Curative and organ-preserving treatment with intra-arterial carboplatin induction followed by surgery and/or radiotherapy for advanced head and neck cancer: single-center five-year results
© Bertino et al; licensee BioMed Central Ltd. 2007
Received: 22 November 2006
Accepted: 11 April 2007
Published: 11 April 2007
This study evaluated the feasibility, toxicity, response rate and survival of neoadjuvant superselective intra-arterial infusion of high dose carboplatin in advanced head and neck cancer.
Forty-six patients with primary head and neck squamous cell carcinoma received 3 cycles of intra-arterial carboplatin (300 to 350 mg/m2 per cycle every 2 weeks), followed by radiotherapy or surgery plus radiotherapy.
No complications or severe toxicity occurred. Sixteen patients (35%) were complete responders, 20 (43%) partial responders while 10 (22%) did not respond to treatment. After completion of the multimodality treatment, 38/46 patients (83%) were complete responders. After a 5-year follow-up period, 18/46 patients (39%) are alive and disease-free, 3 (6,5%) have died of a second primary tumor and 25 (54,5%) have died of the disease.
Intra-arterial carboplatin induction chemotherapy is a safe, well-tolerated technique that discriminates between responders and non-responders and so may have prognostic significance in planning further integrated treatments aimed to organ preservation for advanced head and neck carcinomas.
In recent years chemotherapy has become an essential part of multimodality curative treatments for advanced head and neck cancer, with prolongation of survival and better organ preservation [1–3]. Several strategies have been developed to increase the efficacy of these integrated treatment protocols while decreasing their associated toxicity, e.g. induction or neoadjuvant versus concomitant chemotherapy, intra-arterial versus intravenous systemic administration of the drugs, single or multiple combined chemotherapeutic agents.
According to the detailed meta-analysis by Pignon et al. , today the gold standard therapy for patients with locally advanced head and neck squamous cell carcinoma seems to be concurrent chemotherapy-radiation treatment, with an absolute improvement of 8% in five year-survival compared to other protocols. However, some reports suggest that also induction chemotherapy may improve survival, locoregional control and organ preservation in oropharyngeal and laryngeal cancer [4–8]. According to Al Sarraf further advantages obtained by giving induction chemotherapy first, the incidence of systemic micrometastases is reduced, the cancer is downstaged in approximately 90% of the cases and up 50% of patients may achieve a complete clinical response .
A large body of evidence supports the theoretical attractiveness of intra-arterial chemotherapy, related to the first pass of the drug through the tumor bed and to the possibility of increasing the doses of the chemotherapeutic agent, thus minimizing systemic toxic side effects .
Compared to intravenous systemic chemotherapy protocols, intra-arterial regimens are based on the use of a single chemotherapeutic agent, namely cisplatin. Currently, platinum derivatives are the most effective drugs in the treatment of squamous cell carcinoma of the head and neck, and the second-generation platinum drug, carboplatin, possesses all of the radiopotentiation characteristics of cisplatin with less toxic side effects [2, 10].
Over recent years our group has performed a pilot study of high-dose intra-arterial carboplatin induction chemotherapy on patients with untreated advanced squamous cell carcinoma of the upper aerodigestive tract. Neoadjuvant intra-arterial chemotherapy was part of a multimodality regimen combining radiotherapy in responder patients, surgery plus radiotherapy in resectable non-responder patients and palliative radiotherapy in non-resectable non-responder patients . The purpose of the present study was to assess the feasibility and technical problems of intra-arterial transfemoral superselective perfusion, the maximum-tolerated dose of carboplatin, systemic and local toxicity and the response rate after induction chemotherapy on the same enlarged population after a longer term follow-up. After completing the therapeutic options built into our multimodality protocol, we assessed five-year overall and disease-free survival rates in patients.
Pre-treatment characteristics of the patients
Primary tumour site
Oral cavity + Oropharynx
Oropharynx + Hypopharynx
Pre-treatment tumour (T) and lymph node (N) staging
Patients underwent a complete clinical and laboratory examination including measurement of haematologic (complete blood cell and platelet count, prothrombin time, partial thromboplastin time), hepatic (blood bilirubin, transaminases and alkaline phosphatase level)and renal (blood urea nitrogen, creatinine and electrolytes level, urinanalysis, 24 hours creatinine clearance) parameters, as well as general metabolic functions (blood glucose and lipids level), chest radiography and cervical vessel ultrasonography. The disease was staged by physical examination, panendoscopic examination, biopsy, CT scan and/or MRI.
