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Featured researches published by P. Carde.


Journal of Clinical Oncology | 1988

Clinical stages I and II Hodgkin's disease: a specifically tailored therapy according to prognostic factors.

P. Carde; J.M.V. Burgers; M Henry-Amar; M. Hayat; W. Sizoo; E. van der Schueren; Mathieu Monconduit; Evert M. Noordijk; J Lustman-Marechal; A. Tanguy

The H5 program in clinical stage (CS) I to II supradiaphragmatic Hodgkins disease (HD) was tailored to prognostic factors identified in former European Organization for the Research and Treatment of Cancer (EORTC) studies. Among the 494 adult patients included in the study, the 237 patients belonging to the favorable group (H5F) underwent a staging laparotomy (Sx) in order to select the patients who could be treated with limited radiotherapy (RT) only. Thus, 198 patients (84%) with negative laparotomy were treated with RT alone and randomized to either mantle irradiation (M) or extended field mantle plus para-aortic (M + PA) irradiation. Complete remission (CR) was achieved in 99% of the patients. There was no difference in the 6-year relapse-free survival (RFS) rate (74% and 72%, respectively) or survival rate (96% and 89%). Therefore, Sx helped to define those patients who could be treated with M alone in contrast to those who required more aggressive therapy. The 39 patients with positive laparotomy were treated as the unfavorable group (H5U) from onset and randomized to either total/subtotal nodal irradiation (TNI/STNI) or a sandwiched mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) X 3, M irradiation, MOPP X 3 protocol (3M). Although the RFS rate was higher in the 3M arm (100% v 53%; P = .002), the 6-year survival was not significantly different between the two arms (overall, 92%). In the 257 patients with initial unfavorable disease, the Sx was avoided. They were randomized to either TNI/STNI or 3M. In complete responders (96%), the 6-year RFS was 91% in the 3M arm and 77% in the TNI/STNI arm (P = .02). The pattern of failure differed in the two arms: the inverted Y and spleen irradiation controlled occult infradiaphragmatic disease better than MOPP; conversely, less patients begun on MOPP recurred in the involved mantle areas. The difference in 6-year actuarial total survival (TS) (89% and 82%; P = .05 in favor of the 3M arm) was not retrieved after exclusion of the unrelated deaths from the analysis. The two arms produced similar TS in patients under 40 years of age. TNI retains interest, especially in young men wishing to preserve fertility. The overall result shows that when treatment is tailored to initial prognostic factors, excellent results can be obtained in all patient subgroups at minimal morbidity and toxic cost.


Journal of Clinical Oncology | 1994

A randomized study in stage IIIB and IV Hodgkin's disease comparing eight courses of MOPP versus an alteration of MOPP with ABVD: a European Organization for Research and Treatment of Cancer Lymphoma Cooperative Group and Groupe Pierre-et-Marie-Curie controlled clinical trial.

R. Somers; P. Carde; M Henry-Amar; M. Tarayre; J. Thomas; A. Hagenbeek; Mathieu Monconduit; B.E. de Pauw; W.P.M. Breed; L. Verdonck

