- Research article
- Open Access
- Open Peer Review
Intrinsic resistance to tyrosine kinase inhibitors is associated with poor clinical outcome in metastatic renal cell carcinoma
- Jonas Busch†1,
- Christoph Seidel†2,
- Steffen Weikert1,
- Ingmar Wolff1,
- Carsten Kempkensteffen1,
- Lisa Weinkauf1,
- Stefan Hinz1,
- Ahmed Magheli1,
- Kurt Miller1 and
- Viktor Grünwald2Email author
© Busch et al; licensee BioMed Central Ltd. 2011
- Received: 16 March 2011
- Accepted: 14 July 2011
- Published: 14 July 2011
Data on sequential therapy in patients with metastatic renal cell carcinoma (mRCC) and intrinsic resistance to receptor tyrosine kinase inhibitor (rTKI) treatment remains vague.
We retrospectively studied treatment characteristics and outcome of mRCC patients refractory to first rTKI therapy.
Thirty-five mRCC patients (male, 18; female, 11) with primary resistance to first rTKI therapy (sunitinib, n = 28; sorafenib, n = 7) and a median treatment interval of 2.4 months (1 - 4.6) were identified. In 22 patients, progressive disease (PD) was determined by a new metastatic lesion. Of these, 16 patients received subsequent therapy with 12 patients remaining refractory and 4 patients achieving disease stabilization. In 13 patients continuous growth of existing metastatic lesions determined PD. Of these, 9 received sequential therapy with 6 achieving disease stabilization. Altogether, 25 patients were treated sequentially (rTKI: n = 15; mTOR-inhibitor: n = 10) and achieved a median PFS of 3.2 months (range, 1-16.6). Fifteen patients failed to respond to either line of therapy. Disease control was not associated with type of subsequent therapy. Median OS was 14.9 months (CI: 5.5-24.4).
Intrinsic resistance to rTKI is associated with a low chance of response to sequential therapy and a poor prognosis in mRCC patients.
- Vascular Endothelial Growth Factor
During the last years potent therapeutic options evolved for patients with mRCC [1–4]. The introduction of targeted agents has significantly improved the treatment perspectives and prognosis of these patients. The majority of patients with good and intermediate prognosis according to the MSKCC criteria are treated with rTKI, particularly sunitinib, based on the results of two meta-analyses [5, 6]. In spite of this progress in treatment options, a relevant subset of patients remains refractory to first rTKI therapy. On a molecular level, rTKIs target the vascular endothelial growth factor (VEGF) pathway to induce hypoxia, thereby inhibiting tumor growth. However, recent reports suggest that hypoxia may also select for a more malignant RCC phenotype, which may aggregate metastatic development and prone cells to insensitivity for antiangiogenic treatment . Another possible explanation for the resistance to rTKI treatment could be attributed the fact that tumor cells can overcome the noxious rTKI hypoxic microenvironment by switching to invasive epithelial-mesenchymal transition .
The phenomenon of intrinsic resistance to rTKI is not well understood, and it remains unclear whether patients primary refractory to rTKI might benefit from other treatment regimens during sequential therapy. In the present study we aimed to characterize patients with intrinsic resistance to rTKI treatment and analyse their susceptibility to sequential therapy.
Sunitinib was administered daily either as 50 mg or 37.5 mg orally over 4 weeks followed by a two week wash-out period. Sorafenib was administered continuously at a full dose of 400 mg orally twice a day. Dosing for everolimus was 10 mg daily and for temsirolimus 25 mg intravenously once weekly. All agents were administered until disease progression, death, or intolerable toxicity. Objective response was determined every second cycle of sunitinib or every two to three months for all other agents according to the standard Response Evaluation Criteria in Solid Tumors (RECIST) . PFS and OS were calculated from initiation of first rTKI therapy using the Kaplan-Meier-method.
Furthermore, potential relationships between patients' characteristics (age, gender, MSKCC risk and ECOG performance group) with best response on SL and number of affected organ sites, new metastatic site at PD, localisation of PD and time to progression on prior treatment were assessed in an exploratory manner .
Associations between main characteristics and response to treatment were explored using the chi-square test/Fisher's exact test. A p-value < 0.05 was considered statistically significant. PFS and OS were estimated using the Kaplan-Meier method with the log-rank test.
Response assessment according to line and type of targeted therapy
Line of targeted therapy
PFS in months (range)
In this study we report on 35 patients with intrinsic resistant mRCC to rTKI treatment. This subset of patients seems to be characterized by a low likelihood of response to any form of available targeted therapy, with mTOR inhibitors being equally inefficacious as switching to another TKI. The median OS from initiation of first rTKI therapy was only 14.9 months and the median PFS upon second line targeted therapy was limited to 3.5 months with a disease control rate of roughly 40% in the sequence setting. The primary development of a new metastatic lesion during first rTKI treatment may indicate a particularly unfavourable prognosis.
In spite of recent substantial advances in treatment options the salvage strategy for patients with intrinsic resistance to rTKI treatment is not well defined. According to our data this subgroup of patients may have a low chance of overcoming rTKI resistance or responding to the available sequential treatment options. The rationale for sequential therapy with mTOR inhibitors in rTKI refractory patients lies in the expectation that resistance of the tumor to rTKI treatment may be reversed by targeting a different signaling pathway [11, 12]. In the placebo-controlled phase 3 RECORD-1 trial everolimus turned out to be an efficacious treatment option following failure of rTKI therapy . However, disease control can be achieved by rTKI treatment in the majority of treatment-naïve mRCC patients, suggesting underlying sensitivity to VEGFR-targeted agents. Whether mTOR inhibitors exert superior clinical activity in intrinsic resistant disease remains unknown.
