» Articles » PMID: 23492368

Center of Cancer Systems Biology Second Annual Workshop--tumor Metronomics: Timing and Dose Level Dynamics

Overview
Journal Cancer Res
Specialty Oncology
Date 2013 Mar 16
PMID 23492368
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Metronomic chemotherapy, the delivery of doses in a low, regular manner so as to avoid toxic side effects, was introduced over 12 years ago in the face of substantial clinical and preclinical evidence supporting its tumor-suppressive capability. It constituted a marked departure from the classic maximum-tolerated dose (MTD) strategy, which, given its goal of rapid eradication, uses dosing sufficiently intense to require rest periods between cycles to limit toxicity. Even so, upfront tumor eradication is frequently not achieved with MTD, whereupon a de facto goal of longer-term tumor control is often pursued. As metronomic dosing has shown tumor control capability, even for cancers that have become resistant to the same drug delivered under MTD, the question arises whether it may be a preferable alternative dosing approach from the outset. To date, however, our knowledge of the coupled dynamics underlying metronomic dosing is neither sufficiently well developed nor widely enough disseminated to establish its actual potential. Meeting organizers thus felt the time was right, armed with new quantitative approaches, to call a workshop on "Tumor Metronomics: Timing and Dose Level Dynamics" to explore prospects for gaining a deeper, systems-level appreciation of the metronomics concept. The workshop proved to be a forum in which experts from the clinical, biologic, mathematical, and computational realms could work together to clarify the principles and underpinnings of metronomics. Among other things, the need for significant shifts in thinking regarding endpoints to be used as clinical standards of therapeutic progress was recognized.

Citing Articles

Cyclophosphamide stimulates endoplasmic reticulum stress and induces apoptotic cell death in human glioblastoma cell lines.

Oztatlici M, Oztatlici H, Saygili S, Kaya I, Cingoz I Rom J Morphol Embryol. 2024; 65(1):27-33.

PMID: 38527981 PMC: 11146554. DOI: 10.47162/RJME.65.1.04.


Role of vascular normalization in benefit from metronomic chemotherapy.

Mpekris F, Baish J, Stylianopoulos T, Jain R Proc Natl Acad Sci U S A. 2017; 114(8):1994-1999.

PMID: 28174262 PMC: 5338413. DOI: 10.1073/pnas.1700340114.


Metronomic cyclophosphamide activation of anti-tumor immunity: tumor model, mouse host, and drug schedule dependence of gene responses and their upstream regulators.

Wu J, Jordan M, Waxman D BMC Cancer. 2016; 16:623.

PMID: 27515027 PMC: 4982114. DOI: 10.1186/s12885-016-2597-2.


Computational oncology--mathematical modelling of drug regimens for precision medicine.

Barbolosi D, Ciccolini J, Lacarelle B, Barlesi F, Andre N Nat Rev Clin Oncol. 2015; 13(4):242-54.

PMID: 26598946 DOI: 10.1038/nrclinonc.2015.204.


Transcriptional profiling provides insights into metronomic cyclophosphamide-activated, innate immune-dependent regression of brain tumor xenografts.

Doloff J, Waxman D BMC Cancer. 2015; 15:375.

PMID: 25952672 PMC: 4523019. DOI: 10.1186/s12885-015-1358-y.


References
1.
Ferrari A, Grosso F, Stacchiotti S, Meazza C, Zaffignani E, Marchiano A . Response to vinorelbine and low-dose cyclophosphamide chemotherapy in two patients with desmoplastic small round cell tumor. Pediatr Blood Cancer. 2005; 49(6):864-6. DOI: 10.1002/pbc.20682. View

2.
Folkman J, Hahnfeldt P, Hlatky L . Cancer: looking outside the genome. Nat Rev Mol Cell Biol. 2001; 1(1):76-9. DOI: 10.1038/35036100. View

3.
Kebudi R, Gorgun O, Ayan I . Oral etoposide for recurrent/progressive sarcomas of childhood. Pediatr Blood Cancer. 2004; 42(4):320-4. DOI: 10.1002/pbc.10393. View

4.
Klement G, Baruchel S, Rak J, Man S, Clark K, Hicklin D . Continuous low-dose therapy with vinblastine and VEGF receptor-2 antibody induces sustained tumor regression without overt toxicity. J Clin Invest. 2000; 105(8):R15-24. PMC: 517491. DOI: 10.1172/JCI8829. View

5.
Felgenhauer J, Nieder M, Krailo M, Bernstein M, Henry D, Malkin D . A pilot study of low-dose anti-angiogenic chemotherapy in combination with standard multiagent chemotherapy for patients with newly diagnosed metastatic Ewing sarcoma family of tumors: A Children's Oncology Group (COG) Phase II study NCT00061893. Pediatr Blood Cancer. 2012; 60(3):409-14. PMC: 4583823. DOI: 10.1002/pbc.24328. View