- 1 Department of Medical Oncology, The Royal Marsden Hospital, London, UK
- 2 Translational Cancer Therapeutics Laboratory, Cancer Research UK London Research Institute, London, UK
Medical Therapy for RCC in 2012
There are nearly 9000 new diagnoses of renal cell carcinoma (RCC) each year in the United Kingdom, and nearly 60,000 in the United States (Jemal et al., 2010; UK, 2011; Jemal et al., 2010; Cancer Research UK, 2011). Nephrectomy for localized disease may be curative, but ∼50% of patients present with or subsequently develop metastatic disease (Motzer et al., 1996; Leibovich et al., 2003), which is inevitably fatal. In general, these patients require palliative systemic therapy, but metastatic RCC (mRCC) has historically been refractory to cytotoxic and hormonal therapy (Harris, 1983; Yagoda and Bander, 1989). Prior to 2007, immunotherapy with interferon-alpha or interleukin-2 was the mainstay of treatment, with modest benefits at best (Motzer et al., 2002b; Coppin et al., 2005). Since then, seven molecularly targeted agents have been approved for use in mRCC, all of which have been shown in phase III randomized clinical trials to improve disease control and which now represent the standards of care (Escudier et al., 2007a,b; Hudes et al., 2007; Motzer et al., 2007, 2010; Rini et al., 2008, 2011; Sternberg et al., 2010). Sunitinib, sorafenib, pazopanib, and axitinib are orally administered inhibitors of multiple tyrosine kinase receptors, with variable affinity for the vascular endothelial growth factor receptor (VEGF-R), and provide tumor control through suppression of angiogenesis, as does the monoclonal antibody to VEGF, bevacizumab. Temsirolimus and everolimus are mammalian target of rapamycin (mTOR) inhibitors; the mTOR pathway is a key component of the PI3K/Akt pathway which mediates tumor cell proliferation and survival via cell cycle regulatory proteins (Schmelzle and Hall, 2000; Fingar et al., 2004) and is also thought to influence angiogenesis (Del Bufalo et al., 2006; Thomas et al., 2006). A therapeutic approach which targets critical biological signaling pathways has clearly been the most successful strategy to treat mRCC to date, however, anti-VEGF and anti-mTOR treatments remain inadequate. Furthermore, individualized therapy for mRCC has not been achieved; resistance to treatment is a major problem for which the molecular basis has not been determined, and biomarkers predictive of response or resistance have not been developed.
The Clinico-Pathological Diversity of RCC
Renal cell carcinoma is comprised of distinct pathological subtypes, which to some degree influence tumor behavior. The predominant subtype, clear cell RCC, accounts for 75% of RCCs (Reuter, 2006), and patients with this histology were almost exclusively enrolled in the registration trials for the drugs described above. There is much research into the molecular pathogenesis of clear cell RCC, which is characterized by loss of function in the Von Hippel-Lindau (VHL) gene leading to accumulation of hypoxia-inducible factor (HIF) and a panel of hypoxia-responsive genes such as VEGF (Kim and Kaelin, 2004; Kaelin, 2007). Germline mutations in the MET oncogene are associated with Hereditary Papillary Renal Carcinoma (HRPC) and this gene may also be activated in sporadic Type I papillary RCC (Schmidt et al., 1997; Lubensky et al., 1999). Familial forms of Type 2 papillary RCC result from germline mutations in genes encoding metabolic enzymes, such as the Krebs cycle enzymes fumarate hydratase (FH) and succinate dehydrogenase B (SHDB; Toro et al., 2003; Ricketts et al., 2008). The remaining subtypes – chromophobe, collecting duct, translocation, medullary and mucinous tubular, and spindle cell carcinomas – include some rare entities but there is still considerable knowledge about their pathobiology. Specifically, chromophobe RCCs can occur with hair follicle hamartomas and pulmonary cysts as part of the autosomal dominant Birt–Hogg–Dubé syndrome, caused by mutations in the BHD gene FLCN (Nickerson et al., 2002), and KIT has been reported to be overexpressed in the sporadic form of this subtype (Yamazaki et al., 2003; Pan et al., 2004; Yusenko et al., 2009). Translocation tumors are characterized by a breakpoint at chromosome Xp11 and gene fusions between TFE3 transcription factor and multiple genes (Martignoni et al., 2009).
