Germ Cell Tumors: Updates on Epidemiology, Biology, and Treatment ConsiderationsView this Special Issue
Review Article | Open Access
Robert A. Huddart, Alison M. Reid, "Adjuvant Therapy for Stage IB Germ Cell Tumors: One versus Two Cycles of BEP", Advances in Urology, vol. 2018, Article ID 8781698, 6 pages, 2018. https://doi.org/10.1155/2018/8781698
Adjuvant Therapy for Stage IB Germ Cell Tumors: One versus Two Cycles of BEP
Testicular germ cell tumours are the commonest tumours of young men and are broadly managed either as pure seminomas or as ‘nonseminomas’. The management of Stage 1 nonseminomatous germ cell tumours (NSGCTs), beyond surgical removal of the primary tumour at orchidectomy, is somewhat controversial. Cancer-specific survival rates in these patients are in the order of 99% regardless of whether surveillance, retroperitoneal lymph node dissection, or adjuvant chemotherapy is employed. However, the toxicities of these treatment modalities differ. Undertreating those destined to relapse exposes them to the potentially significant toxicities of 3-4 cycles of bleomycin, etoposide, and cisplatin (BEP) chemotherapy. Conversely, giving adjuvant chemotherapy to all patients following orchidectomy results in overtreatment of a significant proportion. Therefore, the challenge lies in delineating the patient population who require adjuvant chemotherapy and in determining how much chemotherapy to give to adequately reduce relapse risk. This chapter reviews the factors to be considered when adopting a risk-adapted strategy for giving adjuvant chemotherapy in Stage 1B NSGCT sand discusses the data regarding the number of BEP cycles to administer.
Testicular germ cell tumours (TGCTs) are the commonest tumours of young men aged between 20 and 35 years. They are divided into those of pure seminoma subtype (that histologically resemble primordial germ cells) and those with elements that resemble extra embryonic tissue (with or without seminoma components), generally termed “nonseminomas.” Nonseminomatous germ cell tumours (NSGCT) make up roughly 50% of cases and are common in a younger age group than seminomas (median age around 25 years). A characteristic of TGCT is their sensitivity to cisplatin-based chemotherapy which means that, in contrast to most solid tumours, patients with metastasis are usually cured. The most commonly used schedule is “BEP,” consisting of bleomycin, etoposide, and cisplatin. This is highly successful chemotherapy and will cure around 85–90% of patients with metastatic disease and over 95% of those with good prognostic features (i.e., absence of visceral metastasis and low tumour markers) . The cost of this is the risk of significant toxicity, both acute and late (e.g., renal damage, peripheral neuropathy, hearing damage, increased risk of cardiovascular disease, and second cancer; summarised in Table 1). Management of these patients is supported by monitoring tumour markers such as alpha fetoprotein (AFP) and human chorionic gonadotrophin (HCG), which are elevated in patients with metastatic NSGCT in around two-thirds of cases .
Around 75–80% of patients diagnosed with NSGCT present with no other clinical evidence of disease outside the testis on examination, imaging, or on tumour markers. These patients are termed Stage I and have excellent outcomes, with 5-year disease-specific survival over 98% . Without additional treatment though, relapse occurs in around 30%.
Histopathological markers have been used to help predict the risk of recurrence. The best validated of these prognostic markers has been the presence or absence of lymphovascular invasion (LVI). Patients without LVI have around 15–20% risk of relapse, and if LVI is present, there is a 40–50% risk of recurrence . This finding has been consistent across a number of large studies and is current standard of care in dividing patients into higher risk groups despite the modest predictive power; that is, even in low-risk group, 15–20% of patients will relapse and 50% of high-risk patients will remain in remission .
