Hemocyanins: Present and future relevance in superficial bladder carcinoma Don Lamm, M.D. Clinical Professor of Urology, University of Arizona, and Director,

Slides:



Advertisements
Similar presentations
Bladder Cancer Immunotherapy: Progress and Current Limitations
Advertisements

Moskowitz CH et al. Proc ASH 2014;Abstract 290.
Single immediate postoperative instillation of chemotherapy in patients with Ta/T1 bladder TCC Dr Charles Chabert.
 1) For intravesicle therapy:  A) Mitomycin C instillation dose is 40mg for 2 hour  B) Oncotice BCG instillation dose is 81mg for 2hours  C) ImmuCyst.
Immune therapy in NSCLC Presentation – 劉惠文 Supervisor – 劉俊煌教授.
William J. Gradishar MD, FACP Betsy Bramsen Professor of Breast Oncology Director, Maggie Daley Center For Women's Cancer Care Robert H. Lurie Comprehensive.
Immunology in Head and Neck Cancer Stephanie Cordes, MD Christopher Rassekh, MD February 11, 1998.
The University of Texas Health Science Center
Kochenderfer JN et al. Proc ASH 2013;Abstract 168.
Adjuvant therapy for renal cell carcinoma Dr.Mina Tajvidi oncologist.
SUPERFICIAL BLADDER CANCER THERAPY
Bladder Cancer Ishan Parikh. Where and What? The bladder… -stores urine received from the kidneys -is about the size of a pear when empty -is a very elastic.
Electronic Image Safe (Remove for final output). BCG Plus IFN-  Combination Therapy Rationale Evidence of synergistic activity Evidence of synergistic.
Management of High Grade, T1 Bladder Cancer
Phase III Study Comparing Gemcitabine plus Cetuximab versus Gemcitabine in Patients with Locally Advanced or Metastatic Pancreatic Adenocarcinoma Southwest.
Gianni L et al. Proc SABCS 2012;Abstract GS6-7.
CS-1 Results of the Phase 3 Clinical Trials of Abraxane vs. Taxol in Metastatic Breast Cancer William J. Gradishar, MD, FACP Professor of Medicine Northwestern.
Management of Superficial Bladder Cancer Douglas S. Scherr, M.D. Assistant Professor of Urology Clinical Director, Urologic Oncology Weill Medical College-Cornell.
A phase I study on the combination of neoadjuvant radiotherapy plus pazopanib in patients with locally advanced soft tissue sarcoma of the extremities.
 Identify different options of cancer therapy.  Most cancers are treated with a combination of approaches.
T-cell Immunoregulation and the Response to Immunotherapy Harold S. Nelson. MD Professor of Medicine National Jewish Health and University of Colorado.
Insert Program or Hospital Logo Introduction Melanoma is notoriously resistant to chemotherapy. While surgical resection and adjuvant chemotherapy can.
Current Role of Partial Cystectomy: Are we scarifying patient ’ s survival Dr Eric Li Department of Surgery Pamela Youde Nethersole hospital.
1 Management of Difficult Cases of Non-Muscle Invasive Bladder Cancer.
Management of T1G3 Bladder cancer Dr Charles Chabert.
Phase I Study of PLX4032: Proof of Concept for V600E BRAF Mutation as a Therapeutic Target in Human Cancer Flaherty K et al. American Society of Clinical.
NSABP C08 adjuvant colon cancer Best of ASCO, Beirut, July 2009 Prof Eric Van Cutsem, MD, PhD Digestive Oncology Leuven, Belgium.
1Bachelot T et al. Proc SABCS 2010;Abstract S1-6.
Continued Late Conversion to Complete Remission and Durability of Remission in Patients with B-cell Follicular Lymphoma (FL) Treated with Rituximab Followed.
Contemporary Treatment Guidelines on Bladder Cancer
Xeloda ® monotherapy in pancreatic cancer: phase II study  42 patients with advanced/metastatic pancreatic cancer received intermittent Xeloda 1,250mg/m.
CE-1 IRESSA ® Clinical Efficacy Ronald B. Natale, MD Director Cedars Sinai Comprehensive Cancer Center Ronald B. Natale, MD Director Cedars Sinai Comprehensive.
Efficacy of sodium hyaluronate in the management of chemical and radiation cystitis Sommariva et al. Minerrva Urol Nefrol 2010.
Prof. Francesco Boccardo University and National Cancer Research Institute of Genoa, Italy Prof. Francesco Boccardo University and National Cancer Research.
Other Modes of Treatment
Bevacizumab continuation versus no continuation after first-line chemo-bevacizumab therapy in patients with metastatic colorectal cancer: a randomized.
Updated Results of a Phase I First-in-Human Study of the BCL-2 Inhibitor ABT-199 (GDC-0199) in Patients with Relapsed/Refractory (R/R) Chronic Lymphocytic.
1 Agenda  Overview –Burt Adelman MD  Efficacy and Pharmacodynamics –Akshay Vaishnaw MD, PhD  Safety –Gloria Vigliani MD  Alefacept Risk Benefit Profile.
Dyer MJS et al. Proc ASH 2014;Abstract 1743.
Treon SP et al. Proc ASH 2013;Abstract 251.
Cortés J et al. ASCO 2009; Abstract (Poster Discussion)
A Phase 2 Study of Elotuzumab in Combination with Lenalidomide and Low-Dose Dexamethasone in Patients with Relapsed/Refractory Multiple Myeloma Lonial.
TAXOL® (paclitaxel) for Adjuvant Treatment of Node Positive Breast Cancer Oncologic Drugs Advisory Committee TAXOL® (paclitaxel) for Adjuvant Treatment.
Baselga J et al. Proc SABCS 2010;Abstract S3-3.
CON - 1 Conclusions C David R. Parkinson Vice President, Global Head, Clinical Research and Development Novartis Pharmaceuticals Corporation.
Ο ρόλος των μη χειρουργικών θεραπειών στο μη μεταστατικό μυοδιηθητικό καρκίνο ουροδόχου κύστεως Γεώργιος Δ. Λύπας Παθολόγος Ογκολόγος Α’ Ογκολογική Κλινική.
Bladder Cancer R. Zenhäusern.
Wolfram C. M. Dempke SaWo Oncology Ltd May 13, 2017
Reeder CB et al. ASCO 2009; Abstract (Poster)
Farletuzumab in platinum sensitive ovarian cancer with low CA125
Nivolumab in Patients (Pts) with Relapsed or Refractory Classical Hodgkin Lymphoma (R/R cHL): Clinical Outcomes from Extended Follow-up of a Phase 1 Study.
Bladder Cancer: What’s New?
Oki Y et al. Proc ASH 2013;Abstract 252.
Combined Inhibition of PD-L1, MEK, and BRAF Active in Advanced Melanoma CCO Independent Conference Highlights of the 2015 ASCO Annual Meeting* May 29 -
LUCIE Localised Urothelial Carcinoma Immuno-oncology Evaluation Randomised Phase II trial, evaluating safety and efficacy of a combination therapy of.
COMPLICATIONS OF IMMUNOTHERAPY IN THE HOSPITALIZED PATIENT Vivek Batra MD, Emma Weaver MD Division of Medical Oncology, Thomas Jefferson University, Philadelphia.
Intervista a Lucio Crinò
A New Path Forward: Immune Checkpoint Inhibitors in Bladder Cancer
Nat. Rev. Urol. doi: /nrurol
Volume 61, Issue 1, Pages (January 2012)
Volume 54, Issue 3, Pages (September 2008)
Untch M et al. Proc SABCS 2010;Abstract P
Grövdal M et al. Blood 2008;112:Abstract 223.
Domenica 03 giugno Highlight a cura di Filippo de Marinis
Treatment of human MCC tumors with intralesional IFNβ is associated with MHC-I upregulation. Treatment of human MCC tumors with intralesional IFNβ is associated.
Fig. 8 Combining M7824 with radiation or chemotherapy enhances antitumor efficacy. Combining M7824 with radiation or chemotherapy enhances antitumor efficacy.
CD8+ T cells were immunomodulated and required for the efficacy of anti–4-1BB/anti–PD-1 combination treatment. CD8+ T cells were immunomodulated and required.
Efficacy of BSI-201, a PARP Inhibitor, in Combination with Gemcitabine/Carboplatin (GC) in Triple Negative Metastatic Breast Cancer (mTNBC): Results.
Presentation transcript:

