Skip to main content


We’d like to understand how you use our websites in order to improve them. Register your interest.

99mTc-NTP 15-5 assessment of the early therapeutic response of chondrosarcoma to zoledronic acid in the Swarm rat orthotopic model



Since proteoglycans (PGs) appear as key partners in chondrosarcoma biology, PG-targeted imaging using the radiotracer 99mTc-N-(triethylammonium)-3-propyl-[15]ane-N5 (99mTc-NTP 15-5) developed by our group was previously demonstrated to be a good single-photon emission computed tomography tracer for cartilage neoplasms. We therefore initiated this new preclinical study to evaluate the relevance of 99mTc-NTP 15-5 imaging for the in vivo monitoring and quantitative assessment of chondrosarcoma response to zoledronic acid (ZOL) in the Swarm rat orthotopic model.


Rats bearing chondrosarcoma in the orthotopic paratibial location were treated by ZOL (100 μg/kg, subcutaneously) or phosphate-buffered saline, twice a week, from day 4 to day 48 post-tumor implantation. 99mTc-NTP 15-5 imaging was performed at regular intervals with the target-to-background ratio (TBR) determined. Tumor volume was monitored using a calliper, and histology was performed at the end of the study. From day 11 to day 48, mean TBR values ranged from 1.7 ± 0.6 to 2.3 ± 0.6 in ZOL-treated rats and from 2.1 ± 1.0 to 4.9 ± 0.9 in controls. Tumor growth inhibition was evidenced using a calliper from day 24 and associated to a decrease in PG content in treated tumor tissues (confirmed by histology).


This work demonstrated two proofs of concept: (1) biphosphonate therapy could be a promising therapeutic approach for chondrosarcoma; (2) 99mTc-NTP 15-5 is expected to offer a novel imaging modality for the in vivo evaluation of the extracellular matrix features of chondrosarcoma, which could be useful for the follow-up and quantitative assessment of proteoglycan ‘downregulation’ associated to the response to therapeutic attempts.



Considering the 10-year survival rate of chondrosarcoma (from 29% to 83% depending on the subtype and grading), improving its clinical management is a challenge and novel therapeutic approaches are needed [1]. This implies that in vivo markers of the biologic phenotypic features of chondrosarcoma behavior in the bone environment could be used as quantitative criteria of grading, follow-up, and early evaluation of response to therapy.

Since proteoglycans (PGs) appear as key partners in chondrosarcoma biology, PG-targeted imaging using the radiotracer 99mTc-N-(triethylammonium)-3-propyl-[15]ane-N5 (99mTc-NTP 15-5) developed by our group was expected to be a good single-photon emission computed tomography (SPECT) tracer for the molecular imaging of cartilage neoplasms in nuclear medicine [2, 3].

Resistance to chemotherapy is well known to make chondrosarcoma therapeutic management difficult [4]. The bisphosphonate zoledronic acid (ZOL) has demonstrated its therapeutic interest in a variety of tumors affecting the bones, such as osteosarcoma, Ewing's sarcoma, and chondrosarcoma [57].

This study was therefore initiated in the well-characterized Swarm rat chondrosarcoma (SRC) orthotopic model to determine the relevance of 99mTc-NTP 15-5 imaging for an early quantitative characterization of chondrosarcoma response to ZOL.


Protocols were performed under the authorization of the French Directorate of Veterinary Services (Authorization No. C63-113-10) and were conducted under the supervision of authorized investigators in accordance with the institution’s recommendations for the use of laboratory animals.


Experiments were conducted on 24 male Sprague Dawley rats (Charles River, L'Arbresle, France). The SRC model was a generous gift from Dr. P.A. Guerne (Switzerland) as tissue fragments, which were frozen until use. Allograft transplantation of a 10-mm3 SRC fragment was performed on the right hindlimb in the paratibial location of the anesthetized animals (isoflurane (Abbott, Rungis, France) in air (1.5%, 1 L/min)) associated with an intramuscular injection of 100 mg/kg of ketamine (Imalgene®, Rhone Merieux, Lyon, France), as published [3, 6, 8].