Other markers such as proportion of embryonal carcinoma (EC), rete testis invasion, and MIB-1 staining have been proposed, but results have not been fully validated. Tumours with no embryonal components generally have a low rate of recurrence [5–7]. Absence of undifferentiated embryonal carcinoma was one of the original MRC risk factors identified in the first MRC surveillance studies . Some studies have suggested that the proportion of embryonal carcinoma may increase relapse risk [4, 8] though this does correlate with LVI and so has not been fully validated. MIB-1 has also been suggested to be associated with increased relapse risk, but in a recent study , an association could not be validated. Recently, CXCL12 expression has been proposed as a prognostic marker and validated in two data sets. On the basis of this marker and vascular invasion, three risk groups have been proposed including low (10% risk), intermediate (30–40% risk), and high (70%) risk groups though this remains to be validated.
A number of different approaches have been utilised in this patient group. In the past, removing the retroperitoneal lymph nodes has been practiced particularly in the United States and parts of Europe. Patients who are node negative (pN0) have a lower rate of subsequent recurrence (∼10–15%). Node-positive patients (pN1) may be cured by this approach but continue to have a significant rate of recurrence (∼30%). These patients have often been offered subsequent adjuvant chemotherapy (see below). Though undoubtedly some patients may avoid chemotherapy, this is at the cost of a major surgical procedure with the risk of attendant morbidity both immediate and long term. Patients still require follow-up as there remains a significant risk of relapse even in the pN0 group, and even without the use of adjuvant chemotherapy, a substantial number of patients will still be exposed to chemotherapy.
An alternative approach, based on pioneering work of Peckham and colleagues and subsequent MRC trials is to watch patients closely a policy termed active surveillance. This approach watches carefully with the aim of early relapse detection and treatment of recurrence by BEP chemotherapy. This approach has the virtue of avoiding treatment (and its attendant toxicities) except when necessary. The use of surveillance has grown over the years but is not necessarily trouble free. Patients who relapse require the use of full-dose chemotherapy . The surveillance phase can cause psychological stress and can make it difficult for some patients to return to a normal lifestyle for fear of recurrence. Finally, there remains a concern regarding compliance. Several studies have shown a degree of noncompliance with follow-up in GCT patients. The fear is that noncompliers can relapse with more advanced disease with a poorer prognosis. This is a concern as a priori identification of noncompliance is difficult. For these reasons, the role of adjuvant chemotherapy has been explored especially in those at high risk of recurrence.
2. Adjuvant BEP Chemotherapy
An alternative approach to surveillance is to use adjuvant chemotherapy following treatment. This was first explored in the early 1990s after the success of using BEP chemotherapy in metastatic disease. It was argued that using more limited chemotherapy in those at high risk would restrict exposure to chemotherapy and prevent relapse. The key study of this approach was the MRC TE05 study. 114 patients were recruited with a predicted recurrence risk based on MRC risk factors of >50% . Two patients recurred but one patient on histology review was proven to have a non-germ cell cancer, so in the 108 patients with centrally reviewed NSGCT, 1 relapsed and the 95% CI excluded a risk of relapse of 5%. This study was supported by similar smaller studies from Bern and Vienna [10, 11]. These data have been replicated in a number of reported studies totalling almost 1000 patients and a combined risk of relapse of <2% (summarised in Table 2). Most of the studies have used BEP for adjuvant treatment though a few studies have used variants of BEP. MD Anderson reported on substituting carboplatin for cisplatin , and the MRC replaced etoposide with vincristine , both achieving results similar to that achieved by BEP. The lower efficacy of carboplatin in metastatic disease and concerns regarding neurotoxicity, respectively, has meant that these approaches have not been adopted.
MDA high risk: pre-op AFP > 80 ng/ml, VI or >pT2. Chemotherapy drugs: B, bleomycin; C, carboplatin; E, etoposide; O, vincristine; P, cisplatin; V, vinblastine. MRC, Medical Research Council; VI, lymphovascular invasion present; EC, embryonal carcinoma.