Nonetheless, prospective data on the best sequential therapy among the available sequence options in mRCC are still lacking. In their retrospective study Vickers et al. reported that patients receiving another VEGF targeted therapy in the sequence setting may experience a longer progression free survival compared to those treated with mTOR inhibitors . However, among the 216 analyzed patients with a second line therapy only 24 were treated with mTOR inhibitors and as few as three of them received everolimus, so that no valid comparison can be made between everolimus or other options in this setting. In another study Garcia et al. observed a PFS of 4.4 months in 49 patients treated with sorafenib following progression on either sunitinib or bevacizumab . However, the vast majority of these patients had some benefit from first line therapy and developed resistance after several treatment cycles. Compared to these studies our data is based exclusively on patients with intrinsic rTKI resistance. In this subset of patients we observed no convincing efficacy of either of the common sequence therapy regimens. The small number of patients and the retrospective nature of our analysis limit the validity of our observations. The data from prospective randomized trials will certainly clarify some of these issues. However, our data indicate that there is a substantial subset of patients who will not respond to either targeted therapy option available today.
In general, sensitivity to targeted agents occurs when the tumor depends on the constitutive activity of signaling pathways for growth and progression. On the other hand resistance may develop when genetic alterations make the targeted proteins inaccessible to drug binding, activate alternative signaling pathways or upregulate molecule expression to compensate for the inhibition. Indeed, two general modes of resistance to angiogenesis inhibitors targeting the VEGF pathway have been proposed: adaptive (evasive) resistance, which occurs after a period of tumor control, and intrinsic (pre-existing) non-responsiveness without any therapeutic benefit . Alternative pro-angiogenic signaling pathways within the tumor, recruitment of bone marrow-derived pro-angiogenic cells, increased protection of tumor vasculature by pericytes, and increased tumor cell invasiveness to escape oxygen and nutrient deprivation may all constitute escape mechanisms in response to therapy or in response to the selective pressures of the tumor microenvironment during malignant progression . Each targeted agent including the various VEGF pathway inhibitors can cause a different compensatory tumor response, explaining at least in some parts the lack of cross-resistance and the potential benefit of re-challenge strategies .
Despite the proposed common deficiency of VHL function in clear cell RCC, distinct clinical outcome has been reported with current targeted therapies. These findings suggest that underlying genetic abnormalities may be more complex than previously assumed. A recent article by Gordan addressed this crucial question and suggested that HIF2 enhances c-MYC activity and promotes tumor progression in VHL deficient tumors .
In tumors with acquired resistance, distinct mechanisms of resistance have been detected [8, 18, 19]. Furthermore, additional genetic abnormalities have been reported in mRCC. The chromatin remodelling complex gene PBRM1 has been found to be mutated in 41% of 227 clearcell RCC cases . The functional role of PBMR1 in mRCC remains to be determined, but these findings support the notion of a genetic heterogeneity in clear cell mRCC, which may determine intrinsic resistance in mRCC.
However, in intrinsic non-responsiveness the activation of alternative pathways (e.g. TIE2/ANG-2) may be of key relevance [3, 21]. The currently used mTOR inhibitors, i. e. rapalogs, selectively target mTOR complex (TORC)-1, but leave TORC-2 unaffected. Developing inhibitors that target the kinase activity in both TORC1 and TORC2 could result in increased antitumor effects and overcome some of the obstacles associated with the TORC-1 inhibitors. Moreover, mTOR/S6 K activation, insulin receptor substrates 1 and 2 (IRS-1 and IRS-2) and insulin growth factor-1 (IGF-1) signaling, which all result in increased IGFR/PI3K/Akt signaling, appear as attractive targets for further drug development .
Current treatment strategies remain unsatisfactory in patients with intrinsic resistance to VEGF targeted therapies and underscore the medical need to advance the treatment for these patients. Based on the preliminary evidence of different genetic abnormalities in mRCC, clinical trials with agents that interfere with HIF-signalling or the chromatin remodelling complex seem suitable for patients with intrinsic resistant mRCC. However, gemcitabine-based chemotherapy has also been reported effective in single patients and may represent a distinct approach to intrinsic resistance in RCC . Certainly, this subgroup of patients should be explored as a separate entity in clinical trials. Remarkably, the overall patients' prognosis of our study in terms of PFS or OS seems to be comparable to patients of the primary poor prognosis group according to MSKCC criteria.
In conclusion, primary or intrinsic resistance to rTKI therapy indicates a poor prognosis, particularly if new metastatic sites develop. rTKI refractory mRCC patients have a low chance to respond to sequential therapy irrespective of the type of treatment. Further characterization of deregulated key signalling pathways in refractory RCC appears of utmost importance for improving the treatment perspectives. Other potential countermeasures to overcome resistance include combination of VEGF or mTOR inhibition with other signalling inhibitors or with cytotoxic agents.
Publication was assisted by the project "Open-Access-Publizieren" of the Deutsche Forschungsgemeinschaft (DFG).
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