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Larynx NeoplasmsPhase 3NCT00128817

Concurrent Chemoradiation Versus Surgery With Adjuvant Therapy in Advanced Laryngopharyngeal Cancers

A Phase 3 study testing Concurrent Chemoradiation and Laryngectomy + adjuvant radiotherapy/chemoradiotherapy in people with Larynx Neoplasms, run by Tata Memorial Hospital at 1 site in India.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

Surgery with post operative radiotherapy (PORT) had been the mainstay of treatment for advanced laryngeal-pharyngeal cancers (ALHC) until the eighth decade of the past century. Total laryngectomy with post-operative radiotherapy (TL + PORT) used to result in permanent tracheostomy and loss of speech. Read more about this study

Who is it for?
Ages 18 to 75 yearsHealthy volunteers can take part
Conditions the study is for
Larynx Neoplasms
What is being tested?
Concurrent Chemoradiation and Laryngectomy + adjuvant radiotherapy/chemoradiotherapy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
900 participants
Where
1 siteIndia
Study dates
May 2005to May 2015
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Patients with biopsy-proven, previously untreated, T3/T4 tumors (with focal cartilage erosion on computed tomography [CT] scan); squamous cell carcinoma of larynx and hypopharynx.
  • Patients with Karnofsky Performance Scale (KPS) > 80
  • Patients must have resectable tumors which are potentially curable with conventional surgery and radiation therapy.
  • Willing to participate in trial and get randomized

Who cannot join

  • Gross cartilage invasion
  • Extensive soft tissue infiltration
  • Large nodal disease
  • Distant metastases
  • Synchronous primary

Trial locations and contacts

1 site in 1 country.

India1 site
  • Tata Memorial Hospital

    Mumbai, Maharashtra, 400012

Other trials in India

About this study

Official title: Phase III Randomized Clinical Trial to Compare Results of Concurrent Chemo-radiation With Surgery and Postoperative Radiotherapy/Chemoradiotherapy in Advanced Laryngeal and Hypopharyngeal Cancers

Surgery with post operative radiotherapy (PORT) had been the mainstay of treatment for advanced laryngeal-pharyngeal cancers (ALHC) until the eighth decade of the past century. Total laryngectomy with post-operative radiotherapy (TL + PORT) used to result in permanent tracheostomy and loss of speech.

Early trials like the VA or European Organisation for Research and Treatment of Cancer (EORTC) trials compared surgery with post-operative radiotherapy to induction chemotherapy (ICT) and radiotherapy (RT). Subsequent attempts have been focused on the added benefit of including concurrent chemotherapy. There is no randomized trial available in the literature comparing concurrent chemoradiation with the standard treatment, i.e. surgery followed by radiotherapy. However, most of the studies comparing neoadjuvant chemotherapy and radiotherapy reported better locoregional control rates and better survival rates with surgery followed by post-operative chemotherapy. Further, the advances in primary voice rehabilitation have substantially improved the quality of life after laryngectomy. Thus, there is a strong case for comparing the results of concurrent chemo-radiation with surgery and post-operative radiotherapy in a randomized clinical trial. This trial will answer the question - "whether we are saving voice at the cost of life".

The investigators propose to randomize 900 patients of laryngeal and hypopharyngeal cancers in surgery with PORT and a concomitant chemoradiation arm and compare the survival and locoregional control rates.

Read the detailed description

TL + PORT has traditionally been the gold standard in management of ALHC. However, this results in permanent tracheostomy and a possible loss of speech. In case of partial laryngectomy and even in case of TL, there are various options of voice rehabilitation but the successes of all these procedures are highly variable. In 1980s several authors reported interesting possibility of LP with ICT. The first randomized study (RCT) came from VA group who randomized patients to receive either 2 cycles of ICT + RT Vs surgery +PORT. Patients with more than PR received a 3rd cycle followed by definitive RT. There were more local recurrences and fewer distant metastases in the ICT arm. Of the 166 ICT patients, nearly 1/3rd required salvage TL with ultimate LP in 66% surviving patients. These results proved that ICT and definitive RT can be effective in LP without compromising overall survival. European Organization for Research and Treatment of Cancer (EORTC) study randomly assigned hypopharynx cancer patients to receive either immediate surgery with PORT (arm 1) or ICT. Patients with a CR after 2 or 3 cycles of CT were treated there after by RT. Locoregional failures occurred at approximately the same frequencies in both arms but there were fewer distant failures in the ICT arm. The median survival was found to be similar in both arms with LPR of 35% in the ICT arm. This study showed the feasibility of LP in patients with cancer of the hypopharynx. A smaller trial from MSKCC15 reported 52% LPR and another European RCT reported poorer survival in the CT arm with LPR of 20% only. The latter trial had a smaller number of patients and imbalance in randomized groups (4 out of 5 stage IV patients got randomized into CT arm) that could have flawed the outcome. The 3 RCTs (excluding MSKCC trial) were compiled by MACH-NC to obtain a meta analysis that showed similar disease free survival and a non significant trend of higher 6% survival in pooled surgery arm which was counterbalanced by LPR of 58% in the pooled CT arm. Quality of life measures performed as part of the VA study demonstrated that LP offers better speech, good communication skills, lesser pain and depression compared to surgery.

