3-weekly or weekly cisplatin concurrently with radiotherapy for patients with squamous cell carcinoma of the head and neck – a multicentre, retrospective analysis

Prognosis of patients with squamous cell carcinoma of the head and neck (SCCHN) has improved in the last decades [1‐4]. However, most SCCHN patients are diagnosed with loco-regionally advanced (LA-SCCHN) stage disease. In this setting, multimodal therapy including combined radiochemotherapy (RCT) either as adjuvant therapy after tumor resection or as definitive curatively intended treatment approach is recommended. Several Phase III randomized trials confirmed improved loco-regional control and longer survival for high-risk patients with combined versus sequential RCT with cisplatin in the definitive [5‐7] and postoperative setting [8‐10]. For non-surgical cases the meta-analysis by Pignon et al. including 93 trials and more than 17′000 patients demonstrated an overall survival (OS) benefit from the addition of chemotherapy of 6.5% at five years compared to radiotherapy (RT) alone [11]. In a second meta-analysis, these results were confirmed and it was demonstrated that concurrent (but not sequential) RCT improved median OS by one year [12]. The standard treatment regimen consists of three cycles of cisplatin 100 mg/m² given on days 1, 22 and 43 of a 7-week RT course [5, 6, 13]. Due to adverse events (AEs) of this intensive regimen, chemotherapy modifications (dose reductions, delays, and omissions) are required in up to 40% of patients [14, 15]. The main AEs due to cisplatin include renal insufficiency, electrolyte disorders, myelo- and ototoxicity [6, 8, 9, 16]. Suboptimal compliance with cisplatin regimen might negatively impact patient outcome [5, 17, 18]. Therefore, alternative treatment schedules including low-dose cisplatin have been investigated [7, 19‐24]. Based on these studies, weekly cisplatin administered at a dose of 30–40 mg/m² is frequently used [7, 19, 21, 22, 24]. Regardless of the treatment regimen, it has been suggested that a cumulative dose of 200 mg/m² needs to be reached for therapeutic benefit [11, 25]. A retrospective analysis revealed inferior outcome with a cumulative cisplatin dose of ≤200 mg/m² in HPV-negative patients. Recently, a randomized phase III non-inferiority trial suggested that a 3-weekly schedule with cisplatin 100 mg/m² results in superior loco-regional control compared to a weekly dose of 30 mg/m² [23]. However, the higher dose regimen was associated with significantly more acute toxicities of grade 3 or higher. Although this is the first randomized trial, the results have to be interpreted with caution as more than 90% of patients were diagnosed with oral cavity tumors and more than 90% of patients were treated with RCT in the postoperative setting. Several other comparisons between different treatment regimens have been made mainly in retrospective [26‐32] and small prospective trials [33‐35] and showed contradictory findings.

The aim of this multicenter, retrospective analysis was to compare outcome, cumulative cisplatin dose and acute treatment toxicity in patients undergoing RCT for SCCHN receiving 3-weekly or weekly cisplatin concurrently with intensity-modulated radiotherapy (IMRT).

This is one of the largest retrospective studies evaluating different treatment regimens for combined radio-chemotherapy in SCCHN patients undergoing combined RCT with cisplatin. We analysed SCCHN patients treated at three different sites in Switzerland. One advantage of this study was, that treatment allocation was done by site (based on internal guidelines) and not on patient-based criteria, thus excluding an important selection bias. Patients treated according to the 3 weekly cisplatin schedule were more likely to achieve a cumulative cisplatin dose of ≥200 mg/m². However, neither the treatment regimen (three weekly versus once weekly) nor the cumulative cisplatin dose of ≥200 mg/m² was associated with improved PFS or OS. However, the weekly regimen was associated with less renal toxicity.

Most randomized trials investigating the role of concurrent cisplatin-based RCT used a three weekly schedule of cisplatin 100 mg/m² and this treatment regimen is considered the standard therapy in LA-SCCHN patients. However, it is associated with substantial toxicity and many trials showed suboptimal compliance with cisplatin 100 mg/m² potentially negatively influencing the outcome [5, 17, 37]. Therefore, low-dose weekly cisplatin schedules are frequently used in clinical practice despite the lack of evidence from prospective randomized trials [19, 21, 24, 26‐28, 38, 39].

