Skip to main content
Erschienen in: Strahlentherapie und Onkologie 7/2012

01.07.2012 | Original article

Intensity-modulated arc therapy with cisplatin as neo-adjuvant treatment for primary irresectable cervical cancer

Toxicity, tumour response and outcome

verfasst von: K. Vandecasteele, M.D., A. Makar, M.D., Ph.D., R. Van den Broecke, M.D., Ph.D., L. Delrue, M.D., H. Denys, M.D., Ph.D., K. Lambein, M.D., B. Lambert, M.D., Ph.D., M. van Eijkeren, M.D., Ph.D., P. Tummers, M.D., G. De Meerleer, M.D., Ph.D.

Erschienen in: Strahlentherapie und Onkologie | Ausgabe 7/2012

Einloggen, um Zugang zu erhalten

Abstract

Purpose

The goal of this work was to evaluate the feasibility and outcome of intensity-modulated arc therapy ± cisplatin (IMAT ± C) followed by hysterectomy for locally advanced cervical cancer.

Patients and methods

A total of 30 patients were included in the study. The primary tumour and PET-positive lymph node(s) received a simultaneous integrated boost. Four weeks after IMAT ± C treatment, response was evaluated. Resection consisted of hysterectomy with or without lymphadenectomy. Tumour response, acute and late radiation toxicity, postoperative morbidity and outcome were evaluated.

Results

All hysterectomy specimens were macroscopically tumour-free with negative resection margins; pathological complete response was 40%. In 2 patients, one resected lymph node was positive. There was no excess in postoperative morbidity. Apart from two grade 3 hematologic toxicities, no grade 3 or 4 acute radiation toxicity was observed. No grade 3, 1 grade 4 (4%) intestinal, and 4 grade 3 (14%) urinary late toxicities were observed. The 2-year local and regional control rates were 96% and 100%, respectively. The 2-year distant control rate was 92%. Actuarial 2-year progression free survival rate was 89%. Actuarial 1- and 2-year overall survival rates were 96% and 91%, while 3-year overall survival was 84%.