ZOL treatment

ZOL was kindly provided as a research-grade disodium salt by Novartis Pharma AG (Basel, Switzerland). Rats were randomly divided into two groups:

  1. 1.

    ZOL-treated: subcutaneous administration of 100 μg/kg twice a week from day 4 to day 48 after implantation (n = 12)

  2. 2.

    Control: PBS in the same conditions (n = 12)

Tumor growth assessment

Tumor volume was calculated from calliper measurement of the largest (L) and smallest (S) perpendicular tumor diameters, using the formula: V (mm3) = 0.5 × L × S2 [3]. Data were expressed as mean ± standard deviation. At each time point, the tumor volumes of ZOL and controls were compared by analysis of variance (ANOVA) with a level of significance set at p < 0.05.

99mTc-NTP 15-5 imaging

99mTc-NTP 15-5 imaging was performed at days 4 (before treatment), 11, 16, 24, 36, and 48 after implantation. NTP 15-5 was radiolabeled with 99mTc as described [3].

Acquisitions (10-min duration, 15% window at 140 keV) of each hindlimb of anesthetized animals positioned over a 10-cm collimator of a small-animal gamma camera (γImager, Biospace, Paris, France) were performed, 30 min after i.v. administration of 30 MBq of radiotracer. Fixed-size regions of interest (ROIs) were delineated over the tumor, adjacent muscles, and contralateral muscles, and average counts (cpm/mm2) were obtained. The use of activity profile for ROI placement ensured easy, reproducible positioning of the ROI for serial images.

At each time point and for each animal, the target-to-background ratio (TBR) was calculated as follows: TBR = Average count in the tumor (cpm/mm2) / Average count in the contralateral muscle (cpm/mm2). Data were expressed as mean ± standard deviation.

Analysis of data with multiple comparisons was performed by repeated-measures ANOVA followed by Tukey’s post-test, with a level of significance set at p < 0.05.


At the end of the study, tumors fixed in 4% formalin were embedded in paraffin, sectioned (5 μm), and stained with hematoxylin-eosin and alcian blue (AB).


ZOL inhibited tumor growth

As shown in Figure 1, ZOL inhibited tumor growth as compared to controls: From day 24 to day 48, a significant (p < 0.05) difference in tumor volume was observed between control and treated groups.

Figure 1

Representative time course of the mean tumor volume ± standard deviation of ZOL-treated and control groups. Both groups have n = 12 animals. The asterisk indicates p < 0.05.

Tumor regression patterns were clearly evidenced by histology (Figure 2): whereas controls showed nuclear atypia, anisokaryosis, mitosis, lobular arrangement of the tumor, and metachromasia (Figure 2A,B,C), ZOL-treated animals demonstrated fibrous and inflammatory remodeling patterns of tumor regression (Figure 2D,E). Metachromasia, reflecting PG content, was also decreased in ZOL-treated animals as compared to controls (Figure 2F versus Figure 2C).

Figure 2

Histological analysis of tumor tissue at the end of the study: control (A to C) and ZOL-treated (D to F) groups. The tumor slices were stained with hematoxylin-eosin (A, B, D, E) or with alcian blue (C, F). Magnification: ×50 (C), ×100 (B, D, E, F), and ×200 (A). CT, controls; ZOL, zoledronic acid.

99mTc-NTP 15-5 monitoring of in vivo chondrosarcoma response to ZOL

As illustrated in Figure 3A, for representative animals, 99mTc-NTP 15-5 accumulation was observed in the joints and at the sites of tumor implantation as early as day 4. As pathology evolved, a weaker radiotracer accumulation was observed in ZOL-treated tumors as compared to controls.

Figure 3

99m Tc-NTP 15-5 imaging of control and ZOL-treated groups. (A) Representative in vivo scintigraphic images of the tumor-bearing hindlimb obtained for controls and ZOL-treated animals at various stages of the study. (B) Semi-quantitative analysis of 99mTc-NTP 15-5 imaging: results are expressed as mean TBR values ± standard deviation. CT, controls; ZOL, zoledronic acid-treated; TBR, target-to-background ratio. The asterisk indicates p < 0.05.

