Back to Authors

Livingston, J. Andrew

https://orcid.org/0000-0002-1337-3282

Mayo Clinic

The University of Texas MD Anderson Cancer Center

Citations 3

Adolescent and Young Adult (AYA) Oncology, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology
Pappo, Alberto S. , Acquazzino, Melissa , Barnett, Marie , Casey, Robert, Choo, Sun , Dinner, Shira, Fair, Douglas , Federman, Noah , Folbrecht, Jeanelle , Gandhi, Shipra , Germann, Julie N. , Goldsby, Robert E. , Hayashi, Robert J. , Huang, Mary , Jacobs, Linda A. , Lee‐Miller, Cathy , Link, Michael P., Lustberg, Maryam B. , Malogolowkin, Marcio H., Oeffinger, Kevin C. , Pratilas, Christine A. , Mehren, Margaret von , Yeager, Nicholas D. , Hang, Lisa, von Mehren, Margaret , Lustberg, Maryam , Bhatia, Smita , Allen‐Rhoades, Wendy , Borinstein, Scott C. , Chugh, Rashmi , Ermoian, Ralph P. , Huang, Alex Yee-Chen , Livingston, J. Andrew , Reed, Damon R. , Skiles, Jodi L. , Montgomery, Sarah E.

Journal of the National Comprehensive Cancer Network | August 7, 2023 | Volume: 21 | Issue: 8 | Pages: 851-880

10.6004/jnccn.2023.0040 Get It

This selection from the NCCN Guidelines for Adolescent and Young Adult (AYA) Oncology focuses on considerations for the comprehensive care of AYA patients with cancer. Compared with older adults with cancer, AYA patients have unique needs regarding treatment, fertility counseling, psychosocial and behavioral issues, and supportive care services. The complete version of the NCCN Guidelines for Adolescent and Young Adult (AYA) Oncology addresses additional aspects of caring for AYA patients, including risk factors, screening, diagnosis, and survivorship.
Joint Adult and Pediatric Working Group as a Successful Platform to Strengthen Adolescent and Young Adult (AYA) Clinical Trial Collaboration: A Report from the NCTN/SARC AYA Clinical Trials Sarcoma Working Group
Whiteway, Susan L. , Allen‐Rhoades, Wendy , Avutu, Viswatej , Indelicato, Daniel J. , Isakoff, Michael S. , Janeway, Katherine A. , Patel, Shreyaskumar , Riedel, Richard F. , Thornton, Katherine A., Ahmed, Safia K. , Avutu, Viswatej , Reed, Damon R , Riedel, Richard F , Allen-Rhoades, Wendy A , Indelicato, Daniel J , Weiss, Aaron R. , Cardona, Kenneth , Davis, Lara E. , Davis, Elizabeth J. , Livingston, J. Andrew , Reed, Damon R. , Kopp, Lisa M.

Journal of Adolescent and Young Adult Oncology | February 1, 2023 | Volume: 12 | Issue: 5 | Pages: 792-793

10.1089/jayao.2022.0179 Get It

Pregnancy outcomes related to the treatment of sarcomas with anthracyclines and/or ifosfamide during pregnancy
Miller, Devon , Livingston, J. Andrew , Park, Yeonhee , Posey, Kristi, Godbole, Sonia, Skubitz, Keith M. , Agulnik, Mark , Davis, Lara E. , Tine, Brian A. Van , Livingston, John A , Skubitz, Keith , Agulnik, Mark , Davis, Lara E , Van Tine, Brian A , Hirbe, Angela C , Parkes, Amanda , Robinson, Steven I. , Hirbe, Angela C.

Cancer Medicine | March 28, 2022 | Volume: 11 | Issue: 18 | Pages: 3471-3478

10.1002/cam4.4707 Get It

AbstractBackgroundSarcomas are rare diagnoses but are seen with relative frequency in adolescents and young adults and thus can present in pregnancy. We sought to study the administration of anthracyclines and/or ifosfamide in pregnancy‐associated sarcomas.Patients and MethodsWe conducted a multi‐institutional retrospective study, identifying sarcoma patients who received anthracyclines and/or ifosfamide during pregnancy. Chart review identified variables related to demographics, cancer diagnosis, therapies, and outcome of the patient and fetus. Wilcoxon rank‐sum test compared two independent samples.ResultsWe identified 13 patients at seven institutions with sarcoma who received anthracyclines and/or ifosfamide during pregnancy, including four bone sarcomas and nine soft tissue sarcomas diagnosed at a mean gestational age of 16.7 ± 5.9 weeks. Only nine patients had live births (9/13, 69.2%), with mean gestational age of 30.8 ± 3.8 weeks at delivery. The four patients with pregnancy loss all received both doxorubicin and ifosfamide, with chemotherapy initiated at 15.5 weeks as compared with 21.3 weeks for those patients with live births (p = 0.016).ConclusionIn this multi‐institutional study of sarcoma chemotherapy regimens administered during pregnancy, we found a high rate of fetal demise that was seen only in patients receiving both doxorubicin and ifosfamide and statistically more likely with chemotherapy initiation earlier in the second trimester. While limited by a small sample size, our study represents the largest study of sarcoma patients that received anthracyclines and/or ifosfamide in pregnancy thus far reported and supports development of an international registry to study concerns raised by our study.