Abstract #517 Suspected Isolated Pituitary Metastasis Without Other Central Nervous System Metastasis from Extensive Stage Small Cell Lung Carcinoma

2019 ◽  
Vol 25 ◽  
pp. 258
Author(s):  
Christopher Barnes ◽  
Ahmet Can
2020 ◽  
Vol 51 (1) ◽  
pp. 37-44
Author(s):  
Tomoyuki Naito ◽  
Hideaki Shiraishi ◽  
Yutaka Fujiwara

Abstract Major issues in anaplastic lymphoma kinase-positive non-small cell lung carcinoma are acquired resistance against anaplastic lymphoma kinase inhibitors and control of central nervous system metastasis. The development of these inhibitors has changed therapeutic strategy in patients with advanced anaplastic lymphoma kinase-positive non-small cell lung carcinoma. Brigatinib and lorlatinib were designed to penetrate the blood–brain barrier and to inhibit resistant mutations against anaplastic lymphoma kinase inhibitors. We review the clinical data supporting treatment of advanced anaplastic lymphoma kinase-positive non-small cell lung carcinoma with brigatinib and lorlatinib. Brigatinib has shown promising antitumour activity, including substantial activity against central nervous system metastases, in crizotinib-treated (ALTA trial) patients and crizotinib-naïve (ALTA-1L trial) patients with anaplastic lymphoma kinase-positive non-small cell lung carcinoma. In addition, brigatinib improved progression-free survival compared with crizotinib in anaplastic lymphoma kinase inhibitor-naïve patients with anaplastic lymphoma kinase-positive non-small cell lung carcinoma. Lorlatinib has demonstrated clinical antitumour activity against both intracranial and extracranial lesions in patients with anaplastic lymphoma kinase- or c-ros oncogene 1 (ROS1)-positive non-small cell lung carcinoma. Ongoing trials and further studies of these agents’ biological and clinical properties would provide insight into the optimal therapeutic strategy for administering them to achieve the best survival benefit.


Lung Cancer ◽  
2002 ◽  
Vol 36 (3) ◽  
pp. 257-261 ◽  
Author(s):  
Anil Potti ◽  
James Willardson ◽  
Caralee Forseen ◽  
Apar Kishor Ganti ◽  
Michael Koch ◽  
...  

Cancer ◽  
2003 ◽  
Vol 97 (10) ◽  
pp. 2498-2503 ◽  
Author(s):  
James R. Jett ◽  
Alan K. Hatfield ◽  
Shauna Hillman ◽  
Michael D. Bauman ◽  
James A. Mailliard ◽  
...  

Lung Cancer ◽  
1997 ◽  
Vol 18 ◽  
pp. 53
Author(s):  
V. Franciosi ◽  
G. Vasini ◽  
F. Leonardi ◽  
G. Ceci ◽  
A. Mambrini ◽  
...  

2013 ◽  
Vol 1 (1) ◽  
pp. 35 ◽  
Author(s):  
Kamonpun Ussavarungsi ◽  
Minji Kim ◽  
Lukman Tijani

A 64-year-old woman presented with abdominal pain and back pain. Physical examinationrevealed a subcutaneous nodule in the anterior abdominal wall. An ultrasoundguidedbiopsy revealed small cell lung carcinoma (SCLC), and additional workuprevealed extensive stage small cell lung carcinoma with involvement of the left lung andthe abdominal viscera. The patient underwent chemotherapy with a good initial response.Lung carcinoma infrequently metastasizes to the skin. However, these lesions,when present, have important prognostic implications since these patients typicallyrespond poorly to chemotherapy and have a mean survival of about five months. Carefulskin evaluation is essential in the evaluation of patients with possible bronchogeniccarcinoma.


2006 ◽  
Vol 24 (3) ◽  
pp. 407-412 ◽  
Author(s):  
A. William Blackstock ◽  
James E. Herndon ◽  
Electra D. Paskett ◽  
Antonius A. Miller ◽  
Christopher Lathan ◽  
...  

Purpose Among patients with small-cell lung carcinoma, African Americans have lower survival rates than non–African Americans. We investigated whether the disparity in survival would persist when patients were treated with similar therapies (ie, phase II/III Cancer and Leukemia Group B [CALGB] trials). Patients and Methods We assessed 995 patients (928 non–African American and 67 African American) receiving chemotherapy in CALGB studies for extensive-stage small-cell lung cancer (ES-SCLC). Clinical and demographic characteristics, treatment received, and survival data were obtained from the CALGB database. The Cox proportional hazards model was used to assess the effect of race/ethnicity on survival after adjustment for other known prognostic factors. All statistical tests were two sided. Results The unadjusted survival distribution of African American patients was not significantly different from that of non–African American patients; median survival was 11.5 months (95% CI, 9.4 to 13.4 months) for African American patients versus 9.9 months (95% CI, 9.6 to 10.3 months) for non–African American patients. Multivariable adjustment for the effect of treatment arm, histology, and metastatic site at presentation did not alter the outcome for African American patients. Survival was similar even though African American patients were more likely to have a poorer performance status, present with significant weight loss, and be Medicaid recipients (20% v 6%), which is an indicator of lower socioeconomic status. Conclusion African American patients tended to present with prognostic features associated with a worse survival. However, when offered equivalent therapy, the outcome for African American patients was the same as that observed for non–African American patients.


2011 ◽  
Vol 12 (6) ◽  
pp. 375-379 ◽  
Author(s):  
Meredith E. Giuliani ◽  
Soha Atallah ◽  
Alexander Sun ◽  
Andrea Bezjak ◽  
Lisa W. Le ◽  
...  

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