Conclusion

Surgery after IMAT ± C is feasible with low postoperative morbidity and radiation toxicity. Local, regional, distant control and survival rates are promising.
Literatur
1.
Zurück zum Zitat Brocker K, Alt C, Eichbaum M et al (2011) Imaging of female pelvic malignancies regarding MRI, CT, and PET/CT. Strahlenther Onkol 187:611–618PubMedCrossRef Brocker K, Alt C, Eichbaum M et al (2011) Imaging of female pelvic malignancies regarding MRI, CT, and PET/CT. Strahlenther Onkol 187:611–618PubMedCrossRef
2.
Zurück zum Zitat Carcopino X, Houvenaeghel G, Buttarelli M et al (2008) Equivalent survival in patients with advanced stage IB-II and III-IVA cervical cancer treated by adjuvant surgery following chemoradiotherapy. Eur J Surg Oncol 34:569–575PubMedCrossRef Carcopino X, Houvenaeghel G, Buttarelli M et al (2008) Equivalent survival in patients with advanced stage IB-II and III-IVA cervical cancer treated by adjuvant surgery following chemoradiotherapy. Eur J Surg Oncol 34:569–575PubMedCrossRef
3.
Zurück zum Zitat Chassagne D, Sismondi P, Horiot JC et al (1993) A glossary for reporting complications of treatment in gynecological cancers. Radiother Oncol 26:195–202PubMedCrossRef Chassagne D, Sismondi P, Horiot JC et al (1993) A glossary for reporting complications of treatment in gynecological cancers. Radiother Oncol 26:195–202PubMedCrossRef
4.
Zurück zum Zitat Cox JD, Stetz J, Pajak TF (1995) Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC). Int J Radiat Oncol Biol Phys 31:1341–1346PubMedCrossRef Cox JD, Stetz J, Pajak TF (1995) Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC). Int J Radiat Oncol Biol Phys 31:1341–1346PubMedCrossRef
5.
Zurück zum Zitat Cozzi L, Dinshaw KA, Shrivastava SK et al (2008) A treatment planning study comparing volumetric arc modulation with RapidArc and fixed field IMRT for cervix uteri radiotherapy. Radiother Oncol 89:180–191PubMedCrossRef Cozzi L, Dinshaw KA, Shrivastava SK et al (2008) A treatment planning study comparing volumetric arc modulation with RapidArc and fixed field IMRT for cervix uteri radiotherapy. Radiother Oncol 89:180–191PubMedCrossRef
6.
Zurück zum Zitat De Meerleer G, Vakaet L, Meersschout S et al (2004) Intensity-modulated radiotherapy as primary treatment for prostate cancer: acute toxicity in 114 patients. Int J Radiat Oncol Biol Phys 60:777–787CrossRef De Meerleer G, Vakaet L, Meersschout S et al (2004) Intensity-modulated radiotherapy as primary treatment for prostate cancer: acute toxicity in 114 patients. Int J Radiat Oncol Biol Phys 60:777–787CrossRef
7.
Zurück zum Zitat Duthoy W, De Gersem W, Vergote K et al (2004) Clinical implementation of intensity-modulated arc therapy (IMAT) for rectal cancer. Int J Radiat Oncol Biol Phys 60:794–806PubMedCrossRef Duthoy W, De Gersem W, Vergote K et al (2004) Clinical implementation of intensity-modulated arc therapy (IMAT) for rectal cancer. Int J Radiat Oncol Biol Phys 60:794–806PubMedCrossRef
8.
Zurück zum Zitat Ferrandina G, Margariti PA, Smaniotto D et al (2010) Long-term analysis of clinical outcome and complications in locally advanced cervical cancer patients administered concomitant chemoradiation followed by radical surgery. Gynecol Oncol 119:404–410PubMedCrossRef Ferrandina G, Margariti PA, Smaniotto D et al (2010) Long-term analysis of clinical outcome and complications in locally advanced cervical cancer patients administered concomitant chemoradiation followed by radical surgery. Gynecol Oncol 119:404–410PubMedCrossRef
9.
Zurück zum Zitat Fonteyne V, De Neve W, Villeirs G et al (2007) Late radiotherapy-induced lower intestinal toxicity (RILIT) of intensity-modulated radiotherapy for prostate cancer: the need for adapting toxicity scales and the appearance of the sigmoid colon as co-responsible organ for lower intestinal toxicity. Radiother Oncol 84:156–163PubMedCrossRef Fonteyne V, De Neve W, Villeirs G et al (2007) Late radiotherapy-induced lower intestinal toxicity (RILIT) of intensity-modulated radiotherapy for prostate cancer: the need for adapting toxicity scales and the appearance of the sigmoid colon as co-responsible organ for lower intestinal toxicity. Radiother Oncol 84:156–163PubMedCrossRef
10.