PURPOSE We report a prospective randomized study comparing the relative efficacy of alternating chemotherapy mechlorethamine, vincristine, procarbazine, and prednisone/doxorubicin, bleomycin, vinblastine, and dacarbazine (MOPP/ABVD) with the standard MOPP chemotherapy in patients with stage IIIB and IV Hodgkins disease (HD). The purpose is to study the influence of time of remission on clinical outcome. PATIENTS AND METHODS After two courses of MOPP, patients were randomized to receive six further courses of MOPP, or two courses of ABVD followed by two courses of MOPP and two courses of ABVD. Radiotherapy was given to areas presenting with masses > or = 5 cm and to residual masses after course no. 4. Evaluation of response (complete remission [CR]) took place after two courses (CR2), after four courses (CR4), at the end of chemotherapy (CR8), and after additional radiotherapy (CR(CT + RT)). Logistic regression analysis was used to study prognostic factors for response at the end of chemotherapy. Cox analysis was used to study prognostic factors for survival. Two hundred seven patients were registered, 192 (93%) of whom were randomized. RESULTS The CR rate at the end of chemotherapy (CR8) was similar in both arms (57% v 59%). However, there were more progressions in the MOPP arm compared with the MOPP/ABVD arm (23% v 8%, P = .014). A significantly higher failure-free survival (FFS) rate was found in the MOPP/ABVD arm (60% v 43% at 6 years, P = .025). There was no difference in the relapse-free survival (RFS) or survival rate. Of patients not in CR4, only 28% still reached a CR8. RFS at 6 years of patients with CR4 (69%) was not different from that of patients with CR8 (68%); patients with a CR(CT + RT)) had a lower RFS rate (48%). CR4 (P < .001) predicted strongly for final remission at the end of chemotherapy. Cox analysis showed that age more than 50 years, six or more involved lymph node areas, no CR by the fourth cycle, chemotherapy with MOPP alone, and no radiotherapy were unfavorable factors for survival. CONCLUSION MOPP/ABVD chemotherapy significantly improved response and FFS rates, but had no influence on RFS and survival rates. Early CR (CR4) is an important factor for final remission and might be used to select a group of patients with a good prognosis.


Journal of Clinical Oncology | 1998

Maintenance of remission with human recombinant interferon alfa-2a in patients with stages III and IV low-grade malignant non-Hodgkin's lymphoma. European Organization for Research and Treatment of Cancer Lymphoma Cooperative Group.

A. Hagenbeek; P. Carde; J.H. Meerwaldt; R. Somers; J. Thomas; R. de Bock; John Raemaekers; A. van Hoof; C. De Wolf-Peeters; M. van Glabbeke

PURPOSE Interferon alfa has shown significant activity in patients with low-grade malignant non-Hodgkins lymphoma (NHL). In 1985, we initiated a prospective randomized study in which the potential benefit of interferon alfa given as maintenance treatment was investigated after tumor load reduction was achieved with chemoradiotherapy in patients with advanced low-grade malignant non-Hodgkins lymphoma. PATIENTS AND METHODS The study involved 347 patients with stage III or IV disease, 315 satisfying the eligibility criteria. All were treated with a regimen of cyclophosphamide, vincristine, and prednisone (CVP) given every 3 weeks for eight cycles. Thereafter, patients were eligible for iceberg irradiation. Finally, all patients were completely restaged, and responding and stable-disease patients were then randomized, 122 to interferon alfa-2a maintenance, 3 million U three times weekly for 1 year; and 120 to no further treatment. RESULTS Seventy-nine percent of the patients response to CVP, ie, 45% complete remissions (CR) and 34% partial remissions (PR). In the group of randomized patients, the response rate after CVP plus or minus radiotherapy was 90%. As compared with control patients, patients in the interferon (IFN) maintenance group had a tendency toward a prolonged time to progression (TTP) (median, 132 v 87 weeks; P = .054, adjusted for response to CVP). However, overall survival was similar in both groups. Interferon was well tolerated. The median dose of IFN actually received corresponded to 90% of the planned cumulative dose. The treatment had to be stopped because of toxicity in 16 patients (15% of the patients in whom IFN was started). CONCLUSION Interferon maintenance treatment in the phase of minimal residual disease of patients with advanced low-grade malignant NHL increased TTP at the borderline of statistical significance, without remarkable toxicity. However, overall survival was not influenced.