In a pooled analysis from two tertiary academic cancer centres 659 patients with stage III/IV SCCHN treated with single-agent cisplatin RCT were analysed and a survival benefit for patients receiving a cisplatin dose > 200 mg/m² was shown in HPV negative LA-SCCHN [40]. Therefore, a cumulative cisplatin dose of > 200 mg/m² is usually pursued in this setting.

In our study, treatment compliance was lower with the weekly regimen as reflected by a significantly lower cumulative cisplatin dose. With a weekly regimen less than half of patients achieved a cumulative dose of > 200 mg/m² whereas this was the case for three-fourths of patients treated with a 3-weekly regimen. We hypothesize that the flexibility to decide on treatment continuation on a weekly basis might lead to more frequent treatment discontinuation even with low-grade toxicities whereas with a three weekly schedule this decision can only be taken at two time points and many patients might have recovered from chemotherapy associated side effects after three weeks. The retrospective analysis by Geiger et al. was limited to stage III/IV SCCHN patients who had surgery and were treated with adjuvant RCT and compared a conventional three weekly regimen (100 mg/m²) to weekly cisplatin with a dose of 25–30 mg/m² [31]. Of 104 patients, 51 received a three weekly regimen. Similar to our study, the median cisplatin dose was higher with the three weekly regimen. In the retrospective comparison by Rades et al. the proportion of patients achieving a cumulative cisplatin dose of > 200 mg/m² was not different for the two RCT groups [27]. This study was limited to patients undergoing definitive RCT and did not allow for adjuvant RCT therefore representing a more homogenous patient population. Overall, compared to our study much fewer patients reached the threshold of 200 mg/m² with 32 and 41% of patients in the weekly and three weekly group, respectively. The lower cumulative cisplatin dose in the weekly cisplatin group may partially be explained by the weekly dose of 30 mg/m² used in a part of patients. The authors did not provide exact numbers for patients receiving 30 mg/m² or 40 mg/m² weekly, respectively. In our study, two third of patients were treated with a weekly dose of 40 mg/m² and 30% of patients even received a weekly dose of 50 mg/m². Also the randomized trial by Noronha used a weekly cisplatin dose of 30 mg/m² [23]. This dose is frequently used in clinical practice based on retrospective data [38, 41, 42] and two randomized trials from the Indian group [43, 44]. Our study provides additional evidence that the 200 mg/m² cumulative dose can be reached more often by using a three weekly regimen of cisplatin. The more important question of course is, whether this threshold is a valid surrogate marker for PFS or OS.

We did not find an impact of the treatment regimen on the outcome. A recent systematic review compared 4 prospective studies with weekly cisplatin regimen to 7 prospective studies using a 3-weekly high-dose cisplatin treatment and reported superior outcome for the high-dose cisplatin treatment [18]. A small randomized study compared 100 mg/m² cisplatin every 3 weeks to weekly 40 mg/m² [34]. This trial was limited to patients with oral cavity tumors and did not show differences in locoregional control and survival. In addition, with only 50 patients enrolled, this small trial was underpowered to show potential differences. Recently, a large randomized non-inferiority trial (N = 300) compared cisplatin 30 mg/m² given once a week and cisplatin 100 mg/m² given once every 3 weeks concurrently with curative intent RT was published [23]. The primary aim to show non-inferiority for the weekly regimen was not reached. In fact, locoregional tumor control was superior with the high-dose 3-weekly regimen. Most patients (93%) included in the trial had tumor resection before and RCT was given as adjuvant therapy. Moreover, the trial population consisted mainly of oral cavity tumors (87.3%) in patients with smokeless tobacco consumption (71.3%). Only 19.7% of patients were smokers. In our study, oral cavity cancers only account for 18.3% of all tumors and 88.4% of patients were smokers. It is therefore questionable if the results of the randomized trial from a large academic hospital in India are applicable for Western patient populations with a predominance of smoking-associated pharyngeal carcinomas.