Following this work, adjuvant BEP has become an option for high-risk stage 1 NSGCT. Its use has been the subject of much debate. This is centered on the issue of late toxicity from BEP. The acute toxicities of BEP (Table 1) have been recognised for many years. Over the last decade, the risk of long-term effects have been better appreciated especially neuropathy, cardiovascular disease, and second malignancy. This has meant that opponents of adjuvant chemotherapy have advocated avoiding exposure of patients to the hazards of chemotherapy unless there is evidence of defined disease. On the other hand, proponents of adjuvant chemotherapy point to the lower doses used, and assuming this means less risk of toxicity. They also note the benefit of lower use of retroperitoneal lymph node surgery. Originally, the 2 cycles of BEP used adjuvantly was half of the dose of that used for metastatic disease. So, with a ∼50% relapse risk, the total number of cycles of chemotherapy needed to be delivered (“burden” of chemotherapy) was similar with either approach, though distributed differently in the population. However, with a MRC/EORTC randomised trial  showing that 3 cycles of BEP was sufficient for most patients, the balance in terms of burden of chemotherapy was in favour of a surveillance approach (i.e., assuming a 50% relapse risk); for every 100 adjuvant patients, 200 cycles of BEP would be delivered compared to 150 cycles for 100 surveillance patients undergoing 50 relapses. This has led to the exploration as to whether less adjuvant chemotherapy may be sufficient.
3. Single-Cycle Adjuvant BEP
At the Royal Marsden, we initially investigated a single cycle of BEP in patients with intermediate risk of recurrence. In 22 patients with approximately 20% risk of recurrence (i.e., 4-5 patients expected to recur), no active recurrences were noted though 1 patient required resection for teratoma differentiated . In a similar higher risk group (defined as presence of vascular invasion or predominant embryonal carcinoma) in 42 patients, Westermann and colleagues reported a single active relapse compared to an expected rate of around 15 patients  (updated in ).
This approach has now been tested in 3 larger studies (Table 3). In the first of these, Albers and colleagues in the German germ cell cancer study group conducted a randomised trial comparing a single cycle of BEP versus RPLND . In 191 patients randomised to BEP, 2 relapses were seen (1 of which was mature teratoma). In the RPLND arm, 32/173 patients were node positive and received adjuvant chemotherapy, and 15 node-negative patients relapsed (equating to 47 patients with active disease, 27%). The Scandinavian Swenoteca  group adopted a single cycle of BEP for intermediate- and high-risk patients as a population-based treatment protocol. In their latest report on 571 patients and a median follow-up of 7.9 years, 3.2% of patients with lymphovascular invasion (n = 258) and 1.6% patients with no lymphovascular invasion (n = 255) have relapsed with only one patient dying of multiply relapsed TGCT.
The latest study to report is the UK 111 study . This large prospective nonrandomised study was designed to specifically exclude a relapse risk of over 5% after a single cycle of BEP. This study recruited 246 patients and reported after a median follow-up of 39.9 months and with a minimum follow-up of 2 years in 91% of patients. Four patients have had a malignant recurrence and 3 a TD recurrence. The primary end point was 2-year malignant recurrence rate which was 1.3% (95% CI 0.4–4.0%) and thus met its aim to exclude a 2-year recurrence rate of 5%. A full publication is awaited.
4. Current Perspectives
It is our opinion that the data discussed are now robust enough to conclude that 1 cycle of BEP can successfully reduce the risk of recurrence to less than 5%. The additional benefit of adding a second cycle in terms of risk reduction of relapse is small and, in our judgement, is not sufficient to justify the additional toxicity. Using a single cycle of BEP would reduce the overall use of chemotherapy in the “high-risk” vascular invasion population. Using the model described above, treating 100 patients with single-cycle adjuvant BEP would give 100 cycles to this population compared to 150 cycles if it is assumed that 50% relapse on surveillance. In addition to amount of chemotherapy, the balance of who receives is very different either spread across the whole population or concentrating, with greater exposure, in those with proven disease. There is no evidence in any of the studies of adjuvant chemotherapy or surveillance that use of either approach affects overall survival. This has prompted a vigorous debate between supporters [26–28] of adjuvant chemotherapy and surveillance as to the optimal approach, both in seminoma and nonseminoma. To our mind, to exclusively offer either approach, given lack of survival difference, is inappropriate. We attempt to present a balanced argument of the pros and cons of the two approaches stressing the impact on relapse and discussing what is known regarding immediate- and long-term toxicity (including risk of cardiovascular disease and second malignancy). The idea of adjuvant toxicity seems intrinsically attractive to many, with the wish to get treatment over with and avoid future uncertainty of relapse as common levers for deciding on adjuvant chemotherapy.