Blood | 1989

Toward comprehensive management tailored to prognostic factors of patients with clinical stages I and II in Hodgkin's disease. The EORTC Lymphoma Group controlled clinical trials: 1964-1987

M. Tubiana; M Henry-Amar; P. Carde; J.M.V. Burgers; M. Hayat; E Van der Schueren; Evert M. Noordijk; A. Tanguy; J.H. Meerwaldt; José Thomas


Journal of Clinical Oncology | 2005

First results of the EORTC-GELA H9 randomized trials: the H9-F trial (comparing 3 radiation dose levels) and H9-U trial (comparing 3 chemotherapy schemes) in patients with favorable or unfavorable early stage Hodgkin's lymphoma (HL)

Evert M. Noordijk; José Thomas; Christophe Fermé; M. B. Van't Veer; Pauline Brice; Marine Divine; Frank Morschhauser; P. Carde; Houchingue Eghbali; M Henry-Amar


Blood | 2005

Comparison of Three Radiation Dose Levels after EBVP Regimen in Favorable Supradiaphragmatic Clinical Stages (CS) I-II Hodgkin’s Lymphoma (HL): Preliminary Results of the EORTC-GELA H9-F Trial.

Houchingue Eghbali; Pauline Brice; Geert-Yan Creemers; Marinus van Marwijk Kooij; P. Carde; Mars B. Van’t Veer; Elli Lugtenburg; Anne Sonet; Catherine Sebban; Michel M.B. Blanc; J.M.M. Raemaekers; Laurent Voillat; Chantal Rieux; Ed M. Noordijk; M Henry-Amar


Annals of Oncology | 1991

Original article: Superiority of second over first generation chemotherapy in a randomized trial for stage III-IV intermediate and high-grade Non-Hodgkin's Lymphoma (NHL): The 1980–1985 EORTC trial|*

P. Carde; J.H. Meerwaldt; M. van Glabbeke; R. Somers; Mathieu Monconduit; J. Thomas; C. De Wolf-Peeters; B. De Pauw; A. Tanguy; Johanna Kluin-Nelemans; Evert M. Noordijk; R. Regnier; Dominique Bron; J. Lustinan-Marechal; Bernard Caillou; Jacques Bosq; P. van Heerde; J. A. M. van Unnik; J.M.V. Burgers; M. Hayat; Jean-Marc Cosset; E. van der Schueren; J. Wagener; A. Hagenbeek; A. Cattan; Nicole Duez; M. Tubiana


Annals of Oncology | 1994

Preliminary results of the EORTC-GPMC controlled clinical trial H7 in early-stage Hodgkin's disease. EORTC Lymphoma Cooperative Group. Groupe Pierre-et-Marie-Curie.

Evert M. Noordijk; P. Carde; Mandard Am; Mellink Wa; Mathieu Monconduit; Houchingue Eghbali; Umberto Tirelli; José Thomas; R. Somers; N. Dupouy


Annals of Oncology | 1994

EORTC study of non-Hodgkin's lymphoma: Phase III study comparing CHVmP-VB and ProMACE-MOPP in patients with stage II, III, and IV intermediate- and high-grade lymphoma

R. Somers; P. Carde; J. Thomas; Umberto Tirelli; J. J. Keunig; Dominique Bron; A. Delmer; R. de Bock; C. De Wolf-Peeters; M. van Glabbeke; Nicole Duez


European Journal of Cancer | 2004

Long-term efficacy of the CHVmP/BV regimen used for aggressive non-Hodgkin's lymphoma in three randomised EORTC trials

Elizabeth C. Moser; Evert M. Noordijk; M. van Glabbeke; I. Teodorovic; C. De Wolf-Peeters; P. Carde; Joke W. Baars; Umberto Tirelli; J.M.M. Raemaekers; Johanna Kluin-Nelemans

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M Henry-Amar

European Organisation for Research and Treatment of Cancer

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R. Somers

Katholieke Universiteit Leuven

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Evert M. Noordijk

Leiden University Medical Center

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José Thomas

Katholieke Universiteit Leuven

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Mathieu Monconduit

Université catholique de Louvain

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A. Hagenbeek

European Organisation for Research and Treatment of Cancer

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M. van Glabbeke

European Organisation for Research and Treatment of Cancer

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J.M.V. Burgers

Netherlands Cancer Institute

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C. De Wolf-Peeters

Katholieke Universiteit Leuven

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