In three arm study by RTOG (91-11), incidence of laryngectomy was 28% in induction (ICT) chemotherapy arm, 16% in concomitant arm, and 31% in radiation(RT) alone arm. Following TL, the incidence of major and minor complications ranged from 52% to 59% and did not differ significantly among the 3 arms. Fistula was lowest in RT alone arm (15%) and highest in concomitant arm (30%). Similar experience was reported from MSKCC with fistulas occurring in 39%, resulting in prolonged hospitalization. When compared with complication rates of surgery in untreated patients, the complication rates following unsuccessful LP protocol is significantly higher. In spite of higher morbidity, local-regional control is excellent for this group of patients. In RTOG trial, local-regional control following SS was 74% for CT arms and 90% for RT alone arm. At 24 months, the overall survival was equal in all arms.

The necessity of adding chemotherapy to radiotherapy itself is debatable. The MACH -NC reported 4% improvement in overall survival at 2 and 5 yrs with CT. So to prevent death of 400 patients at 5 years, 10,000 patients would have to undergo CT. In O'Sullivan' questionnaire based study, apart from extent of disease the other significant variables that influenced treatment recommendation were physicians specialty and their geographical area of practice. Most LP protocols are often accompanied by increased toxicity and are generally achieved in good performance status patients unlike majority of head and neck cancer patients. In VA trial, 77% patients had Karnofsky performance score (KPS) more than 80 and in RTOG 91-11 trial, 2/3 patients had KPS 90 or more. In RTOG trial, the mucosal toxicity in concurrent CT+RT arm was twice as much as the mucosal toxicity in other two arms. High grade toxic effects occurred more when CT was added to RT but there was no significant difference in rate of toxic effects between concurrent arm and ICT arm. Incidence of treatment modification, treatment interruption and hospitalizations are higher (compared to RT alone) when CT is administered concomitantly or during altered fractionation due to complications such as mucositis, dysphagia, pain, desquamation etc. The indirect costs attributable to non-surgical approaches e.g frequent expensive imagings, duration of treatment , duration of recuperation, cost of chemotherapy drugs, enhanced need for supportive care, stringent follow up and salvage surgery (in one third to half of the patients) may be more than the costs for radical surgery. Careful monitoring of the conservatively treated patient is mandatory to allow for early salvage of failures (in VA trial, induction CT arm had more local recurrences and only 2% patients were lost to follow-up). Given the infirmity and poor compliance of head and neck cancer patients such a stringent follow-up appears difficult (in VA trial patients were followed up every month for 1st year).

Nearly 40-60% patients fail on LPP and predicting this failure before spares these patients of unnecessary chemoradiation and its toxicities, trauma of recurrent disease and complications of salvage surgery. Mutation of the p53 gene has been found to regulate cell proliferation and chemosensitivity. LP is significantly higher in the group of patients whose tumors over expressed p53 but it does not predict survival. A retrospective study nested within the VA study reported that T stage, p53 over-expression and elevated proliferating cell nuclear antigen index were independent predictors of successful LP . Success of RT depends on killing all clonogenic cells that increases linearly with tumor volume (TV). Lesions are classified as T3 or T4 despite a wide variation in TV if one were to perform volumetric analysis for all. TV is one of the most precise and most relevant predictors of RT outcome. This inverse relationship may be explained on the basis of hypoxia due to central tumor necrosis that is detrimental for CT as well as RT. Cartilage invasion, soft tissue extension, volume, extensive nodal involvement, pre epiglottic space invasion, paraglottic space invasion and arytenoids infiltration are some of the radiological parameters that can predict poor outcome to RT.

Recent studies show adjuvant concurrent chemoradiation to the emerging standard of care for high risk tumors providing an estimated five year progression free survival benefit of 11% in advanced stage III and IV tumors or even early stage tumors with extranodal spread, positive resection margins, perineural involvement or vascular embolization. A similar study by RTOG showed an estimated 10% improvement in two year locoregional control in high risk tumors with multiple lymphnodal involvement, extranodal spread and positive resection margins.