All patients received intra-arterial (i.a.) infusions of carboplatin, dissolved in 80 mL of 0,9% saline and infused over 10–15 min by a battery-operated pump (Medrad Mark 5 Plus) with an infusion velocity of 6–8 mL/min. An angiographic catheter (Glidecath Radicofocus 5F Terumo) was introduced percutaneously under local anesthesia (10 mL of 2% lidocaine solution) into the common femoral artery, according to the Seldinger technique. The catheter tip was placed in the external carotid artery, under radiographic control. Diagnostic transfemoral carotid arteriography was performed and the most suitable branch of the artery, providing the main blood supply to the tumour, was selectively catheterised. The catheter was removed immediately after the infusion. A simultaneous intravenous (i.v.) infusion of 250 mL of 0,9% saline was performed. Dexamethasone (4 mg) and ondansetron (1 g) dissolved in 100 mL of 0,9% saline were administered i.v. 1 hour before the infusion. All patients received three cycles of intra-arterial chemotherapy, administered every two weeks. The planned dose of carboplatin per cycle was 300 mg/m2 for the first cohort (3 cases) and 325 mg/m2 for the second cohort (3 cases); subsequently, as no significant toxic effects were observed, the remaining patients (40 cases) received a dose of 350 mg/m2 of carboplatin per cycle. Two weeks after completing chemotherapy, patients were restaged and subsequent treatment was decided upon on the basis of their objective response. Complete responders or partial responders had radiotherapy; non-responders with resectable disease underwent surgery on the tumor site and/or on the neck nodal metastases followed by radiotherapy; non-responders with unresectable disease underwent palliative radiotherapy. Radiation was delivered using conventional fractionation (1,8 – 2 Gy per fraction, five days per week). The total dose was 66 – 70 Gy for PTVI (planning target volume including tumour and encompassing all clinically positive nodes) and 50–56 Gy for PTVII (planning target volume including all anatomical regions at risk of subclinical malignant disease).
Toxicity was evaluated according to WHO criteria  24 hrs after each drug administration. This included: assessment of haematologic, hepatic and renal parameters; assessment of gastrointestinal, otoneurological, cardiac and respiratory function, and the search for signs and symptoms of local toxicity. Response to therapy was assessed two weeks after the last administration of the drug by physical examination, endoscopy, imaging (CT scan and/or MRI) and biopsy, when necessary. A complete response (CR) was defined as the complete disappearance of all demonstrable lesions. A partial response (PR) was defined as a decrease of 50% or greater in the sum of the products of the largest perpendicular diameters of all measurable lesions. No response (NR) was defined as a regression of < 50% in total tumour size or as stable or progressive disease.
The primary efficacy end point was overall survival (i.e, death as a result of any cause). Survival was measured from the start of treatment date to the date of death or the date when the patient was last known to be alive. Yearly estimates were calculated using the Kaplan-Meier method. Secondary efficacy end points were CR rates, loco-regional tumour control and disease-free survival. Time to loco-regional failure was measured from the start of treatment date and the date of disease relapse, the date of disease-related death, or the date when the patient was last known to be alive and disease-free. Loco-regional failure, distant metastases, or disease-related death were all considered failures for disease-free survival. Yearly disease-free survival rates were estimated with the Kaplan-Meier method.
Factors influencing overall and disease-free survival were analyzed and compared by the log-rank test. P values less than 0.05 were considered significant.
One hundred and thirty eight super-selective transfemoral intra-arterial infusions of carboplatin were performed with no significant complications.
Toxicity from chemotherapy
Type of toxicity
N. of patients
Control of disease and survival
No patients were lost to follow-up. The median follow-up time, measured from the start of induction chemotherapy, was 51.3 months (range: 5 to 136 months).
The percentage of organ preservation was 83%, as 8 of the 46 patients underwent salvage surgery at the tumour site.
Our present data confirmed the evidence that regional chemotherapy by superselective transfemoral infusion of high doses of platinum compounds is feasible and that, with the cooperation of an experienced interventional radiologist, can be easily reproduced in a multi-institutional setting, with minimal procedural complications [9, 11, 14–16].
