Targeted therapy for cancer of unknown origin
Press release from Heidelberg University Hospital (UKHD).
Encouraging results from a large international study led by Heidelberg have recently been published in the journal "Lancet": The genetic material of cancer cells with unknown tissue of origin contains numerous targets for targeted drugs that are already available and have been developed to treat other forms of cancer. These suppressed the disease in patients significantly longer than chemotherapy.
If metastases occur in the body but the original tumor remains undetectable, this is referred to as "cancer of unknown primary" (CUP). The problem: if there is no information about the original tissue, neither organ-specific chemotherapy nor targeted drugs are available. A large international study involving more than 630 patients from 34 countries shows how this phantom cancer can nevertheless be treated. The results have now been published in the journal "Lancet": The team led by Professor Dr. Alwin Krämer, Head of the Clinical Cooperation Unit "Molecular Hematology/Oncology" of the Medical Faculty of Heidelberg University and the German Cancer Research Center (DKFZ), Senior Physician at the Department of Hematology, Oncology and Rheumatology, Oncology and Rheumatology at Heidelberg University Hospital (UKHD) and head of the "Carcinoma of Unkown Primary (CUP)" task force at the National Center for Tumor Diseases (NCT) in Heidelberg, examined cancer cells and genetic fragments in the blood of study participants for known cancer mutations for which there are already approved drugs. The team was successful in around a third of those affected. Treatment with the appropriate drug significantly extended the time in which the cancer did not progress and probably also overall survival.
The phase 2 trial "CUPISCO" is registered at ClinicalTrials.gov (NCT03498521) and was funded by Hoffmann-La Roche.
Searching for properties of tumor cells against which suitable weapons already exist
In up to five percent of cancers, no primary tumor can be detected, which massively limits the treatment options for the majority of those affected: they receive non-specific chemotherapy and thus only achieve an average survival time of less than one year. "There have been few new findings on CUP syndrome in recent years," says Professor Alwin Krämer. "Studies have only shown that therapies based on molecular analyses to determine the tissue of origin are no more successful than standard chemotherapy. We took a different approach and looked for molecular characteristics of the tumor cells - more precisely, the underlying gene mutations - that have already proven to be effective targets in other types of cancer and for which targeted drugs are available.
A total of 636 patients were included in the study at more than 150 participating clinics. All were newly diagnosed with a CUP with an unfavorable prognosis. Initially, all patients received three cycles of non-specific standard chemotherapy. The participants in whom the cancer was temporarily halted in this way were then randomly divided into two groups: 110 patients received a further three cycles of standard chemotherapy as a control group. Of the remaining 326 patients, those in whom the scientists found one of twelve selected target mutations were then given the appropriate drug. If none of the sought-after mutations were present, a so-called immune checkpoint inhibitor was given in addition to the chemotherapy, which does not have a targeted effect but stimulates the body's own cancer defenses. During the average two-year follow-up period, the study physicians checked how long the cancer remained dormant under the respective therapy and when it resumed its growth. There were no differences in the severity of the side effects.
Around a third of patients benefited from targeted therapy
"The comparison between the group with mutation-targeted therapy and the control group is particularly interesting from a medical point of view," says Prof. Krämer. The difference in the time until the cancer became active again was just under four months on average - eight months for targeted therapy and four months for standard therapy. "In some of the patients with targeted therapy, the cancer had not progressed any further at the time of the evaluation. It is therefore possible that the disease will remain under control in the longer term if there is a good response to the therapy," says Krämer. "Based on our results, I assume that around a third of patients could benefit from targeted therapy and gain additional months to years of disease-free survival. In patients with suitable genetic changes in the cancer cells, this treatment is clearly superior to standard therapy." The follow-up period of the study continues, so that definitive figures on overall survival will also be available in around a year's time.
The CUPISCO study is not only the largest intervention study of its kind for cancer of unknown origin. For the first time, the scientists have also compiled and published a new guideline for the diagnosis, differential diagnosis and treatment of CUP syndrome as a basis for patient recruitment. Also new is the proof that the genetic analysis of fragments of the tumor genetic material from blood samples is as reliable as corresponding examinations of tissue samples. "This evidence is extremely important, as tumor biopsies often do not provide enough tissue material for all the necessary analyses, especially in CUP syndrome," says Krämer. "For targeted treatment, as we have now successfully carried out in our study, we are therefore dependent in many cases on liquid biopsy, i.e. tumor genetic analysis from the blood. In order to improve the care of CUP patients in the future, this method should be approved with the tests already available for CUP diagnostics."
