirty-nine patients (89%) had lung metastases and 37 (84%) fulfilled the criteria for advanced disease according to the Indiana University classification even without considering the brain metastases. Eighteen patients (41%) presented with brain metastases at primary diagnosis (group 1), four (9%) developed brain metastases at relapse after a previous favorable response to combination chemotherapy (group 2), and 22 (50%) developed brain metastases during or directly after cisplatin-based chemotherapy. Chemotherapy consisted of cisplatin-based combination treatment and radiotherapy was given as whole-brain irradiation of 30 to 40 Gy and in single cases combined with a boost of 10 Gy to single lesions. RESULTS Overall, 10 patients achieved long-term survival (23%; 95% confidence interval [CI], 10.1% to 35.4%). The prognosis was significantly better for patients in groups 1 and 2, with six of 18 (33%) and three of four (75%) patients alive, compared with only one of 22 (5%) in group 3 (P < .01). Patients treated with either chemotherapy or radiotherapy alone did not achieve long-term survival, while nine of 28 (32%) who received treatment with both modalities with or without surgery achieved sustained long-term survival. During univariate analysis, patients with the diagnosis of brain metastases at first presentation (P < .01), patients with a single brain lesion (P < .02), and patients who received combined chemotherapy and radiotherapy (P < .03) had a significantly improved outcome. CONCLUSIONS Long-term survival can be achieved in approximately 25% of patients with brain metastases from testicular cancer by combined treatment with brain irradiation and aggressive cisplatin-based chemotherapy. Patients who develop brain metastases during systemic treatment should receive only palliative radiation therapy, since sustained survival will not be reached.


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