To sum up, CT+RT has the advantages of potential radiosensitization by chemotherapy induced cell cycle redistribution, overcoming radio-resistance within the field of RT, targeting different subpopulation of cells leading to more kill, reduction or delay in distant metastases. Its disadvantages are increased expense, enhanced toxicity and need of good interdisciplinary integration. What needs to be appreciated is the fact that CT+RT has never been evaluated against the standard treatment of TL + PORT. Although the quality of life has been reported to be better after laryngeal preservation, speech rehabilitation has improved steadily over past decade. Time seems to be ripe now to compare LP with CT+RT with TL+PORT and speech rehabilitation with locoregional control and quality of life as endpoint.

DETAILED STUDY PLAN:

Study type: Prospective randomized controlled trial with 900 patients (450 in each arm). Trial size calculated for 392 events with expected improvement of base line survival of 42% by 10% (alpha error of 0.05 and power of 80).

RANDOMIZATION

Arm 1: Radiation Therapy+ CDDP

Arm 2: Surgery + Post operative RT(+ CDDP for high risk cases)

Arms 1 and 2: Cisplatin (CDDP) 100 mg/m2 over 20-30 minutes on days 1, 22, and 43. In arm 2 Cisplatin (CDDP)100 mg/m2 will be given to patients with multiple lymphnodal involvement, extranodal spread, positive resection margins, perineural involvement or vascular embolization.

Surgery: Near total/Total Laryngectomy with bilateral neck dissection with primary speech rehabilitation either by myo-mucosal shunt (NTL) or by primary tracheo-esophageal puncture.

Being tested
Concurrent Chemoradiation, Laryngectomy + adjuvant radiotherapy/chemoradiotherapy
Keywords
neoplasm, larynx, surgery, radiotherapy, chemotherapy
Medical subject headings
Laryngeal Neoplasms, Neoplasms, Laryngeal Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Concurrent ChemoradiationRadiation

    60-70 Gy at 2Gy/5days a week for 6 to 7 weeks Cisplatin (CDDP) 100 mg/m2 over 20-30 minutes on days 1, 22, and 43.

  • Laryngectomy + adjuvant radiotherapy/chemoradiotherapyProcedure or surgery

    Also called Total Laryngectomy, Near-Total Laryngectomy, Adjuvant Radiation Therapy, Adjuvant Chemoradiation

    Surgery: Total Laryngectomy with or without partial pharyngectomy or Near-Total Laryngectomy with or wothout partial pharyngectomy Adjuvant Radiation 2- 3 weeks following surgery: 50-60Gy at 2Gy/5days a week for 5 to 6 weeks Cisplatin (CDDP) 100 mg/m2 over 20-30 minutes on days 1, 22, and 43.

Study groups in NCT00128817
Study groupRoleWhat they receive
1ExperimentalConcurrent Chemoradiation
Receives: Radiation: Concurrent Chemoradiation
2Active comparatorLaryngectomy + adjuvant radiotherapy/chemoradiotherapy
Receives: Procedure: Laryngectomy + adjuvant radiotherapy/chemoradiotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall survival at 3 and 5 years

    Measured: 2015

  2. Disease free survival at 3 and 5 years

    Measured: 2015

  3. Locoregional control rates at 3 and 5 years

    Measured: 2015

Secondary outcomes (5)
  1. Patterns of relapse

    Measured: 2015

  2. Salvage rates

    Measured: 2015

  3. Treatment-related adverse events

    Measured: 2015

  4. Completion of treatment

    Measured: 2015

  5. Quality of life

    Measured: 2015

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Aug 2005 (estimated)
  2. Study startMay 2005
  3. Primary completionMay 2015 (estimated)
  4. Study completionMay 2015 (estimated)

Why it stopped: Slow Accrual

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
900 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00128817
Sponsor's protocol ID
TMH/196/2004
Other IDs
DAECTC/Projno 4/2004-2005
Status last verified
Jan 2013
First submitted
9 Aug 2005
Last updated
23 Jan 2013
Results posted
No
Data monitoring committee
Yes

Publications

  • Badwe RA, D'cruz AK, Mistry RC, Tongaonkar HB, Shastri S, Thorat MA. Developing countries: an evolving opportunity for oncologic research. World J Surg. 2006 Jul;30(7):1173-6. doi: 10.1007/s00268-006-0080-y. No abstract available.

    PubMed 16794899

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Concurrent Chemoradiation and Laryngectomy + adjuvant radiotherapy/chemoradiotherapy in people with Larynx Neoplasms, run by Tata Memorial Hospital at 1 site in India.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 23 Jan 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early (reason given: Slow Accrual). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall survival at 3 and 5 years (time frame: 2015). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00128817, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2013.

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