23/305 equals 7.5% of predicted relapses.
4.1. Future Approaches
Adjuvant chemotherapy has usually been used for patients found to be at higher risk of recurrence. The adoption of single-cycle adjuvant chemotherapy raises the question of whether patients with lower risk should be offered this treatment. The Swenoteca group allowed patients with lower risk of recurrence to receive adjuvant BEP in their protocols and reported a less than 2% relapse risk . We do not offer this approach routinely as this would expose 80% or more of patients to BEP who would not have relapsed and increases the overall burden of chemotherapy. There may be exceptional instances such as when surveillance or full course of BEP would be difficult when it might be considered.
The landscape of adjuvant therapy could be changed if there was better prognostication. We recently reported a new prognostic index that could split stage 1 NSGCT patients into 3 broad groups based on vascular invasion and whether they had expression of CXCL12 or had near 100% embryonal content . Using these criteria, we identified a small group (10–15%) with a very high recurrence risk (>70%) and a significant group (∼40–50%) with a low risk of recurrence (∼10%) with the remainder having a 30–40% recurrence risk. This index needs further validation but may have implications for decision making regarding adjuvant therapy. We believe most clinicians would agree the low-risk group should be surveyed and the high-risk group would benefit from adjuvant therapy. The intermediate group may be more controversial. The total burden of chemotherapy for surveillance and adjuvant chemotherapy would be roughly similar. These patients might reasonably be surveyed but many may consider the risk high enough to justify adjuvant chemotherapy if a single cycle of BEP is used.
This landscape is not static. More sophisticated genetic profiling may be on the horizon , and whilst data are emerging, that microRNA analysis may be a sensitive indicator of subclinical disease [2, 30]. Any impact on prognostication may affect the balance between surveillance and adjuvant therapy.
It is possible that the increasing confidence in the use of adjuvant BEP could change the treatment algorithm in other areas. For instance, could single-cycle BEP with less-invasive surgical techniques lead to a resurgence of surgical management of low-volume (stage 2) NSGCT ?
Single-cycle BEP is effective at reducing the risk of recurrence of stage 1 NSGCT to less than 5% and should be the preferred over two cycles of BEP if adjuvant therapy is chosen rather than surveillance. However, surveillance approaches can legitimately still be offered to all patients.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
The authors acknowledge support of The Royal Marsden/Institute of Cancer Research NIHR Biomedical Research Centre and the Josh Carrick Foundation.
- A. Horwich, D. Nicol, and R. Huddart, “Testicular germ cell tumours,” BMJ, vol. 347, p. f5526, 2013.
- M. J. Murray, R. A. Huddart, and N. Coleman, “The present and future of serum diagnostic tests for testicular germ cell tumours,” Nature Reviews Urology, vol. 13, no. 12, pp. 715–725, 2016.
- M. Chovanec, N. Hanna, K. C. Cary, L. Einhorn, and C. Albany, “Management of stage I testicular germ cell tumours,” Nature Reviews Urology, vol. 13, no. 11, pp. 663–673, 2016.
- Y. Vergouwe, E. W. Steyerberg, M. J. Eijkemans, P. Albers, and J. D. Habbema, “Predictors of occult metastasis in clinical stage I nonseminoma: a systematic review,” Journal of Clinical Oncology, vol. 21, no. 22, pp. 4092–4099, 2003.
- G. Daugaard, M. G. Gundgaard, M. S. Mortensen et al., “Surveillance for stage I nonseminoma testicular cancer: outcomes and long-term follow-up in a population-based cohort,” Journal of Clinical Oncology, vol. 32, no. 34, pp. 3817–3823, 2014.
- L. S. Freedman, M. C. Parkinson, W. G. Jones et al., “Histopathology in the prediction of relapse of patients with stage I testicular teratoma treated by orchidectomy alone,” The Lancet, vol. 2, no. 8554, pp. 294–298, 1987.