Diversity of clinical outcomes in RCC may partly reflect this pathological variation. For example, papillary and chromophobe tumors appear to be less likely to metastasise than clear cell tumors (Leibovich et al., 2010) but might also be less responsive to current therapies when advanced (Motzer et al., 2002a; Choueiri et al., 2008; Plimack et al., 2010). Furthermore, pathologists recognize that within individual renal cell tumors there is regional variation with respect to tumor morphology and grade. It is also apparent that significant heterogeneity of clinical behavior exists within a particular histological subtype of RCC. For example, a subset of patients with clear cell RCC are recognized to have limited and indolent metastatic disease, and may not require initiation of systemic treatment for some years (Fisher et al., 2011). In the landmark phase III trial of sunitinib compared with interferon, ∼25% of patients did not benefit from sunitinib treatment, despite all having at least a clear cell component to their tumor histology (Motzer et al., 2007). Furthermore, a recent trial of sunitinib exclusively in patients with RCC as a result of hereditary VHL disease found a response rate of only 33% in RCCs, and no effect of sunitinib on benign tumors, suggesting a complex relationship between the underlying genetic alteration and treatment of one of its end-targets (Jonasch et al., 2011).
The Challenge of Genetic Heterogeneity in RCC
Could these results, and the challenges associated with current therapies for mRCC be partly explained on the basis of intra and inter-tumoral heterogeneity? This is the concept that distinct sub-populations of cancer cells exist within and between tumors of individual patients respectively, each with distinct genotypes and phenotypes, as a result of clonal evolution of the tumor (Marusyk and Polyak, 2010; Navin et al., 2011). The underlying mechanisms driving intra- and inter-tumor heterogeneity may be different, but it seems likely that their impact on the ability to deliver personalized medicine in mRCC overlaps. The evidence for each will be summarized in the following paragraphs.
Intratumour Heterogeneity
Reports of heterogeneity in DNA content within RCCs date back to 1985 (Ljungberg et al., 1985, 1996; Krech et al., 1990); in one study, intra-tumoural heterogeneity of DNA ploidy assessed by flow and static cytometry was found in 71% of clear cell RCCs (Krech et al., 1990). Some of these studies attempted to correlate spatial variation in DNA ploidy index with prognostic outcomes. Ljungberg et al. (1996) studied multiple samples from each of 200 RCCs and reported a significant proportion of heterogenous tumors (56%) containing both aneuploid and diploid cell populations. A second study also involved multiple samples from individual RCC nephrectomy specimens, including those of clear cell, papillary, and chromophobe histology, and analyzed DNA content by flow cytometry. A lower prevalence of intra-tumoural heterogeneity was found; 27 of 124 tumors (22%) contained both diploid and non-diploid populations (Ruiz-Cerda et al., 1999). Neither of these studies observed a relationship between heterogeneous distribution of aneuploidy within individual tumors, which might reflect ongoing genomic instability as opposed to stably aneuploid tumors, and survival. A negative correlation between the number of DNA losses per RCC tumor, as determined by comparative genomic hybridization, and recurrence-free survival has been demonstrated, but this relationship reflects genomic complexity rather than intra-tumor heterogeneity per se (Moch et al., 1996).
After the cloning of the VHL gene, Moch et al. examined intra-tumor heterogeneity with respect to VHL gene status in RCC. In this study, frozen tumor samples from 53 patients with clear cell and papillary RCC were analyzed by FISH and indicated the presence of intra-tumoural, large sub-populations of malignant cells with and without VHL deletion, in at least one tumor (Moch et al., 1998). This finding was supported by results of an earlier study showing heterogeneous loss of chromosome 3p using conventional cytogenetics (van der Hout et al., 1993). A recent study published in this journal sequenced the VHL gene of paired primary and metastatic clear cell renal tumors stored as paraffin-embedded tissue (Vaziri et al., 2012). Seven of 10 patients’ samples (either primary or metastatic, containing >95% tumor) were found to have VHL gene mutations, and one patient had VHL gene methylation. Four patients had discordant VHL genotype between primary and metastatic lesions, and VHL gene status also varied within different micro-dissected areas of the primary and metastatic tumors in two patients. Acknowledging the difficulty of identifying true somatic mutations in genetically heterogenous specimens, sequence variations of the VHL gene identified in a subset of genomic DNA samples were independently validated by a high-throughput technique which combines endonuclease scanning and Sanger sequencing (Nickerson et al., 2008). This disparity, and results of another study in which 32% of mRCC tumors bore no genetic similarity to the primary (Bissig et al., 1999), might suggest that heterogeneous primary tumors result in the outgrowth of a biologically advantageous low frequency sub-clone which establishes the secondary disease site.