Retrospective studies comparing weekly and three weekly RCT regimens demonstrated conflicting results. The trial by Espeli et al. with 94 patients demonstrated improved OS and similar PFS with cisplatin 100 mg/m² every 3 week compared to 40 mg/m² weekly [30]. Importantly, patients in the weekly cisplatin group were significantly older introducing a potential bias for outcome and toxicities. As in our study cumulative cisplatin dose was significantly lower with the weekly regimen. Significantly more patients in the high-dose cisplatin group developed chronic renal failure whereas in our trial differences in renal toxicity was limited to the acute phase. The retrospective comparison by Rades et al. also showed better locoregional control and OS when using cisplatin 100 mg/m² every three weeks compared to 30–40 mg/m² weekly in 133 patients with LA-SCCHN [27]. In the previously discussed study by Geiger et al. there was no difference in loco-regional control but a trend towards a better survival with 3-weekly cisplatin [31].

In our study, 65% of patients were treated with curative intent definitive RCT, the others received RCT in the adjuvant setting. The heterogeneity of treatment regimens may have confounded our results although the distribution between definitive and adjuvant RCT was similar in the high- and low-dose cisplatin groups in our study. Another limitation of our study is that HPV status was only available in 116 patients (36.9%). Proportions of HPV positive patients were similar in both RCT groups but heterogeneity based on missing HPV analysis in the majority of patients cannot be excluded. The study by Spreafico et al. showed an impact of a cumulative cisplatin dose > 200 mg/m² in patients with HPV negative LA-SCCHN therefore suggesting different sensibility to cisplatin in general or the dose intensity of cisplatin. In the previously discussed analysis by Geiger et al. 50% of patients had HPV-associated oropharyngeal cancer [31]. Although there was a trend towards a better survival for patients treated with a 3-weekly regimen, this difference was not seen in the subgroup of HPV positive patients suggesting that a less intense treatment regimen might be sufficient for patients with HPV-associated LA-SCCHN.

In our study, we found significantly higher renal toxicity with a 3-weekly cisplatin regimen. Interestingly, results from previously discussed studies report conflicting results with regard to toxicity. Several studies reported higher toxicity for 3-weekly cisplatin, mainly renal toxicity [26‐28, 30], but also hematotoxicity [27] and mucositis/dermatitis [28]. In contrast, Tsan et al. reported a higher rate of mucositis and overall toxicity in the weekly cisplatin group [34]. Also the recent comparative analysis of different prospective trials showed less toxicities with the 3-weekly regimen [18]. The fact that this is a retrospective study limits the value of toxicity assessment as we were not able to perform a comprehensive adverse event and toxicity assessment. We therefore decided to investigate oto- and nephrotoxicity as two of the main long-term toxicities in patients treated with cisplatin.

Existing results comparing three weekly and weekly cisplatin regimen combined with RT are conflicting and because they are retrospective they always bear the risk of selection bias. The only statistically powered prospective randomized trial did not prove non-inferiority for a weekly regimen [23]. However, based on the previously discussed issues the validity of the trial for LA-SCCHN in Western countries is questionable. Our study shows a significant higher cumulative cisplatin dose with a 3-weekly regimen. However, we couldn’t find differences in survival outcomes challenging recent data suggesting the prognostic impact of a cumulative cisplatin dose higher than 200 mg/m² [40]. The retrospective design of this large study with all its inherent problems and potential biases makes it difficult to draw definitive conclusions from the analysis. We made every attempt to assess the biases by using multivariable analyses. However, further prospectively randomized trials are needed to establish the most effective RCT treatment regimen. Currently, a randomized phase 3 trial comparing cisplatin 40 mg/m² weekly with 100 mg/m² every three weeks combined with RT is ongoing [45].

This retrospective, multicentre study with more than 300 patients demonstrates that significantly more patients receive a cumulative of dose of ≥200 mg/m², when treated with a 3-weekly schedule compared to weekly dosing. However, we could not find differences in survival between the regimens. Furthermore, we could not confirm previous data suggesting that a cumulative cisplatin dose ≥200 mg/m² is associated with better survival. The 3-weekly regimen led to a higher rate of renal toxicity. Although a 3-weekly regimen allows for a higher cumulative cisplatin dose, weekly cisplatin may be an acceptable alternative treatment considering toxicity. Well-designed prospective trials are needed to establish the most effective RCT treatment regimen and to define patient subgroups that need more intense treatment regimens.