Citations 26

Outcome comparison of allogeneic vs. autologous stem cell transplantation in transformed low grade lymphoid malignancies: A meta-analysis of comparative studies.

Journal of Clinical Oncology | April 19, 2019 | Volume: 33 | Issue: 15_suppl | Pages: 8566-8566

10.1200/jco.2015.33.15_suppl.8566

Overall survival and treatment response in patients with myelodysplastic syndrome and acute myeloid leukemia treated with DNA methyl-transferase inhibitors vs. conventional care regimens: A meta-analysis of 5 randomized trials.

Journal of Clinical Oncology | April 19, 2019 | Volume: 33 | Issue: 15_suppl | Pages: 7037-7037

10.1200/jco.2015.33.15_suppl.7037

Comparison of DNA hypomethylating agents and low dose cytarabine in elderly acute myeloid leukemia patients: A meta-analysis.

Journal of Clinical Oncology | March 7, 2019 | Volume: 33 | Issue: 15_suppl | Pages: e18062-e18062

10.1200/jco.2015.33.15_suppl.e18062

Role of β blocker and angiotensin antagonist for the prophylaxis of early onset anthracycline-induced ventricular dysfunction: A meta-analysis of five randomized controlled trials.

Journal of Clinical Oncology | March 7, 2019 | Volume: 33 | Issue: 15_suppl | Pages: 1021-1021

10.1200/jco.2015.33.15_suppl.1021

Faculty Opinions recommendation of Cancer progression by reprogrammed BCAA metabolism in myeloid leukaemia.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | June 23, 2017 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.727620770.793533377

Faculty Opinions recommendation of SAMHD1 is a biomarker for cytarabine response and a therapeutic target in acute myeloid leukemia.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | January 12, 2017 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.727122838.793526980

Blinatumomab-Induced Donor T-Cell Activation for Post-Stem Cell Transplant-Relapsed Acute Cd19-Positive Biphenotypic Leukemia

Immunotherapy | July 6, 2016 | Volume: 8 | Issue: 8 | Pages: 847-852

10.2217/imt-2015-0023 | PMID 27381683

Faculty Opinions recommendation of Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature | June 17, 2016 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3410/f.726032963.793519532

Multiple Causes of Cardiotoxic Effects in Patients With Chronic Myeloid Leukemia

JAMA Oncology | June 9, 2016 | Volume: 2 | Issue: 6 | Pages: 828

10.1001/jamaoncol.2016.1005 | PMID 27281623

Targeting immune checkpoints in unresectable metastatic cutaneous melanoma: a systematic review and meta‐analysis of anti‐CTLA‐4 and anti‐PD‐1 agents trials

Cancer Medicine | May 11, 2016 | Volume: 5 | Issue: 7 | Pages: 1481-1491

10.1002/cam4.732 | PMID 27167347

AbstractAnti‐cytotoxic T lymphocyte‐associated antigen‐4 (CTLA‐4) and anti‐programmed cell death‐1 (PD‐1) inhibitors have been shown to significantly improve survival in patients with metastatic cutaneous melanoma. However, there was some heterogeneity as well as some variation in the degree of benefit across studies. We reviewed randomized trials and performed a meta‐analysis to determine the efficacy and safety of immune checkpoint inhibitors in comparison with conventional regimens. Eligible studies were limited to randomized controlled trials comparing anti‐CTLA‐4 or anti‐PD‐1 inhibitors to chemotherapy or vaccination treatment in adult patients with unresectable cutaneous metastatic melanoma. Progression‐free survival (PFS) rate at 6 months was 28.5% versus 17.7% (RR: 0.84, 95% CI: 0.76–0.93), overall survival (OS) rate at 1 year was 51.2% versus 38.8% (RR: 0.72, 95% CI: 0.59–0.88), and overall response rate (ORR) at 6 months was 29.6% versus 17.7% (RR: 0.85, 95% CI: 0.76–0.95) favoring immune check point inhibitors over chemotherapies or vaccination. Immune check point inhibitors were associated with more frequent immune‐related adverse events at 13.7% versus 2.4% of treated patients (RR: 6.74, 95% CI: 4.65–9.75). Subgroup analyses demonstrated significant PFS (RR: 0.92 vs. 0.74, P < 0.00001) and ORR (RR: 0.95 vs. 0.76, P = 0.0004) improvement with anti‐PD‐1 treatment compared to anti‐CTLA‐4 when each of them was compared to control treatments. Collectively, these results demonstrate that immune checkpoint inhibitors have superior outcomes compared to conventional chemotherapies or vaccination, and support the results of recent randomized trials that showed superior outcomes with anti‐PD‐1 agents over ipilimumab in unresectable metastatic cutaneous melanoma patients.