Recently we have described the complex somatic mutational, genomic, and transcriptomic landscapes within clear cell RCC tumors from four patients (Gerlinger et al., 2012). Multiple single biopsies of primary and metastatic tumor sites enabled multi-region exome sequencing, revealing that only a minority of somatic mutations were present across all biopsy specimens, and clearly demonstrating the presence of spatial tumor heterogeneity involving nearly all levels of genetic alteration. From this information, a comprehensive phylogenetic tree of branched tumor progression was constructed.
Inter-Tumor Heterogeneity
Whole exome sequencing of clear cell renal tumors has recently identified a number of candidate cancer genes additional to VHL, including PBRM1, SETD2, JARID1C, and UTX (van Haaften et al., 2009; Dalgliesh et al., 2010; Varela et al., 2011; Guo et al., 2012; Larkin et al., 2012). Frequently, these are genes involved in histone and chromatin modification (Larkin et al., 2012). It is apparent though that their mutation rate in clear cell RCC is often low (less than 10%; http://www.sanger.ac.uk/perl/genetics/CGP/cosmic) and therefore mutations are not commonly shared between patients, at least at the current level of sequencing depth possible. This work indicates the presence of significant inter-tumor genetic heterogeneity in the histological subtype of clear cell RCC, previously thought to be dominated by a driver mutation in VHL (Dalgliesh et al., 2010) and may present an obvious limitation to the “one size fits all” approach to systemic therapy which is currently offered to patients with kidney cancer.
The Impact of Tumoural Heterogeneity on Treatment and Research
New evidence such as this clearly has profound implications for clinical practice and research. Inter and intratumour heterogeneity present a major obstacle to further improvements in medical therapy for mRCC. A key issue is the inability to select drug therapy for an individual patient, despite numerous studies investigating candidate biomarkers in RCC (reviewed in Vickers and Heng, 2010). This is in stark contrast to other solid tumor types such as cancers of the breast and lung and melanoma (Slamon et al., 2001; Kwak et al., 2010; Maemondo et al., 2010; Chapman et al., 2011), where patients who will definitely not benefit from targeted treatment are more easily identifiable at the outset. It is possible that limited progress in predictive biomarker discovery and validation in RCC reflects the presence of complex genomic abnormalities which differ within regions of a tumor and between tumor sites. Such intratumour heterogeneity may result in tumor sampling bias and the failure to validate biomarkers discovered through single tumor biopsy genomics analyses. Clinical trial designs which include rigorous tissue collection protocols based on multi-region tumor analyses to define common ubiquitous genetic changes that may serve as more robust predictors of disease biology, such as those used by the Personalized RNA interference to Enhance the Delivery of Individualized Cytotoxic and Targeted therapeutics (PREDICT) consortium (Swanton et al., 2010) are required, but are often complex and demanding in terms of human and financial resources.
The mechanisms of resistance to anti-VEGF and anti-mTOR treatments in mRCC are incompletely understood, but an obvious question which arises from regional genomic variability in tumors is whether intra-tumoural heterogeneity itself fosters treatment resistance and therapeutic failure (Carter et al., 2006; Walther et al., 2008; McClelland et al., 2009; Swanton et al., 2009; Gerlinger and Swanton, 2010; Birkbak et al., 2011; Lee et al., 2011; Roylance et al., 2011). The presence of intra-tumor heterogeneity and its associated multiple tumor dependencies suggest the worrying prospect that multiple drugs will be required to treat one heterogeneous tumor.
Conclusion
In summary, there is a small but increasing body of literature supporting intra- and inter-tumor heterogeneity in RCC, predominantly in the clear cell subtype. Their clinical relevance has not been properly addressed in the era of modern genomic techniques. However, it is our view that the potential impact of tumoural heterogeneity on effective therapy for this disease is such that it is an area worthy of intensive research. Efforts must be focused on adaptation of clinical trial design and the further advancement and accessibility of novel tumor genomics analyses derived from multiple tumor sites to facilitate an understanding of ITH and the clonal evolution of disease through treatment.
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Citation: Fisher R, Larkin J and Swanton C (2012) Inter and intratumour heterogeneity: a barrier to individualized medical therapy in renal cell carcinoma? Front. Oncol. 2:49. doi: 10.3389/fonc.2012.00049
Received: 20 April 2012; Accepted: 01 May 2012;
Published online: 18 May 2012.
Copyright: © 2012 Fisher, Larkin and Swanton. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: charles.swanton@cancer.org.uk