Zurück zum Zitat Green J, Kirwan J, Tierney J et al (2005) Concomitant chemotherapy and radiation therapy for cancer of the uterine cervix. Cochrane Database Syst Rev: CD002225 Green J, Kirwan J, Tierney J et al (2005) Concomitant chemotherapy and radiation therapy for cancer of the uterine cervix. Cochrane Database Syst Rev: CD002225
11.
Zurück zum Zitat Guerrero M, Li XA, Ma L et al (2005) Simultaneous integrated intensity-modulated radiotherapy boost for locally advanced gynecological cancer: radiobiological and dosimetric considerations. Int J Radiat Oncol Biol Phys 62:933–939PubMedCrossRef Guerrero M, Li XA, Ma L et al (2005) Simultaneous integrated intensity-modulated radiotherapy boost for locally advanced gynecological cancer: radiobiological and dosimetric considerations. Int J Radiat Oncol Biol Phys 62:933–939PubMedCrossRef
12.
Zurück zum Zitat Hasselle MD, Rose BS, Kochanski JD et al (2011) Clinical outcomes of intensity-modulated pelvic radiation therapy for carcinoma of the cervix. Int J Radiat Oncol Biol Phys 80:1436–1445PubMedCrossRef Hasselle MD, Rose BS, Kochanski JD et al (2011) Clinical outcomes of intensity-modulated pelvic radiation therapy for carcinoma of the cervix. Int J Radiat Oncol Biol Phys 80:1436–1445PubMedCrossRef
13.
Zurück zum Zitat Keys HM, Bundy BN, Stehman FB et al (2003) Radiation therapy with and without extrafascial hysterectomy for bulky stage IB cervical carcinoma: a randomized trial of the Gynecologic Oncology Group. Gynecol Oncol 89:343–353PubMedCrossRef Keys HM, Bundy BN, Stehman FB et al (2003) Radiation therapy with and without extrafascial hysterectomy for bulky stage IB cervical carcinoma: a randomized trial of the Gynecologic Oncology Group. Gynecol Oncol 89:343–353PubMedCrossRef
14.
Zurück zum Zitat Kirwan JM, Symonds P, Green JA et al (2003) A systematic review of acute and late toxicity of concomitant chemoradiation for cervical cancer. Radiother Oncol 68:217–226PubMedCrossRef Kirwan JM, Symonds P, Green JA et al (2003) A systematic review of acute and late toxicity of concomitant chemoradiation for cervical cancer. Radiother Oncol 68:217–226PubMedCrossRef
15.
Zurück zum Zitat Lammering G, De Ruysscher D, Baardwijk A van et al (2010) The use of FDG-PET to target tumors by radiotherapy. Strahlenther Onkol 186:471–481PubMedCrossRef Lammering G, De Ruysscher D, Baardwijk A van et al (2010) The use of FDG-PET to target tumors by radiotherapy. Strahlenther Onkol 186:471–481PubMedCrossRef
16.
Zurück zum Zitat Loizzi V, Cormio G, Loverro G et al (2003) Chemoradiation: a new approach for the treatment of cervical cancer. Int J Gynecol Cancer 13:580–586PubMedCrossRef Loizzi V, Cormio G, Loverro G et al (2003) Chemoradiation: a new approach for the treatment of cervical cancer. Int J Gynecol Cancer 13:580–586PubMedCrossRef
17.
Zurück zum Zitat Lukka H, Hirte H, Fyles A et al (2002) Concurrent cisplatin-based chemotherapy plus radiotherapy for cervical cancer—a meta-analysis. Clin Oncol (R Coll Radiol) 14:203–212 Lukka H, Hirte H, Fyles A et al (2002) Concurrent cisplatin-based chemotherapy plus radiotherapy for cervical cancer—a meta-analysis. Clin Oncol (R Coll Radiol) 14:203–212
18.
Zurück zum Zitat Marnitz S, Stromberger C, Kawgan-Kagan M et al (2010) Helical tomotherapy in cervical cancer patients: simultaneous integrated boost concept: technique and acute toxicity. Strahlenther Onkol 186:572–579PubMedCrossRef Marnitz S, Stromberger C, Kawgan-Kagan M et al (2010) Helical tomotherapy in cervical cancer patients: simultaneous integrated boost concept: technique and acute toxicity. Strahlenther Onkol 186:572–579PubMedCrossRef
19.
Zurück zum Zitat Morice P, Uzan C, Zafrani Y et al (2007) The role of surgery after chemoradiation therapy and brachytherapy for stage IB2/II cervical cancer. Gynecol Oncol 107:S122–124PubMedCrossRef Morice P, Uzan C, Zafrani Y et al (2007) The role of surgery after chemoradiation therapy and brachytherapy for stage IB2/II cervical cancer. Gynecol Oncol 107:S122–124PubMedCrossRef
20.
Zurück zum Zitat Niibe Y, Hayakawa K, Kanai T et al (2006) Optimal dose for stage IIIB adenocarcinoma of the uterine cervix on the basis of biological effective dose. Eur J Gynaecol Oncol 27:47–49PubMed Niibe Y, Hayakawa K, Kanai T et al (2006) Optimal dose for stage IIIB adenocarcinoma of the uterine cervix on the basis of biological effective dose. Eur J Gynaecol Oncol 27:47–49PubMed