- C. A. Lago-Hernandez, H. Feldman, E. O’Donnell et al., “A refined risk stratification scheme for clinical stage 1 NSGCT based on evaluation of both embryonal predominance and lymphovascular invasion,” Annals of Oncology, vol. 26, no. 7, pp. 1396–1401, 2015.
- D. C. Gilbert, R. Al-Saadi, K. Thway et al., “Defining a new prognostic index for stage I nonseminomatous germ cell tumors using CXCL12 expression and proportion of embryonal carcinoma,” Clinical Cancer Research, vol. 22, no. 5, pp. 1265–1273, 2016.
- M. H. Cullen, S. P. Stenning, M. C. Parkinson et al., “Short-course adjuvant chemotherapy in high-risk stage I nonseminomatous germ cell tumors of the testis: a Medical Research Council report,” Journal of Clinical Oncology, vol. 14, no. 4, pp. 1106–1113, 1996.
- D. Bohlen, M. Borner, R. W. Sonntag, M. F. Fey, and U. E. Studer, “Long-term results following adjuvant chemotherapy in patients with clinical stage I testicular nonseminomatous malignant germ cell tumors with high risk factors,” Journal of Urology, vol. 161, no. 4, pp. 1148–1152, 1999.
- J. Pont, W. Albrecht, G. Postner, F. Sellner, K. Angel, and W. Holtl, “Adjuvant chemotherapy for high-risk clinical stage I nonseminomatous testicular germ cell cancer: long-term results of a prospective trial,” Journal of Clinical Oncology, vol. 14, no. 2, pp. 441–448, 1996.
- R. de Wit, J. T. Roberts, P. M. Wilkinson et al., “Equivalence of three or four cycles of bleomycin, etoposide, and cisplatin chemotherapy and of a 3- or 5-day schedule in good-prognosis germ cell cancer: a randomized study of the European Organization for Research and Treatment of Cancer Genitourinary Tract Cancer Cooperative Group and the Medical Research Council,” Journal of Clinical Oncology, vol. 19, no. 6, pp. 1629–1640, 2001.
- D. P. Dearnaley, S. D. Fossa, S. B. Kaye et al., “Adjuvant bleomycin, vincristine and cisplatin (BOP) for high-risk stage I non-seminomatous germ cell tumours: a prospective trial (MRC TE17),” British Journal of Cancer, vol. 92, no. 12, pp. 2107–2113, 2005.
- J. R. Germa-Lluch, X. Garcia del Muro, P. Maroto et al., “Clinical pattern and therapeutic results achieved in 1490 patients with germ-cell tumours of the testis: the experience of the Spanish Germ-Cell Cancer Group (GG),” European Urology, vol. 42, no. 6, pp. 553–562, 2002.
- C. Chevreau, C. Mazerolles, M. Soulie et al., “Long-term efficacy of two cycles of BEP regimen in high-risk stage I nonseminomatous testicular germ cell tumors with embryonal carcinoma and/or vascular invasion,” European Urology, vol. 46, no. 2, pp. 209–214, 2004.
- R. T. Oliver, J. Ong, J. Shamash et al., “Long-term follow-up of Anglian Germ Cell Cancer Group surveillance versus patients with stage 1 nonseminoma treated with adjuvant chemotherapy,” Urology, vol. 63, no. 3, pp. 556–561, 2004.
- S. Guney, N. Guney, N. C. Sonmez, and E. Ergenekon, “Risk-adapted management for patients with clinical stage I non-seminomatous germ cell tumour of the testis,” Medical Oncology, vol. 26, no. 2, pp. 136–142, 2009.
- A. Bamias, G. Aravantinos, I. Kastriotis et al., “Report of the long-term efficacy of two cycles of adjuvant bleomycin/etoposide/cisplatin in patients with stage I testicular nonseminomatous germ-cell tumors (NSGCT): a risk adapted protocol of the Hellenic Cooperative Oncology Group,” Urologic Oncology, vol. 29, no. 2, pp. 189–193, 2011.