Hemocyanins: Present and future relevance in superficial bladder carcinoma Don Lamm, M.D. Clinical Professor of Urology, University of Arizona, and Director, BCG Oncology, (Bladder Cancer, Genitourinary Oncology) Phoenix, AZ BCGOncology.com

KLH and Olsson’s Serendipitous Discovery 1970’s: Cellular immune response is shown to be important in cancer KLH: used to determine cellular response by skin test reaction 1974: Olsson immunizes 10 BT patients with 5mg KLH to determine immunocompetence No correlation possible: only 3/10 have BT recurrence, compared with 7/10 before KLH

KLH and Olsson’s Serendipitous Discovery 1974: Olsson follows with a controlled trial 9 get 5mg KLH sc, 10 controls Follow: 204 and 228 pt months, respectively Recurrence 1/9 (11%) with KLH versus 7/10(70%) with control. A 59% reduction of tumor recurrence with a single, innocuous cutaneous immunization! Olsson CA. J Urol. 1974, 111:173-6

KLH and Olsson’s Serendipitous Discovery Olsson did not pursue his finding. Why? Moving from Boston (Boston U) to New York ( Columbia U) he lost his data. We evaluated KLH in the animal model, publishing positive results in 1981, but believed BCG was more effective … Klippel and Jurincic, hearing Olsson lecture in Germany, developed KLH from animal models to clinical trials* Lamm DL. Urol Res 9:227, 1981.*Jurincic CD. J Urol 139:723, 1988.

Lamm DL. Urol Res 9:227, 1981.

