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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1204821 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type5 l$ D" z& F/ |  I
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 % Z' B1 Z8 V* ?2 I# U. n" t; F$ e
+ Author Affiliations
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1 _. C5 K: K: `: F1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
4 a! v/ t8 r7 R  {3 O4 I2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 2 h  w+ P/ s" {7 d1 c6 {
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : ]$ |! J8 o* f$ }
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
) R. }- X8 X/ q  ?4 a- E# Q5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
, P6 `; \1 |( y: [5 m. R( N6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 1 H& q6 u$ Z; S1 x! L( B' L: G4 K
7Kinki University School of Medicine, Osaka 589-8511, Japan
1 B: w# X+ Q3 L5 a3 ], F/ e8 x7 J- u3 J8Izumi Municipal Hospital, Osaka 594-0071, Japan 3 G6 M& O: ]" E) T
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . d& i- r7 L( v5 r6 J( B* j0 ^
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
. d+ t& U2 p) a* S" @0 `AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. ) ~5 A, A6 Y* @: A- Q3 M. [: S' ~4 W

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type 7 l/ z* C$ n! s# F" S5 ], p

' d1 Z# q6 ~, m! CAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
# D6 g% L7 j) K+ Z- e
; l7 p; }5 S6 I3 J* d4 Q; |Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    K4 D$ @; d: ?7 E* Z8 e

% f, j) C0 r3 i5 cPublished online on: Thursday, December 1, 2011
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5 {! t* A  {8 a* j& m: sDoi: 10.3892/ol.2011.507
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Pages: 405-410 % W9 d! b* s1 ]1 Y

; j+ c2 X7 t/ p( ]3 f/ s# ?/ VAbstract:5 A6 r& m. S7 E$ O$ }. X; c% R
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.4 F& d1 ^3 a' |' ~% l. f4 R. K* r
9 K* }  {6 ~. E6 S# ~: r1 z- _
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population. c& A  d. b& A# z. }
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 E! o- X' E6 L# T2 U( s! l5 Y
+ Author Affiliations
7 i# m9 j0 L6 [. h, X& d# e% x& a) W1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- y4 T" M5 a0 y$ _+ m! s2Department of Thoracic Surgery, Kyoto University, Kyoto
8 [$ ?" |' P1 D3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ) K6 X% }, q7 |
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp ) C, _7 i5 q& ]/ M, {, ~' \
Received September 3, 2010. % u# f. Z7 E2 k6 a0 ]
Revision received November 11, 2010.
: q; r! f; t! d8 F6 x5 BAccepted November 17, 2010. ' H; I) Q/ V5 v1 C+ _& p7 X
Abstract' Z4 P$ e1 `/ T" @! c0 a* u; i
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
5 p0 R; A! S' V& NPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
. B0 _/ _7 S: iResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.   S  E. _2 v  F, _$ q4 x2 |6 R9 `8 ^
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。# _6 O, ^% g% F$ R& }
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?' L3 ~7 n6 |6 x( a2 k$ D
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
' D9 g3 i, q- ~2 F7 J' J4 A" r) J3 C3 X) Xhttp://clinicaltrials.gov/ct2/show/NCT01523587
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9 L1 Y# ?* q. ]9 y8 A- ?) @BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC" n2 N6 {9 G9 A
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 . a0 M9 N7 V6 F5 e( X$ j/ q

1 |7 [) I; h/ d' V5 d- s从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。- q2 }3 ^* S4 U& R+ s
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
* A, ?' l5 B- E, l5 H( m5 l9 Y$ g从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
' J* `6 c* l4 S1 m  r% b; A( o* w* X至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
; q! D4 U( e) l6 I不错。

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