K. Chau
Memorial Sloan Kettering Cancer Center
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Featured researches published by K. Chau.
International Journal of Radiation Oncology Biology Physics | 2017
Andreas Rimner; S. Lovie; Meier Hsu; Monica Chelius; Zhigang Zhang; K. Chau; Alison J. Moskowitz; Matthew J. Matasar; Craig H. Moskowitz; Joachim Yahalom
PURPOSEnWe report the long-term results of integrated accelerated involved field radiation therapy (IFRT) followed by total lymphoid irradiation (TLI) as part of the high-dose salvage regimen followed by autologous bone marrow transplantation or autologous stem cell transplantation in patients with relapsed or refractory Hodgkin lymphoma (HL).nnnMETHODS AND MATERIALSnFrom November 1985 to July 2008, 186 previously unirradiated patients with relapsed or refractory HL underwent salvage therapy on 4 consecutive institutional review board-approved protocols. All patients had biopsy-proven primary refractory or relapsed HL. After standard-dose salvage chemotherapy (SC), accelerated IFRT (18-20xa0Gy) was given to relapsed or refractory sites, followed by TLI (15-18xa0Gy) and high-dose chemotherapy. Overall survival (OS) and event-free survival (EFS) were analyzed by Cox analysis and disease-specific survival (DSS) by competing-risk regression.nnnRESULTSnWith a median follow-up period of 57xa0months among survivors, 5- and 10-year OS rates were 68% and 56%, respectively; 5- and 10-year EFS rates were 62% and 56%, respectively; and 5- and 10-year cumulative incidences of HL-related deaths were 21% and 29%, respectively. On multivariate analysis, complete response to SC was independently associated with improved OS and EFS. Primary refractory disease and extranodal disease were independently associated with poor DSS. Eight patients had grade 3 or higher cardiac toxicity, with 3 deaths. Second malignancies developed in 10 patients, 5 of whom died.nnnCONCLUSIONSnAccelerated IFRT followed by TLI and high-dose chemotherapy is an effective, feasible, and safe salvage strategy for patients with relapsed or refractory HL with excellent long-term OS, EFS, and DSS. Complete response to SC is the most important prognostic factor.
Blood Advances | 2018
Shunan Qi; May Y. Huang; Yong Yang; Heiko Schöder; Sewit Teckie; Ariela Noy; K. Chau; Joachim Yahalom
The role of [18F]fluorodeoxyglucose (FDG) positron-emission tomography (PET) in mucosa-associated lymphoid tissue (MALT) of marginal zone lymphoma remains poorly defined. We correlated initial PET with pathology, clinical factors, and outcome. From January 2001 to July 2012, 173 MALT lymphoma patients with a biopsied lesion identified on PET within 90 days of tissue biopsy were analyzed. PET positivity and intensity of FDG uptake were correlated with clinical factors and patient outcome. Among 173 accrued cases, biopsied site was PET avid in 123 patients (71%); median standardized uptake value (SUV) was 6.0 (range: 0.7-28.0), and SUV >10.0 in 20 patients (16%). PET avidity varied by organ sites. PET positivity correlated with higher International Prognostic Index, but not with 5-year overall survival (OS; 96% vs 88%, PET negative vs positive, P = .229) or 5-year progression-free survival (67% vs 56%, P = .493). SUV was an independent prognostic factor of OS, and an increased SUV was associated with a decreasing 5-year OS. Patients who presented with SUV ≥10 had a higher rate of subsequent large cell transformation (20% vs 5%, P = .035) and inferior OS (78% vs 92%, P = .008). The exact role of FDG PET in the management of MALT lymphoma, beyond initial staging, remains to be defined.
International Journal of Radiation Oncology Biology Physics | 2017
James Laird; Jennifer Ma; K. Chau; M. Chelius; Weiji Shi; Zhigang Zhang; Benjamin H. Lok; Joachim Yahalom
PURPOSEnTo characterize the efficacy and safety of radiation therapy in a contemporary Langerhans cell histiocytosis (LCH) cohort and to explore whether there are sites at higher risk for local recurrence.nnnPATIENTS AND METHODSnBetween 1995 and 2015 we identified 39 consecutive LCH patients who were treated primarily with radiation therapy. Patients were staged by single/multisystem involvement and established risk organ criteria. In 46 irradiated lesions, clinical and radiologic responses were evaluated at multiple time points after radiation therapy. Patient demographics, treatment, and local failure were compared by site of lesion.nnnRESULTSnMedian age at radiation therapy was 35xa0years (range, 1.5-67xa0years). Twelve patients had multisystem involvement, and of those, 5 patients had disease in organs considered to be high risk. The following sites were irradiated: bone (31), brain (6), skin (3), lymph node (3), thyroid (2), and nasopharynx (1). Median dose was 11.4xa0Gy (range, 7.5-50.4xa0Gy). At a median follow-up of 45xa0months (range, 6-199xa0months), local recurrence or progression was noted in 5 of 46 lesions (11%). There were no local failures of the 31 bone lesions evaluated, whereas the 3-year freedom from local failure in the 15 non-bone lesions was 63% (95% confidence interval 32-83%; P=.0008). Local failures occurred in 2 of 3 skin lesions, in 2 of 6 brain lesions, and 1 of 3 lymph node lesions. Deaths were recorded in 5 of 39 patients (13%), all of whom were adults with multisystem disease.nnnCONCLUSIONnRadiation therapy is a safe and effective measure for providing local control of LCH involving the bone. Whereas bone lesions are well controlled with low doses of radiation, disease in other tissues, such as the skin and brain, may require higher doses of radiation or additional treatment modalities.
Journal of Clinical Oncology | 2018
J.C. Yang; K. Chau; Michael Scordo; Craig S. Sauter; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
M. Chelius; K. Chau; J.C. Yang; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
A.J. Xu; M. Chelius; K. Chau; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
Jennifer Ma; James Laird; K. Chau; M. Chelius; Benjamin H. Lok; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
T. Beckham; J.C. Yang; K. Chau; Ariela Noy; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
J.C. Yang; K. Chau; M. Scordo; C.S. Sauter; Joachim Yahalom
International Journal of Radiation Oncology Biology Physics | 2018
K. Chau; J.C. Yang; C. Hajj; M. Chelius; Joachim Yahalom