The advantage of carboplatin is that it has an antitumour activity comparable with that of cisplatin but a toxicology profile with lower renal and gastrointestinal effects [10, 17–19]. We administered far higher doses of carboplatin than those used by Vieitez et al. , according to our preliminary phase I study  that led us escalating the cycle doses of carboplatin from 300 mg/m2 to 350 mg/m2. These doses were comparable to the cisplatin "decadoses" used by Robbins et al. [21–24], without relying on simultaneous i.v. treatment with sodium thiosulphate to achieve systemic neutralisation of the platinum compound.
Systemic toxicity was low in our study population: all patients completed the three cycles of chemotherapy with no chemotherapy-related deaths, only 4 cases of moderate (grade 1–2) hematologic toxicity, and one case each of high (grade 3–4) hepatic and neurological toxicity. Local toxicity occurred in some cases, mainly at the level of skin and oral mucosa, but of short duration and of low/moderate degree. The higher systemic toxicity observed in other studies based on the same intra-arterial chemotherapy approach could be due to the different activity/toxicity profile of cisplatin versus carboplatin or to the potentiation of toxic effects in concurrent chemotherapy-radiotherapy regimens.
With respect to a classic neoadjuvant intravenous chemotherapy protocol (Al Sarraf) our protocol presents the advantage of a reduced systemic toxicity and of a reduced duration (one day vs. three days administration, two weeks vs. three weeks interval), with a significant improvement of patient's compliance.
A true neoadjuvant intra-arterial chemotherapy approach for head and neck cancer treatment is rare and the results of many trials are difficult to compare, owing to a number of methodological differences . Limiting our comparison to the latest studies conducted with platinum compounds, our response rates at the end of induction chemotherapy (CR 35% and PR 43%) are similar to those observed by Kovacs  (CR 38% and PR 31%) and lower than those observed by Wilson et al  (CR 68% and PR 23%).
Our five-year overall and disease-free survival rates (50% and 49,8%) may be compared with those observed by Kovacs  (77% and 59%). Even if concurrent chemoradiation treatments seem to achieve the best overall survival rate , our results (50% and 49,8%) are similar to those obtained with the RADPLAT protocol (38,8% and 53,6%) .
According to our previous results  and the opinion of other authors [2, 27], we consider the response to induction chemotherapy to be an important prognostic factor which may determine the sequence and timing of further planned definitive therapy: patients with a lesser response will require total surgical resection of the disease or the remaining disease, followed by post-surgical radiation therapy; patients with a good response may avoid surgery and be treated with radiotherapy alone. Therefore, on the basis of the evaluation made after induction chemotherapy, we adopted a flexible protocol, based not only on the patient's compliance and general conditions, but mainly on their response to neoadjuvant chemotherapy. A similar but less customized multimodality treatment has been followed by Kovacs et al.  in a large series of oral and oropharyngeal cancer patients.
Our present experience suggests that in the treatment of head and neck cancer, superselective intra-arterial infusion with high doses of carboplatin delivered directly to the tumour bed is a safe and well-tolerated technique with no major systemic or local toxic side effects. It proves once again that, compared to other protocols (e.g. concurrent chemoradiotherapy), systemic or intra-arterial induction chemotherapy, does not have a significant advantage in terms of overall or disease-free survival. However, in some patients with bulky head and neck tumours, this technique, adopted as part of a first-line multidisciplinary approach, can achieve a high response rate, which may have a prognostic significance. This is a prospective study of a cohort of patients treated in a unique fashion in which carboplatin was given as an intra-arterial infusion. Those patients who had a major response were than treated with radiation therapy only. Non-responders were treated with surgery. The protocol introduces a novel algorithm for management of patients with advanced head and neck cancer. It is designed to triage patients who are sensitive to chemotherapy to non-surgical regimen whereas those who are not sensitive are treated with surgery.
The authors gratefully acknowledge Dr. Th. Robbins for the revision of the manuscript.