From day 11 to day 48, mean TBR values ranged from 1.7 ± 0.6 to 2.3 ± 0.6 in ZOL-treated rats and from 2.1 ± 1.0 to 4.9 ± 0.9 in controls (Figure 3B). Differences in TBR between treated rats and controls were statistically significant (p < 0.05) from day 24 to day 48. Repeated-measures ANOVA revealed both a significant ‘between-group effect’ as well as a within-subject effect (group * time).


A few years ago, Heymann's group published the therapeutic relevance of using ZOL in the SRC model [6]. Since then, others have reported the promising effects of bisphosphonates not only on chondrosarcoma proliferation and invasion in vitro, but also in clinical practice [7, 9, 10]. In clinics, chondrosarcoma therapeutic response is still evaluated by conventional imaging by measuring anatomical tumor size reduction [11]. Unlike the late effects of anticancer therapy on tumor size, molecular and metabolic changes are well recognized to be induced much earlier, before morphological changes occur [12].

Our previous study demonstrated 99mTc-NTP 15-5 to be a promising SPECT tracer for the molecular imaging of cartilage neoplasms in nuclear medicine [3]. 99mTc-NTP 15-5 appeared of particular interest since radiotracers currently available in clinics such as 201Tl, 99mTc-MIBI, 99mTc-tetrofosmin, 99mTc-DMSA(V), and 18F-FDG have evidenced limitations for imaging chondrosarcoma with low cellularity and high chondrogenic matrix [13].

The results reported in this new study bring additional data in favor of 99mTc-NTP 15-5 imaging for the in vivo follow-up of chondrosarcoma and more especially the semi-quantitative assessment of therapeutic response in vivo, with TBR values being significantly decreased in the treated group with respect to controls from day 24. Chondrosarcoma growth inhibition was confirmed by calliper measurement from day 24 and characterized at the tissue level by histology: interestingly, AB staining evidenced a huge decrease in glycosaminoglycan content in ZOL as compared to controls. Such PG ‘downregulation’ reflects the tumor proliferation inhibition at the extracellular matrix level and is expected to be at the origin of the decreased accumulation of the 99mTc-NTP 15-5 radiotracer in tumors responding to ZOL.


99mTc-NTP 15-5 is expected to offer a novel imaging modality for the semi-quantitative evaluation of PG in vivo as markers of the extracellular matrix features of chondrosarcoma, which could be useful for the follow-up and evaluation of the response to therapeutic attempts. Combining chondrosarcoma functional imaging at the PG level with relevant targeted therapies may represent the opportunity to bridge the gap between preclinical and clinical testing, which is of real need for improving the management of this pathology.


  1. 1.

    World Health Organization: Cartilage tumors. In Pathology and Genetics of Tumours of Soft Tissue and Bone. Edited by: Fletcher CDM, Unni KK, Mertens F. Lyon: IARC; 2002:234–257. [Kleihues P, Sobin LH (Series Editors): World Health Organization Classification of Tumors]

  2. 2.

    Velasco CR, Colliec-Jouault S, Redini F, Heymann D, Padrines M: Proteoglycans on bone tumor development. Drug Discov Today 2010, 13–14: 553–560.

  3. 3.

    Miot-Noirault E, Gouin F, Vidal A, Rapp M, Maublant J, Askienazy S, Chezal JM, Heymann D, Redini F, Moins N: First preclinical imaging of primary cartilage neoplasm and its local recurrence using 99m Tc-NTP 15–5 radiotracer. J Nucl Med 2009, 50: 1541–1547. 10.2967/jnumed.108.056721

  4. 4.

    Onishi AC, Hincker AM, Lee FY: Surmounting chemotherapy and radioresistance in chondrosarcoma: molecular mechanisms and therapeutic targets. Sarcoma 2011, 2011: 381564.

  5. 5.