Results have already been incorporated into European guidelines
Based on the results of the CUPISCO study, the scientists conclude that all patients with newly diagnosed CUP syndrome should undergo a genetic analysis of the tumor genome either on biopsy material or a liquid biopsy in order to identify targeted therapy options. This recommendation for tumor genetic analysis and subsequent targeted treatment of patients with CUP syndrome was recently included in the newly formulated European guidelines for precision medicine treatment of advanced tumor diseases.
Literature
Krämer A, Bochtler T, Pauli C, Shiu KK, Cook N, Janoski de Menezes J, Pazo-Cid RA, Losa F, Robbrecht DGJ, Tomášek J, Arslan C, Özgüroğlu M, Stahl M, Bigot F, Kim SY, Naito Y, Italiano A, Chalabi N, Durán-Pacheco G, Michaud C, Scarato J, Thomas M, Ross JS, Moch H, Mileshkin L: Molecularly guided therapy versus chemotherapy after disease control in unfavourable cancer of unknown primary (CUPISCO): an open-label, randomized, phase 2 study. Lancet, Epub 2024 July 31; doi:10.1016/S0140-6736(24)00814-6.
Krämer A, Bochtler T, Pauli C, et al. Cancer of unknown primary: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2023;34(3):228-246. doi:10.1016/j.annonc.2022.11.013
Mosele MF, Westphalen CB, Stenzinger A, et al. Recommendations for the use of next-generation sequencing (NGS) for patients with advanced cancer in 2024: a report from the ESMO Precision Medicine Working Group. Ann Oncol. 2024;35(7):588-606. doi:10.1016/j.annonc.2024.04.005
Contact
Prof. Dr. Alwin Krämer
Medical Clinic V (Hematology, Oncology and Rheumatology), Heidelberg University Hospital
Head of the Clinical Cooperation Unit Molecular Hematology/Oncology
Heidelberg Medical Faculty of Heidelberg University and German Cancer Research Center (DKFZ)
Head of the Task Force "Carcinoma of Unkown Primary (CUP)" at the National Center for Tumor Diseases (NCT) Heidelberg
E-mail: alwin.kraemer(at)med.uni-heidelberg.de; a.kraemer(at)dkfz.de
Targeted therapy for cancer of unknown origin
Press release from Heidelberg University Hospital (UKHD).
Encouraging results from a large international study led by Heidelberg have recently been published in the journal "Lancet": The genetic material of cancer cells with unknown tissue of origin contains numerous targets for targeted drugs that are already available and have been developed to treat other forms of cancer. These suppressed the disease in patients significantly longer than chemotherapy.
If metastases occur in the body but the original tumor remains undetectable, this is referred to as "cancer of unknown primary" (CUP). The problem: if there is no information about the original tissue, neither organ-specific chemotherapy nor targeted drugs are available. A large international study involving more than 630 patients from 34 countries shows how this phantom cancer can nevertheless be treated. The results have now been published in the journal "Lancet": The team led by Professor Dr. Alwin Krämer, Head of the Clinical Cooperation Unit "Molecular Hematology/Oncology" of the Medical Faculty of Heidelberg University and the German Cancer Research Center (DKFZ), Senior Physician at the Department of Hematology, Oncology and Rheumatology, Oncology and Rheumatology at Heidelberg University Hospital (UKHD) and head of the "Carcinoma of Unkown Primary (CUP)" task force at the National Center for Tumor Diseases (NCT) in Heidelberg, examined cancer cells and genetic fragments in the blood of study participants for known cancer mutations for which there are already approved drugs. The team was successful in around a third of those affected. Treatment with the appropriate drug significantly extended the time in which the cancer did not progress and probably also overall survival.
The phase 2 trial "CUPISCO" is registered at ClinicalTrials.gov (NCT03498521) and was funded by Hoffmann-La Roche.
Searching for properties of tumor cells against which suitable weapons already exist
In up to five percent of cancers, no primary tumor can be detected, which massively limits the treatment options for the majority of those affected: they receive non-specific chemotherapy and thus only achieve an average survival time of less than one year. "There have been few new findings on CUP syndrome in recent years," says Professor Alwin Krämer. "Studies have only shown that therapies based on molecular analyses to determine the tissue of origin are no more successful than standard chemotherapy. We took a different approach and looked for molecular characteristics of the tumor cells - more precisely, the underlying gene mutations - that have already proven to be effective targets in other types of cancer and for which targeted drugs are available.