- Pignon JP, Bourhis J, Domenge C, Designe L: Chemotherapy added to locoregional treatment for head and neck squamous-cell carcinoma: three meta-analyses of updated individual data. Lancet. 2000, 355: 949-955.View ArticlePubMedGoogle Scholar
- Al-Sarraf M: Treatment of locally advanced head and neck cancer: historical and critical review. Cancer Control. 2002, 9: 387-399.PubMedGoogle Scholar
- Argiris A: Update on chemoradiotherapy for head and neck cancer. Curr Opin Oncol. 2002, 14: 323-329. 10.1097/00001622-200205000-00012.View ArticlePubMedGoogle Scholar
- The Department of Veterans Affairs Laryngeal Cancer Study Group: Induction chemotherapy plus radiation compared with surgery plus radiation in patients with advanced laryngeal cancer. N Engl J Med. 1991, 324: 1685-1690.View ArticleGoogle Scholar
- Domenge C, Hill C, Lefebvre JL, De Raucourt D, Rhein B, Wibault P, Marandas P, Coche-Dequeant B, Stromboni-Luboinski M, Sancho-Garnier H, Luboinski B: Randomized trial of neoadjuvant chemotherapy in oropharyngeal carcinoma. Br J Cancer. 2002, 83: 1594-1598. 10.1054/bjoc.2000.1512.View ArticleGoogle Scholar
- Kim S, Wu HG, Heo DS, Kim KH, Sung MW, Park CI: Advanced hypopharyngeal carcinoma treatment results according to treatment modalities. Head Neck. 2001, 23: 713-717. 10.1002/hed.1101.View ArticlePubMedGoogle Scholar
- Vokes EE, Stenson K, Rosen FR, Kies MS, Rademaker AW, Witt ME, Brockstein BE, List MA, Fung BB, Portugal L, Mittal BB, Pelzer H, Weichselbaum RR, Haraf DJ: Weekly carboplatin and paclitaxel followed by concomitant paclitaxel, fluorouracil, and hydroxyurea chemoradiotherapy: curative and organ-preserving therapy for advanced head and neck cancer. J Clin Oncol. 2003, 21: 320-326. 10.1200/JCO.2003.06.006.View ArticlePubMedGoogle Scholar
- Altundag O, Gullu I, Altundag K, Yalcin S, Ozyar E, Cengia M, Akyol F, Yucel T, Hosal S, Sozeri B: Induction chemotherapy with cisplatin and 5-fluorouracil followed by chemoradiotherapy or radiotherapy alone in the treatment of locoregionally advanced resectable cancers of the larynx and hypopharynx: results of single-center study of 45 patients. Head Neck. 2005, 27: 15-21. 10.1002/hed.20107.View ArticlePubMedGoogle Scholar
- Robbins KT, Kumar P, Harris J, McCulloch T, Cmelak A, Sofferman R, Levine P, Weisman R, Wilson W, Weymuller E, Fu K: Supradose intra-arterial cisplatin and concurrent radiation therapy for the treatment of stage IV head and neck squamous cell carcinoma is feasible and efficacious in multi-institutional setting: results of radiation therapy oncology group trial 9615. J Clin Oncol. 2005, 23: 1447-1454. 10.1200/JCO.2005.03.168.View ArticlePubMedGoogle Scholar
- Volling P, Schroder M, Rauschning W, Achterrath W, Stennert E: Carboplatin. The better platinum in head and neck cancer?. Arch Otolaryngol Head Neck Surg. 1989, 115: 695-698.View ArticlePubMedGoogle Scholar
- Benazzo M, Caracciolo G, Zappoli F, Bernardo G, Mira E: Induction chemotherapy by superselective intra-arterial high-dose carboplatin infusion for head and neck cancer. Eur Arch Otorhinolaryngol. 2000, 257: 279-282. 10.1007/s004050050240.View ArticlePubMedGoogle Scholar
- International Union Against Cancer: TNM Classification of malignant tumours. 1987, New York: Wiley-Liss, FourthGoogle Scholar
- World Health Organization: WHO Handbook for Reporting Results of Cancer Treatment. 1979, WHO offset publication. Geneva: World Health Organization, 48-Google Scholar
- Robbins KT, Kumar P, Harris J, McCulloch T, Cmelak A, Sofferman R, Levine P, Weisman R, Wilson W, Weymuller E, Fu K: Supradose intra-arterial cisplatin and concurrent radiation therapy for the treatment of stage IV head and neck squamous cell carcinoma is feasible and efficacious in a multi-institutional setting: results if radiation therapy oncology group trial 9615. J Clin Oncol. 2005, 23: 1447-1454. 10.1200/JCO.2005.03.168.View ArticlePubMedGoogle Scholar