KLH Immune Effects Studies in 9 animal species show strong cellular and humoral immune stimulation Doses ranging from to 250mg/kg Lymphoblastogenesis, T cells, KLH specific T helper cells, Macrophages, Basophils, IgA, IgG, IgM Toll immunity Thomsen Freidenreich Antigen

Anti-Tumor Effects of KLH in Animal Models Following Olsson’s demonstration of significant reduction in BT recurrence with ID KLH immunization, animal studies have consistently demonstrated and confirmed the anti-tumor efficacy of KLH. In summary: –Pre-immunization and intralesional KLH inhibits transplanted bladder cancer –Endotoxin enhances the efficacy of KLH –Combination therapy, eg KLH plus IL-2, Ifn alpha or Ifn gamma improves response: as high as 100% with Interferon alpha +KLH –Minimal dose/response relationship exists –Minimal toxicity observed Local immune response and anti-tumor effect is confirmed, but what about the systemic effect reported by Olsson?

Saline IM KLH BCG Crude KLH

BCG Crude KLH Immucothel BCG

High LPS Purified KLH Crude KLH pKLH +LPS BCG pKLH+LPS Low LPS Saline

Anti-Tumor Effects of KLH in Animal Models Following Olsson’s demonstration of significant reduction in BT recurrence with ID KLH immunization, animal studies have consistently demonstrated and confirmed the anti-tumor efficacy of KLH. In summary: –Pre-immunization and intralesional KLH inhibits transplanted bladder cancer –Endotoxin enhances the efficacy of KLH –Combination therapy, eg KLH plus IL-2, Ifn alpha or Ifn gamma improves response: as high as 100% endotoxin + purified KLH –Minimal dose/response relationship exists –Minimal toxicity observed Local immune response and anti-tumor effect is confirmed, but what about the systemic effect reported by Olsson?

Evidence of Systemic KLH Immunity to Bladder Cancer BBN 0.05% in drinking water: bladder cancer model model in rats. 1mg KLH s.c. plus 12.5 intraves significantly reduces BT formation.* Pre-sensitization 1mg KLH followed by twice weekly 1mg SC or 12.5mg intraves beginning on day 15: 50% tumor in SC group compared with 74% in the intravesical group!** *Recker and Rubben, 1989**Linn and Rubben et al:, 1998

Hemocyanin Clinical Studies

KLH Uncontrolled Trials 548 patients with Ta, T1, T2 TCC or CIS followed for an average of 21.5 months 28.5% recurrence at 21.5 months CIS: Jurincic’1995: 52% CR (11/21) CIS: Bassi’2000: 50% CR (14/28) CIS: Lamm’2000: 50% CR (9/18) CIS alone plus 33% (4/12) in CIS plus papillary TCC

Complete Response to KLH by Disease Category StageCR (N)CR (%) CIS 9 50% Ta, T1, CIS 4 33% Ta, T1 3 20% Total 16 36%

Side Effects of KLH in 54 Evaluable Patients KLH *BCG Dysuria: 24% 60% Hematuria: 7% 26% Malaise: 7% 33% *Contemporary series

KLH in CIS/Residual Papillary TCC DoseCR (N)CR (%) 0.4 mg 4 29% 2.0 mg 8 42% 10 mg 4 29% 50 mg 6 35% Total: 22 34% No dose/response observed. All patients received the same 1mg dose of S.C. KLH!

KLH in Refractory TCC DoseCR (N)CR (%) 0.4 mg 1 25% 2.0 mg 3 30% 10 mg 3 30% 50 mg 2 29% Total: 9 26%

KLH Controlled Clinical Trials 393 patients in 8 trials; 188 KLH, 205 other KLH: 25.7% recurrence, 21.1 months, versus 41.0% recurrence with chemo, TUR, or BCG BCG: 14% rec. (3/21) vs. 41% (7/17) KLH MMC: 33% (21/64) vs. 13% (9/71), p<0.01 KLH vs. Chemo/non- BCG: 24% vs 44% rec.

KLH vs Mitomycin C Author/yrNKLH Klippel’85503/30 (10%) Jurincic’88443/21 (14%) Al-Naieb’90 413/20 (15%) Total:1359/71 (13%) % rec MMCP (20%) 4/20NS (39%) 9/ (38%) 8/21NS (33%) 21/640.01

What is the Future of Hemocyanins in Bladder Cancer? Systemic efficacy in bladder cancer was first reported in 1974 by Olsson and HAS BEEN CONFIRMED IN ANIMAL MODELS! Percutaneous hemocyanin appears to be effective in CIS, and therefore may be effective in upper tract TCC Hemocyanin should be tried as an adjuvant to cystectomy- with or without chemotherapy!

Conclusions Hemocyanins have a broad range of beneficial immune effects, both cellular and humoral KLH is clearly effective in the prevention and treatment of bladder cancer Unlike BCG, KLH appears to have a very significant systemic effect While hemocyanins may be less effective than BCG in the treatment of local TCC, they are clearly less toxic

Conclusions Hemocyanins, like other immunotherapies, appear to be more effective when used in combination with other immunotherapy With a systemic effect: Hemocyanins should be studied as an adjuvant to the treatment of upper tract TCC Hemocyanins should be studied as an adjuvant to cystectomy.

Thanks, Don Lamm, Phoenix BCGOncology.com