A total of 636 patients were included in the study at more than 150 participating clinics. All were newly diagnosed with a CUP with an unfavorable prognosis. Initially, all patients received three cycles of non-specific standard chemotherapy. The participants in whom the cancer was temporarily halted in this way were then randomly divided into two groups: 110 patients received a further three cycles of standard chemotherapy as a control group. Of the remaining 326 patients, those in whom the scientists found one of twelve selected target mutations were then given the appropriate drug. If none of the sought-after mutations were present, a so-called immune checkpoint inhibitor was given in addition to the chemotherapy, which does not have a targeted effect but stimulates the body's own cancer defenses. During the average two-year follow-up period, the study physicians checked how long the cancer remained dormant under the respective therapy and when it resumed its growth. There were no differences in the severity of the side effects.
Around a third of patients benefited from targeted therapy
"The comparison between the group with mutation-targeted therapy and the control group is particularly interesting from a medical point of view," says Prof. Krämer. The difference in the time until the cancer became active again was just under four months on average - eight months for targeted therapy and four months for standard therapy. "In some of the patients with targeted therapy, the cancer had not progressed any further at the time of the evaluation. It is therefore possible that the disease will remain under control in the longer term if there is a good response to the therapy," says Krämer. "Based on our results, I assume that around a third of patients could benefit from targeted therapy and gain additional months to years of disease-free survival. In patients with suitable genetic changes in the cancer cells, this treatment is clearly superior to standard therapy." The follow-up period of the study continues, so that definitive figures on overall survival will also be available in around a year's time.
The CUPISCO study is not only the largest intervention study of its kind for cancer of unknown origin. For the first time, the scientists have also compiled and published a new guideline for the diagnosis, differential diagnosis and treatment of CUP syndrome as a basis for patient recruitment. Also new is the proof that the genetic analysis of fragments of the tumor genetic material from blood samples is as reliable as corresponding examinations of tissue samples. "This evidence is extremely important, as tumor biopsies often do not provide enough tissue material for all the necessary analyses, especially in CUP syndrome," says Krämer. "For targeted treatment, as we have now successfully carried out in our study, we are therefore dependent in many cases on liquid biopsy, i.e. tumor genetic analysis from the blood. In order to improve the care of CUP patients in the future, this method should be approved with the tests already available for CUP diagnostics."
Results have already been incorporated into European guidelines
Based on the results of the CUPISCO study, the scientists conclude that all patients with newly diagnosed CUP syndrome should undergo a genetic analysis of the tumor genome either on biopsy material or a liquid biopsy in order to identify targeted therapy options. This recommendation for tumor genetic analysis and subsequent targeted treatment of patients with CUP syndrome was recently included in the newly formulated European guidelines for precision medicine treatment of advanced tumor diseases.
Literature
Krämer A, Bochtler T, Pauli C, Shiu KK, Cook N, Janoski de Menezes J, Pazo-Cid RA, Losa F, Robbrecht DGJ, Tomášek J, Arslan C, Özgüroğlu M, Stahl M, Bigot F, Kim SY, Naito Y, Italiano A, Chalabi N, Durán-Pacheco G, Michaud C, Scarato J, Thomas M, Ross JS, Moch H, Mileshkin L: Molecularly guided therapy versus chemotherapy after disease control in unfavourable cancer of unknown primary (CUPISCO): an open-label, randomized, phase 2 study. Lancet, Epub 2024 July 31; doi:10.1016/S0140-6736(24)00814-6.
Krämer A, Bochtler T, Pauli C, et al. Cancer of unknown primary: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2023;34(3):228-246. doi:10.1016/j.annonc.2022.11.013
Mosele MF, Westphalen CB, Stenzinger A, et al. Recommendations for the use of next-generation sequencing (NGS) for patients with advanced cancer in 2024: a report from the ESMO Precision Medicine Working Group. Ann Oncol. 2024;35(7):588-606. doi:10.1016/j.annonc.2024.04.005
Contact
Prof. Dr. Alwin Krämer
Medical Clinic V (Hematology, Oncology and Rheumatology), Heidelberg University Hospital
Head of the Clinical Cooperation Unit Molecular Hematology/Oncology
Heidelberg Medical Faculty of Heidelberg University and German Cancer Research Center (DKFZ)
Head of the Task Force "Carcinoma of Unkown Primary (CUP)" at the National Center for Tumor Diseases (NCT) Heidelberg
E-mail: alwin.kraemer(at)med.uni-heidelberg.de; a.kraemer(at)dkfz.de