21.
Zurück zum Zitat Pasler M, Wirtz H, Lutterbach J (2011) Impact of gantry rotation time on plan quality and dosimetric verification – volumetric modulated arc therapy (VMAT) vs. intensity modulated radiotherapy (IMRT). Strahlenther Onkol 187:812–819PubMedCrossRef Pasler M, Wirtz H, Lutterbach J (2011) Impact of gantry rotation time on plan quality and dosimetric verification – volumetric modulated arc therapy (VMAT) vs. intensity modulated radiotherapy (IMRT). Strahlenther Onkol 187:812–819PubMedCrossRef
22.
Zurück zum Zitat Perez CA, Breaux S, Madoc-Jones H et al (1983) Radiation therapy alone in the treatment of carcinoma of uterine cervix. I. Analysis of tumor recurrence. Cancer 51:1393–1402PubMedCrossRef Perez CA, Breaux S, Madoc-Jones H et al (1983) Radiation therapy alone in the treatment of carcinoma of uterine cervix. I. Analysis of tumor recurrence. Cancer 51:1393–1402PubMedCrossRef
23.
Zurück zum Zitat Perez CA, Grigsby PW, Chao KS et al (1998) Tumor size, irradiation dose, and long-term outcome of carcinoma of uterine cervix. Int J Radiat Oncol Biol Phys 41:307–317PubMedCrossRef Perez CA, Grigsby PW, Chao KS et al (1998) Tumor size, irradiation dose, and long-term outcome of carcinoma of uterine cervix. Int J Radiat Oncol Biol Phys 41:307–317PubMedCrossRef
24.
Zurück zum Zitat Potter R, Dimopoulos J, Georg P et al (2007) Clinical impact of MRI assisted dose volume adaptation and dose escalation in brachytherapy of locally advanced cervix cancer. Radiother Oncol 83:148–155PubMedCrossRef Potter R, Dimopoulos J, Georg P et al (2007) Clinical impact of MRI assisted dose volume adaptation and dose escalation in brachytherapy of locally advanced cervix cancer. Radiother Oncol 83:148–155PubMedCrossRef
25.
Zurück zum Zitat Small W, Jr, Mell LK, Anderson P et al (2008) Consensus guidelines for delineation of clinical target volume for intensity-modulated pelvic radiotherapy in postoperative treatment of endometrial and cervical cancer. Int J Radiat Oncol Biol Phys 71:428–434PubMedCrossRef Small W, Jr, Mell LK, Anderson P et al (2008) Consensus guidelines for delineation of clinical target volume for intensity-modulated pelvic radiotherapy in postoperative treatment of endometrial and cervical cancer. Int J Radiat Oncol Biol Phys 71:428–434PubMedCrossRef
26.
Zurück zum Zitat Vandecasteele K, De Neve W, De Gersem W et al (2009) Intensity-modulated arc therapy with simultaneous ntegrated boost in the treatment of primary irresectable cervical cancer. Strahlenther Onkol 185:799–807PubMedCrossRef Vandecasteele K, De Neve W, De Gersem W et al (2009) Intensity-modulated arc therapy with simultaneous ntegrated boost in the treatment of primary irresectable cervical cancer. Strahlenther Onkol 185:799–807PubMedCrossRef
27.
Zurück zum Zitat Yeoh EE, Fraser RJ, McGowan RE et al (2003) Evidence for efficacy without increased toxicity of hypofractionated radiotherapy for prostate carcinoma: early results of a phase III randomized trial. Int J Radiat Oncol Biol Phys 55:943–955PubMedCrossRef Yeoh EE, Fraser RJ, McGowan RE et al (2003) Evidence for efficacy without increased toxicity of hypofractionated radiotherapy for prostate carcinoma: early results of a phase III randomized trial. Int J Radiat Oncol Biol Phys 55:943–955PubMedCrossRef
Metadaten
Titel
Intensity-modulated arc therapy with cisplatin as neo-adjuvant treatment for primary irresectable cervical cancer
Toxicity, tumour response and outcome
verfasst von
K. Vandecasteele, M.D.
A. Makar, M.D., Ph.D.
R. Van den Broecke, M.D., Ph.D.
L. Delrue, M.D.
H. Denys, M.D., Ph.D.
K. Lambein, M.D.
B. Lambert, M.D., Ph.D.
M. van Eijkeren, M.D., Ph.D.
P. Tummers, M.D.
G. De Meerleer, M.D., Ph.D.
Publikationsdatum
01.07.2012
Verlag
Springer-Verlag
Erschienen in
Strahlentherapie und Onkologie / Ausgabe 7/2012
Print ISSN: 0179-7158
Elektronische ISSN: 1439-099X
DOI
https://doi.org/10.1007/s00066-012-0097-0

Weitere Artikel der Ausgabe 7/2012

Strahlentherapie und Onkologie 7/2012 Zur Ausgabe

Mitteilungen der Fachgesellschaften

Mitteilungen

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.