- Vieitez JM, Bilbao JI, Hidalgo OF, Martin S, Manzano RG, Tangco E: Intra-arterial chemotherapy with carboplatin and 5-fluorouracil in epidermoid cancer of the oropharynx and oral cavity. Reg Cancer Treat. 1991, 4: 152-155.Google Scholar
- Kovacs AF: Intra-arterial induction high-dose chemotherapy with cisplatin for oral and oropharyngeal cancer: long-term results. Br J Cancer. 2004, 90: 1323-1328. 10.1038/sj.bjc.6601674.View ArticlePubMedPubMed CentralGoogle Scholar
- Calvert AH, Harland SJ, Newell DR, Siddik ZH, Harrap KR: Phase I studies with carboplatin at the Royal Marsden Hospital. Cancer Treat Rev. 1985, 12: 51-57. 10.1016/0305-7372(85)90018-0.View ArticlePubMedGoogle Scholar
- Foster BJ, Clagget-Carr K, Leyland-Jones B, Hoth D: Results of NCI-sponsored phase I trials with carboplatin. Cancer Treat Rev. 1985, 12: 43-49. 10.1016/0305-7372(85)90017-9.View ArticlePubMedGoogle Scholar
- Rose WC, Schuring JE: Preclinical antitumor and toxicologic profile of carboplatin. Cancer Treat Rev. 1985, 12: 1-19. 10.1016/0305-7372(85)90014-3.View ArticlePubMedGoogle Scholar
- Benazzo M, Bernardo G, Corbella F, Danova M, Lanza L, Zappoli F, Uggetti C, Mira E: La chemioterapia intraarteriosa neo-adiuvante superselettiva con carboplatino ad alte dosi nei tumori avanzati cervico-facciali. Acta Otorhinol Ital. 1996, 16: 30-34.Google Scholar
- Robbins KT, Storniolo M, Kerber C, Seagren S, Berson A, Howell SB: Rapid superselective high-dose cisplatin infusion for advanced head and neck malignancies. Head Neck. 1992, 14: 364-371. 10.1002/hed.2880140505.View ArticlePubMedGoogle Scholar
- Robbins KT, Storniolo AM, Kerber C, Vicario D, Seagren S, Shea M, Hanchett C, Los G, Howell SB: Phase I study of highly selective supradose cisplatin infusion for advanced head and neck cancer. J Clin Oncol. 1994, 12: 2113-2120.PubMedGoogle Scholar
- Robbins KT, Fontanesi J, Wong FS, Vicario D, Seagren S, Kumar P, Weisman R, Pellitteri P, Thomas JR, Flick P, Palmer R, Weir AB, Kerber C, Murry T, Ferguson R, Los G, Orloff L, Howell SB: A novel organ preservation protocol for advanced carcinoma of the larynx and pharynx. Arch Otolaryngol Head Neck Surg. 1996, 122: 853-857.View ArticlePubMedGoogle Scholar
- Robbins KT, Kumar P, Regine WF, Wong FS, Weir AB, Flick P, Kun LE, Palmer R, Murry T, Fontanesi J, Ferguson R, Thomas R, Harstell WF, Paig CU, Salazar G, Norfleet L, Hanchett CB, Harrington V, Neill HB: Efficacy of targeted supradose cisplatin and concomitant radiation therapy for advanced head and neck cancer: the Memphis experience. Int J Radiat Oncol Biol Phys. 1997, 38: 263-271. 10.1016/S0360-3016(97)00092-8.View ArticlePubMedGoogle Scholar
- Wilson WR, Siegel RS, Harisiadis LA, Davis DO, Nguyen HH, Bank WO: High-dose intra-arterial cisplatin therapy followed by radiation therapy for advanced squamous cell carcinoma of the head and neck. Arch Otolaryngol Head Neck Surg. 2001, 127: 809-812.PubMedGoogle Scholar
- Robbins KT, Kumar P, Wong FSH, Harstell WF, Flick P, Palmer R, Weir AB, Neill HB, Murry T, Ferguson R, Hanchett C, Vieira F, Bush A, Howell SB: Targeted chemoradiation for advanced head and neck cancer: analysis of 213 patients. Head Neck. 2000, 22: 687-693. 10.1002/1097-0347(200010)22:7<687::AID-HED8>3.0.CO;2-W.View ArticlePubMedGoogle Scholar
- Kovacs AF: Intra-arterial chemotherapy and chemoembolization in head neck cancer. Establishment as a neoadjuvant routine method. Cancer Ther. 2003, 1: 1-9.Google Scholar
- Kovacs AF, Schiemann M, Turowski B: Combined modality treatment of oral and oropharyngeal cancer including neoadiuvant intra-arterial cisplatin and radical surgery followed by concurrent radiation and chemotherapy with weekly docebaxel – three year results of a pilot study. J Cranio-Maxillofac Surg. 2002, 30: 112-120. 10.1054/jcms.2002.0283.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/7/62/prepub
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