    Moriceau G, Ory B, Gobin B, Verrecchia F, Gouin F, Blanchard F, Redini F, Heymann D: Therapeutic approach of primary bone tumours by bisphosphonates. Curr Pharm Des 2010, 16: 2981–2987. 10.2174/138161210793563554

  6. 6.

    Gouin F, Ory B, Rédini F, Heymann D: Zoledronic acid slows down rat primary chondrosarcoma development, recurrent tumor progression after intralesional curretage and increases overall survival. Int J Cancer 2006, 119: 980–984. 10.1002/ijc.21951

  7. 7.

    Streitbuerger A, Henrichs M, Ahrens H, Lanvers-Kaminzky C, Gouin F, Gosheger G, Hardes J: Cytotoxic effect of clodronate and zoledronate on the chondrosarcoma cell lines HTB-94 and CAL-78. Int Orthop 2011, 35: 1369–1373. 10.1007/s00264-010-1130-5

  8. 8.

    Grimaud E, Damiens C, Rousselle AV, Passuti N, Heymann D, Gouin F: Bone remodelling and tumor grade modifications induced by interactions between bone and swarm rat chondrosarcoma. Histol Histopathol 2002, 17: 1103–1111.

  9. 9.

    Odri GA, Dumoucel S, Picarda G, Battaglia S, Lamoureux F, Corradini N, Rousseau J, Tirode F, Laud K, Delattre O, Gouin F, Heymann D, Redini F: Zoledronic acid as a new adjuvant therapeutic strategy for Ewing’s sarcoma patients. Cancer Res 2010, 70: 7610–7619. 10.1158/0008-5472.CAN-09-4272

  10. 10.

    Montella L, Addeo R, Faiola V, Cennamo G, Guarrasi R, Capasso E, Mamone R, Caraglia M, Del Prete S: Zoledronic acid in metastatic chondrosarcoma and advanced sacrum chordoma: two case reports. J Exp Clin Cancer Res 2009, 28: 7. 10.1186/1756-9966-28-7

  11. 11.

    Fox E, Patel S, Wathen JK, Schuetze S, Chawla S, Harmon D, Reinke D, Chugh R, Benjamin RS, Helman LJ: Phase II study of sequential gemcitabine followed by docetaxel for recurrent Ewing sarcoma, osteosarcoma, or unresectable or locally recurrent chondrosarcoma: results of sarcoma alliance for research through collaboration study 003. Oncologist 2012, 17: 321. 10.1634/theoncologist.2010-0265

  12. 12.

    Chiti A, Oyen WJG: Imaging of therapy response in oncology. Q J Nucl Med 2011, 55: 587–588.

  13. 13.

    Arsos G, Venizelos I, Karatzas N, Koukoulidis A, Karakatsanis C: Low-grade chondrosarcomas: a difficult target for radionuclide imaging. Case report and review of the literature. Eur J Radiol 2002, 43: 66–72. 10.1016/S0720-048X(01)00427-2

Download references


This work was supported by the Ligue contre le Cancer Auvergne, Auvergne Region for Contrat de Projets Etat Region/Regional Innovation Fund FRI2/OSEO and in collaboration with Cyclopharma.



The authors thank G. Hamery and P. Monmousseau from the Experimental Therapy Unit facility core (Nantes, France).

Author information



Corresponding author

Correspondence to Elisabeth Miot-Noirault.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

EMN, CP, and SB carried out the experimental treatments and imaging studies. ED and FG carried out the development of the SRC orthotopic model. AV and JMC carried out the synthesis and radiolabeling of NTP 15-5. MMD carried out the histology. MFH participated in the histology analysis. DH and FR conceived of the study and participated in its design and in the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Authors’ original file for figure 3

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 2.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and Permissions

About this article

Cite this article

Miot-Noirault, E., David, E., Vidal, A. et al. 99mTc-NTP 15-5 assessment of the early therapeutic response of chondrosarcoma to zoledronic acid in the Swarm rat orthotopic model. EJNMMI Res 3, 40 (2013).

Download citation


  • Chondrosarcoma
  • Zoledronic acid
  • 99mTc-NTP 15-5 radiotracer
  • Proteoglycans