» Articles » PMID: 23999218

Drug Rechallenge and Treatment Beyond Progression--implications for Drug Resistance

Overview
Specialty Oncology
Date 2013 Sep 4
PMID 23999218
Citations 111
Authors
Affiliations
Soon will be listed here.
Abstract

The established dogma in oncology for managing recurrent or refractory disease dictates that therapy is changed at disease progression, because the cancer is assumed to have become drug-resistant. Drug resistance, whether pre-existing or acquired, is largely thought to be a stable and heritable process; thus, reuse of therapeutic agents that have failed is generally contraindicated. Over the past few decades, clinical evidence has suggested a role for unstable, non-heritable mechanisms of acquired drug resistance pertaining to chemotherapy and targeted agents. There are many examples of circumstances where patients respond to reintroduction of the same therapy (drug rechallenge) after a drug holiday following disease relapse or progression during therapy. Additional, albeit limited, evidence suggests that, in certain circumstances, continuing a therapy beyond disease progression can also have antitumour activity. In this Review, we describe the anticancer agents used in these treatment strategies and discuss the potential mechanisms explaining the apparent tumour re-sensitization with reintroduced or continued therapy. The extensive number of malignancies and drugs that challenge the custom of permanently switching to different drugs at each line of therapy warrants a more in-depth examination of the definitions of disease progression and drug resistance and the resulting implications for patient care.

Citing Articles

Efficacy and safety analysis of atezolizumab continuation beyond progression in extensive-stage small cell lung cancer.

Shi W, Bao X, Xiong J, Wu Y, Sun J, Xu Z Clin Exp Med. 2025; 25(1):71.

PMID: 40038111 PMC: 11880126. DOI: 10.1007/s10238-025-01606-1.


Vincristine-induced ptosis in pediatric patients: a systematic review and practice recommendations.

Ahmed H, Thrishulamurthy C Eur J Pediatr. 2025; 184(3):209.

PMID: 39994116 DOI: 10.1007/s00431-025-06039-2.


Efficacy and Safety of Immune Checkpoint Inhibitor Rechallenge in the Treatment of Esophageal Squamous Cell Cancer.

Zhang X, Zhang J, He J, Zhong X, Yu J, Wang L J Cancer. 2025; 16(3):943-951.

PMID: 39781362 PMC: 11705047. DOI: 10.7150/jca.104380.


Anti-EGFR Rechallenge in Metastatic Colorectal Cancer and the Role of ctDNA: A Systematic Review and Meta-analysis.

da Silva L, Saldanha E, da Conceicao L, Noronha M, da Silva M, Peixoto R J Gastrointest Cancer. 2024; 56(1):28.

PMID: 39623250 DOI: 10.1007/s12029-024-01152-1.


Anti-anemic potential of L. in iron-deficient rat model; network pharmacology profiling.

Javed S, Shahzadi Z, Yousaf Z, Anjum I, Aftab A, Hanif S Food Sci Nutr. 2024; 12(10):7331-7346.

PMID: 39479620 PMC: 11521654. DOI: 10.1002/fsn3.4314.


References
1.
Simon G, Wagner H . Small cell lung cancer. Chest. 2003; 123(1 Suppl):259S-271S. DOI: 10.1378/chest.123.1_suppl.259s. View

2.
Loriot Y, Massard C, Gross-Goupil M, Palma M, Escudier B, Bossi A . The interval from the last cycle of docetaxel-based chemotherapy to progression is associated with the efficacy of subsequent docetaxel in patients with prostate cancer. Eur J Cancer. 2010; 46(10):1770-2. DOI: 10.1016/j.ejca.2010.04.010. View

3.
Dalton W, Crowley J, Salmon S, Grogan T, Laufman L, Weiss G . A phase III randomized study of oral verapamil as a chemosensitizer to reverse drug resistance in patients with refractory myeloma. A Southwest Oncology Group study. Cancer. 1995; 75(3):815-20. DOI: 10.1002/1097-0142(19950201)75:3<815::aid-cncr2820750311>3.0.co;2-r. View

4.
Di Lorenzo G, Buonerba C, Faiella A, Rescigno P, Rizzo M, Autorino R . Phase II study of docetaxel re-treatment in docetaxel-pretreated castration-resistant prostate cancer. BJU Int. 2010; 107(2):234-9. DOI: 10.1111/j.1464-410X.2010.09498.x. View

5.
Faehling M, Eckert R, Kamp T, Kuom S, Griese U, Strater J . EGFR-tyrosine kinase inhibitor treatment beyond progression in long-term Caucasian responders to erlotinib in advanced non-small cell lung cancer: a case-control study of overall survival. Lung Cancer. 2013; 80(3):306-12. DOI: 10.1016/j.lungcan.2013.02.010. View