- Z. Mezvrishvili and L. Managadze, “Is bleomycin necessary in adjuvant chemotherapy of clinical stage I non-seminomatous testicular cancer?” Georgian Medical News, vol. 134, pp. 25–28, 2006.
- D. C. Gilbert, A. R. Norman, J. Nicholl, D. P. Dearnaley, A. Horwich, and R. A. Huddart, “Treating stage I nonseminomatous germ cell tumours with a single cycle of chemotherapy,” BJU International, vol. 98, no. 1, pp. 67–69, 2006.
- D. H. Westermann, H. Schefer, G. N. Thalmann, E. Karamitopoulou-Diamantis, M. F. Fey, and U. E. Studer, “Long-term followup results of 1 cycle of adjuvant bleomycin, etoposide and cisplatin chemotherapy for high risk clinical stage I nonseminomatous germ cell tumors of the testis,” Journal of Urology, vol. 179, no. 1, pp. 163–166, 2008.
- A. D. Vidal, G. N. Thalmann, E. Karamitopoulou-Diamantis, M. F. Fey, and U. E. Studer, “Long-term outcome of patients with clinical stage I high-risk nonseminomatous germ-cell tumors 15 years after one adjuvant cycle of bleomycin, etoposide, and cisplatin chemotherapy,” Annals of Oncology, vol. 26, no. 2, pp. 374–377, 2015.
- P. Albers, R. Siener, S. Krege et al., “Randomized phase III trial comparing retroperitoneal lymph node dissection with one course of bleomycin and etoposide plus cisplatin chemotherapy in the adjuvant treatment of clinical stage I nonseminomatous testicular germ cell tumors: AUO trial AH 01/94 by the German Testicular Cancer Study Group,” Journal of Clinical Oncology, vol. 26, no. 18, pp. 2966–2972, 2008.
- T. Tandstad, O. Dahl, G. Cohn-Cedermark et al., “Risk-adapted treatment in clinical stage I nonseminomatous germ cell testicular cancer: the SWENOTECA management program,” Journal of Clinical Oncology, vol. 27, no. 13, pp. 2122–2128, 2009.
- R. A. Huddart, J. D. White, P. Hutton et al., “111: a single-arm trial evaluating one cycle of BEP as adjuvant chemotherapy in high-risk, stage 1 non-seminomatous or combined germ cell tumors of the testis (NSGCTT),” Journal of Clinical Oncology, vol. 35, no. 6, p. 400, 2017.
- J. Oldenburg, J. Aparicio, J. Beyer et al., “Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer,” Annals of Oncology, vol. 26, no. 5, pp. 833–838, 2015.
- C. R. Nichols, B. Roth, P. Albers et al., “Active surveillance is the preferred approach to clinical stage I testicular cancer,” Journal of Clinical Oncology, vol. 31, no. 28, pp. 3490–3493, 2013.
- R. de Wit and G. J. Bosl, “Optimal management of clinical stage I testis cancer: one size does not fit all,” Journal of Clinical Oncology, vol. 31, no. 28, pp. 3477–3479, 2013.
- J. E. Korkola, S. Heck, A. B. Olshen et al., “Development and validation of a gene-based model for outcome prediction in germ cell tumors using a combined genomic and expression profiling approach,” PLoS One, vol. 10, no. 12, Article ID e0142846, 2015.
- K. P. Dieckmann, A. Radtke, M. Spiekermann et al., “Serum levels of microRNA miR-371a-3p: a sensitive and specific new biomarker for germ cell tumours,” European Urology, vol. 71, no. 2, pp. 213–220, 2017.
- M. Behnia, R. Foster, L. H. Einhorn, J. Donohue, and C. R. Nichols, “Adjuvant bleomycin, etoposide and cisplatin in pathological stage II non-seminomatous testicular cancer. The Indiana University experience,” European Journal of Cancer, vol. 36, no. 4, pp. 472–475, 2000.
Copyright © 2018 Robert A. Huddart and Alison M. Reid. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.